| geneid | 5357 |
|---|---|
| ensemblid | ENSG00000120756.13 |
| hgncid | 9090 |
| symbol | PLS1 |
| name | plastin 1 |
| refseq_nuc | NM_001145319.2 |
| refseq_prot | NP_001138791.1 |
| ensembl_nuc | ENST00000457734.7 |
| ensembl_prot | ENSP00000387890.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 142596393 |
| end | 142713664 |
| strand | + |
| ver | v1.2 |
| region | chr3:142596393-142713664 |
| region5000 | chr3:142591393-142718664 |
| regionname0 | PLS1_chr3_142596393_142713664 |
| regionname5000 | PLS1_chr3_142591393_142718664 |
| 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 | 629 | 255 | 65 | 50 | 106 | 12 | 20 | 78 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0002 | 0/0 | 629 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0003 | 0/0 | 629 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0004 | 0/0 | 629 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0005 | 0/0 | 629 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1890 | 176 | 60 | 33 | 60 | 10 | 13 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0002 | 1/1 | 1890 | 73 | 4 | 12 | 46 | 2 | 7 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0003 | 0/0 | 1890 | 14 | 14 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0004 | 0/0 | 1890 | 4 | 0 | 4 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0005 | 0/0 | 1890 | 4 | 3 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0006 | 0/0 | 1890 | 2 | 2 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0007 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0008 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| c0009 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1811 | 183 | 27 | 37 | 90 | 9 | 18 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0002 | 0/0 | 1811 | 31 | 25 | 3 | 1 | 0 | 2 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0003 | 0/0 | 1811 | 18 | 6 | 3 | 8 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0004 | 0/0 | 1811 | 8 | 8 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0005 | 0/0 | 1809 | 7 | 7 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0006 | 0/0 | 1811 | 5 | 4 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0007 | 0/0 | 1810 | 4 | 0 | 4 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0008 | 0/0 | 1811 | 3 | 3 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0009 | 0/0 | 1811 | 3 | 2 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0010 | 0/0 | 1811 | 3 | 0 | 0 | 3 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0011 | 0/0 | 1811 | 2 | 0 | 2 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0012 | 0/0 | 1811 | 2 | 2 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0013 | 0/0 | 1811 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0014 | 0/0 | 1811 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0015 | 0/0 | 1811 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0016 | 0/0 | 1811 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0017 | 0/0 | 1811 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0018 | 0/0 | 1811 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| t0019 | 0/0 | 1811 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1890 | 176 | 60 | 33 | 60 | 10 | 13 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002 | 1/1 | 1890 | 73 | 4 | 12 | 46 | 2 | 7 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0004 | 0/0 | 1890 | 4 | 0 | 4 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0008 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0009 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0002c0003 | 0/0 | 1890 | 14 | 14 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0003c0005 | 0/0 | 1890 | 4 | 3 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0004c0006 | 0/0 | 1890 | 2 | 2 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0005c0007 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3700 | 120 | 18 | 26 | 58 | 7 | 11 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0002 | 0/0 | 3700 | 21 | 16 | 2 | 1 | 0 | 2 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0003 | 0/0 | 3700 | 9 | 6 | 1 | 1 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0004 | 0/0 | 3700 | 6 | 6 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0005 | 0/0 | 3698 | 7 | 7 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0006 | 0/0 | 3700 | 5 | 4 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0008 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0009 | 0/0 | 3700 | 3 | 2 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0011 | 0/0 | 3700 | 2 | 0 | 2 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0015 | 0/0 | 3700 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0001t0018 | 0/0 | 3700 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0001 | 1/1 | 3700 | 56 | 3 | 10 | 32 | 2 | 7 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0003 | 0/0 | 3700 | 9 | 0 | 2 | 7 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0010 | 0/0 | 3700 | 3 | 0 | 0 | 3 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0012 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0013 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0014 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0016 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0002t0019 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0004t0007 | 0/0 | 3699 | 4 | 0 | 4 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0008t0017 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0001c0009t0001 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0002c0003t0001 | 0/0 | 3700 | 4 | 4 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0002c0003t0002 | 0/0 | 3700 | 9 | 9 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0002c0003t0008 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0003c0005t0001 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0003c0005t0002 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0003c0005t0008 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0003c0005t0012 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0004c0006t0004 | 0/0 | 3700 | 2 | 2 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| a0005c0007t0001 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | copy fasta | chr3 | 142591393 | 142718664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0011g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0010g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0013g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0014g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0016g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0002t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0004t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0004t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0004t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0004t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0008t0017g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0001c0009t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0002c0003t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0003c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0003c0005t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0003c0005t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0003c0005t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0004c0006t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| a0005c0007t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0057 | EUR | GBR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0273 | EUR | GBR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0061 | EUR | FIN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0017 | EUR | FIN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00323 | hp2 | a0001 | c0001 | t0018 | g0070 | EUR | FIN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00639 | hp2 | a0001 | c0004 | t0007 | g0093 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG00741 | hp2 | a0005 | c0007 | t0001 | g0084 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01081 | hp2 | a0001 | c0004 | t0007 | g0033 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01255 | hp1 | a0003 | c0005 | t0002 | g0127 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01256 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01358 | hp2 | a0001 | c0004 | t0007 | g0030 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01433 | hp1 | a0001 | c0008 | t0017 | g0111 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0153 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01891 | hp1 | a0001 | c0002 | t0012 | g0088 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01934 | hp2 | a0001 | c0004 | t0007 | g0045 | AMR | PEL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02056 | hp1 | a0001 | c0002 | t0019 | g0040 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CDX | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02257 | hp1 | a0002 | c0003 | t0002 | g0114 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0152 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0023 | AMR | PEL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02280 | hp1 | a0002 | c0003 | t0002 | g0255 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02280 | hp2 | a0004 | c0006 | t0004 | g0001 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0115 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0121 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0119 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02717 | hp1 | a0002 | c0003 | t0002 | g0118 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02818 | hp2 | a0003 | c0005 | t0008 | g0128 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02886 | hp1 | a0002 | c0003 | t0002 | g0154 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02895 | hp2 | a0001 | c0009 | t0001 | g0136 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02965 | hp2 | a0002 | c0003 | t0002 | g0117 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02970 | hp1 | a0003 | c0005 | t0001 | g0129 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02970 | hp2 | a0002 | c0003 | t0008 | g0097 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0272 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0120 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03453 | hp2 | a0004 | c0006 | t0004 | g0001 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | ESN | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | STU | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | BEB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | BEB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0191 | AFR | YRI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | CHB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0103 | AFR | YRI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | YRI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18971 | hp2 | a0001 | c0002 | t0010 | g0047 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18973 | hp2 | a0001 | c0002 | t0010 | g0048 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19006 | hp1 | a0001 | c0002 | t0014 | g0067 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | LWK | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | LWK | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19060 | hp2 | a0001 | c0002 | t0010 | g0058 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19062 | hp2 | a0001 | c0002 | t0016 | g0059 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19084 | hp2 | a0001 | c0002 | t0013 | g0054 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0065 | EAS | JPT | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | YRI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | YRI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0116 | AFR | ASW | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ASW | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0265 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0266 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | MSL | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | USA | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| HG06807 | hp2 | a0003 | c0005 | t0012 | g0133 | AFR | USA | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | USA | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0254 | AFR | LWK | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0072 | REF | REF | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0074 | REF | REF | PLS1_chr3_142591393_142718664 | PLS1 | chr3 | 142591393 | 142718664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142676230
|
A | G | 1 | a0003 | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.438A>G | p.Ile146Met | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/16 | 591/3700 | 438/1890 | 146/629 | chr3 | 142676230 | ||
| chr3:142684073
|
C | T | 1 | a0002 | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
missense_variant | MODERATE | c.647C>T | p.Ser216Leu | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 7/16 | 800/3700 | 647/1890 | 216/629 | chr3 | 142684073 | ||
| chr3:142684133
|
T | C | 1 | a0005 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.707T>C | p.Val236Ala | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 7/16 | 860/3700 | 707/1890 | 236/629 | chr3 | 142684133 | ||
| chr3:142704533
|
G | A | 1 | a0004 | 2 | HG02280.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.1576G>A | p.Val526Ile | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/16 | 1729/3700 | 1576/1890 | 526/629 | chr3 | 142704533 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142671067
|
T | G | 1 | a0001c0004 | 4 | HG00639.hp2 HG01081.hp2 HG01358.hp2 others(1): Show |
synonymous_variant | LOW | c.309T>G | p.Thr103Thr | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/16 | 462/3700 | 309/1890 | 103/629 | chr3 | 142671067 | ||
| chr3:142689764
|
G | A | 6 | a0001c0001a0001c0008a0001c0009others(3): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
synonymous_variant | LOW | c.1128G>A | p.Pro376Pro | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/16 | 1281/3700 | 1128/1890 | 376/629 | chr3 | 142689764 | ||
| chr3:142711875
|
C | T | 1 | a0001c0009 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1758C>T | p.Tyr586Tyr | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 1911/3700 | 1758/1890 | 586/629 | chr3 | 142711875 | ||
| chr3:142711992
|
G | T | 1 | a0001c0008 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1875G>T | p.Leu625Leu | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 2028/3700 | 1875/1890 | 625/629 | chr3 | 142711992 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142596432
|
A | T | 2 | a0001c0002t0010a0001c0002t0019 | 4 | HG02056.hp1 NA18971.hp2 NA18973.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-114A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/16 | chr3 | 142596432 | ||||||
| chr3:142596467
|
A | G | 1 | a0001c0001t0018 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/16 | 67771 | chr3 | 142596467 | |||||
| chr3:142712027
|
G | T | 1 | a0001c0002t0010 | 3 | NA18971.hp2 NA18973.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 20 | chr3 | 142712027 | |||||
| chr3:142712158
|
G | C | 8 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(5): Show | 29 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*151G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 151 | chr3 | 142712158 | |||||
| chr3:142712301
|
C | T | 1 | a0001c0008t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 294 | chr3 | 142712301 | |||||
| chr3:142712366
|
GA | G | 1 | a0001c0004t0007 | 4 | HG00639.hp2 HG01081.hp2 HG01358.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*360delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 360 | chr3 | 142712366 | |||||
| chr3:142712590
|
T | A | 3 | a0001c0001t0008a0002c0003t0008a0003c0005t0008 | 3 | HG02630.hp2 HG02818.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*583T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 583 | chr3 | 142712590 | |||||
| chr3:142712691
|
T | A | 3 | a0001c0001t0002a0002c0003t0002a0003c0005t0002 | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*684T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 684 | chr3 | 142712691 | |||||
| chr3:142712766
|
A | G | 3 | a0001c0001t0011a0001c0002t0012a0003c0005t0012 | 4 | HG01256.hp2 HG01258.hp2 HG01891.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*759A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 759 | chr3 | 142712766 | |||||
| chr3:142712805
|
G | A | 1 | a0001c0002t0013 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 798 | chr3 | 142712805 | |||||
| chr3:142712915
|
C | T | 1 | a0001c0001t0006 | 5 | HG01123.hp1 HG02109.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*908C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 908 | chr3 | 142712915 | |||||
| chr3:142712991
|
T | C | 2 | a0001c0001t0004a0004c0006t0004 | 8 | HG02280.hp2 HG02451.hp2 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*984T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 984 | chr3 | 142712991 | |||||
| chr3:142713002
|
T | G | 1 | a0001c0008t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 995 | chr3 | 142713002 | |||||
| chr3:142713117
|
C | T | 4 | a0001c0001t0002a0001c0001t0009a0002c0003t0002others(1): Show | 34 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1110C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 1110 | chr3 | 142713117 | |||||
| chr3:142713134
|
G | A | 1 | a0001c0002t0014 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1127G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 1127 | chr3 | 142713134 | |||||
| chr3:142713182
|
T | A | 1 | a0001c0001t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 1175 | chr3 | 142713182 | |||||
| chr3:142713223
|
C | G | 1 | a0001c0002t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1216C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 1216 | chr3 | 142713223 | |||||
| chr3:142713500
|
TAA | T | 1 | a0001c0001t0005 | 7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1494_*1495delAA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 16/16 | 1494 | chr3 | 142713500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142596604
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(14): Show | 17 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+95G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142596604 | ||||||
| chr3:142596706
|
C | A | 1 | a0001c0002t0001g0020 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-37+197C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142596706 | ||||||
| chr3:142597086
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+577A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597086 | ||||||
| chr3:142597178
|
C | T | 16 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(13): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37+669C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597178 | ||||||
| chr3:142597194
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-37+685A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597194 | ||||||
| chr3:142597200
|
C | T | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+691C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597200 | ||||||
| chr3:142597253
|
A | T | 1 | a0001c0001t0001g0258 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-37+744A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597253 | ||||||
| chr3:142597422
|
T | C | 1 | a0001c0002t0001g0021 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-37+913T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597422 | ||||||
| chr3:142597457
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG00673.hp2 HG02071.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+948T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597457 | ||||||
| chr3:142597461
|
T | G | 14 | a0001c0001t0001g0262a0001c0001t0002g0259a0001c0001t0002g0260others(11): Show | 15 | HG00738.hp1 HG01123.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+952T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597461 | ||||||
| chr3:142597463
|
T | G | 22 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0262others(19): Show | 23 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.-37+954T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597463 | ||||||
| chr3:142597465
|
G | T | 4 | a0001c0001t0001g0256a0001c0002t0001g0257a0002c0003t0002g0254others(1): Show | 4 | HG02280.hp1 HG03540.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+956G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597465 | ||||||
| chr3:142597552
|
C | G | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+1043C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597552 | ||||||
| chr3:142597601
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-37+1092C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597601 | ||||||
| chr3:142597818
|
C | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-37+1309C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597818 | ||||||
| chr3:142597836
|
T | C | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37+1327T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597836 | ||||||
| chr3:142597963
|
A | C | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+1454A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597963 | ||||||
| chr3:142597971
|
C | A | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+1462C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142597971 | ||||||
| chr3:142598406
|
A | T | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+1897A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142598406 | ||||||
| chr3:142598409
|
T | C | 19 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(16): Show | 19 | HG01175.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37+1900T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142598409 | ||||||
| chr3:142598494
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+1985A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142598494 | ||||||
| chr3:142598507
|
A | G | 35 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(32): Show | 35 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-37+1998A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142598507 | ||||||
| chr3:142598928
|
G | A | 6 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0008g0130others(3): Show | 6 | HG01255.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+2419G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142598928 | ||||||
| chr3:142599167
|
C | CATGA | 5 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG00621.hp2 HG02027.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+2669_-37+2672d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599167 | |||||
| chr3:142599178
|
G | GAATA | 46 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-37+2704_-37+2707d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599178 | |||||
| chr3:142599178
|
G | GAATAAAT others(1): Show |
17 | a0001c0001t0001g0105a0001c0001t0001g0125a0001c0001t0001g0159others(14): Show | 17 | HG00735.hp1 HG01106.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37+2700_-37+2707d others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599178 | |||||
| chr3:142599178
|
GAATA | G | 33 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0104others(30): Show | 34 | HG00099.hp2 HG00738.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-37+2704_-37+2707d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599178 | |||||
| chr3:142599182
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(92): Show | 96 | HG00280.hp1 HG00597.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.-37+2673A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599182 | ||||||
| chr3:142599186
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+2677A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599186 | ||||||
| chr3:142599320
|
ATTCT | A | 6 | a0001c0001t0003g0156a0001c0001t0003g0157a0001c0001t0009g0153others(3): Show | 6 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+2814_-37+2817d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599320 | |||||
| chr3:142599320
|
ATTCTTTT others(3): Show |
A | 2 | a0001c0001t0001g0214a0001c0001t0001g0253 | 2 | HG00741.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-37+2814_-37+2823d others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599320 | |||||
| chr3:142599320
|
ATTCTTTT others(4): Show |
A | 96 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(93): Show | 97 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.-37+2814_-37+2824d others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599320 | |||||
| chr3:142599320
|
ATTCTTTT others(5): Show |
A | 1 | a0001c0001t0001g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-37+2814_-37+2825d others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599320 | |||||
| chr3:142599323
|
C | CT | 16 | a0001c0001t0006g0270a0001c0001t0006g0272a0001c0002t0001g0081others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37+2838dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599323 | |||||
| chr3:142599323
|
CT | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 62 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.-37+2838delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599323 | |||||
| chr3:142599351
|
A | T | 6 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0008g0130others(3): Show | 6 | HG01255.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+2842A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599351 | ||||||
| chr3:142599390
|
C | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+2881C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599390 | ||||||
| chr3:142599455
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+2946G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599455 | ||||||
| chr3:142599475
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+2966G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599475 | ||||||
| chr3:142599490
|
C | T | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+2981C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599490 | ||||||
| chr3:142599620
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 180 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-37+3111C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599620 | ||||||
| chr3:142599750
|
TTTTA | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(56): Show | 59 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-37+3257_-37+3260d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142599750 | |||||
| chr3:142599787
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(96): Show | 100 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.-37+3278C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142599787 | ||||||
| chr3:142600032
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-37+3523G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600032 | ||||||
| chr3:142600069
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(96): Show | 100 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.-37+3560G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600069 | ||||||
| chr3:142600169
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37+3660T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600169 | ||||||
| chr3:142600371
|
G | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-37+3862G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600371 | ||||||
| chr3:142600378
|
A | T | 1 | a0001c0001t0015g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-37+3869A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600378 | ||||||
| chr3:142600552
|
T | C | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+4043T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600552 | ||||||
| chr3:142600596
|
T | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+4087T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600596 | ||||||
| chr3:142600684
|
G | A | 1 | a0002c0003t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-37+4175G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600684 | ||||||
| chr3:142600876
|
TCATATAT others(3): Show |
T | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+4368_-37+4377d others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600876 | ||||||
| chr3:142600877
|
C | CAT | 3 | a0001c0001t0001g0031a0001c0002t0016g0059a0003c0005t0012g0133 | 3 | HG06807.hp2 NA19062.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-37+4407_-37+4408d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
C | CATAT | 3 | a0001c0001t0001g0032a0001c0002t0001g0035a0001c0004t0007g0045 | 3 | HG01934.hp2 HG02735.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-37+4405_-37+4408d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-37+4399_-37+4408d others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
C | CATATATA others(5): Show |
1 | a0001c0002t0001g0081 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37+4397_-37+4408d others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
CATATAT | C | 6 | a0001c0001t0001g0262a0001c0001t0002g0260a0001c0001t0006g0264others(3): Show | 6 | HG00738.hp1 HG01123.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+4403_-37+4408d others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-37+4399_-37+4408d others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
CATATATA others(5): Show |
C | 3 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0252 | 3 | HG00597.hp2 HG02683.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-37+4397_-37+4408d others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-37+4395_-37+4408d others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600877
|
CATATATA others(9): Show |
C | 5 | a0001c0001t0001g0125a0001c0001t0002g0123a0001c0001t0002g0124others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+4393_-37+4408d others(18): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600877 | |||||
| chr3:142600891
|
T | C | 1 | a0001c0002t0001g0028 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-37+4382T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600891 | ||||||
| chr3:142600894
|
ATATATAT others(18): Show |
A | 1 | a0001c0002t0001g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-37+4387_-37+4411d others(27): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600894 | |||||
| chr3:142600894
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0003g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-37+4387_-37+4412d others(28): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600894 | |||||
| chr3:142600894
|
ATATATAT others(20): Show |
A | 6 | a0001c0001t0003g0147a0001c0001t0003g0156a0001c0001t0003g0157others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+4387_-37+4413d others(29): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600894 | |||||
| chr3:142600895
|
TATATATA others(10): Show |
T | 2 | a0001c0001t0004g0131a0001c0001t0008g0130 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-37+4387_-37+4403d others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600895 | ||||||
| chr3:142600896
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0009g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-37+4389_-37+4415d others(29): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600896 | |||||
| chr3:142600899
|
TATATATA others(10): Show |
T | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-37+4391_-37+4407d others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600899 | ||||||
| chr3:142600900
|
A | T | 1 | a0001c0001t0002g0269 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+4391A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600900 | ||||||
| chr3:142600900
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-37+4393_-37+4409d others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600900 | |||||
| chr3:142600900
|
ATATATAT others(12): Show |
A | 1 | a0001c0002t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-37+4393_-37+4411d others(21): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600900 | |||||
| chr3:142600902
|
A | T | 5 | a0001c0001t0002g0267a0001c0001t0002g0269a0001c0001t0004g0001others(2): Show | 6 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+4393A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600902 | ||||||
| chr3:142600902
|
ATATATAT others(8): Show |
A | 3 | a0001c0001t0001g0014a0001c0001t0002g0102a0001c0002t0001g0079 | 3 | HG01175.hp2 HG01433.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-37+4395_-37+4409d others(17): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600902 | |||||
| chr3:142600904
|
A | T | 5 | a0001c0001t0002g0267a0001c0001t0002g0269a0001c0001t0004g0001others(2): Show | 6 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+4395A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600904 | ||||||
| chr3:142600904
|
ATATATAT others(6): Show |
A | 3 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0162 | 3 | HG02615.hp2 HG02647.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-37+4397_-37+4409d others(15): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600904 | |||||
| chr3:142600904
|
ATATATAT others(7): Show |
A | 14 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37+4397_-37+4410d others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600904 | |||||
| chr3:142600904
|
ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01081.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-37+4397_-37+4411d others(17): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600904 | |||||
| chr3:142600904
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-37+4397_-37+4412d others(18): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600904 | |||||
| chr3:142600906
|
A | T | 6 | a0001c0001t0002g0267a0001c0001t0002g0269a0001c0001t0003g0263others(3): Show | 7 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+4397A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600906 | ||||||
| chr3:142600906
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0078 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-37+4399_-37+4409d others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600906 | |||||
| chr3:142600906
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-37+4399_-37+4410d others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600906 | |||||
| chr3:142600906
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0004a0002c0003t0002g0120 | 2 | HG00639.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-37+4399_-37+4411d others(15): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600906 | |||||
| chr3:142600906
|
ATATATAT others(7): Show |
A | 5 | a0001c0001t0001g0135a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+4399_-37+4412d others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600906 | |||||
| chr3:142600908
|
A | T | 8 | a0001c0001t0001g0271a0001c0001t0002g0267a0001c0001t0002g0269others(5): Show | 9 | HG01884.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+4399A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600908 | ||||||
| chr3:142600908
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-37+4401_-37+4411d others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600908 | |||||
| chr3:142600908
|
ATATATAT others(5): Show |
A | 8 | a0001c0001t0001g0076a0001c0001t0001g0105a0002c0003t0002g0103others(5): Show | 8 | HG02165.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37+4401_-37+4412d others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600908 | |||||
| chr3:142600908
|
ATATATAT others(6): Show |
A | 1 | a0002c0003t0002g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-37+4401_-37+4413d others(15): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600908 | |||||
| chr3:142600908
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-37+4401_-37+4415d others(17): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600908 | |||||
| chr3:142600910
|
A | ATTT | 3 | a0001c0001t0001g0134a0001c0001t0001g0213a0001c0001t0005g0250 | 3 | HG02735.hp2 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-37+4402_-37+4403i others(5): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600910 | |||||
| chr3:142600910
|
A | T | 16 | a0001c0001t0001g0252a0001c0001t0001g0271a0001c0001t0002g0261others(13): Show | 17 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37+4401A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600910 | ||||||
| chr3:142600910
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0215 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-37+4403_-37+4415d others(15): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600910 | |||||
| chr3:142600912
|
A | ATTTT | 3 | a0001c0001t0001g0002a0001c0001t0001g0203a0001c0001t0001g0204 | 4 | HG01257.hp1 HG01258.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+4404_-37+4405i others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600912 | |||||
| chr3:142600912
|
A | ATTTTTT | 10 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0205others(7): Show | 10 | HG00597.hp1 HG01243.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37+4404_-37+4405i others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600912 | |||||
| chr3:142600912
|
A | T | 29 | a0001c0001t0001g0134a0001c0001t0001g0211a0001c0001t0001g0212others(26): Show | 30 | HG00621.hp2 HG00738.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37+4403A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600912 | ||||||
| chr3:142600914
|
A | ATTTT | 9 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(6): Show | 9 | HG01167.hp2 HG01256.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+4406_-37+4407i others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600914 | |||||
| chr3:142600914
|
A | ATTTTT | 9 | a0001c0001t0001g0101a0001c0001t0001g0193a0001c0001t0001g0194others(6): Show | 9 | HG01257.hp2 HG01346.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+4406_-37+4407i others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600914 | |||||
| chr3:142600914
|
A | ATTTTTT | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | NA18612.hp2 NA18950.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-37+4406_-37+4407i others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600914 | |||||
| chr3:142600914
|
A | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0001t0001g0139others(49): Show | 54 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-37+4405A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600914 | ||||||
| chr3:142600916
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-37+4408_-37+4409i others(32): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0107 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-37+4408_-37+4409i others(21): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(22): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-37+4408_-37+4409i others(20): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | NA18957.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG01255.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-37+4408_-37+4409i others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATATTT others(7): Show |
1 | a0001c0008t0017g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-37+4408_-37+4409i others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATATTTTT others(5): Show |
2 | a0001c0001t0001g0106a0001c0002t0001g0257 | 2 | HG02886.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATTTTT | 6 | a0001c0001t0001g0100a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG00673.hp2 HG00741.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+4428_-37+4432d others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATTTTTT | 9 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+4427_-37+4432d others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | ATTTTTTT | 5 | a0001c0001t0001g0137a0001c0001t0001g0237a0001c0001t0005g0238others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+4426_-37+4432d others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
A | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0134others(77): Show | 82 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.-37+4407A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600916 | ||||||
| chr3:142600916
|
AT | A | 9 | a0001c0001t0001g0163a0001c0002t0001g0028a0001c0002t0001g0034others(6): Show | 9 | HG00423.hp1 HG01496.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+4432delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
ATT | A | 6 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0095others(3): Show | 6 | HG01361.hp2 HG02622.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+4431_-37+4432d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600916
|
ATTT | A | 5 | a0001c0002t0001g0027a0001c0002t0001g0055a0001c0002t0001g0063others(2): Show | 5 | HG01074.hp1 HG01891.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+4430_-37+4432d others(5): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142600916 | |||||
| chr3:142600917
|
T | TA | 13 | a0001c0001t0001g0050a0001c0002t0001g0020a0001c0002t0001g0021others(10): Show | 13 | HG00621.hp1 HG00741.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(3): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600917 | ||||||
| chr3:142600917
|
T | TATA | 10 | a0001c0001t0001g0052a0001c0002t0001g0041a0001c0002t0001g0042others(7): Show | 10 | HG01123.hp2 HG02056.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(5): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600917 | ||||||
| chr3:142600917
|
T | TATATATA | 4 | a0001c0002t0001g0036a0001c0002t0001g0082a0001c0004t0007g0030others(1): Show | 4 | HG01081.hp2 HG01358.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+4408_-37+4409i others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600917 | ||||||
| chr3:142600918
|
T | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 11 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37+4409T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600918 | ||||||
| chr3:142600919
|
T | A | 28 | a0001c0001t0001g0050a0001c0001t0001g0163a0001c0002t0001g0028others(25): Show | 28 | HG00280.hp2 HG00621.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-37+4410T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600919 | ||||||
| chr3:142600920
|
T | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 6 | HG00639.hp2 HG01361.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+4411T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600920 | ||||||
| chr3:142600921
|
T | A | 8 | a0001c0001t0001g0163a0001c0002t0001g0034a0001c0002t0001g0037others(5): Show | 8 | HG01358.hp2 HG01496.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37+4412T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600921 | ||||||
| chr3:142600922
|
T | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | NA18953.hp2 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-37+4413T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600922 | ||||||
| chr3:142600923
|
T | A | 3 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0060 | 3 | HG02071.hp2 NA18977.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-37+4414T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600923 | ||||||
| chr3:142600924
|
T | A | 1 | a0001c0001t0001g0031 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-37+4415T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600924 | ||||||
| chr3:142600925
|
T | A | 1 | a0001c0002t0001g0034 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-37+4416T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600925 | ||||||
| chr3:142600942
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37+4433G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600942 | ||||||
| chr3:142600955
|
G | A | 1 | a0001c0002t0019g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-37+4446G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142600955 | ||||||
| chr3:142601059
|
G | A | 1 | a0001c0001t0006g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-37+4550G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601059 | ||||||
| chr3:142601069
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-37+4560A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601069 | ||||||
| chr3:142601073
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+4564G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601073 | ||||||
| chr3:142601077
|
C | T | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+4568C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601077 | ||||||
| chr3:142601090
|
A | AT | 6 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(3): Show | 6 | HG01358.hp2 HG01433.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+4591dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142601090 | |||||
| chr3:142601099
|
T | G | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+4590T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601099 | ||||||
| chr3:142601116
|
G | A | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+4607G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601116 | ||||||
| chr3:142601211
|
C | T | 1 | a0001c0002t0001g0257 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-37+4702C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601211 | ||||||
| chr3:142601226
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-37+4717A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601226 | ||||||
| chr3:142601239
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(29): Show | 32 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-37+4730A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601239 | ||||||
| chr3:142601422
|
AT | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | NA18961.hp2 NA18998.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-37+4915delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142601422 | |||||
| chr3:142601690
|
A | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-37+5181A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601690 | ||||||
| chr3:142601717
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(37): Show | 40 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-37+5208A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601717 | ||||||
| chr3:142601815
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(95): Show | 99 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.-37+5306C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601815 | ||||||
| chr3:142601937
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(14): Show | 17 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+5428T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601937 | ||||||
| chr3:142601985
|
A | G | 3 | a0001c0001t0005g0248a0001c0001t0005g0249a0001c0001t0005g0250 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-37+5476A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142601985 | ||||||
| chr3:142602056
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-37+5547T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602056 | ||||||
| chr3:142602107
|
G | GT | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-37+5612dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142602107 | |||||
| chr3:142602107
|
G | GTT | 16 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0161others(13): Show | 16 | HG00621.hp2 HG01106.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37+5611_-37+5612d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142602107 | |||||
| chr3:142602486
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+5977C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602486 | ||||||
| chr3:142602545
|
G | C | 9 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(6): Show | 9 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+6036G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602545 | ||||||
| chr3:142602574
|
C | G | 4 | a0001c0001t0001g0125a0001c0001t0002g0126a0001c0001t0004g0132others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+6065C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602574 | ||||||
| chr3:142602626
|
T | G | 1 | a0001c0001t0004g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-37+6117T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602626 | ||||||
| chr3:142602635
|
G | C | 3 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273 | 3 | HG00099.hp2 NA18947.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-37+6126G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602635 | ||||||
| chr3:142602809
|
A | AGGGCCTC others(6): Show |
63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-37+6302_-37+6303i others(15): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142602809 | |||||
| chr3:142602875
|
C | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-37+6366C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602875 | ||||||
| chr3:142602905
|
G | A | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+6396G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142602905 | ||||||
| chr3:142603053
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-37+6544G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603053 | ||||||
| chr3:142603213
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 66 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-37+6704G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603213 | ||||||
| chr3:142603217
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-37+6708C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603217 | ||||||
| chr3:142603267
|
C | T | 6 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(3): Show | 6 | HG01175.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+6758C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603267 | ||||||
| chr3:142603271
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273 | 3 | HG00099.hp2 NA18947.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-37+6762G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603271 | ||||||
| chr3:142603447
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-37+6938T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603447 | ||||||
| chr3:142603491
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 66 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-37+6982G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603491 | ||||||
| chr3:142603714
|
G | T | 4 | a0001c0001t0001g0181a0001c0001t0002g0174a0001c0001t0002g0182others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+7205G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603714 | ||||||
| chr3:142603769
|
C | CA | 102 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(99): Show | 103 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.-37+7275dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142603769 | |||||
| chr3:142603769
|
CA | C | 11 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(8): Show | 11 | HG01496.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37+7275delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142603769 | |||||
| chr3:142603769
|
CAA | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-37+7274_-37+7275d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142603769 | |||||
| chr3:142603905
|
A | C | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+7396A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603905 | ||||||
| chr3:142603907
|
A | G | 1 | a0001c0004t0007g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-37+7398A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603907 | ||||||
| chr3:142603966
|
G | A | 2 | a0002c0003t0001g0152a0002c0003t0002g0154 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-37+7457G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142603966 | ||||||
| chr3:142604116
|
A | G | 8 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(5): Show | 8 | HG01496.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37+7607A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604116 | ||||||
| chr3:142604362
|
A | T | 1 | a0001c0002t0001g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-37+7853A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604362 | ||||||
| chr3:142604710
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273others(7): Show | 11 | HG00099.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37+8201G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604710 | ||||||
| chr3:142604743
|
G | A | 4 | a0001c0002t0010g0047a0001c0002t0010g0048a0001c0002t0010g0058others(1): Show | 4 | HG02056.hp1 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+8234G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604743 | ||||||
| chr3:142604796
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0006g0272 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-37+8287G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604796 | ||||||
| chr3:142604839
|
G | A | 1 | a0001c0002t0001g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-37+8330G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604839 | ||||||
| chr3:142604860
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-37+8351G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604860 | ||||||
| chr3:142604928
|
T | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 66 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-37+8419T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604928 | ||||||
| chr3:142604929
|
C | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-37+8420C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142604929 | ||||||
| chr3:142604935
|
C | CA | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(53): Show | 56 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.-37+8441dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142604935 | |||||
| chr3:142604935
|
CA | C | 12 | a0001c0001t0001g0224a0001c0001t0001g0262a0001c0001t0001g0271others(9): Show | 12 | HG00738.hp1 HG01123.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+8441delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142604935 | |||||
| chr3:142605056
|
A | T | 1 | a0001c0002t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-37+8547A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142605056 | ||||||
| chr3:142605088
|
G | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG00673.hp2 HG02071.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+8579G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142605088 | ||||||
| chr3:142605737
|
G | A | 12 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(9): Show | 12 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+9228G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142605737 | ||||||
| chr3:142605900
|
T | A | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-37+9391T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142605900 | ||||||
| chr3:142606070
|
T | C | 19 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0108others(16): Show | 19 | HG01255.hp1 HG01433.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37+9561T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606070 | ||||||
| chr3:142606125
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-37+9616C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606125 | ||||||
| chr3:142606185
|
C | T | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37+9676C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606185 | ||||||
| chr3:142606234
|
T | G | 1 | a0001c0002t0001g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-37+9725T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606234 | ||||||
| chr3:142606338
|
C | T | 1 | a0001c0002t0003g0065 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-37+9829C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606338 | ||||||
| chr3:142606378
|
A | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(26): Show | 29 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37+9869A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606378 | ||||||
| chr3:142606384
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0160 | 3 | HG02056.hp2 HG02165.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-37+9875T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606384 | ||||||
| chr3:142606776
|
CTTCTT | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+10271_-37+1027 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142606776 | |||||
| chr3:142606906
|
A | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+10397A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606906 | ||||||
| chr3:142606975
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-37+10466G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142606975 | ||||||
| chr3:142607004
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+10495G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607004 | ||||||
| chr3:142607233
|
T | A | 1 | a0001c0001t0002g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-37+10724T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607233 | ||||||
| chr3:142607279
|
C | CAT | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-37+10783_-37+1078 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142607279 | |||||
| chr3:142607279
|
C | CATAT | 3 | a0002c0003t0001g0152a0002c0003t0002g0103a0002c0003t0002g0154 | 3 | HG02258.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-37+10781_-37+1078 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142607279 | |||||
| chr3:142607336
|
G | A | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+10827G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607336 | ||||||
| chr3:142607423
|
T | G | 1 | a0001c0002t0003g0065 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-37+10914T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607423 | ||||||
| chr3:142607433
|
C | T | 13 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(10): Show | 13 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-37+10924C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607433 | ||||||
| chr3:142607553
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0126 | 3 | HG01175.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-37+11044C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607553 | ||||||
| chr3:142607573
|
C | T | 7 | a0001c0001t0005g0236a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+11064C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142607573 | ||||||
| chr3:142607878
|
A | AT | 6 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(3): Show | 6 | HG01496.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+11382dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142607878 | |||||
| chr3:142608115
|
G | A | 1 | a0001c0002t0001g0247 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-37+11606G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608115 | ||||||
| chr3:142608265
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+11756C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608265 | ||||||
| chr3:142608398
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+11889C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608398 | ||||||
| chr3:142608435
|
G | T | 1 | a0001c0002t0001g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-37+11926G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608435 | ||||||
| chr3:142608463
|
C | G | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+11954C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608463 | ||||||
| chr3:142608501
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-37+11992G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608501 | ||||||
| chr3:142608540
|
G | A | 1 | a0001c0002t0001g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-37+12031G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608540 | ||||||
| chr3:142608575
|
G | A | 1 | a0002c0003t0002g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-37+12066G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608575 | ||||||
| chr3:142608640
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+12131G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608640 | ||||||
| chr3:142608778
|
C | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+12269C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608778 | ||||||
| chr3:142608841
|
T | C | 4 | a0001c0002t0010g0047a0001c0002t0010g0048a0001c0002t0010g0058others(1): Show | 4 | HG02056.hp1 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+12332T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608841 | ||||||
| chr3:142608982
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+12473T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142608982 | ||||||
| chr3:142609067
|
A | G | 13 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(10): Show | 13 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-37+12558A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142609067 | ||||||
| chr3:142609435
|
A | AC | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+12927dupC | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142609435 | |||||
| chr3:142609533
|
C | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0269 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-37+13024C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142609533 | ||||||
| chr3:142609739
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273 | 3 | HG00099.hp2 NA18947.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-37+13230G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142609739 | ||||||
| chr3:142609860
|
G | A | 4 | a0001c0002t0001g0035a0001c0002t0001g0061a0001c0002t0001g0082others(1): Show | 4 | HG00280.hp2 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+13351G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142609860 | ||||||
| chr3:142609987
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG01934.hp1 HG02273.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-37+13478G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142609987 | ||||||
| chr3:142609991
|
C | T | 1 | a0001c0002t0003g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-37+13482C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142609991 | ||||||
| chr3:142610077
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+13568C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610077 | ||||||
| chr3:142610115
|
C | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+13606C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610115 | ||||||
| chr3:142610194
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-37+13685G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610194 | ||||||
| chr3:142610457
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-37+13948A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610457 | ||||||
| chr3:142610485
|
A | G | 1 | a0001c0002t0019g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-37+13976A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610485 | ||||||
| chr3:142610517
|
A | G | 2 | a0001c0002t0001g0035a0001c0002t0001g0082 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-37+14008A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610517 | ||||||
| chr3:142610715
|
G | T | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+14206G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610715 | ||||||
| chr3:142610782
|
C | A | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-37+14273C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610782 | ||||||
| chr3:142610930
|
G | T | 1 | a0001c0002t0003g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-37+14421G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142610930 | ||||||
| chr3:142611243
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-37+14734C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611243 | ||||||
| chr3:142611346
|
G | C | 1 | a0002c0003t0002g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-37+14837G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611346 | ||||||
| chr3:142611433
|
G | A | 4 | a0001c0001t0001g0181a0001c0001t0002g0174a0001c0001t0002g0182others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+14924G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611433 | ||||||
| chr3:142611646
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37+15137G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611646 | ||||||
| chr3:142611710
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-37+15201C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611710 | ||||||
| chr3:142611717
|
A | T | 2 | a0001c0001t0011g0010a0001c0001t0011g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-37+15208A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611717 | ||||||
| chr3:142611740
|
G | A | 2 | a0002c0003t0001g0152a0002c0003t0002g0154 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-37+15231G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611740 | ||||||
| chr3:142611860
|
C | T | 1 | a0001c0001t0004g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-37+15351C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142611860 | ||||||
| chr3:142612017
|
A | G | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+15508A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612017 | ||||||
| chr3:142612021
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+15512T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612021 | ||||||
| chr3:142612125
|
A | G | 8 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37+15616A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612125 | ||||||
| chr3:142612360
|
ATTGTAT | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37+15858_-37+1586 others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142612360 | |||||
| chr3:142612470
|
C | T | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-37+15961C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612470 | ||||||
| chr3:142612518
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+16009A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612518 | ||||||
| chr3:142612531
|
C | A | 1 | a0003c0005t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-37+16022C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612531 | ||||||
| chr3:142612662
|
G | A | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+16153G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612662 | ||||||
| chr3:142612729
|
GA | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+16230delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142612729 | |||||
| chr3:142612780
|
A | T | 4 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0110others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+16271A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612780 | ||||||
| chr3:142612820
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-37+16311G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612820 | ||||||
| chr3:142612877
|
G | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+16368G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142612877 | ||||||
| chr3:142613036
|
G | C | 3 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273 | 3 | HG00099.hp2 NA18947.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-37+16527G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613036 | ||||||
| chr3:142613174
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-37+16665C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613174 | ||||||
| chr3:142613268
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(55): Show | 58 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-37+16759A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613268 | ||||||
| chr3:142613534
|
C | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(34): Show | 37 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.-37+17025C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613534 | ||||||
| chr3:142613683
|
G | C | 3 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37+17174G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613683 | ||||||
| chr3:142613793
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+17284C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613793 | ||||||
| chr3:142613795
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-37+17286C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142613795 | ||||||
| chr3:142614183
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+17674G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614183 | ||||||
| chr3:142614222
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+17713T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614222 | ||||||
| chr3:142614322
|
A | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+17813A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614322 | ||||||
| chr3:142614323
|
G | A | 3 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37+17814G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614323 | ||||||
| chr3:142614350
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0253 | 2 | HG01070.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-37+17841G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614350 | ||||||
| chr3:142614695
|
A | C | 9 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+18186A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614695 | ||||||
| chr3:142614757
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-37+18248G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614757 | ||||||
| chr3:142614778
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37+18269C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614778 | ||||||
| chr3:142614893
|
T | G | 1 | a0001c0002t0001g0041 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-37+18384T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614893 | ||||||
| chr3:142614923
|
TG | T | 17 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0108others(14): Show | 17 | HG01255.hp1 HG01433.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+18418delG | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142614923 | |||||
| chr3:142614980
|
T | C | 1 | a0001c0002t0001g0022 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-37+18471T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142614980 | ||||||
| chr3:142615127
|
A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+18618A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142615127 | ||||||
| chr3:142615151
|
G | A | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+18642G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142615151 | ||||||
| chr3:142615248
|
G | A | 17 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0108others(14): Show | 17 | HG01255.hp1 HG01433.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+18739G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142615248 | ||||||
| chr3:142615598
|
G | A | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+19089G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142615598 | ||||||
| chr3:142615620
|
A | G | 17 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0108others(14): Show | 17 | HG01255.hp1 HG01433.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+19111A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142615620 | ||||||
| chr3:142615888
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+19379T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142615888 | ||||||
| chr3:142615955
|
AG | A | 9 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273others(6): Show | 10 | HG00099.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37+19448delG | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142615955 | |||||
| chr3:142616335
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37+19826A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142616335 | ||||||
| chr3:142616490
|
A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+19981A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142616490 | ||||||
| chr3:142616568
|
T | C | 2 | a0001c0001t0002g0267a0001c0001t0002g0269 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-37+20059T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142616568 | ||||||
| chr3:142616706
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(31): Show | 34 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.-37+20197G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142616706 | ||||||
| chr3:142616732
|
A | G | 7 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0108others(4): Show | 7 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+20223A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142616732 | ||||||
| chr3:142616897
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0260 | 2 | HG03017.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-37+20388C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142616897 | ||||||
| chr3:142617026
|
C | G | 6 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(3): Show | 6 | HG01496.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+20517C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617026 | ||||||
| chr3:142617089
|
A | G | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37+20580A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617089 | ||||||
| chr3:142617145
|
G | GGT | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(32): Show | 35 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.-37+20636_-37+2063 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617145 | ||||||
| chr3:142617146
|
A | AT | 40 | a0001c0001t0001g0125a0001c0001t0001g0151a0001c0001t0001g0224others(37): Show | 41 | HG00099.hp2 HG01175.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-37+20652dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142617146 | |||||
| chr3:142617146
|
A | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-37+20637A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617146 | ||||||
| chr3:142617445
|
A | C | 1 | a0001c0002t0001g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-37+20936A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617445 | ||||||
| chr3:142617519
|
T | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-37+21010T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617519 | ||||||
| chr3:142617520
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(34): Show | 37 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.-37+21011G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617520 | ||||||
| chr3:142617739
|
AGGCTGAG others(20): Show |
A | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+21231_-37+2125 others(31): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617739 | ||||||
| chr3:142617766
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-37+21257T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142617766 | ||||||
| chr3:142618588
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-37+22079A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142618588 | ||||||
| chr3:142618830
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-37+22321C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142618830 | ||||||
| chr3:142618888
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-37+22379T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142618888 | ||||||
| chr3:142618962
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(105): Show | 109 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.-37+22453G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142618962 | ||||||
| chr3:142619029
|
G | T | 1 | a0001c0002t0012g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-37+22520G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619029 | ||||||
| chr3:142619322
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-37+22813C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619322 | ||||||
| chr3:142619335
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-37+22826A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619335 | ||||||
| chr3:142619418
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37+22909T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619418 | ||||||
| chr3:142619599
|
T | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-37+23090T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619599 | ||||||
| chr3:142619694
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+23185G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619694 | ||||||
| chr3:142619835
|
T | C | 1 | a0003c0005t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-37+23326T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619835 | ||||||
| chr3:142619909
|
T | G | 21 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(18): Show | 21 | HG01175.hp2 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-37+23400T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619909 | ||||||
| chr3:142619913
|
A | G | 2 | a0002c0003t0002g0114a0002c0003t0002g0120 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-37+23404A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142619913 | ||||||
| chr3:142620122
|
CT | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0143a0003c0005t0001g0129others(2): Show | 5 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+23627delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142620122 | |||||
| chr3:142620208
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+23699T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142620208 | ||||||
| chr3:142620308
|
G | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0269 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-37+23799G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142620308 | ||||||
| chr3:142620756
|
T | A | 1 | a0001c0001t0003g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37+24247T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142620756 | ||||||
| chr3:142620825
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-37+24316C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142620825 | ||||||
| chr3:142620973
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+24464T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142620973 | ||||||
| chr3:142620981
|
T | G | 19 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(16): Show | 19 | HG00673.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37+24472T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142620981 | ||||||
| chr3:142621272
|
A | G | 12 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(9): Show | 12 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+24763A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621272 | ||||||
| chr3:142621337
|
A | G | 2 | a0001c0001t0002g0259a0001c0001t0002g0261 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-37+24828A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621337 | ||||||
| chr3:142621359
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+24850G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621359 | ||||||
| chr3:142621560
|
A | G | 1 | a0001c0002t0001g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-37+25051A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621560 | ||||||
| chr3:142621610
|
A | T | 2 | a0001c0001t0001g0125a0001c0001t0002g0126 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-37+25101A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621610 | ||||||
| chr3:142621622
|
T | C | 1 | a0001c0002t0001g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-37+25113T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621622 | ||||||
| chr3:142621733
|
A | T | 1 | a0001c0008t0017g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-37+25224A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621733 | ||||||
| chr3:142621814
|
TG | T | 21 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(18): Show | 21 | HG01175.hp2 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-37+25310delG | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142621814 | |||||
| chr3:142621825
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-37+25316A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621825 | ||||||
| chr3:142621965
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(106): Show | 110 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37+25456A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142621965 | ||||||
| chr3:142622037
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+25528A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622037 | ||||||
| chr3:142622137
|
TTTC | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+25633_-37+2563 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142622137 | |||||
| chr3:142622304
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+25795G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622304 | ||||||
| chr3:142622305
|
C | T | 21 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(18): Show | 21 | HG01175.hp2 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-37+25796C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622305 | ||||||
| chr3:142622310
|
A | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+25801A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622310 | ||||||
| chr3:142622359
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+25850C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622359 | ||||||
| chr3:142622466
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+25957T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622466 | ||||||
| chr3:142622557
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-37+26048C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622557 | ||||||
| chr3:142622750
|
G | A | 9 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0206others(6): Show | 9 | HG00621.hp2 HG02027.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+26241G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622750 | ||||||
| chr3:142622859
|
T | G | 48 | a0001c0001t0001g0169a0001c0001t0001g0175a0001c0001t0001g0183others(45): Show | 48 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-37+26350T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622859 | ||||||
| chr3:142622975
|
T | A | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-37+26466T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622975 | ||||||
| chr3:142622990
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-37+26481C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142622990 | ||||||
| chr3:142623054
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(26): Show | 29 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37+26545G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142623054 | ||||||
| chr3:142623270
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(106): Show | 110 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37+26761C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142623270 | ||||||
| chr3:142623314
|
G | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-37+26805G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142623314 | ||||||
| chr3:142623322
|
A | AT | 37 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0196others(34): Show | 37 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-37+26820dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142623322 | |||||
| chr3:142624029
|
A | G | 2 | a0001c0002t0001g0034a0001c0002t0001g0037 | 2 | HG02071.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-37+27520A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624029 | ||||||
| chr3:142624100
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273others(6): Show | 10 | HG00099.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37+27591C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624100 | ||||||
| chr3:142624103
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+27594A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624103 | ||||||
| chr3:142624368
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0253 | 2 | HG01070.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-37+27859G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624368 | ||||||
| chr3:142624549
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+28040G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624549 | ||||||
| chr3:142624559
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+28050A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624559 | ||||||
| chr3:142624710
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-37+28201C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624710 | ||||||
| chr3:142624798
|
A | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37+28289A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624798 | ||||||
| chr3:142624849
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-37+28340C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624849 | ||||||
| chr3:142624939
|
AG | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(51): Show | 55 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.-37+28432delG | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142624939 | |||||
| chr3:142624939
|
AGGAG | A | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37+28432_-37+2843 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142624939 | |||||
| chr3:142624949
|
T | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+28440T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624949 | ||||||
| chr3:142624996
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37+28487A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142624996 | ||||||
| chr3:142625138
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+28629T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625138 | ||||||
| chr3:142625149
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-37+28640G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625149 | ||||||
| chr3:142625197
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(34): Show | 37 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.-37+28688G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625197 | ||||||
| chr3:142625205
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37+28696C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625205 | ||||||
| chr3:142625247
|
A | AT | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-37+28744dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142625247 | |||||
| chr3:142625254
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-37+28745C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625254 | ||||||
| chr3:142625415
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG03688.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-37+28906C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625415 | ||||||
| chr3:142625523
|
A | C | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-37+29014A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625523 | ||||||
| chr3:142625847
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 84 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-37+29338G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625847 | ||||||
| chr3:142625856
|
C | T | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37+29347C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142625856 | ||||||
| chr3:142626044
|
G | A | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37+29535G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626044 | ||||||
| chr3:142626142
|
G | A | 35 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0198others(32): Show | 35 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-37+29633G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626142 | ||||||
| chr3:142626271
|
T | A | 1 | a0003c0005t0008g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-37+29762T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626271 | ||||||
| chr3:142626361
|
G | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(75): Show | 79 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-37+29852G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626361 | ||||||
| chr3:142626555
|
A | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-37+30046A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626555 | ||||||
| chr3:142626747
|
T | C | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37+30238T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626747 | ||||||
| chr3:142626781
|
A | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-37+30272A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626781 | ||||||
| chr3:142626838
|
G | T | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37+30329G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626838 | ||||||
| chr3:142626973
|
T | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+30464T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626973 | ||||||
| chr3:142626975
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-37+30466C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142626975 | ||||||
| chr3:142627290
|
A | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-37+30781A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142627290 | ||||||
| chr3:142627712
|
C | G | 48 | a0001c0001t0001g0169a0001c0001t0001g0175a0001c0001t0001g0183others(45): Show | 48 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-37+31203C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142627712 | ||||||
| chr3:142627796
|
CT | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(181): Show | 185 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-37+31301delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142627796 | |||||
| chr3:142627922
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-37+31413T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142627922 | ||||||
| chr3:142628070
|
C | T | 1 | a0001c0004t0007g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-37+31561C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628070 | ||||||
| chr3:142628204
|
G | C | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-37+31695G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628204 | ||||||
| chr3:142628335
|
G | GTGTGTGC others(24): Show |
1 | a0001c0002t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-37+31865_-37+3189 others(35): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142628335 | |||||
| chr3:142628335
|
GTGTGTGC others(24): Show |
G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 190 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.-37+31865_-37+3189 others(35): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142628335 | |||||
| chr3:142628359
|
AGTGTGCA others(32): Show |
A | 3 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273 | 3 | HG00099.hp2 NA18947.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-37+31860_-37+3189 others(43): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142628359 | |||||
| chr3:142628368
|
GTGTGCGC others(5): Show |
G | 1 | a0001c0001t0001g0016 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-37+31865_-37+3187 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142628368 | |||||
| chr3:142628374
|
G | A | 1 | a0001c0002t0001g0022 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-37+31865G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628374 | ||||||
| chr3:142628375
|
C | T | 5 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+31866C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628375 | ||||||
| chr3:142628471
|
T | TTTACATT others(14): Show |
4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+31963_-37+3196 others(25): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142628471 | |||||
| chr3:142628635
|
T | C | 1 | a0001c0001t0006g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-37+32126T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628635 | ||||||
| chr3:142628915
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-37+32406A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628915 | ||||||
| chr3:142628994
|
T | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0131a0001c0001t0004g0132others(3): Show | 7 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+32485T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142628994 | ||||||
| chr3:142629114
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37+32605A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142629114 | ||||||
| chr3:142629199
|
A | AT | 16 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(13): Show | 16 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37+32705dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142629199 | |||||
| chr3:142629199
|
AT | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 169 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-37+32705delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142629199 | |||||
| chr3:142629220
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-37+32711A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142629220 | ||||||
| chr3:142629279
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-37+32770T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142629279 | ||||||
| chr3:142629472
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-37+32963T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142629472 | ||||||
| chr3:142629658
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-37+33149C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142629658 | ||||||
| chr3:142629858
|
G | A | 6 | a0001c0001t0002g0104a0001c0001t0002g0190a0003c0005t0001g0129others(3): Show | 6 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+33349G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142629858 | ||||||
| chr3:142630068
|
A | C | 2 | a0001c0002t0001g0039a0001c0002t0001g0046 | 2 | NA18964.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-37+33559A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630068 | ||||||
| chr3:142630105
|
C | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0002t0001g0068 | 3 | HG03491.hp1 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-37+33596C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630105 | ||||||
| chr3:142630327
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0175a0001c0001t0003g0144others(1): Show | 4 | HG00099.hp2 NA18947.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+33818G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630327 | ||||||
| chr3:142630420
|
CA | C | 84 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(81): Show | 85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-36-33762delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630420 | |||||
| chr3:142630420
|
CAA | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0135others(17): Show | 20 | HG00423.hp2 HG00735.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-36-33763_-36-3376 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630420 | |||||
| chr3:142630420
|
CAAA | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 103 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.-36-33764_-36-3376 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630420 | |||||
| chr3:142630420
|
CAAAA | C | 46 | a0001c0001t0001g0169a0001c0001t0001g0175a0001c0001t0001g0183others(43): Show | 46 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.-36-33765_-36-3376 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630420 | |||||
| chr3:142630437
|
A | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-33765A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630437 | ||||||
| chr3:142630519
|
G | A | 4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-33683G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630519 | ||||||
| chr3:142630537
|
T | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-33665T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630537 | ||||||
| chr3:142630608
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-36-33594G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630608 | ||||||
| chr3:142630825
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-36-33377A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630825 | ||||||
| chr3:142630938
|
A | AAC | 14 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(11): Show | 14 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-36-33230_-36-3322 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACAC | 4 | a0001c0001t0001g0181a0001c0001t0002g0174a0001c0001t0002g0182others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-33232_-36-3322 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACAC | 4 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0001t0001g0198others(1): Show | 4 | HG00735.hp2 HG01106.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-33234_-36-3322 others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(1): Show |
53 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0076others(50): Show | 54 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-36-33236_-36-3322 others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(3): Show |
28 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(25): Show | 28 | HG00597.hp2 HG00673.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.-36-33238_-36-3322 others(14): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(5): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 29 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-36-33240_-36-3322 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(7): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0135others(15): Show | 18 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-36-33242_-36-3322 others(18): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(9): Show |
4 | a0001c0001t0002g0190a0001c0001t0004g0131a0001c0001t0004g0268others(1): Show | 4 | HG01496.hp1 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-33244_-36-3322 others(20): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(11): Show |
3 | a0001c0001t0004g0113a0001c0001t0008g0130a0003c0005t0012g0133 | 3 | HG02630.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-36-33246_-36-3322 others(22): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(13): Show |
7 | a0001c0001t0001g0216a0001c0001t0004g0112a0001c0001t0009g0155others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-33248_-36-3322 others(24): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(15): Show |
5 | a0001c0001t0002g0102a0001c0001t0002g0126a0002c0003t0002g0254others(2): Show | 5 | HG01175.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-33250_-36-3322 others(26): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(17): Show |
3 | a0002c0003t0002g0103a0002c0003t0002g0117a0002c0003t0002g0154 | 3 | HG02886.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-36-33252_-36-3322 others(28): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(19): Show |
6 | a0001c0001t0001g0125a0001c0001t0002g0122a0001c0001t0002g0123others(3): Show | 6 | HG02615.hp1 HG02723.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-33254_-36-3322 others(30): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | AACACACA others(21): Show |
3 | a0001c0001t0002g0104a0002c0003t0001g0121a0002c0003t0002g0114 | 3 | HG02257.hp1 HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-36-33256_-36-3322 others(32): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630938
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0202 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-36-33264_-36-3326 others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630938 | ||||||
| chr3:142630938
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-36-33264_-36-3326 others(21): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630938 | ||||||
| chr3:142630938
|
A | ACACACAC others(14): Show |
1 | a0003c0005t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-36-33264_-36-3326 others(25): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630938 | ||||||
| chr3:142630938
|
A | ACACACAC others(20): Show |
1 | a0002c0003t0001g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-36-33264_-36-3326 others(31): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630938 | ||||||
| chr3:142630938
|
AACAC | A | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-33232_-36-3322 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142630938 | |||||
| chr3:142630974
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-36-33228T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630974 | ||||||
| chr3:142630987
|
A | C | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-36-33215A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142630987 | ||||||
| chr3:142631202
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(93): Show | 97 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.-36-33000T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631202 | ||||||
| chr3:142631237
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-36-32965A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631237 | ||||||
| chr3:142631561
|
T | G | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-32641T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631561 | ||||||
| chr3:142631594
|
G | A | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-32608G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631594 | ||||||
| chr3:142631651
|
G | A | 1 | a0003c0005t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-36-32551G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631651 | ||||||
| chr3:142631664
|
G | GA | 87 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0076others(84): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-36-32512dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142631664 | |||||
| chr3:142631664
|
G | GAA | 18 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(15): Show | 18 | HG00673.hp2 HG02027.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-32513_-36-3251 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142631664 | |||||
| chr3:142631664
|
GA | G | 24 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0104others(21): Show | 24 | HG00280.hp2 HG00621.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-36-32512delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142631664 | |||||
| chr3:142631665
|
A | G | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG03688.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-36-32537A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631665 | ||||||
| chr3:142631666
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36-32536A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631666 | ||||||
| chr3:142631778
|
T | A | 1 | a0001c0002t0001g0053 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-36-32424T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631778 | ||||||
| chr3:142631801
|
G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-32401G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631801 | ||||||
| chr3:142631822
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0135others(7): Show | 10 | HG00423.hp2 HG01934.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36-32380G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631822 | ||||||
| chr3:142631878
|
C | G | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-36-32324C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631878 | ||||||
| chr3:142631914
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-36-32288C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142631914 | ||||||
| chr3:142632180
|
A | T | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-36-32022A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632180 | ||||||
| chr3:142632255
|
T | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-36-31947T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632255 | ||||||
| chr3:142632315
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0135others(7): Show | 10 | HG00423.hp2 HG01934.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36-31887G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632315 | ||||||
| chr3:142632597
|
A | AT | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-36-31591dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142632597 | |||||
| chr3:142632611
|
T | C | 4 | a0001c0002t0001g0035a0001c0002t0001g0061a0001c0002t0001g0082others(1): Show | 4 | HG00280.hp2 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-31591T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632611 | ||||||
| chr3:142632621
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-36-31581C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632621 | ||||||
| chr3:142632624
|
G | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-36-31578G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632624 | ||||||
| chr3:142632797
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-36-31405C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632797 | ||||||
| chr3:142632807
|
C | T | 1 | a0001c0002t0001g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-36-31395C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632807 | ||||||
| chr3:142632936
|
T | A | 1 | a0001c0002t0003g0066 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-36-31266T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142632936 | ||||||
| chr3:142633088
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 190 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.-36-31114C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142633088 | ||||||
| chr3:142633266
|
A | C | 2 | a0001c0001t0009g0153a0001c0001t0009g0155 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-36-30936A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142633266 | ||||||
| chr3:142633554
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-36-30648G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142633554 | ||||||
| chr3:142633655
|
TCAAA | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(46): Show | 49 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36-30534_-36-3053 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142633655 | |||||
| chr3:142633983
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(37): Show | 41 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.-36-30219A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142633983 | ||||||
| chr3:142634025
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG03688.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-36-30177A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142634025 | ||||||
| chr3:142634136
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(93): Show | 97 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.-36-30066A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142634136 | ||||||
| chr3:142634232
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-36-29970A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142634232 | ||||||
| chr3:142634552
|
C | T | 10 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0259others(7): Show | 10 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36-29650C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142634552 | ||||||
| chr3:142634843
|
A | G | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-29359A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142634843 | ||||||
| chr3:142634888
|
C | T | 89 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(86): Show | 89 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.-36-29314C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142634888 | ||||||
| chr3:142634915
|
CT | C | 12 | a0001c0001t0001g0031a0001c0002t0001g0042a0002c0003t0001g0152others(9): Show | 12 | HG01123.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-29272delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142634915 | |||||
| chr3:142635207
|
A | G | 2 | a0002c0003t0001g0152a0002c0003t0002g0154 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-36-28995A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635207 | ||||||
| chr3:142635268
|
G | A | 1 | a0001c0001t0004g0131 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-36-28934G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635268 | ||||||
| chr3:142635416
|
C | G | 2 | a0002c0003t0001g0152a0002c0003t0002g0154 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-36-28786C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635416 | ||||||
| chr3:142635435
|
CA | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 120 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-36-28749delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142635435 | |||||
| chr3:142635435
|
CAA | C | 39 | a0001c0001t0001g0125a0001c0001t0001g0151a0001c0001t0001g0208others(36): Show | 40 | HG00099.hp2 HG01070.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.-36-28750_-36-2874 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142635435 | |||||
| chr3:142635566
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-36-28636A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635566 | ||||||
| chr3:142635635
|
A | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-28567A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635635 | ||||||
| chr3:142635715
|
C | G | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-36-28487C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635715 | ||||||
| chr3:142635750
|
A | T | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-36-28452A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635750 | ||||||
| chr3:142635833
|
G | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-28369G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142635833 | ||||||
| chr3:142636055
|
A | AT | 10 | a0001c0001t0001g0151a0001c0001t0002g0107a0001c0001t0002g0108others(7): Show | 10 | HG00099.hp2 HG01891.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36-28134dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142636055 | |||||
| chr3:142636055
|
A | ATT | 4 | a0001c0001t0004g0001a0001c0001t0004g0131a0001c0001t0004g0268others(1): Show | 5 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-28135_-36-2813 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142636055 | |||||
| chr3:142636055
|
AT | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(93): Show | 97 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.-36-28134delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142636055 | |||||
| chr3:142636547
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-27655A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142636547 | ||||||
| chr3:142636568
|
G | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-36-27634G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142636568 | ||||||
| chr3:142636723
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-36-27479A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142636723 | ||||||
| chr3:142636797
|
G | A | 1 | a0001c0002t0013g0054 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-36-27405G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142636797 | ||||||
| chr3:142637024
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-36-27178T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637024 | ||||||
| chr3:142637084
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-36-27118G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637084 | ||||||
| chr3:142637384
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-36-26818C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637384 | ||||||
| chr3:142637524
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36-26678G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637524 | ||||||
| chr3:142637654
|
T | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-36-26548T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637654 | ||||||
| chr3:142637759
|
A | T | 2 | a0002c0003t0001g0152a0002c0003t0002g0154 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-36-26443A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637759 | ||||||
| chr3:142637870
|
C | A | 1 | a0001c0008t0017g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-36-26332C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637870 | ||||||
| chr3:142637872
|
C | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-36-26330C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637872 | ||||||
| chr3:142637874
|
A | C | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-36-26328A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637874 | ||||||
| chr3:142637895
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0182a0001c0001t0009g0191 | 3 | HG02965.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-36-26307C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637895 | ||||||
| chr3:142637942
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG03688.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-36-26260C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637942 | ||||||
| chr3:142637981
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-36-26221C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637981 | ||||||
| chr3:142637987
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-36-26215C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142637987 | ||||||
| chr3:142638076
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-36-26126C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638076 | ||||||
| chr3:142638108
|
A | T | 1 | a0001c0001t0004g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-36-26094A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638108 | ||||||
| chr3:142638220
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0003g0273others(7): Show | 11 | HG00099.hp2 HG01433.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-25982G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638220 | ||||||
| chr3:142638282
|
C | G | 4 | a0001c0001t0001g0106a0001c0001t0002g0260a0001c0001t0002g0267others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-25920C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638282 | ||||||
| chr3:142638335
|
C | T | 11 | a0001c0001t0001g0125a0001c0001t0001g0262a0001c0001t0001g0271others(8): Show | 11 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-25867C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638335 | ||||||
| chr3:142638381
|
G | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 191 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-36-25821G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638381 | ||||||
| chr3:142638712
|
C | CATTTT | 3 | a0001c0002t0001g0055a0001c0002t0001g0081a0001c0002t0001g0192 | 3 | HG02976.hp1 HG03579.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-36-25449_-36-2544 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142638712 | |||||
| chr3:142638712
|
CATTTT | C | 18 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(15): Show | 18 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-25449_-36-2544 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142638712 | |||||
| chr3:142638712
|
CATTTTAT others(8): Show |
C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-36-25459_-36-2544 others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142638712 | |||||
| chr3:142638723
|
ATTTTATT others(5): Show |
A | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-25476_-36-2546 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142638723 | |||||
| chr3:142638804
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-36-25398C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638804 | ||||||
| chr3:142638804
|
C | T | 1 | a0001c0002t0001g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-36-25398C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638804 | ||||||
| chr3:142638856
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(29): Show | 32 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-36-25346C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638856 | ||||||
| chr3:142638873
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 167 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-36-25329G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638873 | ||||||
| chr3:142638894
|
G | A | 7 | a0001c0001t0001g0149a0001c0001t0002g0267a0001c0001t0002g0269others(4): Show | 7 | HG01255.hp1 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-25308G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142638894 | ||||||
| chr3:142639432
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-36-24770C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639432 | ||||||
| chr3:142639436
|
T | A | 7 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(4): Show | 7 | HG01175.hp2 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-24766T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639436 | ||||||
| chr3:142639469
|
A | G | 11 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-24733A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639469 | ||||||
| chr3:142639688
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(89): Show | 93 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-36-24514A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639688 | ||||||
| chr3:142639759
|
G | C | 36 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0198others(33): Show | 36 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-36-24443G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639759 | ||||||
| chr3:142639862
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG00621.hp2 HG02027.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-24340A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639862 | ||||||
| chr3:142639897
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0002g0267a0001c0001t0002g0269 | 3 | HG02055.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36-24305A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639897 | ||||||
| chr3:142639982
|
G | A | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-24220G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142639982 | ||||||
| chr3:142640050
|
A | T | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-24152A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640050 | ||||||
| chr3:142640162
|
A | T | 1 | a0001c0002t0001g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-36-24040A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640162 | ||||||
| chr3:142640331
|
A | G | 1 | a0001c0002t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-36-23871A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640331 | ||||||
| chr3:142640570
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-36-23632C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640570 | ||||||
| chr3:142640585
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-36-23617A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640585 | ||||||
| chr3:142640654
|
A | T | 8 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(5): Show | 9 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-36-23548A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640654 | ||||||
| chr3:142640696
|
T | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-36-23506T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640696 | ||||||
| chr3:142640721
|
G | C | 4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-23481G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640721 | ||||||
| chr3:142640790
|
T | C | 4 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0077others(1): Show | 4 | HG01167.hp1 HG01192.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-23412T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640790 | ||||||
| chr3:142640819
|
T | A | 1 | a0001c0002t0001g0046 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-36-23383T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640819 | ||||||
| chr3:142640888
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0052 | 3 | HG01358.hp1 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-36-23314C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142640888 | ||||||
| chr3:142641117
|
T | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-36-23085T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641117 | ||||||
| chr3:142641157
|
A | ATT | 8 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(5): Show | 9 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-36-23044_-36-2304 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142641157 | |||||
| chr3:142641158
|
T | TTA | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-36-23028_-36-2302 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142641158 | |||||
| chr3:142641175
|
T | TATTA | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-23027_-36-2302 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641175 | ||||||
| chr3:142641176
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-36-23026T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641176 | ||||||
| chr3:142641177
|
A | T | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-36-23025A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641177 | ||||||
| chr3:142641531
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-36-22671G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641531 | ||||||
| chr3:142641591
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | NA18943.hp2 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-22611T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641591 | ||||||
| chr3:142641915
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0131a0001c0001t0004g0132others(3): Show | 7 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-22287C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142641915 | ||||||
| chr3:142642062
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18961.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-36-22140A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142642062 | ||||||
| chr3:142642071
|
C | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.-36-22131C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142642071 | ||||||
| chr3:142642471
|
T | G | 4 | a0001c0004t0007g0030a0001c0004t0007g0033a0001c0004t0007g0045others(1): Show | 4 | HG00639.hp2 HG01081.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-21731T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142642471 | ||||||
| chr3:142642685
|
T | G | 3 | a0001c0001t0001g0149a0001c0001t0002g0267a0001c0001t0002g0269 | 3 | HG02055.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36-21517T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142642685 | ||||||
| chr3:142642778
|
T | C | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-21424T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142642778 | ||||||
| chr3:142643034
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36-21168G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643034 | ||||||
| chr3:142643337
|
A | G | 8 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36-20865A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643337 | ||||||
| chr3:142643366
|
G | A | 11 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-20836G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643366 | ||||||
| chr3:142643401
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-36-20801G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643401 | ||||||
| chr3:142643560
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 166 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-36-20642C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643560 | ||||||
| chr3:142643663
|
G | T | 2 | a0002c0003t0002g0114a0002c0003t0002g0120 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-36-20539G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643663 | ||||||
| chr3:142643824
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-36-20378C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643824 | ||||||
| chr3:142643825
|
A | AT | 11 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 11 | HG00741.hp2 HG01243.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-20356dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142643825 | |||||
| chr3:142643825
|
AT | A | 23 | a0001c0001t0001g0125a0001c0001t0001g0271a0001c0001t0002g0102others(20): Show | 23 | HG00621.hp1 HG01123.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.-36-20356delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142643825 | |||||
| chr3:142643825
|
ATT | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-36-20357_-36-2035 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142643825 | |||||
| chr3:142643825
|
ATTT | A | 66 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0169others(63): Show | 67 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-36-20358_-36-2035 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142643825 | |||||
| chr3:142643825
|
ATTTT | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(51): Show | 55 | HG00323.hp2 HG00621.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36-20359_-36-2035 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142643825 | |||||
| chr3:142643830
|
T | C | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-36-20372T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643830 | ||||||
| chr3:142643831
|
T | A | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-36-20371T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643831 | ||||||
| chr3:142643849
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-36-20353A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142643849 | ||||||
| chr3:142644289
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG01934.hp1 HG02273.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-36-19913C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644289 | ||||||
| chr3:142644490
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0002g0267a0001c0001t0002g0269 | 3 | HG02055.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36-19712C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644490 | ||||||
| chr3:142644491
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-36-19711G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644491 | ||||||
| chr3:142644532
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-19670C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644532 | ||||||
| chr3:142644569
|
A | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-19633A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644569 | ||||||
| chr3:142644590
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 166 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-36-19612C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644590 | ||||||
| chr3:142644778
|
G | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-19424G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644778 | ||||||
| chr3:142644809
|
T | C | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-19393T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142644809 | ||||||
| chr3:142645226
|
G | T | 5 | a0001c0001t0002g0174a0001c0001t0002g0182a0001c0001t0002g0184others(2): Show | 5 | HG02965.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-18976G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142645226 | ||||||
| chr3:142645650
|
T | C | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-18552T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142645650 | ||||||
| chr3:142645827
|
T | G | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-18375T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142645827 | ||||||
| chr3:142646079
|
T | C | 1 | a0002c0003t0002g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-36-18123T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646079 | ||||||
| chr3:142646384
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-36-17818G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646384 | ||||||
| chr3:142646389
|
C | G | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-17813C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646389 | ||||||
| chr3:142646521
|
C | G | 1 | a0001c0009t0001g0136 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-36-17681C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646521 | ||||||
| chr3:142646563
|
G | A | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-17639G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646563 | ||||||
| chr3:142646764
|
T | C | 4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-17438T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646764 | ||||||
| chr3:142646788
|
A | G | 7 | a0001c0001t0005g0236a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-17414A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646788 | ||||||
| chr3:142646927
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-17275A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142646927 | ||||||
| chr3:142647055
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-36-17147A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647055 | ||||||
| chr3:142647056
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-36-17146A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647056 | ||||||
| chr3:142647076
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-17126C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647076 | ||||||
| chr3:142647232
|
G | T | 15 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(12): Show | 16 | HG00099.hp2 HG01070.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-16970G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647232 | ||||||
| chr3:142647357
|
T | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-16845T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647357 | ||||||
| chr3:142647499
|
T | TTTTC | 19 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(16): Show | 20 | HG00099.hp2 HG01070.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-36-16699_-36-1669 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142647499 | |||||
| chr3:142647503
|
C | CT | 90 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(87): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-36-16685dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142647503 | |||||
| chr3:142647503
|
C | CTTTCT | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 67 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.-36-16696_-36-1669 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142647503 | |||||
| chr3:142647528
|
A | C | 1 | a0001c0001t0015g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-36-16674A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647528 | ||||||
| chr3:142647784
|
T | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-16418T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647784 | ||||||
| chr3:142647827
|
C | T | 2 | a0001c0001t0002g0104a0001c0001t0002g0190 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-16375C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647827 | ||||||
| chr3:142647897
|
G | C | 11 | a0002c0003t0001g0115a0002c0003t0001g0152a0002c0003t0002g0103others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36-16305G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647897 | ||||||
| chr3:142647897
|
G | T | 2 | a0002c0003t0001g0116a0002c0003t0001g0121 | 2 | HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-36-16305G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647897 | ||||||
| chr3:142647983
|
A | G | 7 | a0001c0001t0001g0125a0001c0001t0002g0102a0001c0001t0002g0122others(4): Show | 7 | HG01175.hp2 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-16219A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142647983 | ||||||
| chr3:142648214
|
G | A | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-15988G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142648214 | ||||||
| chr3:142648219
|
AAGAACGG others(7): Show |
A | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-15978_-36-1596 others(18): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142648219 | |||||
| chr3:142648317
|
CT | C | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-15880delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142648317 | |||||
| chr3:142648383
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-15819C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142648383 | ||||||
| chr3:142648453
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0181a0001c0001t0003g0199 | 3 | HG03225.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-36-15749C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142648453 | ||||||
| chr3:142648524
|
T | C | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-15678T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142648524 | ||||||
| chr3:142648708
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-15494A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142648708 | ||||||
| chr3:142649100
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-36-15102T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649100 | ||||||
| chr3:142649159
|
G | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-15043G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649159 | ||||||
| chr3:142649199
|
G | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | NA18953.hp2 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-36-15003G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649199 | ||||||
| chr3:142649229
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-14973A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649229 | ||||||
| chr3:142649335
|
C | CA | 11 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0002g0104others(8): Show | 11 | HG00738.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-14849dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649335 | |||||
| chr3:142649335
|
C | CAA | 9 | a0001c0001t0001g0165a0001c0001t0002g0267a0001c0001t0002g0269others(6): Show | 9 | HG00323.hp1 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-14850_-36-1484 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649335 | |||||
| chr3:142649335
|
C | CAAA | 46 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(43): Show | 46 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-36-14851_-36-1484 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649335 | |||||
| chr3:142649335
|
C | CAAAA | 97 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0031others(94): Show | 98 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.-36-14852_-36-1484 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649335 | |||||
| chr3:142649335
|
C | CAAAAA | 31 | a0001c0001t0001g0151a0001c0001t0001g0169a0001c0001t0001g0181others(28): Show | 32 | HG00099.hp2 HG01070.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.-36-14853_-36-1484 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649335 | |||||
| chr3:142649364
|
G | T | 4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-14838G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649364 | ||||||
| chr3:142649458
|
G | A | 1 | a0001c0002t0019g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-36-14744G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649458 | ||||||
| chr3:142649493
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-36-14709C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649493 | ||||||
| chr3:142649559
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-14643G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649559 | ||||||
| chr3:142649733
|
AG | A | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-14467delG | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649733 | |||||
| chr3:142649819
|
C | CT | 12 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0038others(9): Show | 12 | HG00639.hp2 HG01081.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.-36-14382dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142649819 | |||||
| chr3:142649892
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-14310C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649892 | ||||||
| chr3:142649900
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-14302G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142649900 | ||||||
| chr3:142650001
|
G | T | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-14201G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650001 | ||||||
| chr3:142650211
|
C | CT | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(126): Show | 131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-36-13966dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142650211 | |||||
| chr3:142650211
|
C | CTT | 18 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0170others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-13967_-36-1396 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142650211 | |||||
| chr3:142650211
|
C | CTTT | 8 | a0001c0001t0001g0015a0001c0001t0001g0106a0001c0001t0001g0125others(5): Show | 8 | HG01175.hp2 HG02135.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36-13968_-36-1396 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142650211 | |||||
| chr3:142650211
|
CT | C | 13 | a0001c0001t0002g0104a0001c0001t0002g0190a0001c0001t0006g0272others(10): Show | 13 | HG00673.hp1 HG01081.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-13966delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142650211 | |||||
| chr3:142650219
|
T | C | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-36-13983T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650219 | ||||||
| chr3:142650220
|
T | C | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-13982T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650220 | ||||||
| chr3:142650369
|
C | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-36-13833C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650369 | ||||||
| chr3:142650378
|
C | T | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-13824C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650378 | ||||||
| chr3:142650380
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-36-13822G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650380 | ||||||
| chr3:142650535
|
C | T | 2 | a0001c0001t0009g0153a0001c0001t0009g0155 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-36-13667C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650535 | ||||||
| chr3:142650997
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-13205G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142650997 | ||||||
| chr3:142651075
|
G | A | 2 | a0001c0002t0001g0039a0001c0002t0001g0046 | 2 | NA18964.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-36-13127G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142651075 | ||||||
| chr3:142651197
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0261 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-36-13005C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142651197 | ||||||
| chr3:142651226
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-36-12976G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142651226 | ||||||
| chr3:142651257
|
C | T | 4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-12945C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142651257 | ||||||
| chr3:142651308
|
A | G | 9 | a0001c0001t0001g0271a0001c0001t0002g0259a0001c0001t0002g0261others(6): Show | 9 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-36-12894A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142651308 | ||||||
| chr3:142651462
|
C | CA | 25 | a0001c0001t0003g0148a0001c0002t0001g0020a0001c0002t0001g0022others(22): Show | 25 | HG01175.hp1 HG01192.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-36-12715dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142651462 | |||||
| chr3:142651462
|
CA | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0002g0261others(10): Show | 13 | HG00673.hp1 HG01123.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-36-12715delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142651462 | |||||
| chr3:142651462
|
CAAAA | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0145others(3): Show | 6 | HG00597.hp2 HG01934.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-12718_-36-1271 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142651462 | |||||
| chr3:142651462
|
CAAAAA | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.-36-12719_-36-1271 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142651462 | |||||
| chr3:142651462
|
CAAAAAA | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(116): Show | 121 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-36-12720_-36-1271 others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142651462 | |||||
| chr3:142651481
|
A | C | 2 | a0001c0001t0006g0265a0001c0001t0006g0266 | 2 | HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-36-12721A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142651481 | ||||||
| chr3:142652024
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.-36-12178A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652024 | ||||||
| chr3:142652174
|
C | T | 1 | a0001c0001t0009g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-36-12028C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652174 | ||||||
| chr3:142652347
|
A | T | 2 | a0002c0003t0002g0118a0002c0003t0002g0119 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-36-11855A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652347 | ||||||
| chr3:142652732
|
A | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(12): Show | 15 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-11470A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652732 | ||||||
| chr3:142652792
|
CTTGTTTG others(5): Show |
C | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-11409_-36-1139 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652792 | ||||||
| chr3:142652835
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-36-11367G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652835 | ||||||
| chr3:142652853
|
A | T | 2 | a0001c0001t0004g0001a0004c0006t0004g0001 | 3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-36-11349A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142652853 | ||||||
| chr3:142653314
|
C | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-36-10888C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142653314 | ||||||
| chr3:142653364
|
CT | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.-36-10822delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142653364 | |||||
| chr3:142653364
|
CTT | C | 11 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(8): Show | 11 | HG00099.hp2 HG00323.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36-10823_-36-1082 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142653364 | |||||
| chr3:142653561
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-36-10641A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142653561 | ||||||
| chr3:142653584
|
C | T | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-36-10618C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142653584 | ||||||
| chr3:142653934
|
T | C | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-10268T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142653934 | ||||||
| chr3:142654027
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-10175A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654027 | ||||||
| chr3:142654116
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-36-10086G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654116 | ||||||
| chr3:142654476
|
G | A | 1 | a0001c0001t0015g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-36-9726G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654476 | ||||||
| chr3:142654518
|
A | AC | 10 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0002g0102others(7): Show | 10 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36-9684_-36-9683i others(3): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654518 | ||||||
| chr3:142654634
|
T | C | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-9568T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654634 | ||||||
| chr3:142654814
|
G | A | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-36-9388G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654814 | ||||||
| chr3:142654885
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-36-9317C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142654885 | ||||||
| chr3:142654947
|
AAGAGAAA others(4): Show |
A | 1 | a0001c0002t0001g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-36-9242_-36-9232d others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142654947 | |||||
| chr3:142655055
|
C | A | 1 | a0001c0002t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-36-9147C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655055 | ||||||
| chr3:142655098
|
G | A | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-9104G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655098 | ||||||
| chr3:142655466
|
A | G | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-36-8736A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655466 | ||||||
| chr3:142655516
|
T | G | 3 | a0001c0001t0003g0018a0001c0001t0011g0010a0001c0001t0011g0011 | 3 | HG01070.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-36-8686T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655516 | ||||||
| chr3:142655518
|
C | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(40): Show | 43 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-36-8684C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655518 | ||||||
| chr3:142655518
|
C | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-8684C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655518 | ||||||
| chr3:142655539
|
A | G | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-8663A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655539 | ||||||
| chr3:142655583
|
G | A | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-8619G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655583 | ||||||
| chr3:142655594
|
C | CGCCT | 12 | a0001c0001t0001g0175a0001c0001t0001g0181a0001c0001t0001g0196others(9): Show | 12 | HG00621.hp2 HG02027.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.-36-8605_-36-8602d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142655594 | |||||
| chr3:142655636
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-36-8566C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655636 | ||||||
| chr3:142655637
|
G | A | 1 | a0001c0004t0007g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-36-8565G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655637 | ||||||
| chr3:142655722
|
C | CA | 6 | a0001c0001t0001g0151a0001c0001t0003g0144a0001c0001t0005g0238others(3): Show | 6 | HG02056.hp1 HG02572.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-8460dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142655722 | |||||
| chr3:142655722
|
CA | C | 34 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0125others(31): Show | 35 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-36-8460delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142655722 | |||||
| chr3:142655722
|
CAA | C | 12 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-8461_-36-8460d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142655722 | |||||
| chr3:142655722
|
CAAA | C | 22 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(19): Show | 22 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36-8462_-36-8460d others(5): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142655722 | |||||
| chr3:142655758
|
A | G | 1 | a0001c0002t0003g0066 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-36-8444A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655758 | ||||||
| chr3:142655798
|
G | C | 3 | a0001c0001t0003g0018a0001c0001t0011g0010a0001c0001t0011g0011 | 3 | HG01070.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-36-8404G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142655798 | ||||||
| chr3:142656070
|
T | C | 1 | a0001c0002t0001g0037 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-36-8132T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656070 | ||||||
| chr3:142656208
|
T | C | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-36-7994T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656208 | ||||||
| chr3:142656213
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-7989T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656213 | ||||||
| chr3:142656240
|
G | A | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-7962G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656240 | ||||||
| chr3:142656251
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-7951T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656251 | ||||||
| chr3:142656498
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36-7704T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656498 | ||||||
| chr3:142656552
|
A | G | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-36-7650A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656552 | ||||||
| chr3:142656678
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-36-7524A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656678 | ||||||
| chr3:142656756
|
G | A | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-7446G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656756 | ||||||
| chr3:142656906
|
T | G | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-7296T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656906 | ||||||
| chr3:142656975
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 178 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.-36-7227G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142656975 | ||||||
| chr3:142657124
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019 | 3 | HG00597.hp2 HG02135.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-36-7078C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657124 | ||||||
| chr3:142657125
|
G | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-7077G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657125 | ||||||
| chr3:142657212
|
G | T | 1 | a0001c0002t0003g0024 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-36-6990G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657212 | ||||||
| chr3:142657268
|
G | T | 1 | a0001c0009t0001g0136 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-36-6934G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657268 | ||||||
| chr3:142657286
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 178 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.-36-6916A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657286 | ||||||
| chr3:142657366
|
C | A | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-36-6836C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657366 | ||||||
| chr3:142657428
|
T | C | 5 | a0001c0001t0002g0174a0001c0001t0002g0182a0001c0001t0002g0184others(2): Show | 5 | HG02965.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-6774T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657428 | ||||||
| chr3:142657664
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-6538A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657664 | ||||||
| chr3:142657678
|
C | T | 2 | a0001c0001t0002g0102a0001c0001t0002g0260 | 2 | HG01175.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-36-6524C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657678 | ||||||
| chr3:142657688
|
C | T | 10 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0002g0102others(7): Show | 10 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36-6514C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142657688 | ||||||
| chr3:142658293
|
T | C | 1 | a0003c0005t0008g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-36-5909T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658293 | ||||||
| chr3:142658299
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012 | 3 | NA18747.hp1 NA19005.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-36-5903C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658299 | ||||||
| chr3:142658333
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(93): Show | 96 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-36-5869A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658333 | ||||||
| chr3:142658368
|
C | T | 2 | a0001c0001t0009g0153a0001c0001t0009g0155 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-36-5834C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658368 | ||||||
| chr3:142658381
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-5821T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658381 | ||||||
| chr3:142658386
|
A | G | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-5816A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658386 | ||||||
| chr3:142658441
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-5761A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658441 | ||||||
| chr3:142658476
|
C | CA | 21 | a0001c0001t0001g0196a0001c0001t0001g0205a0001c0001t0001g0206others(18): Show | 21 | HG00621.hp2 HG01123.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-36-5710dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142658476 | |||||
| chr3:142658476
|
C | CAA | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-5711_-36-5710d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 142658476 | |||||
| chr3:142658824
|
G | T | 1 | a0002c0003t0002g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-36-5378G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658824 | ||||||
| chr3:142658965
|
A | T | 6 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-5237A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142658965 | ||||||
| chr3:142659367
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-4835T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659367 | ||||||
| chr3:142659421
|
G | T | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36-4781G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659421 | ||||||
| chr3:142659481
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG03688.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-36-4721A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659481 | ||||||
| chr3:142659715
|
A | T | 1 | a0001c0002t0003g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-36-4487A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659715 | ||||||
| chr3:142659825
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-4377T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659825 | ||||||
| chr3:142659956
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG01074.hp2 HG01516.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-4246G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659956 | ||||||
| chr3:142659956
|
G | T | 10 | a0001c0001t0002g0104a0001c0001t0002g0190a0001c0001t0004g0001others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36-4246G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142659956 | ||||||
| chr3:142660049
|
C | A | 1 | a0001c0001t0001g0202 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-36-4153C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660049 | ||||||
| chr3:142660109
|
G | C | 35 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(32): Show | 35 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.-36-4093G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660109 | ||||||
| chr3:142660146
|
A | G | 1 | a0001c0008t0017g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-36-4056A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660146 | ||||||
| chr3:142660147
|
G | T | 3 | a0001c0001t0005g0248a0001c0001t0005g0249a0001c0001t0005g0250 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-36-4055G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660147 | ||||||
| chr3:142660278
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.-36-3924C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660278 | ||||||
| chr3:142660289
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG03688.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-36-3913A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660289 | ||||||
| chr3:142660409
|
G | C | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-36-3793G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660409 | ||||||
| chr3:142660415
|
G | A | 3 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-36-3787G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660415 | ||||||
| chr3:142660415
|
G | C | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-36-3787G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660415 | ||||||
| chr3:142660719
|
C | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-3483C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660719 | ||||||
| chr3:142660750
|
C | T | 1 | a0001c0004t0007g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-36-3452C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142660750 | ||||||
| chr3:142661247
|
A | C | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-2955A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142661247 | ||||||
| chr3:142661377
|
G | A | 4 | a0001c0001t0004g0001a0001c0001t0004g0131a0001c0001t0004g0268others(1): Show | 5 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-2825G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142661377 | ||||||
| chr3:142661666
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.-36-2536A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142661666 | ||||||
| chr3:142661709
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-36-2493T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142661709 | ||||||
| chr3:142661923
|
G | C | 2 | a0001c0001t0009g0153a0001c0001t0009g0155 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-36-2279G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142661923 | ||||||
| chr3:142662114
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 48 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.-36-2088C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662114 | ||||||
| chr3:142662347
|
C | T | 13 | a0001c0001t0001g0271a0001c0001t0002g0259a0001c0001t0002g0261others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-36-1855C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662347 | ||||||
| chr3:142662383
|
C | G | 1 | a0001c0002t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-36-1819C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662383 | ||||||
| chr3:142662555
|
C | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0194others(3): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-1647C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662555 | ||||||
| chr3:142662730
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-36-1472A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662730 | ||||||
| chr3:142662801
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-1401T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662801 | ||||||
| chr3:142662926
|
G | A | 1 | a0001c0001t0004g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-36-1276G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662926 | ||||||
| chr3:142662949
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-1253T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662949 | ||||||
| chr3:142662972
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-36-1230G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142662972 | ||||||
| chr3:142663039
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0015g0017 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-36-1163G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663039 | ||||||
| chr3:142663168
|
T | A | 1 | a0001c0002t0012g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-36-1034T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663168 | ||||||
| chr3:142663268
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-36-934T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663268 | ||||||
| chr3:142663273
|
T | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-929T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663273 | ||||||
| chr3:142663322
|
G | A | 4 | a0001c0004t0007g0030a0001c0004t0007g0033a0001c0004t0007g0045others(1): Show | 4 | HG00639.hp2 HG01081.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-880G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663322 | ||||||
| chr3:142663387
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-815G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663387 | ||||||
| chr3:142663584
|
A | G | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-618A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663584 | ||||||
| chr3:142663696
|
ACATGGGG others(10): Show |
A | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-505_-36-489del others(17): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142663696 | ||||||
| chr3:142664036
|
G | C | 3 | a0001c0001t0004g0001a0001c0001t0004g0268a0004c0006t0004g0001 | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-166G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142664036 | ||||||
| chr3:142664153
|
A | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-49A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 1/15 | chr3 | 142664153 | ||||||
| chr3:142664448
|
G | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0163others(7): Show | 11 | HG00323.hp2 HG00741.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+141G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142664448 | ||||||
| chr3:142664476
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+169G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142664476 | ||||||
| chr3:142664655
|
T | G | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+348T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142664655 | ||||||
| chr3:142665167
|
C | T | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+860C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142665167 | ||||||
| chr3:142665291
|
G | A | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+984G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142665291 | ||||||
| chr3:142665297
|
C | CA | 16 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.70+1004dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 142665297 | |||||
| chr3:142665297
|
CA | C | 18 | a0001c0001t0001g0105a0001c0001t0001g0149a0001c0001t0001g0165others(15): Show | 18 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.70+1004delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 142665297 | |||||
| chr3:142665521
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.70+1214A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142665521 | ||||||
| chr3:142665802
|
A | AT | 23 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(20): Show | 23 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.70+1508dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 142665802 | |||||
| chr3:142665802
|
AT | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(89): Show | 93 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.70+1508delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 142665802 | |||||
| chr3:142665987
|
CTTTA | C | 3 | a0001c0002t0001g0233a0001c0002t0001g0251a0001c0002t0001g0257 | 3 | HG02027.hp1 HG02523.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.70+1685_70+1688del others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 142665987 | |||||
| chr3:142666093
|
G | A | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.70+1786G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666093 | ||||||
| chr3:142666216
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.70+1909T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666216 | ||||||
| chr3:142666234
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70+1927A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666234 | ||||||
| chr3:142666759
|
A | G | 1 | a0001c0002t0001g0022 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.70+2452A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666759 | ||||||
| chr3:142666858
|
C | A | 1 | a0002c0003t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.71-2532C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666858 | ||||||
| chr3:142666985
|
T | G | 1 | a0001c0002t0001g0005 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.71-2405T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666985 | ||||||
| chr3:142666998
|
C | T | 1 | a0001c0002t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.71-2392C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142666998 | ||||||
| chr3:142667392
|
C | T | 2 | a0001c0001t0002g0267a0001c0001t0002g0269 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.71-1998C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142667392 | ||||||
| chr3:142667473
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-1917C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142667473 | ||||||
| chr3:142667948
|
G | A | 1 | a0002c0003t0002g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71-1442G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142667948 | ||||||
| chr3:142668077
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-1313A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142668077 | ||||||
| chr3:142668521
|
G | T | 1 | a0001c0002t0003g0024 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.71-869G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142668521 | ||||||
| chr3:142668566
|
G | T | 5 | a0001c0001t0002g0174a0001c0001t0002g0182a0001c0001t0002g0184others(2): Show | 5 | HG02965.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-824G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142668566 | ||||||
| chr3:142668606
|
CT | C | 20 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(17): Show | 20 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.71-771delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 142668606 | |||||
| chr3:142668872
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0146others(1): Show | 4 | HG00423.hp2 NA18960.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-518G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142668872 | ||||||
| chr3:142668905
|
C | G | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-485C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142668905 | ||||||
| chr3:142668967
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 212 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.71-423A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142668967 | ||||||
| chr3:142669106
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | NA18961.hp2 NA18998.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.71-284G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142669106 | ||||||
| chr3:142669122
|
C | T | 1 | a0001c0001t0015g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.71-268C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142669122 | ||||||
| chr3:142669326
|
A | T | 1 | a0005c0007t0001g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.71-64A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 2/15 | chr3 | 142669326 | ||||||
| chr3:142669671
|
AATG | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.234+135_234+137del others(3): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 142669671 | |||||
| chr3:142669680
|
G | T | 13 | a0001c0001t0001g0271a0001c0001t0002g0259a0001c0001t0002g0261others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.234+127G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142669680 | ||||||
| chr3:142669785
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.234+232A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142669785 | ||||||
| chr3:142669977
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.234+424G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142669977 | ||||||
| chr3:142670047
|
G | GT | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+494_234+495ins others(1): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670047 | ||||||
| chr3:142670482
|
TA | T | 10 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0002g0102others(7): Show | 10 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-502delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 142670482 | |||||
| chr3:142670483
|
A | T | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-510A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670483 | ||||||
| chr3:142670554
|
A | C | 3 | a0001c0001t0003g0147a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02055.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.235-439A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670554 | ||||||
| chr3:142670654
|
G | T | 39 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0183others(36): Show | 39 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.235-339G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670654 | ||||||
| chr3:142670783
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-210A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670783 | ||||||
| chr3:142670827
|
G | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(33): Show | 36 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.235-166G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670827 | ||||||
| chr3:142670833
|
T | C | 6 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-160T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 3/15 | chr3 | 142670833 | ||||||
| chr3:142671159
|
G | T | 13 | a0001c0001t0001g0271a0001c0001t0002g0259a0001c0001t0002g0261others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.364+37G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142671159 | ||||||
| chr3:142671184
|
A | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG01934.hp1 HG02273.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.364+62A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142671184 | ||||||
| chr3:142671296
|
C | A | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.364+174C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142671296 | ||||||
| chr3:142671568
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.364+446C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142671568 | ||||||
| chr3:142671620
|
T | G | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.364+498T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142671620 | ||||||
| chr3:142672173
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.364+1051C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142672173 | ||||||
| chr3:142672339
|
C | CT | 22 | a0001c0001t0001g0015a0001c0001t0001g0204a0001c0001t0001g0208others(19): Show | 22 | HG01123.hp1 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.364+1238dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 142672339 | |||||
| chr3:142672339
|
CT | C | 11 | a0001c0001t0001g0125a0001c0001t0001g0181a0001c0001t0002g0126others(8): Show | 11 | HG01074.hp1 HG01255.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.364+1238delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 142672339 | |||||
| chr3:142672368
|
C | T | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+1246C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142672368 | ||||||
| chr3:142672373
|
C | T | 1 | a0001c0001t0005g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.364+1251C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142672373 | ||||||
| chr3:142672436
|
A | G | 35 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(32): Show | 35 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.364+1314A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142672436 | ||||||
| chr3:142672894
|
G | A | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.364+1772G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142672894 | ||||||
| chr3:142672924
|
AT | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+1805delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 142672924 | |||||
| chr3:142673005
|
A | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.364+1883A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673005 | ||||||
| chr3:142673164
|
C | T | 2 | a0001c0001t0009g0153a0001c0001t0009g0155 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.364+2042C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673164 | ||||||
| chr3:142673177
|
C | A | 13 | a0001c0001t0001g0271a0001c0001t0002g0259a0001c0001t0002g0261others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.364+2055C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673177 | ||||||
| chr3:142673350
|
C | T | 3 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364+2228C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673350 | ||||||
| chr3:142673367
|
T | C | 1 | a0001c0002t0001g0043 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.364+2245T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673367 | ||||||
| chr3:142673474
|
T | C | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.364+2352T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673474 | ||||||
| chr3:142673554
|
T | A | 39 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0183others(36): Show | 39 | HG00280.hp1 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.364+2432T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673554 | ||||||
| chr3:142673754
|
T | TC | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.365-2400dupC | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 142673754 | |||||
| chr3:142673901
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.365-2256A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142673901 | ||||||
| chr3:142674140
|
G | C | 6 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.365-2017G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142674140 | ||||||
| chr3:142674568
|
T | C | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-1589T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142674568 | ||||||
| chr3:142674833
|
A | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0160 | 2 | HG02056.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.365-1324A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142674833 | ||||||
| chr3:142674946
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.365-1211G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142674946 | ||||||
| chr3:142675384
|
TTTTTTG | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(27): Show | 31 | HG00323.hp2 HG00673.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.365-760_365-755del others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 142675384 | |||||
| chr3:142675531
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.365-626C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675531 | ||||||
| chr3:142675682
|
C | T | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-475C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675682 | ||||||
| chr3:142675684
|
G | GT | 13 | a0001c0001t0001g0150a0001c0001t0002g0104a0001c0001t0002g0190others(10): Show | 14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.365-462dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 142675684 | |||||
| chr3:142675729
|
G | C | 1 | a0001c0002t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.365-428G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675729 | ||||||
| chr3:142675778
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 181 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.365-379A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675778 | ||||||
| chr3:142675840
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-317A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675840 | ||||||
| chr3:142675864
|
G | A | 1 | a0002c0003t0008g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.365-293G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675864 | ||||||
| chr3:142675961
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.365-196G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142675961 | ||||||
| chr3:142676111
|
A | G | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.365-46A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 4/15 | chr3 | 142676111 | ||||||
| chr3:142676405
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.497+116C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/15 | chr3 | 142676405 | ||||||
| chr3:142677051
|
C | T | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+762C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/15 | chr3 | 142677051 | ||||||
| chr3:142677396
|
A | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(40): Show | 43 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.498-636A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/15 | chr3 | 142677396 | ||||||
| chr3:142677454
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.498-578G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/15 | chr3 | 142677454 | ||||||
| chr3:142677738
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.498-294A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/15 | chr3 | 142677738 | ||||||
| chr3:142677819
|
C | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0002g0102others(7): Show | 10 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-213C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 5/15 | chr3 | 142677819 | ||||||
| chr3:142678417
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.579+304C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678417 | ||||||
| chr3:142678420
|
C | G | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.579+307C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678420 | ||||||
| chr3:142678507
|
G | A | 13 | a0001c0001t0001g0271a0001c0001t0002g0259a0001c0001t0002g0261others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+394G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678507 | ||||||
| chr3:142678586
|
T | C | 6 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0179others(3): Show | 6 | HG00738.hp2 HG01074.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+473T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678586 | ||||||
| chr3:142678596
|
A | G | 3 | a0001c0002t0001g0233a0001c0002t0001g0251a0001c0002t0001g0257 | 3 | HG02027.hp1 HG02523.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.579+483A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678596 | ||||||
| chr3:142678600
|
A | G | 1 | a0001c0001t0004g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.579+487A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678600 | ||||||
| chr3:142678631
|
C | T | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.579+518C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678631 | ||||||
| chr3:142678771
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.579+658C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678771 | ||||||
| chr3:142678778
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.579+665A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678778 | ||||||
| chr3:142678837
|
C | G | 11 | a0001c0001t0001g0151a0001c0001t0003g0018a0001c0001t0003g0144others(8): Show | 11 | HG00099.hp2 HG00639.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.579+724C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678837 | ||||||
| chr3:142678882
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.579+769C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142678882 | ||||||
| chr3:142679160
|
G | A | 21 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(18): Show | 21 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+1047G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679160 | ||||||
| chr3:142679171
|
T | A | 14 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+1058T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679171 | ||||||
| chr3:142679197
|
C | T | 1 | a0001c0002t0003g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.579+1084C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679197 | ||||||
| chr3:142679228
|
T | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(40): Show | 43 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.579+1115T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679228 | ||||||
| chr3:142679242
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.579+1129T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679242 | ||||||
| chr3:142679275
|
T | G | 3 | a0001c0001t0001g0145a0001c0001t0002g0104a0001c0001t0002g0190 | 3 | HG01934.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.579+1162T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679275 | ||||||
| chr3:142679346
|
C | T | 1 | a0003c0005t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.579+1233C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679346 | ||||||
| chr3:142679383
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1270C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679383 | ||||||
| chr3:142679496
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0100 | 2 | HG00673.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.579+1383A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679496 | ||||||
| chr3:142679559
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.579+1446A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679559 | ||||||
| chr3:142679588
|
A | G | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.579+1475A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679588 | ||||||
| chr3:142679631
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.579+1518A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679631 | ||||||
| chr3:142679686
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.579+1573A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679686 | ||||||
| chr3:142679768
|
G | A | 1 | a0001c0002t0003g0026 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.579+1655G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679768 | ||||||
| chr3:142679782
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.579+1669T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679782 | ||||||
| chr3:142679830
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+1717C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679830 | ||||||
| chr3:142679881
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.579+1768T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679881 | ||||||
| chr3:142679882
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.579+1769G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142679882 | ||||||
| chr3:142680004
|
G | T | 11 | a0002c0003t0001g0152a0002c0003t0002g0103a0002c0003t0002g0114others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.579+1891G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680004 | ||||||
| chr3:142680039
|
G | A | 2 | a0001c0001t0011g0010a0001c0001t0011g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.579+1926G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680039 | ||||||
| chr3:142680111
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.579+1998G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680111 | ||||||
| chr3:142680152
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.579+2039C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680152 | ||||||
| chr3:142680626
|
C | T | 1 | a0001c0001t0006g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.579+2513C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680626 | ||||||
| chr3:142680736
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+2623C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680736 | ||||||
| chr3:142680845
|
G | A | 5 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+2732G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680845 | ||||||
| chr3:142680867
|
G | A | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+2754G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680867 | ||||||
| chr3:142680873
|
C | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.579+2760C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142680873 | ||||||
| chr3:142681049
|
T | C | 10 | a0001c0001t0002g0104a0001c0001t0002g0190a0001c0001t0004g0001others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+2936T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681049 | ||||||
| chr3:142681240
|
C | T | 1 | a0001c0001t0009g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.580-2766C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681240 | ||||||
| chr3:142681249
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.580-2757G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681249 | ||||||
| chr3:142681308
|
AG | A | 11 | a0002c0003t0001g0152a0002c0003t0002g0103a0002c0003t0002g0114others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-2697delG | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681308 | ||||||
| chr3:142681335
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.580-2671A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681335 | ||||||
| chr3:142681488
|
A | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | NA18953.hp2 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.580-2518A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681488 | ||||||
| chr3:142681578
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.580-2428G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142681578 | ||||||
| chr3:142682296
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.580-1710G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142682296 | ||||||
| chr3:142682440
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.580-1566T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142682440 | ||||||
| chr3:142682527
|
T | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1479T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142682527 | ||||||
| chr3:142682646
|
A | C | 17 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.580-1360A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142682646 | ||||||
| chr3:142682702
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | NA18943.hp2 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-1304T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142682702 | ||||||
| chr3:142683198
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0150 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.580-808A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142683198 | ||||||
| chr3:142683241
|
A | C | 1 | a0001c0001t0001g0256 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.580-765A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142683241 | ||||||
| chr3:142683329
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 53 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.580-677G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142683329 | ||||||
| chr3:142683429
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.580-577A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142683429 | ||||||
| chr3:142683559
|
G | A | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-447G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142683559 | ||||||
| chr3:142683855
|
G | GT | 20 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(17): Show | 20 | HG00738.hp1 HG01123.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-140dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 142683855 | |||||
| chr3:142683856
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0137 | 2 | HG02683.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.580-150T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 6/15 | chr3 | 142683856 | ||||||
| chr3:142684400
|
A | G | 8 | a0001c0001t0002g0104a0001c0001t0002g0190a0001c0001t0004g0001others(5): Show | 9 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.888+5A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142684400 | ||||||
| chr3:142684410
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.888+15G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142684410 | ||||||
| chr3:142684573
|
A | T | 11 | a0001c0001t0001g0271a0001c0001t0003g0147a0001c0001t0003g0148others(8): Show | 11 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.888+178A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142684573 | ||||||
| chr3:142684832
|
G | A | 15 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(12): Show | 15 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.888+437G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142684832 | ||||||
| chr3:142684909
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.888+514A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142684909 | ||||||
| chr3:142685041
|
A | G | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.888+646A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685041 | ||||||
| chr3:142685244
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.888+849C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685244 | ||||||
| chr3:142685272
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.888+877G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685272 | ||||||
| chr3:142685467
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.889-817A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685467 | ||||||
| chr3:142685552
|
G | A | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-732G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685552 | ||||||
| chr3:142685641
|
C | T | 1 | a0001c0002t0001g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.889-643C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685641 | ||||||
| chr3:142685662
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.889-622A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685662 | ||||||
| chr3:142685672
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-612A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142685672 | ||||||
| chr3:142686040
|
G | T | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.889-244G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142686040 | ||||||
| chr3:142686053
|
G | A | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-231G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142686053 | ||||||
| chr3:142686201
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.889-83C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142686201 | ||||||
| chr3:142686225
|
C | T | 11 | a0001c0001t0001g0271a0001c0001t0003g0147a0001c0001t0003g0148others(8): Show | 11 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.889-59C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 8/15 | chr3 | 142686225 | ||||||
| chr3:142686506
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(41): Show | 44 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.981+130T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142686506 | ||||||
| chr3:142686573
|
C | A | 2 | a0001c0002t0001g0068a0001c0002t0001g0096 | 2 | HG01346.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.981+197C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142686573 | ||||||
| chr3:142686607
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.981+231G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142686607 | ||||||
| chr3:142686669
|
T | C | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+293T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142686669 | ||||||
| chr3:142686862
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.981+486C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142686862 | ||||||
| chr3:142687144
|
C | G | 1 | a0001c0001t0002g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.981+768C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142687144 | ||||||
| chr3:142687222
|
T | TA | 26 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(23): Show | 26 | HG00423.hp2 HG00738.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.981+860dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142687222 | |||||
| chr3:142687222
|
T | TAAA | 11 | a0001c0001t0001g0271a0001c0001t0003g0147a0001c0001t0003g0148others(8): Show | 11 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+858_981+860dup others(3): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142687222 | |||||
| chr3:142687615
|
A | G | 3 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.981+1239A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142687615 | ||||||
| chr3:142687758
|
C | T | 15 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(12): Show | 15 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.981+1382C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142687758 | ||||||
| chr3:142687929
|
C | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.981+1553C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142687929 | ||||||
| chr3:142687951
|
G | GT | 37 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(34): Show | 38 | HG00323.hp2 HG00621.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.981+1590dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142687951 | |||||
| chr3:142687951
|
G | T | 3 | a0001c0001t0004g0112a0001c0001t0004g0113a0001c0002t0001g0096 | 3 | HG01346.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.981+1575G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142687951 | ||||||
| chr3:142688190
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0146others(1): Show | 4 | HG00423.hp2 NA18960.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-1428C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688190 | ||||||
| chr3:142688228
|
A | G | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-1390A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688228 | ||||||
| chr3:142688235
|
A | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.982-1383A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688235 | ||||||
| chr3:142688258
|
A | G | 1 | a0001c0001t0018g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.982-1360A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688258 | ||||||
| chr3:142688275
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.982-1343A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688275 | ||||||
| chr3:142688521
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.982-1097T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688521 | ||||||
| chr3:142688539
|
C | T | 15 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(12): Show | 15 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.982-1079C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688539 | ||||||
| chr3:142688615
|
T | G | 1 | a0001c0001t0004g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.982-1003T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688615 | ||||||
| chr3:142688817
|
G | A | 15 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(12): Show | 15 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.982-801G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688817 | ||||||
| chr3:142688995
|
G | A | 13 | a0002c0003t0001g0115a0002c0003t0001g0116a0002c0003t0001g0121others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.982-623G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142688995 | ||||||
| chr3:142689160
|
T | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 200 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.982-458T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689160 | ||||||
| chr3:142689185
|
G | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.982-433G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689185 | ||||||
| chr3:142689193
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012 | 3 | NA18747.hp1 NA19005.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.982-425G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689193 | ||||||
| chr3:142689209
|
G | A | 4 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128others(1): Show | 4 | HG01255.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-409G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689209 | ||||||
| chr3:142689222
|
G | A | 15 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0271others(12): Show | 15 | HG00738.hp1 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.982-396G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689222 | ||||||
| chr3:142689380
|
G | A | 2 | a0001c0002t0001g0039a0001c0002t0001g0046 | 2 | NA18964.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.982-238G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689380 | ||||||
| chr3:142689429
|
C | CATAA | 115 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(112): Show | 116 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.982-163_982-160dup others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142689429 | |||||
| chr3:142689429
|
C | CATAAATA others(1): Show |
32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(29): Show | 32 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.982-167_982-160dup others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142689429 | |||||
| chr3:142689429
|
C | CATAAATA others(5): Show |
13 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(10): Show | 13 | HG01243.hp2 HG02145.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.982-171_982-160dup others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142689429 | |||||
| chr3:142689429
|
C | CATAAATA others(9): Show |
1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.982-175_982-160dup others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 142689429 | |||||
| chr3:142689496
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.982-122G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689496 | ||||||
| chr3:142689566
|
A | C | 2 | a0001c0001t0009g0153a0001c0001t0009g0155 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.982-52A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 9/15 | chr3 | 142689566 | ||||||
| chr3:142689969
|
G | C | 1 | a0001c0002t0001g0044 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1177+156G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142689969 | ||||||
| chr3:142690027
|
A | G | 1 | a0001c0002t0003g0023 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1177+214A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690027 | ||||||
| chr3:142690109
|
A | G | 1 | a0001c0002t0012g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1177+296A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690109 | ||||||
| chr3:142690277
|
T | C | 1 | a0002c0003t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1177+464T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690277 | ||||||
| chr3:142690347
|
A | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177+534A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690347 | ||||||
| chr3:142690386
|
G | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1177+573G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690386 | ||||||
| chr3:142690551
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1177+738T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690551 | ||||||
| chr3:142690695
|
T | C | 4 | a0001c0001t0005g0236a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+882T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142690695 | ||||||
| chr3:142691003
|
A | G | 11 | a0001c0001t0001g0106a0001c0001t0002g0102a0001c0001t0002g0122others(8): Show | 11 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1177+1190A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691003 | ||||||
| chr3:142691020
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1177+1207T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691020 | ||||||
| chr3:142691041
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1177+1228C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691041 | ||||||
| chr3:142691100
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | NA18961.hp2 NA18998.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1177+1287G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691100 | ||||||
| chr3:142691179
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0002g0267others(1): Show | 4 | HG00738.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+1366C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691179 | ||||||
| chr3:142691283
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 153 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1177+1470C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691283 | ||||||
| chr3:142691516
|
C | T | 3 | a0003c0005t0001g0129a0003c0005t0002g0127a0003c0005t0008g0128 | 3 | HG01255.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1177+1703C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691516 | ||||||
| chr3:142691602
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1177+1789A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691602 | ||||||
| chr3:142691935
|
A | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(98): Show | 102 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1177+2122A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142691935 | ||||||
| chr3:142692030
|
T | C | 11 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+2217T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692030 | ||||||
| chr3:142692100
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0262 | 2 | HG00738.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1177+2287G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692100 | ||||||
| chr3:142692154
|
A | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 64 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1178-2315A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692154 | ||||||
| chr3:142692176
|
G | A | 1 | a0001c0001t0003g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1178-2293G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692176 | ||||||
| chr3:142692192
|
C | T | 40 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0134others(37): Show | 41 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1178-2277C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692192 | ||||||
| chr3:142692331
|
T | G | 14 | a0001c0001t0001g0175a0001c0001t0001g0181a0001c0001t0001g0196others(11): Show | 14 | HG00621.hp2 HG02027.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1178-2138T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692331 | ||||||
| chr3:142692358
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(42): Show | 46 | HG00323.hp2 HG00621.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1178-2111T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692358 | ||||||
| chr3:142692374
|
A | G | 11 | a0001c0001t0001g0271a0001c0001t0003g0147a0001c0001t0003g0148others(8): Show | 11 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1178-2095A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692374 | ||||||
| chr3:142692445
|
A | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1178-2024A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692445 | ||||||
| chr3:142692893
|
A | G | 2 | a0001c0001t0001g0106a0002c0003t0001g0152 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1178-1576A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692893 | ||||||
| chr3:142692954
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0258 | 2 | HG03942.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1178-1515C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142692954 | ||||||
| chr3:142693263
|
G | C | 1 | a0001c0001t0002g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1178-1206G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142693263 | ||||||
| chr3:142693369
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1178-1100C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142693369 | ||||||
| chr3:142693382
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 25 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1178-1087C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142693382 | ||||||
| chr3:142693809
|
T | TTACTATG others(1): Show |
5 | a0001c0001t0001g0271a0002c0003t0001g0115a0002c0003t0001g0116others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1178-658_1178-651d others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 142693809 | |||||
| chr3:142694119
|
ATT | A | 29 | a0001c0001t0003g0018a0001c0001t0003g0144a0001c0001t0003g0147others(26): Show | 29 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1178-347_1178-346d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 142694119 | |||||
| chr3:142694423
|
G | C | 1 | a0001c0002t0001g0081 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1178-46G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 10/15 | chr3 | 142694423 | ||||||
| chr3:142694565
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 214 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1256+18C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142694565 | ||||||
| chr3:142694758
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 25 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1256+211C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142694758 | ||||||
| chr3:142694805
|
A | C | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1256+258A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142694805 | ||||||
| chr3:142695079
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0002g0107a0001c0001t0002g0108others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1256+532G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695079 | ||||||
| chr3:142695117
|
TTC | T | 31 | a0001c0001t0003g0018a0001c0001t0003g0144a0001c0001t0003g0147others(28): Show | 31 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1256+576_1256+577d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695117 | |||||
| chr3:142695132
|
A | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0182 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1256+585A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695132 | ||||||
| chr3:142695532
|
AAC | A | 3 | a0001c0001t0009g0153a0001c0001t0009g0155a0001c0001t0009g0191 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1256+989_1256+990d others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695532 | |||||
| chr3:142695597
|
T | A | 2 | a0001c0001t0001g0106a0002c0003t0001g0152 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1256+1050T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695597 | ||||||
| chr3:142695755
|
GACTT | G | 23 | a0001c0001t0001g0171a0001c0001t0001g0271a0001c0001t0002g0104others(20): Show | 23 | HG00323.hp2 HG00735.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1256+1214_1256+121 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695755 | |||||
| chr3:142695757
|
CTTACTTA others(1): Show |
C | 57 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0164others(54): Show | 57 | HG00423.hp1 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1256+1214_1256+122 others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695757 | |||||
| chr3:142695757
|
CTTACTTA others(5): Show |
C | 8 | a0001c0001t0001g0002a0001c0001t0001g0194a0001c0001t0001g0204others(5): Show | 10 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1256+1214_1256+122 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695757 | |||||
| chr3:142695757
|
CTTACTTA others(9): Show |
C | 7 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0106others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256+1214_1256+122 others(20): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695757 | |||||
| chr3:142695757
|
CTTACTTA others(13): Show |
C | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(31): Show | 34 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1256+1214_1256+123 others(24): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695757 | |||||
| chr3:142695757
|
CTTACTTA others(21): Show |
C | 14 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(11): Show | 14 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1256+1214_1256+124 others(32): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695757 | |||||
| chr3:142695761
|
C | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+1214C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695761 | ||||||
| chr3:142695761
|
CTTAT | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0076a0001c0001t0001g0101others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1256+1261_1256+126 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695761 | |||||
| chr3:142695761
|
CTTATTTA others(1): Show |
C | 13 | a0001c0001t0001g0125a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00673.hp1 HG01123.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1256+1257_1256+126 others(12): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695761 | |||||
| chr3:142695761
|
CTTATTTA others(5): Show |
C | 6 | a0001c0002t0001g0027a0001c0002t0001g0072a0001c0002t0001g0073others(3): Show | 6 | HG01167.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256+1253_1256+126 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695761 | |||||
| chr3:142695761
|
CTTATTTA others(17): Show |
C | 7 | a0001c0001t0005g0236a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256+1241_1256+126 others(28): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142695761 | |||||
| chr3:142695765
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1256+1218T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695765 | ||||||
| chr3:142695769
|
T | C | 2 | a0001c0001t0001g0009a0001c0002t0001g0192 | 2 | HG02976.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1256+1222T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695769 | ||||||
| chr3:142695864
|
G | A | 2 | a0001c0001t0001g0106a0002c0003t0001g0152 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1256+1317G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695864 | ||||||
| chr3:142695865
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 50 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1256+1318G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695865 | ||||||
| chr3:142695901
|
T | C | 5 | a0001c0001t0001g0271a0002c0003t0001g0115a0002c0003t0001g0116others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+1354T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695901 | ||||||
| chr3:142695936
|
A | G | 1 | a0001c0001t0004g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1256+1389A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142695936 | ||||||
| chr3:142696046
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(54): Show | 58 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1256+1499G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142696046 | ||||||
| chr3:142696476
|
T | G | 1 | a0001c0001t0002g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1257-1477T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142696476 | ||||||
| chr3:142696659
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1257-1294A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142696659 | ||||||
| chr3:142696720
|
A | AAAT | 93 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0098others(90): Show | 94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1257-1195_1257-119 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
A | AAATAAT | 25 | a0001c0001t0001g0099a0001c0001t0001g0151a0001c0001t0001g0171others(22): Show | 25 | HG00323.hp2 HG00741.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1257-1198_1257-119 others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
A | AAATAATA others(2): Show |
11 | a0001c0001t0001g0149a0001c0001t0001g0175a0001c0001t0001g0220others(8): Show | 11 | HG01123.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-1201_1257-119 others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
A | AAATAATA others(5): Show |
1 | a0003c0005t0008g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1257-1204_1257-119 others(16): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
A | AAATAATA others(8): Show |
1 | a0001c0002t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1257-1207_1257-119 others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
AAAT | A | 21 | a0001c0001t0001g0106a0001c0001t0001g0181a0001c0001t0001g0224others(18): Show | 21 | HG01255.hp2 HG01496.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1257-1195_1257-119 others(7): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
AAATAAT | A | 23 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(20): Show | 23 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1257-1198_1257-119 others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
AAATAATA others(2): Show |
A | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(15): Show | 18 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1257-1201_1257-119 others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696720
|
AAATAATA others(8): Show |
A | 1 | a0001c0002t0001g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1257-1207_1257-119 others(19): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 142696720 | |||||
| chr3:142696758
|
A | C | 33 | a0001c0001t0001g0106a0001c0001t0002g0102a0001c0001t0002g0104others(30): Show | 33 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1257-1195A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142696758 | ||||||
| chr3:142696759
|
T | C | 33 | a0001c0001t0001g0106a0001c0001t0002g0102a0001c0001t0002g0104others(30): Show | 33 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1257-1194T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142696759 | ||||||
| chr3:142696854
|
GA | G | 3 | a0001c0001t0002g0158a0001c0001t0002g0267a0001c0001t0002g0269 | 3 | HG00735.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1257-1098delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142696854 | ||||||
| chr3:142697011
|
A | G | 1 | a0001c0002t0001g0044 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1257-942A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142697011 | ||||||
| chr3:142697299
|
G | A | 3 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124 | 3 | HG03017.hp2 HG03688.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1257-654G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142697299 | ||||||
| chr3:142697657
|
G | A | 1 | a0001c0002t0012g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1257-296G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142697657 | ||||||
| chr3:142697731
|
G | A | 16 | a0001c0001t0003g0018a0001c0001t0003g0144a0001c0001t0003g0273others(13): Show | 16 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1257-222G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 11/15 | chr3 | 142697731 | ||||||
| chr3:142698214
|
G | T | 16 | a0001c0001t0003g0018a0001c0001t0003g0144a0001c0001t0003g0273others(13): Show | 16 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1371+147G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142698214 | ||||||
| chr3:142698228
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1371+161G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142698228 | ||||||
| chr3:142698420
|
C | G | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1371+353C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142698420 | ||||||
| chr3:142698437
|
T | TA | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 61 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1371+385dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 142698437 | |||||
| chr3:142698437
|
TA | T | 43 | a0001c0001t0001g0227a0001c0001t0001g0252a0001c0001t0002g0102others(40): Show | 43 | HG00735.hp1 HG01070.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.1371+385delA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 142698437 | |||||
| chr3:142698853
|
G | A | 1 | a0002c0003t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1371+786G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142698853 | ||||||
| chr3:142698858
|
A | G | 6 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 6 | HG01192.hp2 NA18971.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1371+791A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142698858 | ||||||
| chr3:142698962
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1371+895T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142698962 | ||||||
| chr3:142699384
|
G | A | 2 | a0001c0001t0001g0106a0002c0003t0001g0152 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1371+1317G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142699384 | ||||||
| chr3:142699410
|
G | A | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1371+1343G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142699410 | ||||||
| chr3:142699789
|
A | T | 2 | a0001c0001t0001g0106a0002c0003t0001g0152 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1371+1722A>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142699789 | ||||||
| chr3:142699927
|
A | G | 3 | a0001c0001t0008g0130a0002c0003t0008g0097a0003c0005t0008g0128 | 3 | HG02630.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1371+1860A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142699927 | ||||||
| chr3:142700317
|
T | TTTTA | 29 | a0001c0001t0002g0102a0001c0001t0002g0107a0001c0001t0002g0108others(26): Show | 29 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1371+2270_1371+227 others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 142700317 | |||||
| chr3:142700408
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1371+2341T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700408 | ||||||
| chr3:142700413
|
C | G | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1371+2346C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700413 | ||||||
| chr3:142700471
|
C | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 84 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1371+2404C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700471 | ||||||
| chr3:142700483
|
C | T | 2 | a0001c0001t0006g0265a0001c0001t0006g0266 | 2 | HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1371+2416C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700483 | ||||||
| chr3:142700531
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1371+2464G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700531 | ||||||
| chr3:142700532
|
C | A | 1 | a0001c0002t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1371+2465C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700532 | ||||||
| chr3:142700581
|
G | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 273 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.1371+2514G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700581 | ||||||
| chr3:142700818
|
C | G | 1 | a0001c0002t0001g0257 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1371+2751C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142700818 | ||||||
| chr3:142701371
|
C | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 25 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1372-2497C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701371 | ||||||
| chr3:142701467
|
T | A | 5 | a0001c0001t0001g0271a0002c0003t0001g0115a0002c0003t0001g0116others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-2401T>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701467 | ||||||
| chr3:142701629
|
G | A | 7 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 8 | HG02280.hp2 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1372-2239G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701629 | ||||||
| chr3:142701775
|
G | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0163others(16): Show | 20 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1372-2093G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701775 | ||||||
| chr3:142701841
|
C | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1372-2027C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701841 | ||||||
| chr3:142701958
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1372-1910A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701958 | ||||||
| chr3:142701985
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1372-1883C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142701985 | ||||||
| chr3:142702044
|
A | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 50 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1372-1824A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702044 | ||||||
| chr3:142702117
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1372-1751C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702117 | ||||||
| chr3:142702145
|
C | G | 1 | a0001c0002t0001g0021 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1372-1723C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702145 | ||||||
| chr3:142702395
|
C | A | 1 | a0001c0002t0001g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1372-1473C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702395 | ||||||
| chr3:142702743
|
G | A | 4 | a0001c0001t0002g0102a0001c0001t0002g0259a0001c0001t0002g0260others(1): Show | 4 | HG01175.hp2 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-1125G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702743 | ||||||
| chr3:142702787
|
G | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0160a0001c0002t0001g0034 | 3 | HG02056.hp2 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1372-1081G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702787 | ||||||
| chr3:142702889
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 25 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1372-979C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702889 | ||||||
| chr3:142702985
|
T | C | 17 | a0001c0001t0001g0175a0001c0001t0001g0181a0001c0001t0001g0196others(14): Show | 17 | HG00621.hp2 HG02027.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1372-883T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142702985 | ||||||
| chr3:142703163
|
T | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 118 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1372-705T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142703163 | ||||||
| chr3:142703172
|
T | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(15): Show | 18 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1372-696T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142703172 | ||||||
| chr3:142703289
|
AT | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0032others(107): Show | 110 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.1372-556delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 142703289 | |||||
| chr3:142703289
|
ATTT | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(21): Show | 24 | HG00673.hp2 HG00738.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1372-558_1372-556d others(5): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 142703289 | |||||
| chr3:142703289
|
ATTTT | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1372-559_1372-556d others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 142703289 | |||||
| chr3:142703823
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1372-45T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 12/15 | chr3 | 142703823 | ||||||
| chr3:142704363
|
A | G | 8 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0137others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-100A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 13/15 | chr3 | 142704363 | ||||||
| chr3:142704635
|
A | AT | 30 | a0001c0001t0001g0009a0001c0001t0001g0101a0001c0001t0001g0134others(27): Show | 30 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1629+79dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
A | ATT | 7 | a0001c0001t0001g0219a0001c0001t0002g0109a0001c0001t0002g0126others(4): Show | 7 | HG00621.hp2 HG01261.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1629+78_1629+79dup others(2): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
A | ATTTT | 16 | a0001c0001t0001g0106a0001c0001t0001g0159a0001c0001t0001g0198others(13): Show | 16 | HG00597.hp1 HG01070.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1629+76_1629+79dup others(4): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
A | ATTTTT | 13 | a0001c0001t0001g0162a0001c0001t0001g0169a0001c0001t0001g0183others(10): Show | 13 | HG01243.hp1 HG01255.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.1629+75_1629+79dup others(5): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
A | ATTTTTTT others(1): Show |
10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG00099.hp2 HG01243.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1629+72_1629+79dup others(8): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
A | ATTTTTTT others(2): Show |
11 | a0001c0001t0003g0018a0001c0001t0003g0199a0001c0001t0006g0264others(8): Show | 11 | HG00423.hp1 HG01070.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1629+71_1629+79dup others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
A | ATTTTTTT others(3): Show |
6 | a0001c0001t0006g0265a0001c0001t0006g0270a0001c0001t0008g0130others(3): Show | 6 | HG01123.hp1 HG01258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1629+70_1629+79dup others(10): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
AT | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 51 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1629+79delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
ATT | A | 7 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0145others(4): Show | 7 | HG01884.hp2 HG01934.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1629+78_1629+79del others(2): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704635
|
ATTTTTTT others(6): Show |
A | 5 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+67_1629+79del others(13): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704635 | |||||
| chr3:142704692
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1629+106A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142704692 | ||||||
| chr3:142704752
|
C | G | 1 | a0001c0002t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1629+166C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142704752 | ||||||
| chr3:142704815
|
AT | A | 33 | a0001c0001t0001g0106a0001c0001t0003g0018a0001c0001t0003g0144others(30): Show | 33 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1629+245delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142704815 | |||||
| chr3:142704866
|
G | T | 2 | a0001c0002t0003g0062a0001c0002t0003g0064 | 2 | NA18950.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1629+280G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142704866 | ||||||
| chr3:142704901
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 25 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1629+315G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142704901 | ||||||
| chr3:142705094
|
C | T | 3 | a0001c0001t0009g0153a0001c0001t0009g0155a0001c0001t0009g0191 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1629+508C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142705094 | ||||||
| chr3:142705699
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(116): Show | 120 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1629+1113C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142705699 | ||||||
| chr3:142705915
|
T | G | 29 | a0001c0001t0003g0018a0001c0001t0003g0144a0001c0001t0003g0147others(26): Show | 29 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1629+1329T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142705915 | ||||||
| chr3:142705953
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0261 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1629+1367C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142705953 | ||||||
| chr3:142706183
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1629+1597A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706183 | ||||||
| chr3:142706306
|
G | A | 7 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 8 | HG02280.hp2 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+1720G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706306 | ||||||
| chr3:142706384
|
G | A | 7 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 8 | HG02280.hp2 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+1798G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706384 | ||||||
| chr3:142706482
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1629+1896C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706482 | ||||||
| chr3:142706510
|
T | C | 3 | a0001c0001t0009g0153a0001c0001t0009g0155a0001c0001t0009g0191 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1629+1924T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706510 | ||||||
| chr3:142706631
|
G | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(83): Show | 87 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1629+2045G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706631 | ||||||
| chr3:142706683
|
G | T | 1 | a0001c0002t0001g0068 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1629+2097G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706683 | ||||||
| chr3:142706740
|
A | G | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1629+2154A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706740 | ||||||
| chr3:142706921
|
A | G | 8 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1629+2335A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142706921 | ||||||
| chr3:142707054
|
A | G | 2 | a0002c0003t0002g0254a0002c0003t0002g0255 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1629+2468A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142707054 | ||||||
| chr3:142707118
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1629+2532G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142707118 | ||||||
| chr3:142707218
|
G | A | 13 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(10): Show | 13 | HG00673.hp2 HG00738.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1629+2632G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142707218 | ||||||
| chr3:142707352
|
C | CATAAA | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1629+2767_1629+277 others(9): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142707352 | |||||
| chr3:142707638
|
A | G | 3 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124 | 3 | HG03017.hp2 HG03688.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1629+3052A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142707638 | ||||||
| chr3:142708041
|
T | C | 8 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0137others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+3455T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708041 | ||||||
| chr3:142708155
|
G | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0094 | 2 | HG00621.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1630-3346G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708155 | ||||||
| chr3:142708241
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1630-3260T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708241 | ||||||
| chr3:142708258
|
T | C | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1630-3243T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708258 | ||||||
| chr3:142708447
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1630-3054C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708447 | ||||||
| chr3:142708495
|
CTTGGCCT others(9): Show |
C | 3 | a0001c0001t0008g0130a0002c0003t0008g0097a0003c0005t0008g0128 | 3 | HG02630.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1630-3001_1630-298 others(20): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142708495 | |||||
| chr3:142708761
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1630-2740G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708761 | ||||||
| chr3:142708894
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 118 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1630-2607A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708894 | ||||||
| chr3:142708967
|
C | A | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1630-2534C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708967 | ||||||
| chr3:142708967
|
C | G | 2 | a0001c0001t0001g0271a0003c0005t0001g0129 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1630-2534C>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142708967 | ||||||
| chr3:142709539
|
G | A | 1 | a0001c0002t0003g0065 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1630-1962G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709539 | ||||||
| chr3:142709571
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1630-1930C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709571 | ||||||
| chr3:142709573
|
G | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(89): Show | 93 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1630-1928G>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709573 | ||||||
| chr3:142709598
|
C | T | 2 | a0001c0001t0001g0106a0002c0003t0001g0152 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1630-1903C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709598 | ||||||
| chr3:142709636
|
G | A | 3 | a0001c0001t0008g0130a0002c0003t0008g0097a0003c0005t0008g0128 | 3 | HG02630.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1630-1865G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709636 | ||||||
| chr3:142709686
|
C | T | 1 | a0001c0002t0019g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1630-1815C>T | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709686 | ||||||
| chr3:142709722
|
C | A | 7 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 8 | HG02280.hp2 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630-1779C>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709722 | ||||||
| chr3:142709816
|
C | CA | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1630-1669dupA | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142709816 | |||||
| chr3:142709816
|
C | CAA | 10 | a0001c0001t0002g0126a0001c0001t0004g0001a0001c0001t0004g0112others(7): Show | 11 | HG01255.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1630-1670_1630-166 others(6): Show |
PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142709816 | |||||
| chr3:142709834
|
T | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0207 | 2 | NA18973.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1630-1667T>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709834 | ||||||
| chr3:142709852
|
A | G | 6 | a0001c0001t0001g0237a0001c0002t0001g0036a0001c0002t0001g0037others(3): Show | 6 | HG00673.hp1 NA18943.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630-1649A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709852 | ||||||
| chr3:142709994
|
A | G | 31 | a0001c0001t0002g0102a0001c0001t0002g0104a0001c0001t0002g0107others(28): Show | 31 | HG00735.hp1 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1630-1507A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142709994 | ||||||
| chr3:142710084
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1630-1417G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710084 | ||||||
| chr3:142710153
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1630-1348T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710153 | ||||||
| chr3:142710167
|
C | CT | 10 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0004g0001others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1630-1316dupT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142710167 | |||||
| chr3:142710167
|
CT | C | 6 | a0001c0001t0001g0105a0001c0001t0001g0213a0001c0002t0012g0088others(3): Show | 6 | HG01255.hp1 HG01433.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630-1316delT | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 142710167 | |||||
| chr3:142710330
|
G | A | 7 | a0001c0001t0004g0001a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 8 | HG02280.hp2 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630-1171G>A | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710330 | ||||||
| chr3:142710447
|
G | C | 4 | a0001c0001t0009g0153a0001c0001t0009g0155a0001c0001t0009g0191others(1): Show | 4 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-1054G>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710447 | ||||||
| chr3:142710462
|
A | G | 2 | a0001c0002t0001g0037a0001c0002t0001g0069 | 2 | NA18999.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1630-1039A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710462 | ||||||
| chr3:142710510
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1630-991T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710510 | ||||||
| chr3:142710592
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1630-909A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710592 | ||||||
| chr3:142710604
|
T | C | 1 | a0003c0005t0012g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1630-897T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710604 | ||||||
| chr3:142710638
|
T | C | 2 | a0001c0002t0012g0088a0003c0005t0012g0133 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1630-863T>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710638 | ||||||
| chr3:142710912
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1630-589A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710912 | ||||||
| chr3:142710938
|
A | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 50 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1630-563A>C | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142710938 | ||||||
| chr3:142711329
|
A | G | 5 | a0001c0001t0001g0271a0002c0003t0001g0115a0002c0003t0001g0116others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-172A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142711329 | ||||||
| chr3:142711422
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1630-79A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 14/15 | chr3 | 142711422 | ||||||
| chr3:142711655
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1754+30A>G | PLS1 | ENSG00000120756.13 | transcript | ENST00000457734.7 | protein_coding | 15/15 | chr3 | 142711655 |