Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5830 |
|---|---|
| ensemblid | ENSG00000139197.11 |
| hgncid | 9719 |
| symbol | PEX5 |
| name | peroxisomal biogenesis factor 5 |
| refseq_nuc | NM_001351132.2 |
| refseq_prot | NP_001338061.1 |
| ensembl_nuc | ENST00000675855.1 |
| ensembl_prot | ENSP00000502374.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7189686 |
| end | 7211459 |
| strand | + |
| ver | v1.2 |
| region | chr12:7189686-7211459 |
| region5000 | chr12:7184686-7216459 |
| regionname0 | PEX5_chr12_7189686_7211459 |
| regionname5000 | PEX5_chr12_7184686_7216459 |
| 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 | 0/0 | 635 | 379 | 80 | 64 | 183 | 15 | 37 | 148 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002 | 1/0 | 639 | 36 | 14 | 4 | 10 | 1 | 6 | 3 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0003 | 0/0 | 635 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0004 | 0/0 | 654 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0005 | 0/0 | 639 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0006 | 0/0 | 635 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0007 | 0/1 | 635 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0008 | 0/0 | 635 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0009 | 0/0 | 635 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| 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 | 1908 | 376 | 79 | 64 | 181 | 15 | 37 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0002 | 1/0 | 1920 | 36 | 14 | 4 | 10 | 1 | 6 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0003 | 0/0 | 1908 | 4 | 4 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0004 | 0/0 | 1965 | 3 | 0 | 0 | 2 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0005 | 0/0 | 1908 | 2 | 1 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0006 | 0/0 | 1920 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0007 | 0/1 | 1908 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0008 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0009 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0010 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| c0011 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| 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 | 0/0 | 1318 | 144 | 16 | 39 | 66 | 4 | 19 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0002 | 1/0 | 1318 | 124 | 20 | 13 | 75 | 8 | 7 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0003 | 0/1 | 1319 | 53 | 3 | 8 | 31 | 1 | 9 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0004 | 0/0 | 1319 | 39 | 36 | 3 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0005 | 0/0 | 1319 | 24 | 5 | 4 | 6 | 2 | 7 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0006 | 0/0 | 1318 | 12 | 0 | 0 | 12 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0007 | 0/0 | 1320 | 8 | 8 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0008 | 0/0 | 1318 | 8 | 8 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0009 | 0/0 | 1318 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0010 | 0/0 | 1318 | 3 | 0 | 0 | 2 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0011 | 0/0 | 1319 | 2 | 0 | 0 | 0 | 0 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0012 | 0/0 | 1318 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0013 | 0/0 | 1319 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0014 | 0/0 | 1318 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0015 | 0/0 | 1318 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0016 | 0/0 | 1318 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0017 | 0/0 | 1319 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0018 | 0/0 | 1318 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| t0019 | 0/0 | 1321 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| 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 | 7 | 0 | 0 | 7 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0328 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| 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 | 1908 | 376 | 79 | 64 | 181 | 15 | 37 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0005 | 0/0 | 1908 | 2 | 1 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0010 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002 | 1/0 | 1920 | 36 | 14 | 4 | 10 | 1 | 6 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0003c0003 | 0/0 | 1908 | 4 | 4 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0004c0004 | 0/0 | 1965 | 3 | 0 | 0 | 2 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0005c0006 | 0/0 | 1920 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0006c0009 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0007c0007 | 0/1 | 1908 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0008c0008 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0009c0011 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3225 | 140 | 15 | 39 | 63 | 4 | 19 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0002 | 0/0 | 3225 | 109 | 10 | 12 | 72 | 8 | 7 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0003 | 0/0 | 3226 | 51 | 3 | 8 | 30 | 1 | 9 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0004 | 0/0 | 3226 | 34 | 31 | 3 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0005 | 0/0 | 3226 | 4 | 2 | 1 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0006 | 0/0 | 3225 | 12 | 0 | 0 | 12 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0007 | 0/0 | 3227 | 7 | 7 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0008 | 0/0 | 3225 | 8 | 8 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0010 | 0/0 | 3225 | 3 | 0 | 0 | 2 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0011 | 0/0 | 3226 | 2 | 0 | 0 | 0 | 0 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0013 | 0/0 | 3226 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0015 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0016 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0017 | 0/0 | 3226 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0018 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0001t0019 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0005t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0005t0012 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0001c0010t0002 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0001 | 0/0 | 3237 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0002 | 1/0 | 3237 | 10 | 8 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0004 | 0/0 | 3238 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0005 | 0/0 | 3238 | 19 | 3 | 3 | 6 | 1 | 6 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0007 | 0/0 | 3239 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0009 | 0/0 | 3237 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0002c0002t0014 | 0/0 | 3237 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0003c0003t0004 | 0/0 | 3226 | 4 | 4 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0004c0004t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0004c0004t0003 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0004c0004t0005 | 0/0 | 3283 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0005c0006t0002 | 0/0 | 3237 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0006c0009t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0007c0007t0003 | 0/1 | 3226 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0008c0008t0002 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| a0009c0011t0002 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | copy fasta | chr12 | 7184686 | 7216459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0007g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0008g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0010g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0010g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0011g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0013g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0015g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0017g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0018g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0005t0012g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0001c0010t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0328 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0009g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0009g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0009g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0002c0002t0014g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0003c0003t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0003c0003t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0003c0003t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0004c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0004c0004t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0004c0004t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0005c0006t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0005c0006t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0006c0009t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0007c0007t0003g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0008c0008t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| a0009c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0200 | EUR | GBR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | GBR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0207 | EUR | FIN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0264 | EUR | FIN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00408 | hp2 | a0008 | c0008 | t0002 | g0252 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00597 | hp2 | a0002 | c0002 | t0005 | g0324 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00621 | hp2 | a0002 | c0002 | t0005 | g0322 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0187 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00735 | hp2 | a0002 | c0002 | t0005 | g0020 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01070 | hp2 | a0002 | c0002 | t0005 | g0313 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01109 | hp2 | a0002 | c0002 | t0005 | g0316 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0208 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | IBS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0231 | EUR | IBS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | IBS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0288 | EUR | IBS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02056 | hp2 | a0002 | c0002 | t0009 | g0335 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02080 | hp1 | a0009 | c0011 | t0002 | g0002 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02083 | hp1 | a0002 | c0002 | t0005 | g0045 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02129 | hp2 | a0002 | c0002 | t0005 | g0323 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02155 | hp1 | a0002 | c0002 | t0005 | g0045 | EAS | CDX | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CDX | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02165 | hp2 | a0002 | c0002 | t0005 | g0310 | EAS | CDX | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0327 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0306 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02280 | hp1 | a0002 | c0002 | t0005 | g0312 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02451 | hp1 | a0002 | c0002 | t0005 | g0315 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02572 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0307 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0301 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02717 | hp1 | a0001 | c0005 | t0012 | g0294 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02735 | hp1 | a0002 | c0002 | t0005 | g0020 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02886 | hp1 | a0002 | c0002 | t0004 | g0326 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02970 | hp2 | a0003 | c0003 | t0004 | g0293 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0226 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0308 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03486 | hp1 | a0002 | c0002 | t0007 | g0325 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03486 | hp2 | a0005 | c0006 | t0002 | g0330 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03579 | hp2 | a0001 | c0001 | t0017 | g0204 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03654 | hp2 | a0004 | c0004 | t0005 | g0311 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03688 | hp2 | a0001 | c0001 | t0011 | g0021 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03710 | hp1 | a0002 | c0002 | t0005 | g0319 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03831 | hp2 | a0002 | c0002 | t0005 | g0314 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03927 | hp2 | a0002 | c0002 | t0005 | g0321 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03942 | hp1 | a0002 | c0002 | t0005 | g0318 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04204 | hp2 | a0002 | c0002 | t0005 | g0320 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0021 | SAS | STU | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | YRI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | YRI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18612 | hp2 | a0001 | c0005 | t0001 | g0008 | EAS | CHB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CHB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | YRI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18906 | hp2 | a0005 | c0006 | t0002 | g0331 | AFR | YRI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18940 | hp2 | a0001 | c0001 | t0016 | g0012 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18952 | hp1 | a0004 | c0004 | t0001 | g0161 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18977 | hp2 | a0001 | c0010 | t0002 | g0019 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18988 | hp2 | a0001 | c0001 | t0018 | g0052 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19004 | hp2 | a0002 | c0002 | t0009 | g0332 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19005 | hp1 | a0006 | c0009 | t0001 | g0102 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0230 | AFR | LWK | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19043 | hp2 | a0003 | c0003 | t0004 | g0299 | AFR | LWK | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19056 | hp1 | a0001 | c0001 | t0010 | g0295 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0060 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19064 | hp2 | a0004 | c0004 | t0003 | g0309 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19081 | hp2 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19084 | hp2 | a0002 | c0002 | t0014 | g0333 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19085 | hp1 | a0002 | c0002 | t0009 | g0334 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0329 | AFR | YRI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | ASW | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20129 | hp2 | a0003 | c0003 | t0004 | g0044 | AFR | ASW | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20752 | hp2 | a0002 | c0002 | t0005 | g0020 | EUR | TSI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0168 | EUR | TSI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20805 | hp2 | a0001 | c0001 | t0010 | g0296 | EUR | TSI | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | GIH | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02486 | hp1 | a0003 | c0003 | t0004 | g0044 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0317 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | ACB | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | MSL | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | USA | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | USA | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | LWK | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | LWK | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0007 | t0003 | g0197 | REF | REF | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0328 | REF | REF | PEX5_chr12_7184686_7216459 | PEX5 | chr12 | 7184686 | 7216459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7202252
|
C | G | 1 | a0009 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.654C>G | p.Phe218Leu | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 8/16 | 735/3237 | 654/1920 | 218/639 | chr12 | 7202252 | ||
| chr12:7202673
|
T | C | 1 | a0003 | 4 | HG02486.hp1 HG02970.hp2 NA19043.hp2 others(1): Show |
missense_variant | MODERATE | c.815T>C | p.Met272Thr | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/16 | 896/3237 | 815/1920 | 272/639 | chr12 | 7202673 | ||
| chr12:7207690
|
G | A | 1 | a0005 | 2 | HG03486.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.998G>A | p.Arg333His | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 11/16 | 1079/3237 | 998/1920 | 333/639 | chr12 | 7207690 | ||
| chr12:7208644
|
C | T | 1 | a0006 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1369C>T | p.Arg457Cys | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 13/16 | 1450/3237 | 1369/1920 | 457/639 | chr12 | 7208644 | ||
| chr12:7209169
|
A | G | 1 | a0008 | 1 | HG00408.hp2 | missense_variant&splice_region_variant | MODERATE | c.1559A>G | p.Asn520Ser | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/16 | 1640/3237 | 1559/1920 | 520/639 | chr12 | 7209169 | ||
| chr12:7210117
|
G | A | 1 | a0007 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1814G>A | p.Ser605Asn | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 1895/3237 | 1814/1920 | 605/639 | chr12 | 7210117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7202291
|
C | T | 1 | a0001c0010 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.693C>T | p.Ser231Ser | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 8/16 | 774/3237 | 693/1920 | 231/639 | chr12 | 7202291 | ||
| chr12:7209754
|
G | A | 1 | a0001c0005 | 2 | HG02717.hp1 NA18612.hp2 |
synonymous_variant | LOW | c.1632G>A | p.Ala544Ala | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 15/16 | 1713/3237 | 1632/1920 | 544/639 | chr12 | 7209754 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7189747
|
C | G | 9 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(6): Show | 160 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(157): Show |
5_prime_UTR_variant | MODIFIER | c.-20C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/16 | 631 | chr12 | 7189747 | |||||
| chr12:7210243
|
G | C | 1 | a0001c0005t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 20 | chr12 | 7210243 | |||||
| chr12:7210298
|
G | A | 2 | a0001c0001t0007a0002c0002t0007 | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*75G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 75 | chr12 | 7210298 | |||||
| chr12:7210337
|
C | T | 1 | a0001c0001t0017 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 114 | chr12 | 7210337 | |||||
| chr12:7210364
|
G | A | 4 | a0001c0001t0003a0001c0001t0013a0004c0004t0003others(1): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 141 | chr12 | 7210364 | |||||
| chr12:7210685
|
G | C | 2 | a0002c0002t0009a0002c0002t0014 | 4 | HG02056.hp2 NA19004.hp2 NA19084.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*462G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 462 | chr12 | 7210685 | |||||
| chr12:7210851
|
G | A | 4 | a0001c0001t0005a0001c0001t0011a0002c0002t0005others(1): Show | 26 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*628G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 628 | chr12 | 7210851 | |||||
| chr12:7210851
|
G | C | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 628 | chr12 | 7210851 | |||||
| chr12:7210866
|
C | T | 1 | a0001c0001t0016 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 643 | chr12 | 7210866 | |||||
| chr12:7210918
|
G | C | 1 | a0001c0001t0018 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 695 | chr12 | 7210918 | |||||
| chr12:7210978
|
C | G | 13 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(10): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*755C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 755 | chr12 | 7210978 | |||||
| chr12:7210990
|
G | A | 1 | a0001c0001t0013 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 767 | chr12 | 7210990 | |||||
| chr12:7211016
|
A | AAG | 3 | a0001c0001t0007a0001c0001t0019a0002c0002t0007 | 9 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*794_*795dupAG | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 796 | INFO_REALIGN_3_PRIME | chr12 | 7211016 | ||||
| chr12:7211183
|
C | G | 1 | a0001c0001t0008 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 960 | chr12 | 7211183 | |||||
| chr12:7211260
|
G | T | 1 | a0002c0002t0014 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1037G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 1037 | chr12 | 7211260 | |||||
| chr12:7211320
|
T | C | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1097T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 1097 | chr12 | 7211320 | |||||
| chr12:7211347
|
A | AT | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(10): Show | 121 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1134dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 16/16 | 1135 | INFO_REALIGN_3_PRIME | chr12 | 7211347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7189771
|
GGGCCCGG others(10): Show |
G | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 156 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-17+22_-17+38delGG others(15): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7189771 | ||||||
| chr12:7189790
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 156 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-17+40T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7189790 | ||||||
| chr12:7189852
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-17+102G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7189852 | ||||||
| chr12:7189901
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 12 | NA18940.hp1 NA18942.hp2 NA18966.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17+151G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7189901 | ||||||
| chr12:7189938
|
T | C | 5 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(2): Show | 6 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17+188T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7189938 | ||||||
| chr12:7190023
|
G | T | 1 | a0001c0001t0002g0048 | 2 | NA18971.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-17+273G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7190023 | ||||||
| chr12:7190040
|
T | A | 9 | a0001c0001t0002g0029a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 10 | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17+290T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7190040 | ||||||
| chr12:7190262
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056 | 5 | HG00642.hp2 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16-100G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 1/15 | chr12 | 7190262 | ||||||
| chr12:7190512
|
G | GGCCTCTG others(38): Show |
3 | a0004c0004t0001g0161a0004c0004t0003g0309a0004c0004t0005g0311 | 3 | HG03654.hp2 NA18952.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.147+77_147+121dupC others(44): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 7190512 | |||||
| chr12:7190512
|
GGCCTCTG others(38): Show |
G | 303 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.147+77_147+121delC others(44): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 7190512 | |||||
| chr12:7190628
|
A | C | 5 | a0001c0001t0002g0304a0001c0001t0004g0003a0001c0001t0004g0302others(2): Show | 11 | HG02055.hp2 HG02451.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+104A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 2/15 | chr12 | 7190628 | ||||||
| chr12:7190672
|
T | G | 3 | a0002c0002t0002g0306a0002c0002t0002g0307a0002c0002t0002g0308 | 3 | HG02258.hp2 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.147+148T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 2/15 | chr12 | 7190672 | ||||||
| chr12:7190785
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.148-103C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 2/15 | chr12 | 7190785 | ||||||
| chr12:7190821
|
A | T | 2 | a0001c0001t0003g0300a0001c0001t0003g0301 | 2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.148-67A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 2/15 | chr12 | 7190821 | ||||||
| chr12:7191090
|
G | A | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.184-136G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 3/15 | chr12 | 7191090 | ||||||
| chr12:7191823
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.448+123A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7191823 | ||||||
| chr12:7191869
|
A | G | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.448+169A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7191869 | ||||||
| chr12:7191874
|
A | T | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.448+174A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7191874 | ||||||
| chr12:7192109
|
G | A | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+409G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192109 | ||||||
| chr12:7192141
|
A | G | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+441A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192141 | ||||||
| chr12:7192157
|
T | C | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+457T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192157 | ||||||
| chr12:7192206
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.448+506A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192206 | ||||||
| chr12:7192220
|
C | G | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+520C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192220 | ||||||
| chr12:7192344
|
T | C | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+644T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192344 | ||||||
| chr12:7192440
|
A | C | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+740A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192440 | ||||||
| chr12:7192604
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.448+904G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192604 | ||||||
| chr12:7192612
|
T | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(218): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.448+912T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192612 | ||||||
| chr12:7192666
|
G | A | 3 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178 | 3 | HG01099.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.448+966G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192666 | ||||||
| chr12:7192762
|
C | G | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+1062C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192762 | ||||||
| chr12:7192964
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+1264A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192964 | ||||||
| chr12:7192988
|
C | T | 1 | a0001c0005t0012g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.448+1288C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7192988 | ||||||
| chr12:7193234
|
C | CT | 17 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0002g0291others(14): Show | 20 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.448+1553dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7193234 | |||||
| chr12:7193234
|
C | CTT | 6 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+1552_448+1553d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7193234 | |||||
| chr12:7193234
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+1542_448+1553d others(14): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7193234 | |||||
| chr12:7193234
|
CT | C | 167 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.448+1553delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7193234 | |||||
| chr12:7193234
|
CTT | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 12 | HG03041.hp2 NA18940.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.448+1552_448+1553d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7193234 | |||||
| chr12:7193292
|
G | A | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.448+1592G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193292 | ||||||
| chr12:7193313
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0297 | 3 | HG02895.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.448+1613A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193313 | ||||||
| chr12:7193433
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.448+1733C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193433 | ||||||
| chr12:7193509
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.448+1809C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193509 | ||||||
| chr12:7193526
|
G | A | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.448+1826G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193526 | ||||||
| chr12:7193534
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.448+1834G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193534 | ||||||
| chr12:7193595
|
A | T | 44 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(41): Show | 63 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.448+1895A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193595 | ||||||
| chr12:7193934
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(145): Show | 174 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.448+2234G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193934 | ||||||
| chr12:7193952
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0297 | 3 | HG02895.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.448+2252T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7193952 | ||||||
| chr12:7194038
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.448+2338G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194038 | ||||||
| chr12:7194249
|
A | G | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+2549A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194249 | ||||||
| chr12:7194395
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.448+2695T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194395 | ||||||
| chr12:7194567
|
TGAA | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+2869_448+2871d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7194567 | |||||
| chr12:7194575
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.448+2875A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194575 | ||||||
| chr12:7194614
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.448+2914G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194614 | ||||||
| chr12:7194682
|
T | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.448+2982T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194682 | ||||||
| chr12:7194843
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.448+3143G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194843 | ||||||
| chr12:7194911
|
T | G | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.448+3211T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194911 | ||||||
| chr12:7194913
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.448+3213A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194913 | ||||||
| chr12:7194938
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.448+3238G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194938 | ||||||
| chr12:7194948
|
G | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+3248G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194948 | ||||||
| chr12:7194948
|
G | T | 1 | a0001c0001t0004g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.448+3248G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7194948 | ||||||
| chr12:7195008
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.448+3308T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195008 | ||||||
| chr12:7195147
|
T | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.448+3447T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195147 | ||||||
| chr12:7195206
|
C | T | 3 | a0001c0001t0002g0231a0001c0001t0002g0287a0001c0001t0002g0288 | 3 | HG01255.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.448+3506C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195206 | ||||||
| chr12:7195409
|
C | T | 20 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0049others(17): Show | 24 | HG00735.hp1 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.449-3602C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195409 | ||||||
| chr12:7195522
|
G | A | 4 | a0001c0001t0004g0003a0001c0001t0004g0302a0001c0001t0004g0303others(1): Show | 10 | HG02055.hp2 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.449-3489G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195522 | ||||||
| chr12:7195525
|
C | G | 1 | a0001c0001t0002g0286 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.449-3486C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195525 | ||||||
| chr12:7195607
|
T | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-3404T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195607 | ||||||
| chr12:7195613
|
G | GT | 15 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(12): Show | 15 | HG00597.hp2 HG01175.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.449-3385dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7195613 | |||||
| chr12:7195613
|
G | GTT | 4 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226others(1): Show | 9 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-3386_449-3385d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7195613 | |||||
| chr12:7195780
|
A | C | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.449-3231A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195780 | ||||||
| chr12:7195859
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-3152C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7195859 | ||||||
| chr12:7196024
|
C | CATTATAT | 106 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0011others(103): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.449-2977_449-2971d others(9): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196024 | |||||
| chr12:7196033
|
T | A | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.449-2978T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196033 | ||||||
| chr12:7196033
|
T | TTATATAA | 224 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(221): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.449-2972_449-2971i others(9): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196033 | |||||
| chr12:7196063
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 162 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.449-2948T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196063 | ||||||
| chr12:7196104
|
TTTC | T | 40 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(37): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.449-2904_449-2902d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196104 | |||||
| chr12:7196132
|
GTA | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 162 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.449-2877_449-2876d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196132 | |||||
| chr12:7196145
|
CAT | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2863_449-2862d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196145 | |||||
| chr12:7196187
|
A | G | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2824A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196187 | ||||||
| chr12:7196212
|
ATTATATA others(50): Show |
A | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.449-2761_449-2705d others(59): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196212 | |||||
| chr12:7196213
|
TTA | T | 24 | a0001c0001t0002g0042a0001c0001t0002g0280a0001c0001t0002g0281others(21): Show | 29 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.449-2792_449-2791d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196213 | |||||
| chr12:7196215
|
ATATATGT others(72): Show |
A | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2768_449-2690d others(81): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196215 | |||||
| chr12:7196232
|
TTTAATTA others(76): Show |
T | 1 | a0001c0001t0004g0218 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.449-2775_449-2693d others(85): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196232 | |||||
| chr12:7196250
|
T | A | 84 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(81): Show | 106 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.449-2761T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196250 | ||||||
| chr12:7196253
|
A | AT | 61 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(58): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.449-2756dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196253 | |||||
| chr12:7196254
|
TTATATAT others(54): Show |
T | 20 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(17): Show | 23 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.449-2755_449-2695d others(63): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196254 | |||||
| chr12:7196255
|
TA | T | 3 | a0001c0001t0003g0202a0001c0001t0005g0205a0001c0001t0005g0206 | 3 | HG02145.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.449-2755delA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196255 | ||||||
| chr12:7196294
|
T | TTA | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2713_449-2712d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196294 | |||||
| chr12:7196301
|
T | A | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2710T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196301 | ||||||
| chr12:7196312
|
T | G | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2699T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196312 | ||||||
| chr12:7196317
|
T | A | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2694T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196317 | ||||||
| chr12:7196318
|
A | AT | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2692dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196318 | |||||
| chr12:7196322
|
A | G | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2689A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196322 | ||||||
| chr12:7196328
|
TA | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-2681delA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196328 | |||||
| chr12:7196331
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-2680T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196331 | ||||||
| chr12:7196332
|
T | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-2679T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196332 | ||||||
| chr12:7196333
|
T | C | 1 | a0002c0002t0005g0324 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.449-2678T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196333 | ||||||
| chr12:7196338
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-2673A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196338 | ||||||
| chr12:7196342
|
C | G | 1 | a0002c0002t0005g0324 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.449-2669C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196342 | ||||||
| chr12:7196343
|
A | T | 1 | a0002c0002t0005g0324 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.449-2668A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196343 | ||||||
| chr12:7196344
|
T | C | 1 | a0002c0002t0005g0324 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.449-2667T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196344 | ||||||
| chr12:7196347
|
A | AATG | 21 | a0001c0001t0005g0205a0001c0001t0005g0206a0001c0001t0005g0207others(18): Show | 25 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.449-2664_449-2663i others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196347 | ||||||
| chr12:7196350
|
ATT | A | 21 | a0001c0001t0005g0205a0001c0001t0005g0206a0001c0001t0005g0207others(18): Show | 25 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.449-2659_449-2658d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196350 | |||||
| chr12:7196351
|
T | TGTA | 41 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(38): Show | 56 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.449-2660_449-2659i others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196351 | ||||||
| chr12:7196352
|
T | A | 41 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(38): Show | 56 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.449-2659T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196352 | ||||||
| chr12:7196352
|
T | G | 2 | a0001c0001t0003g0201a0002c0002t0005g0324 | 2 | HG00597.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.449-2659T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196352 | ||||||
| chr12:7196362
|
A | G | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2649A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196362 | ||||||
| chr12:7196365
|
A | C | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2646A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196365 | ||||||
| chr12:7196376
|
GTAA | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2630_449-2628d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196376 | |||||
| chr12:7196395
|
C | A | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2616C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196395 | ||||||
| chr12:7196395
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-2616C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196395 | ||||||
| chr12:7196398
|
AT | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-2612delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196398 | ||||||
| chr12:7196399
|
T | A | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2612T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196399 | ||||||
| chr12:7196400
|
A | T | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2611A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196400 | ||||||
| chr12:7196402
|
G | A | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2609G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196402 | ||||||
| chr12:7196402
|
G | GTAATAA | 20 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(17): Show | 24 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.449-2608_449-2607i others(8): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196402 | |||||
| chr12:7196403
|
T | C | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2608T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196403 | ||||||
| chr12:7196403
|
T | TAATAATT others(2): Show |
43 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(40): Show | 58 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.449-2608_449-2607i others(11): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196403 | ||||||
| chr12:7196404
|
G | A | 44 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(41): Show | 59 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.449-2607G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196404 | ||||||
| chr12:7196404
|
G | T | 20 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(17): Show | 24 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.449-2607G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196404 | ||||||
| chr12:7196405
|
T | A | 20 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(17): Show | 24 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.449-2606T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196405 | ||||||
| chr12:7196405
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0002g0238a0001c0001t0008g0004others(2): Show | 10 | HG00673.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.449-2606T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196405 | ||||||
| chr12:7196416
|
GTAA | G | 4 | a0001c0001t0002g0235a0001c0001t0003g0176a0001c0001t0003g0177others(1): Show | 4 | HG01099.hp2 HG03017.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2590_449-2588d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196416 | |||||
| chr12:7196421
|
AATT | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0297 | 3 | HG02895.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.449-2587_449-2585d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196421 | |||||
| chr12:7196427
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.449-2584A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196427 | ||||||
| chr12:7196429
|
G | A | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2582G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196429 | ||||||
| chr12:7196429
|
GTGCCATA others(122): Show |
G | 1 | a0001c0001t0015g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.449-2579_449-2451d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196429 | |||||
| chr12:7196432
|
C | T | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2579C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196432 | ||||||
| chr12:7196437
|
T | C | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2574T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196437 | ||||||
| chr12:7196450
|
T | TTA | 27 | a0001c0001t0004g0220a0001c0001t0004g0298a0001c0001t0005g0205others(24): Show | 32 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.449-2559_449-2558d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196450 | |||||
| chr12:7196451
|
TATGTGTC others(20): Show |
T | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2557_449-2531d others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196451 | |||||
| chr12:7196454
|
G | A | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2557G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196454 | ||||||
| chr12:7196461
|
A | C | 1 | a0002c0002t0005g0323 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.449-2550A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196461 | ||||||
| chr12:7196462
|
T | C | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2549T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196462 | ||||||
| chr12:7196478
|
C | T | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2533C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196478 | ||||||
| chr12:7196479
|
A | ATATG | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2531_449-2530i others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196479 | |||||
| chr12:7196479
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2532A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196479 | ||||||
| chr12:7196483
|
T | TATATAAT others(20): Show |
1 | a0001c0001t0002g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.449-2443_449-2417d others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196483 | |||||
| chr12:7196484
|
A | C | 1 | a0002c0002t0005g0323 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.449-2527A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196484 | ||||||
| chr12:7196485
|
T | C | 64 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(61): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-2526T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196485 | ||||||
| chr12:7196510
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-2501C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196510 | ||||||
| chr12:7196512
|
T | C | 88 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(85): Show | 115 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.449-2499T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196512 | ||||||
| chr12:7196518
|
GTAA | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.449-2488_449-2486d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196518 | |||||
| chr12:7196518
|
GTAATAAT others(102): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.449-2488_449-2380d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196518 | |||||
| chr12:7196518
|
GTAATAAT others(129): Show |
G | 2 | a0001c0001t0001g0096a0001c0001t0001g0114 | 2 | HG04199.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.449-2488_449-2353d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196518 | |||||
| chr12:7196525
|
TTA | T | 12 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(9): Show | 13 | HG01099.hp2 HG01891.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.449-2480_449-2479d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196525 | |||||
| chr12:7196536
|
A | ATACATAA others(15): Show |
4 | a0001c0001t0003g0005a0001c0001t0003g0031a0001c0001t0003g0183others(1): Show | 9 | NA18946.hp1 NA18949.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-2475_449-2474i others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196536 | ||||||
| chr12:7196537
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(214): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.449-2474C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196537 | ||||||
| chr12:7196539
|
T | C | 84 | a0001c0001t0001g0024a0001c0001t0003g0010a0001c0001t0003g0016others(81): Show | 107 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.449-2472T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196539 | ||||||
| chr12:7196539
|
T | TAC | 4 | a0001c0001t0003g0005a0001c0001t0003g0031a0001c0001t0003g0183others(1): Show | 9 | NA18946.hp1 NA18949.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-2471_449-2470i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196539 | |||||
| chr12:7196545
|
GTAA | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(101): Show | 121 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.449-2461_449-2459d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196545 | |||||
| chr12:7196549
|
TAATTA | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0025others(19): Show | 28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.449-2461_449-2457d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196549 | ||||||
| chr12:7196550
|
AATT | A | 5 | a0001c0001t0003g0030a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 6 | NA18944.hp1 NA18945.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2458_449-2456d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196550 | |||||
| chr12:7196564
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(219): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.449-2447C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196564 | ||||||
| chr12:7196566
|
T | C | 94 | a0001c0001t0001g0027a0001c0001t0001g0069a0001c0001t0001g0070others(91): Show | 122 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.449-2445T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196566 | ||||||
| chr12:7196572
|
GTAA | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 148 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.449-2434_449-2432d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196572 | |||||
| chr12:7196582
|
T | TGTCATAC others(12): Show |
1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2429_449-2428i others(21): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196582 | ||||||
| chr12:7196583
|
A | G | 1 | a0001c0001t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.449-2428A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196583 | ||||||
| chr12:7196583
|
A | T | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2428A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196583 | ||||||
| chr12:7196585
|
A | G | 12 | a0001c0001t0003g0005a0001c0001t0003g0031a0001c0001t0003g0034others(9): Show | 18 | HG00099.hp1 HG00733.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2426A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196585 | ||||||
| chr12:7196587
|
G | C | 12 | a0001c0001t0003g0005a0001c0001t0003g0031a0001c0001t0003g0034others(9): Show | 18 | HG00099.hp1 HG00733.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2424G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196587 | ||||||
| chr12:7196588
|
T | A | 19 | a0001c0001t0003g0005a0001c0001t0003g0031a0001c0001t0003g0034others(16): Show | 26 | HG00099.hp1 HG00733.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.449-2423T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196588 | ||||||
| chr12:7196589
|
C | CAT | 187 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 225 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.449-2421_449-2420i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | CATACATA others(125): Show |
1 | a0001c0001t0003g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.449-2421_449-2420i others(134): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | CATACATA others(128): Show |
2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.449-2421_449-2420i others(137): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | CATACATA others(123): Show |
4 | a0001c0001t0005g0207a0002c0002t0005g0312a0002c0002t0005g0313others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2421_449-2420i others(132): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | CATACATA others(20): Show |
12 | a0001c0001t0003g0010a0001c0001t0003g0016a0001c0001t0003g0032others(9): Show | 19 | HG00438.hp2 HG00642.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.449-2421_449-2420i others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | CATACATA others(45): Show |
2 | a0001c0001t0003g0195a0001c0001t0003g0196 | 2 | HG01192.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.449-2421_449-2420i others(54): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | CATACATA others(125): Show |
1 | a0001c0001t0003g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.449-2421_449-2420i others(134): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196589 | |||||
| chr12:7196589
|
C | T | 12 | a0001c0001t0003g0005a0001c0001t0003g0031a0001c0001t0003g0034others(9): Show | 18 | HG00099.hp1 HG00733.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2422C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196589 | ||||||
| chr12:7196591
|
C | CAT | 9 | a0001c0001t0002g0042a0001c0001t0002g0238a0001c0001t0002g0279others(6): Show | 10 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.449-2418_449-2417d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196591 | |||||
| chr12:7196591
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(73): Show | 89 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.449-2420C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196591 | ||||||
| chr12:7196597
|
GTAA | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(86): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.449-2409_449-2407d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196597 | |||||
| chr12:7196602
|
AATTAT | A | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.449-2406_449-2402d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196602 | |||||
| chr12:7196604
|
TTA | T | 14 | a0001c0001t0003g0030a0001c0001t0003g0034a0001c0001t0003g0180others(11): Show | 16 | HG01175.hp2 HG02145.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-2401_449-2400d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196604 | |||||
| chr12:7196615
|
A | ATACATAA others(38): Show |
1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-2396_449-2395i others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196615 | ||||||
| chr12:7196615
|
A | ATACATAA others(92): Show |
4 | a0002c0002t0005g0314a0002c0002t0005g0315a0002c0002t0005g0316others(1): Show | 4 | HG01109.hp2 HG02129.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2396_449-2395i others(101): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196615 | ||||||
| chr12:7196615
|
A | ATACATAA others(38): Show |
1 | a0001c0001t0004g0037 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.449-2396_449-2395i others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196615 | ||||||
| chr12:7196616
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(213): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.449-2395C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196616 | ||||||
| chr12:7196616
|
CAT | C | 7 | a0001c0001t0002g0042a0001c0001t0002g0239a0001c0001t0002g0280others(4): Show | 8 | HG00408.hp1 HG02015.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2391_449-2390d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196616 | |||||
| chr12:7196618
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(147): Show | 190 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.449-2393T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196618 | ||||||
| chr12:7196618
|
T | TAC | 6 | a0001c0001t0004g0037a0002c0002t0005g0314a0002c0002t0005g0315others(3): Show | 7 | HG01109.hp2 HG01884.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2392_449-2391i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196618 | |||||
| chr12:7196620
|
T | TAATGTAA others(284): Show |
2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG01952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.449-2230_449-2229i others(293): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196620 | |||||
| chr12:7196624
|
GTAA | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0050others(34): Show | 45 | HG00438.hp1 HG00544.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.449-2382_449-2380d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196624 | |||||
| chr12:7196626
|
A | AATAATTA others(40): Show |
2 | a0001c0001t0005g0208a0002c0002t0005g0322 | 2 | HG00621.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.449-2375_449-2374i others(49): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196626 | |||||
| chr12:7196642
|
A | ATACATAA others(65): Show |
4 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0317others(1): Show | 6 | HG00597.hp2 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2369_449-2368i others(74): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196642 | ||||||
| chr12:7196642
|
A | ATACATAA others(63): Show |
4 | a0002c0002t0005g0020a0002c0002t0005g0319a0002c0002t0005g0320others(1): Show | 6 | HG00735.hp2 HG02735.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2369_449-2368i others(72): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196642 | ||||||
| chr12:7196642
|
A | ATACATAA others(38): Show |
5 | a0001c0001t0004g0036a0001c0001t0004g0215a0001c0001t0004g0216others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2369_449-2368i others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196642 | ||||||
| chr12:7196643
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.449-2368C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196643 | ||||||
| chr12:7196645
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(111): Show | 141 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.449-2366T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196645 | ||||||
| chr12:7196645
|
T | TAC | 13 | a0001c0001t0004g0036a0001c0001t0004g0215a0001c0001t0004g0216others(10): Show | 18 | HG00597.hp2 HG00735.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.449-2365_449-2364i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196645 | |||||
| chr12:7196651
|
GTAA | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0050others(12): Show | 23 | HG02027.hp2 HG02056.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.449-2355_449-2353d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196651 | |||||
| chr12:7196653
|
A | AATAATTA others(40): Show |
1 | a0002c0002t0005g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.449-2348_449-2347i others(49): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196653 | |||||
| chr12:7196658
|
TTA | T | 3 | a0001c0001t0002g0278a0001c0001t0002g0285a0001c0001t0004g0298 | 3 | HG02559.hp2 NA18946.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.449-2347_449-2346d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196658 | |||||
| chr12:7196658
|
TTATA | T | 8 | a0001c0001t0004g0035a0001c0001t0004g0211a0001c0001t0004g0213others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-2349_449-2346d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196658 | |||||
| chr12:7196658
|
TTATATA | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2351_449-2346d others(8): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196658 | |||||
| chr12:7196670
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-2341C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196670 | ||||||
| chr12:7196672
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(89): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.449-2339T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196672 | ||||||
| chr12:7196678
|
GTAA | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0001g0138others(2): Show | 5 | HG02056.hp1 HG02486.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-2328_449-2326d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196678 | |||||
| chr12:7196680
|
A | AATAATTA others(40): Show |
1 | a0002c0002t0005g0310 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.449-2321_449-2320i others(49): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196680 | |||||
| chr12:7196687
|
A | G | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.449-2324A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196687 | ||||||
| chr12:7196689
|
A | ATGTCATA others(59): Show |
1 | a0001c0001t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.449-2321_449-2320i others(68): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196689 | |||||
| chr12:7196692
|
TGTCACAT others(106): Show |
T | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.449-2318_449-2206d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196692 | ||||||
| chr12:7196697
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(221): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.449-2314C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196697 | ||||||
| chr12:7196699
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(75): Show | 108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.449-2312T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196699 | ||||||
| chr12:7196705
|
GTAA | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0001g0156others(1): Show | 4 | HG02486.hp2 HG04199.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2301_449-2299d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196705 | |||||
| chr12:7196712
|
TTATATA | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2297_449-2292d others(8): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196712 | |||||
| chr12:7196712
|
TTATATAT others(128): Show |
T | 1 | a0001c0001t0015g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.449-2293_449-2159d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196712 | |||||
| chr12:7196714
|
ATATATGT others(205): Show |
A | 1 | a0001c0001t0001g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.449-2266_449-2055d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196714 | |||||
| chr12:7196714
|
ATATATGT others(230): Show |
A | 5 | a0001c0001t0001g0008a0001c0001t0001g0075a0001c0001t0001g0131others(2): Show | 7 | HG03239.hp1 NA18612.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2220_449-1984d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196714 | |||||
| chr12:7196724
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.449-2287C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196724 | ||||||
| chr12:7196726
|
T | C | 64 | a0001c0001t0001g0156a0001c0001t0003g0005a0001c0001t0003g0010others(61): Show | 88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.449-2285T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196726 | ||||||
| chr12:7196726
|
TATAATGT others(72): Show |
T | 1 | a0001c0001t0001g0027 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.449-2202_449-2124d others(81): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196726 | |||||
| chr12:7196732
|
GTAA | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0001g0156others(1): Show | 4 | HG04199.hp1 HG06807.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2274_449-2272d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196732 | |||||
| chr12:7196741
|
ATATATGT others(203): Show |
A | 6 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0073others(3): Show | 7 | HG00642.hp2 HG01099.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2202_449-1993d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196741 | |||||
| chr12:7196742
|
T | TGTCATAT others(34): Show |
1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2269_449-2268i others(43): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196742 | ||||||
| chr12:7196743
|
A | ATGTCATA others(59): Show |
3 | a0001c0001t0004g0037a0001c0001t0004g0298a0002c0002t0004g0326 | 4 | HG01884.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2267_449-2266i others(68): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196743 | |||||
| chr12:7196743
|
A | T | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-2268A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196743 | ||||||
| chr12:7196748
|
TCA | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2260_449-2259d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196748 | |||||
| chr12:7196750
|
A | ATATACAA others(11): Show |
1 | a0001c0001t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.449-2261_449-2260i others(20): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196750 | ||||||
| chr12:7196751
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(200): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.449-2260C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196751 | ||||||
| chr12:7196751
|
CAT | C | 13 | a0001c0001t0002g0029a0001c0001t0002g0167a0001c0001t0002g0168others(10): Show | 14 | HG00140.hp2 HG00673.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.449-2256_449-2255d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196751 | |||||
| chr12:7196753
|
T | C | 56 | a0001c0001t0001g0096a0001c0001t0001g0156a0001c0001t0003g0005others(53): Show | 73 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.449-2258T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196753 | ||||||
| chr12:7196753
|
T | TAATGTAA others(16): Show |
1 | a0001c0001t0002g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.449-2257_449-2256i others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196753 | |||||
| chr12:7196753
|
T | TATAATGT others(18): Show |
17 | a0001c0001t0002g0017a0001c0001t0002g0039a0001c0001t0002g0048others(14): Show | 20 | HG00558.hp1 HG00558.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.449-2254_449-2230d others(27): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196753 | |||||
| chr12:7196753
|
TATAATGT others(228): Show |
T | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.449-2254_449-2020d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196753 | |||||
| chr12:7196759
|
GTAA | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0114others(4): Show | 8 | HG01361.hp2 HG02486.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2247_449-2245d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196759 | |||||
| chr12:7196759
|
GTAATAAT others(233): Show |
G | 4 | a0001c0001t0001g0024a0001c0001t0001g0083a0001c0001t0001g0137others(1): Show | 5 | NA18945.hp2 NA18997.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2247_449-2008d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196759 | |||||
| chr12:7196762
|
ATAATTAT others(254): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.449-2220_449-1960d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196762 | |||||
| chr12:7196762
|
ATAATTAT others(278): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.449-2220_449-1936d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196762 | |||||
| chr12:7196768
|
ATATATGT others(176): Show |
A | 11 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 13 | HG00741.hp2 HG01081.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.449-2202_449-2020d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196768 | |||||
| chr12:7196770
|
A | ATGTCATA others(59): Show |
8 | a0001c0001t0004g0036a0001c0001t0004g0215a0001c0001t0004g0216others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-2240_449-2239i others(68): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196770 | |||||
| chr12:7196771
|
T | TGTCATAT others(133): Show |
1 | a0001c0001t0004g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.449-2240_449-2239i others(142): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196771 | ||||||
| chr12:7196777
|
ACATATAA others(324): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.449-2217_449-1887d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196777 | |||||
| chr12:7196778
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(190): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.449-2233C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196778 | ||||||
| chr12:7196778
|
CAT | C | 54 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0011others(51): Show | 74 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.449-2229_449-2228d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196778 | |||||
| chr12:7196780
|
T | C | 46 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0001g0156others(43): Show | 61 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.449-2231T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196780 | ||||||
| chr12:7196782
|
T | C | 2 | a0001c0001t0004g0220a0001c0001t0004g0224 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.449-2229T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196782 | ||||||
| chr12:7196786
|
GTAATAAT others(179): Show |
G | 10 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0066others(7): Show | 13 | HG02056.hp2 HG02074.hp2 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.449-2220_449-2035d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196786 | |||||
| chr12:7196786
|
GTAATAAT others(206): Show |
G | 5 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG01167.hp2 HG03831.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-2220_449-2008d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196786 | |||||
| chr12:7196789
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.449-2222A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196789 | ||||||
| chr12:7196789
|
ATAATTAT others(227): Show |
A | 9 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 9 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-2202_449-1969d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196789 | |||||
| chr12:7196789
|
ATAATTAT others(251): Show |
A | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0119 | 3 | HG01258.hp2 HG01517.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.449-2202_449-1945d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196789 | |||||
| chr12:7196791
|
A | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG01106.hp2 HG01169.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.449-2220A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196791 | ||||||
| chr12:7196792
|
ATTATATA others(152): Show |
A | 3 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG01106.hp2 HG01169.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.449-2217_449-2059d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196792 | |||||
| chr12:7196795
|
ATATATGT others(124): Show |
A | 12 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0064others(9): Show | 12 | HG02965.hp1 HG03041.hp2 HG03130.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-2202_449-2072d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196795 | |||||
| chr12:7196795
|
ATATATGT others(149): Show |
A | 14 | a0001c0001t0001g0009a0001c0001t0001g0072a0001c0001t0001g0074others(11): Show | 17 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.449-2202_449-2047d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196795 | |||||
| chr12:7196797
|
A | ATGTCATA others(59): Show |
1 | a0001c0001t0004g0211 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.449-2213_449-2212i others(68): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196797 | |||||
| chr12:7196797
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.449-2214A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196797 | ||||||
| chr12:7196798
|
T | TGTCATAT others(133): Show |
1 | a0001c0001t0004g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.449-2213_449-2212i others(142): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196798 | ||||||
| chr12:7196799
|
A | G | 11 | a0001c0001t0002g0173a0001c0001t0004g0035a0001c0001t0004g0213others(8): Show | 18 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2212A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196799 | ||||||
| chr12:7196801
|
G | C | 11 | a0001c0001t0002g0173a0001c0001t0004g0035a0001c0001t0004g0213others(8): Show | 18 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2210G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196801 | ||||||
| chr12:7196802
|
T | A | 11 | a0001c0001t0002g0173a0001c0001t0004g0035a0001c0001t0004g0213others(8): Show | 18 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2209T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196802 | ||||||
| chr12:7196803
|
C | CAT | 119 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0049others(116): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.449-2207_449-2206i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196803 | |||||
| chr12:7196803
|
C | T | 11 | a0001c0001t0004g0035a0001c0001t0004g0213a0001c0001t0004g0219others(8): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2208C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196803 | ||||||
| chr12:7196805
|
C | CAT | 82 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0011others(79): Show | 108 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.449-2204_449-2203d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196805 | |||||
| chr12:7196805
|
C | CATAATGT others(20): Show |
1 | a0001c0001t0004g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.449-2106_449-2080d others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196805 | |||||
| chr12:7196805
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0049others(117): Show | 153 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.449-2206C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196805 | ||||||
| chr12:7196807
|
T | C | 1 | a0001c0001t0004g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.449-2204T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196807 | ||||||
| chr12:7196807
|
T | TACAATGT others(15): Show |
4 | a0001c0001t0004g0037a0001c0001t0004g0212a0001c0001t0004g0298others(1): Show | 5 | HG01884.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-2203_449-2202i others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196807 | |||||
| chr12:7196809
|
A | T | 1 | a0001c0001t0005g0208 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.449-2202A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196809 | ||||||
| chr12:7196810
|
T | A | 1 | a0001c0001t0005g0208 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.449-2201T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196810 | ||||||
| chr12:7196811
|
GTAATAAT others(154): Show |
G | 1 | a0001c0001t0001g0098 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.449-2195_449-2035d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196811 | |||||
| chr12:7196814
|
A | ATTATATA others(158): Show |
1 | a0002c0002t0009g0332 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.449-2196_449-2195i others(167): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196814 | |||||
| chr12:7196814
|
ATAATTAT others(202): Show |
A | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0010g0296 | 3 | HG01261.hp2 HG01496.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.449-2168_449-1960d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196814 | |||||
| chr12:7196818
|
TTA | T | 7 | a0001c0001t0004g0003a0001c0001t0004g0213a0001c0001t0004g0302others(4): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2187_449-2186d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196818 | |||||
| chr12:7196820
|
ATATATGT others(124): Show |
A | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.449-2114_449-1984d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196820 | |||||
| chr12:7196822
|
A | G | 1 | a0001c0001t0004g0035 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.449-2189A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196822 | ||||||
| chr12:7196823
|
T | TCATATAT others(108): Show |
1 | a0001c0001t0004g0035 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.449-2188_449-2187i others(117): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196823 | ||||||
| chr12:7196829
|
A | ATATACAA others(11): Show |
6 | a0001c0001t0004g0215a0001c0001t0004g0217a0001c0001t0004g0218others(3): Show | 6 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-2182_449-2181i others(20): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196829 | ||||||
| chr12:7196829
|
A | ATATACAA others(38): Show |
2 | a0001c0001t0004g0036a0001c0001t0004g0216 | 3 | HG01167.hp1 HG01169.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.449-2182_449-2181i others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196829 | ||||||
| chr12:7196830
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0043others(124): Show | 161 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.449-2181C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196830 | ||||||
| chr12:7196832
|
T | C | 7 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0186others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2179T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196832 | ||||||
| chr12:7196834
|
T | C | 10 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(7): Show | 13 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.449-2177T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196834 | ||||||
| chr12:7196834
|
T | TAC | 6 | a0001c0001t0004g0215a0001c0001t0004g0217a0001c0001t0004g0218others(3): Show | 6 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-2176_449-2175i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196834 | |||||
| chr12:7196838
|
GTAATAAT others(127): Show |
G | 3 | a0001c0001t0001g0049a0001c0001t0001g0139a0001c0001t0001g0146 | 3 | HG03654.hp1 HG03669.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.449-2168_449-2035d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196838 | |||||
| chr12:7196841
|
ATAATTAT others(175): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.449-2141_449-1960d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196841 | |||||
| chr12:7196845
|
TTATA | T | 5 | a0001c0001t0004g0213a0001c0001t0011g0021a0002c0002t0005g0045others(2): Show | 7 | HG00597.hp2 HG00621.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2162_449-2159d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196845 | |||||
| chr12:7196849
|
A | ATATGTCA others(11): Show |
1 | a0001c0001t0004g0219 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.449-2155_449-2154i others(20): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196849 | |||||
| chr12:7196854
|
TCA | T | 3 | a0001c0001t0004g0215a0001c0001t0004g0217a0001c0001t0004g0218 | 3 | HG02257.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.449-2154_449-2153d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196854 | |||||
| chr12:7196856
|
A | ATATACAA others(38): Show |
1 | a0001c0001t0004g0211 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.449-2155_449-2154i others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196856 | ||||||
| chr12:7196856
|
ACATAT | A | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2154_449-2150d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196856 | ||||||
| chr12:7196857
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0043others(123): Show | 157 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.449-2154C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196857 | ||||||
| chr12:7196861
|
T | C | 17 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(14): Show | 20 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.449-2150T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196861 | ||||||
| chr12:7196862
|
A | T | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2149A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196862 | ||||||
| chr12:7196865
|
GTAA | G | 13 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0103others(10): Show | 13 | HG00438.hp1 HG01433.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.449-2141_449-2139d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196865 | |||||
| chr12:7196865
|
GTAATAAT others(100): Show |
G | 2 | a0001c0001t0001g0142a0001c0001t0001g0159 | 2 | HG01993.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.449-2141_449-2035d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196865 | |||||
| chr12:7196868
|
ATAAT | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2140_449-2137d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196868 | |||||
| chr12:7196868
|
ATAATTAT others(148): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0107 | 2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.449-2114_449-1960d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196868 | |||||
| chr12:7196871
|
ATTATATA others(73): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.449-2138_449-2059d others(82): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196871 | |||||
| chr12:7196872
|
TTA | T | 58 | a0001c0001t0002g0017a0001c0001t0002g0029a0001c0001t0002g0039others(55): Show | 75 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.449-2133_449-2132d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196872 | |||||
| chr12:7196872
|
TTATA | T | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2135_449-2132d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196872 | |||||
| chr12:7196874
|
A | ATATGTCA others(16): Show |
1 | a0001c0001t0002g0279 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.449-2134_449-2133i others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196874 | |||||
| chr12:7196876
|
A | ATATGTCA others(11): Show |
1 | a0001c0001t0004g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.449-2128_449-2127i others(20): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196876 | |||||
| chr12:7196883
|
ACATATAA others(218): Show |
A | 1 | a0001c0001t0001g0297 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.449-2111_449-1887d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196883 | |||||
| chr12:7196884
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0043others(121): Show | 160 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.449-2127C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196884 | ||||||
| chr12:7196888
|
T | C | 16 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(13): Show | 19 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.449-2123T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196888 | ||||||
| chr12:7196889
|
A | T | 2 | a0001c0001t0008g0225a0002c0002t0009g0332 | 2 | HG03098.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.449-2122A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196889 | ||||||
| chr12:7196892
|
GTAA | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0051others(6): Show | 16 | HG02135.hp2 HG02922.hp1 HG03139.hp1 others(13): Show |
intron_variant | MODIFIER | c.449-2114_449-2112d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196892 | |||||
| chr12:7196892
|
GTAATAAT others(73): Show |
G | 7 | a0001c0001t0001g0090a0001c0001t0001g0108a0001c0001t0001g0143others(4): Show | 7 | HG01433.hp2 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2114_449-2035d others(82): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196892 | |||||
| chr12:7196895
|
ATAAT | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2113_449-2110d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196895 | |||||
| chr12:7196895
|
ATAATTAT others(145): Show |
A | 5 | a0001c0001t0001g0088a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG00438.hp1 NA18952.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2087_449-1936d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196895 | |||||
| chr12:7196899
|
TTA | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0011others(59): Show | 83 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.449-2106_449-2105d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196899 | |||||
| chr12:7196901
|
A | ATATGTCA others(16): Show |
1 | a0001c0001t0002g0266 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.449-2107_449-2106i others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196901 | |||||
| chr12:7196910
|
A | ATATACAA others(11): Show |
1 | a0001c0001t0004g0219 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.449-2101_449-2100i others(20): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196910 | ||||||
| chr12:7196910
|
ACATAT | A | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2100_449-2096d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196910 | ||||||
| chr12:7196910
|
ACATATAA others(191): Show |
A | 1 | a0001c0001t0001g0043 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.449-2084_449-1887d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196910 | |||||
| chr12:7196911
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0051others(107): Show | 140 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.449-2100C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196911 | ||||||
| chr12:7196915
|
T | C | 19 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(16): Show | 24 | HG00597.hp2 HG00621.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.449-2096T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196915 | ||||||
| chr12:7196916
|
A | T | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2095A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196916 | ||||||
| chr12:7196919
|
GTAA | G | 4 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0322others(1): Show | 6 | HG00597.hp2 HG00621.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2087_449-2085d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196919 | |||||
| chr12:7196919
|
GTAATAAT others(73): Show |
G | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.449-2087_449-2008d others(82): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196919 | |||||
| chr12:7196921
|
AATAATTA others(118): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.449-2089_449-1965d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196921 | ||||||
| chr12:7196922
|
ATAATTAT others(118): Show |
A | 6 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0054others(3): Show | 12 | HG02135.hp2 NA18940.hp1 NA18966.hp1 others(9): Show |
intron_variant | MODIFIER | c.449-2079_449-1955d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196922 | |||||
| chr12:7196924
|
A | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0004g0036others(7): Show | 12 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.449-2087A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196924 | ||||||
| chr12:7196924
|
AAT | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-2086_449-2085d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196924 | ||||||
| chr12:7196925
|
AT | A | 10 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0004g0036others(7): Show | 12 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.449-2084delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196925 | |||||
| chr12:7196926
|
T | TTA | 93 | a0001c0001t0001g0027a0001c0001t0001g0156a0001c0001t0002g0002others(90): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.449-2081_449-2080d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196926 | |||||
| chr12:7196926
|
T | TTATATAT others(47): Show |
1 | a0001c0001t0002g0239 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.449-2080_449-2079i others(56): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196926 | |||||
| chr12:7196926
|
TTA | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0226a0002c0002t0005g0313 | 8 | HG01070.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-2081_449-2080d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196926 | |||||
| chr12:7196927
|
T | C | 4 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0322others(1): Show | 6 | HG00597.hp2 HG00621.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2084T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196927 | ||||||
| chr12:7196927
|
T | TATGTCAT others(112): Show |
2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.449-2082_449-2081i others(121): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196927 | |||||
| chr12:7196928
|
ATATGTCA others(16): Show |
A | 4 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0138others(1): Show | 4 | HG02056.hp1 HG02572.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-2079_449-2057d others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196928 | |||||
| chr12:7196932
|
G | A | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-2079G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196932 | ||||||
| chr12:7196934
|
C | G | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-2077C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196934 | ||||||
| chr12:7196935
|
A | T | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-2076A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196935 | ||||||
| chr12:7196936
|
C | T | 113 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0056others(110): Show | 142 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.449-2075C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196936 | ||||||
| chr12:7196940
|
T | C | 16 | a0001c0001t0004g0035a0001c0001t0004g0211a0001c0001t0004g0213others(13): Show | 19 | HG00597.hp2 HG00621.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.449-2071T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196940 | ||||||
| chr12:7196940
|
TAATGTAA others(434): Show |
T | 1 | a0001c0001t0002g0018 | 3 | HG01261.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.449-2054_449-1614d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196940 | |||||
| chr12:7196946
|
A | AATATATA others(6): Show |
2 | a0001c0001t0007g0166a0001c0001t0007g0209 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.449-2062_449-2061i others(15): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196946 | |||||
| chr12:7196947
|
ATAAT | A | 4 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0165others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2061_449-2058d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196947 | |||||
| chr12:7196949
|
A | T | 22 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0064others(19): Show | 24 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.449-2062A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196949 | ||||||
| chr12:7196949
|
AAT | A | 3 | a0001c0001t0002g0265a0001c0001t0006g0022a0001c0001t0007g0164 | 4 | HG01891.hp2 HG02083.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2061_449-2060d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196949 | ||||||
| chr12:7196950
|
AT | A | 22 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0064others(19): Show | 24 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.449-2059delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196950 | |||||
| chr12:7196951
|
T | TTA | 109 | a0001c0001t0001g0050a0001c0001t0001g0106a0001c0001t0001g0114others(106): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.449-2056_449-2055d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196951
|
T | TTATATAT others(22): Show |
10 | a0001c0001t0002g0042a0001c0001t0002g0243a0001c0001t0002g0244others(7): Show | 11 | HG00408.hp1 HG00741.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.449-2055_449-2054i others(31): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196951
|
T | TTATATAT others(49): Show |
2 | a0001c0001t0002g0019a0001c0010t0002g0019 | 3 | NA18949.hp2 NA18968.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.449-2055_449-2054i others(58): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196951
|
T | TTATATAT others(44): Show |
1 | a0002c0002t0005g0310 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.449-2055_449-2054i others(53): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196951
|
T | TTATATAT others(216): Show |
1 | a0007c0007t0003g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.449-2055_449-2054i others(225): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196951
|
T | TTATATGT others(20): Show |
1 | a0001c0001t0002g0277 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.449-2010_449-1984d others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196951
|
T | TTATGTCA others(139): Show |
1 | a0004c0004t0005g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.449-2057_449-2056i others(148): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196951 | |||||
| chr12:7196952
|
T | TATATATG others(189): Show |
6 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0186others(3): Show | 6 | HG00099.hp1 HG00733.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-2055_449-2054i others(198): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196952 | |||||
| chr12:7196952
|
T | TATGTCAT others(112): Show |
5 | a0001c0001t0005g0207a0002c0002t0005g0312a0002c0002t0005g0315others(2): Show | 5 | HG00280.hp1 HG01109.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2057_449-2056i others(121): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196952 | |||||
| chr12:7196952
|
T | TATGTCAT others(135): Show |
5 | a0002c0002t0005g0020a0002c0002t0005g0317a0002c0002t0005g0319others(2): Show | 7 | HG00735.hp2 HG02559.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2057_449-2056i others(144): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196952 | |||||
| chr12:7196952
|
T | TGTCATAT others(34): Show |
1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-2059_449-2058i others(43): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196952 | ||||||
| chr12:7196953
|
A | ATATATGT others(13): Show |
1 | a0002c0002t0005g0313 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.449-2055_449-2054i others(22): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196953 | |||||
| chr12:7196953
|
A | ATGTCATA others(36): Show |
3 | a0002c0002t0005g0314a0003c0003t0004g0044a0003c0003t0004g0299 | 4 | HG02486.hp1 HG03831.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-2057_449-2056i others(45): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196953 | |||||
| chr12:7196953
|
A | T | 1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-2058A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196953 | ||||||
| chr12:7196954
|
T | C | 1 | a0001c0001t0004g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.449-2057T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196954 | ||||||
| chr12:7196957
|
G | A | 4 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0165others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2054G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196957 | ||||||
| chr12:7196961
|
C | T | 159 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(156): Show | 196 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.449-2050C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196961 | ||||||
| chr12:7196965
|
T | C | 27 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0186others(24): Show | 31 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.449-2046T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196965 | ||||||
| chr12:7196965
|
T | TAATGTAA others(189): Show |
1 | a0001c0001t0013g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.449-2030_449-2029i others(198): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196965 | |||||
| chr12:7196965
|
T | TAATGTAA others(243): Show |
1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.449-2030_449-2029i others(252): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196965 | |||||
| chr12:7196969
|
GTAA | G | 17 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0072others(14): Show | 18 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.449-2037_449-2035d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196969 | |||||
| chr12:7196969
|
GTAATAAT | G | 4 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0165others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2039_449-2033d others(9): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196969 | |||||
| chr12:7196972
|
A | ATAATTAT others(215): Show |
1 | a0001c0001t0003g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.449-2024_449-2023i others(224): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196972 | |||||
| chr12:7196972
|
A | ATAATTAT others(240): Show |
2 | a0001c0001t0003g0030a0001c0001t0003g0210 | 3 | NA18997.hp1 NA19070.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.449-2030_449-2029i others(249): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196972 | |||||
| chr12:7196972
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.449-2039A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196972 | ||||||
| chr12:7196972
|
ATAATTAT others(44): Show |
A | 1 | a0001c0001t0001g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.449-2010_449-1960d others(53): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196972 | |||||
| chr12:7196974
|
AATT | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0091a0001c0001t0001g0097others(2): Show | 5 | HG02572.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-2034_449-2032d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196974 | |||||
| chr12:7196979
|
T | TGTCATAT others(110): Show |
1 | a0002c0002t0005g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.449-2032_449-2031i others(119): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196979 | ||||||
| chr12:7196979
|
T | TGTCATAT others(133): Show |
1 | a0001c0001t0005g0208 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.449-2032_449-2031i others(142): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196979 | ||||||
| chr12:7196984
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.449-2027G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196984 | ||||||
| chr12:7196985
|
T | A | 2 | a0001c0001t0004g0221a0001c0001t0004g0222 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.449-2026T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196985 | ||||||
| chr12:7196987
|
A | ATATGTAA others(108): Show |
5 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(2): Show | 5 | HG01099.hp2 HG01243.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-2024_449-2023i others(117): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196987 | ||||||
| chr12:7196987
|
A | ATATGTAA others(135): Show |
23 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0031others(20): Show | 33 | HG00438.hp2 HG00642.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.449-2024_449-2023i others(144): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196987 | ||||||
| chr12:7196987
|
A | ATATGTAA others(228): Show |
1 | a0001c0001t0003g0010 | 4 | NA18989.hp2 NA19074.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-2024_449-2023i others(237): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196987 | ||||||
| chr12:7196988
|
C | T | 152 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 179 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.449-2023C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196988 | ||||||
| chr12:7196989
|
A | G | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.449-2022A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196989 | ||||||
| chr12:7196992
|
T | C | 26 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0186others(23): Show | 28 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.449-2019T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7196992 | ||||||
| chr12:7196992
|
T | TAC | 29 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(26): Show | 42 | HG00438.hp2 HG00642.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.449-2018_449-2017i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196992 | |||||
| chr12:7196996
|
GTAA | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0062others(65): Show | 77 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.449-2010_449-2008d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196996 | |||||
| chr12:7196999
|
A | ATAATTAT others(17): Show |
7 | a0001c0001t0002g0017a0001c0001t0002g0039a0001c0001t0002g0247others(4): Show | 8 | HG00408.hp2 HG02129.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-1924_449-1901d others(26): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196999 | |||||
| chr12:7196999
|
A | ATAATTAT others(41): Show |
2 | a0001c0001t0002g0245a0001c0001t0002g0289 | 2 | HG02027.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.449-1948_449-1901d others(50): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196999 | |||||
| chr12:7196999
|
A | ATTATATA others(14): Show |
1 | a0001c0001t0002g0264 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.449-2011_449-2010i others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196999 | |||||
| chr12:7196999
|
ATAAT | A | 6 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0165others(3): Show | 7 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2009_449-2006d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7196999 | |||||
| chr12:7197004
|
TATATATG others(111): Show |
T | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-1996_449-1879d others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197004 | |||||
| chr12:7197013
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.449-1998C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197013 | ||||||
| chr12:7197015
|
C | T | 191 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(188): Show | 232 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(229): Show |
intron_variant | MODIFIER | c.449-1996C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197015 | ||||||
| chr12:7197019
|
T | C | 48 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(45): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.449-1992T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197019 | ||||||
| chr12:7197023
|
G | GTAA | 71 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(68): Show | 92 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.449-1986_449-1984d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197023 | |||||
| chr12:7197023
|
G | GTAATCAT others(18): Show |
1 | a0002c0002t0005g0314 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.449-1984_449-1983i others(27): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197023 | |||||
| chr12:7197026
|
AT | A | 10 | a0001c0001t0005g0205a0001c0001t0005g0206a0001c0001t0007g0028others(7): Show | 11 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.449-1983delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197026 | |||||
| chr12:7197027
|
TTA | T | 5 | a0001c0001t0010g0233a0002c0002t0001g0162a0002c0002t0005g0313others(2): Show | 6 | HG01070.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-1978_449-1977d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197027 | |||||
| chr12:7197027
|
TTATATAT others(67): Show |
T | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1978_449-1905d others(76): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197027 | |||||
| chr12:7197028
|
T | A | 3 | a0001c0001t0004g0221a0001c0001t0004g0222a0001c0001t0004g0223 | 3 | HG01243.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.449-1983T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197028 | ||||||
| chr12:7197029
|
A | AT | 3 | a0001c0001t0004g0221a0001c0001t0004g0222a0001c0001t0004g0223 | 3 | HG01243.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.449-1981dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197029 | |||||
| chr12:7197029
|
A | ATATATGT others(15): Show |
3 | a0001c0001t0004g0003a0001c0001t0004g0302a0001c0001t0004g0305 | 9 | HG02055.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-1976_449-1955d others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197029 | |||||
| chr12:7197030
|
T | C | 3 | a0002c0002t0005g0313a0003c0003t0004g0044a0003c0003t0004g0299 | 4 | HG01070.hp2 HG02486.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1981T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197030 | ||||||
| chr12:7197032
|
T | C | 1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-1979T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197032 | ||||||
| chr12:7197036
|
T | A | 1 | a0001c0001t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.449-1975T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197036 | ||||||
| chr12:7197039
|
C | T | 204 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(201): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.449-1972C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197039 | ||||||
| chr12:7197043
|
T | C | 43 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(40): Show | 57 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.449-1968T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197043 | ||||||
| chr12:7197047
|
G | GTAA | 59 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0114others(56): Show | 71 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.449-1962_449-1960d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197047 | |||||
| chr12:7197050
|
AT | A | 8 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(5): Show | 9 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-1959delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197050 | |||||
| chr12:7197050
|
ATTATATA others(14): Show |
A | 1 | a0001c0001t0001g0050 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.449-1959_449-1939d others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197050 | |||||
| chr12:7197050
|
ATTATATA others(38): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.449-1959_449-1915d others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197050 | |||||
| chr12:7197052
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.449-1959T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197052 | ||||||
| chr12:7197058
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.449-1953T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197058 | ||||||
| chr12:7197060
|
TCA | T | 4 | a0001c0001t0004g0303a0001c0001t0015g0230a0002c0002t0002g0307others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1948_449-1947d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197060 | |||||
| chr12:7197063
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(214): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.449-1948C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197063 | ||||||
| chr12:7197067
|
T | C | 12 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(9): Show | 13 | HG01070.hp2 HG01099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.449-1944T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197067 | ||||||
| chr12:7197071
|
G | GTAA | 78 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0001g0151others(75): Show | 96 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.449-1938_449-1936d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197071 | |||||
| chr12:7197071
|
G | GTAATTAT others(42): Show |
1 | a0001c0001t0002g0262 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.449-1925_449-1924i others(51): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197071 | |||||
| chr12:7197071
|
GTAATTAT others(66): Show |
G | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.449-1924_449-1852d others(75): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197071 | |||||
| chr12:7197074
|
AT | A | 8 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(5): Show | 9 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-1935delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197074 | |||||
| chr12:7197074
|
ATTATATA others(14): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0107 | 2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.449-1935_449-1915d others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197074 | |||||
| chr12:7197076
|
T | A | 8 | a0001c0001t0003g0010a0001c0001t0003g0034a0001c0001t0003g0191others(5): Show | 12 | HG02622.hp2 HG02809.hp2 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-1935T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197076 | ||||||
| chr12:7197077
|
A | AT | 4 | a0001c0001t0003g0010a0001c0001t0003g0034a0001c0001t0003g0191others(1): Show | 8 | NA18962.hp2 NA18973.hp1 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-1933dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197077 | |||||
| chr12:7197084
|
TCA | T | 17 | a0001c0001t0002g0011a0001c0001t0002g0029a0001c0001t0002g0167others(14): Show | 21 | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.449-1924_449-1923d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197084 | |||||
| chr12:7197087
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(217): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.449-1924C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197087 | ||||||
| chr12:7197091
|
T | C | 4 | a0002c0002t0005g0314a0003c0003t0004g0044a0003c0003t0004g0293others(1): Show | 5 | HG02486.hp1 HG02970.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1920T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197091 | ||||||
| chr12:7197095
|
G | GTAA | 87 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(84): Show | 109 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.449-1914_449-1912d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197095 | |||||
| chr12:7197095
|
GTAATTAT others(42): Show |
G | 12 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0089others(9): Show | 14 | HG01081.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.449-1896_449-1848d others(51): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197095 | |||||
| chr12:7197098
|
AT | A | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-1911delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197098 | |||||
| chr12:7197098
|
ATTATATA others(12): Show |
A | 2 | a0002c0002t0002g0307a0002c0002t0002g0308 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.449-1911_449-1893d others(21): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197098 | |||||
| chr12:7197100
|
T | A | 17 | a0001c0001t0002g0011a0001c0001t0002g0029a0001c0001t0002g0167others(14): Show | 21 | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.449-1911T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197100 | ||||||
| chr12:7197100
|
TATATATG others(15): Show |
T | 20 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(17): Show | 22 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.449-1896_449-1875d others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197100 | |||||
| chr12:7197102
|
T | C | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1909T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197102 | ||||||
| chr12:7197105
|
A | G | 1 | a0001c0001t0007g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.449-1906A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197105 | ||||||
| chr12:7197107
|
G | C | 1 | a0001c0001t0007g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.449-1904G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197107 | ||||||
| chr12:7197108
|
T | A | 2 | a0001c0001t0004g0223a0001c0001t0007g0209 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.449-1903T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197108 | ||||||
| chr12:7197109
|
C | CAT | 204 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(201): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.449-1898_449-1897d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197109 | |||||
| chr12:7197109
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0132a0001c0001t0001g0297others(1): Show | 5 | HG01361.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-1902C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197109 | ||||||
| chr12:7197113
|
T | TAC | 5 | a0001c0001t0008g0004a0001c0001t0008g0226a0003c0003t0004g0044others(2): Show | 11 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.449-1897_449-1896i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197113 | |||||
| chr12:7197121
|
TAA | T | 6 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0165others(3): Show | 7 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1889_449-1888d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197121 | ||||||
| chr12:7197122
|
A | AATT | 100 | a0001c0001t0002g0011a0001c0001t0002g0029a0001c0001t0002g0167others(97): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.449-1887_449-1886i others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197122 | |||||
| chr12:7197122
|
A | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(106): Show | 125 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.449-1889A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197122 | ||||||
| chr12:7197124
|
T | TC | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1887_449-1886i others(3): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197124 | ||||||
| chr12:7197137
|
T | C | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1874T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197137 | ||||||
| chr12:7197141
|
GTAA | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.449-1865_449-1863d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197141 | |||||
| chr12:7197144
|
A | ATAATTAT others(17): Show |
6 | a0001c0001t0002g0174a0001c0001t0002g0265a0001c0001t0002g0278others(3): Show | 7 | HG00558.hp1 HG01934.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1800_449-1777d others(26): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATAATTAT others(41): Show |
48 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0012others(45): Show | 67 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.449-1824_449-1777d others(50): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATAATTAT others(65): Show |
6 | a0001c0001t0002g0017a0001c0001t0002g0254a0001c0001t0002g0267others(3): Show | 8 | HG02074.hp1 HG03486.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-1848_449-1777d others(74): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATAATTAT others(89): Show |
2 | a0001c0001t0002g0229a0001c0001t0002g0253 | 2 | NA18954.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.449-1777_449-1776i others(98): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATAATTAT others(113): Show |
1 | a0001c0001t0002g0287 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.449-1777_449-1776i others(122): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATTATATA others(14): Show |
10 | a0001c0001t0002g0011a0001c0001t0002g0029a0001c0001t0002g0167others(7): Show | 14 | HG01070.hp1 HG01081.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1866_449-1865i others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATTATATA others(38): Show |
1 | a0001c0001t0002g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.449-1866_449-1865i others(47): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | ATTATATA others(86): Show |
1 | a0001c0005t0012g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.449-1866_449-1865i others(95): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197144 | |||||
| chr12:7197144
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.449-1867A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197144 | ||||||
| chr12:7197145
|
TAATTA | T | 7 | a0001c0001t0001g0086a0001c0001t0007g0028a0001c0001t0007g0163others(4): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-1865_449-1861d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197145 | ||||||
| chr12:7197153
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.449-1858T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197153 | ||||||
| chr12:7197163
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0153 | 3 | HG01978.hp1 HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.449-1848A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197163 | ||||||
| chr12:7197164
|
T | C | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1847T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197164 | ||||||
| chr12:7197165
|
AATGTAAT others(80): Show |
A | 2 | a0001c0001t0008g0004a0001c0001t0008g0226 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1838_449-1752d others(89): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197165 | |||||
| chr12:7197166
|
ATG | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0153 | 3 | HG01978.hp1 HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.449-1843_449-1842d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197166 | |||||
| chr12:7197168
|
G | GTAA | 83 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(80): Show | 105 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.449-1841_449-1839d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197168 | |||||
| chr12:7197171
|
ATTATATA others(14): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.449-1838_449-1818d others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197171 | |||||
| chr12:7197172
|
TTA | T | 11 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0153others(8): Show | 12 | HG01891.hp2 HG01978.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-1833_449-1832d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197172 | |||||
| chr12:7197173
|
T | A | 3 | a0001c0001t0004g0212a0001c0001t0004g0220a0002c0002t0004g0326 | 3 | HG02886.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.449-1838T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197173 | ||||||
| chr12:7197174
|
A | ATATATGT others(15): Show |
3 | a0001c0001t0002g0019a0001c0001t0004g0302a0001c0010t0002g0019 | 4 | HG02055.hp2 NA18949.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1831_449-1810d others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197174 | |||||
| chr12:7197174
|
A | ATATATGT others(39): Show |
1 | a0008c0008t0002g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.449-1831_449-1786d others(48): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197174 | |||||
| chr12:7197175
|
T | C | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-1836T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197175 | ||||||
| chr12:7197175
|
TA | T | 3 | a0001c0001t0004g0212a0001c0001t0004g0220a0002c0002t0004g0326 | 3 | HG02886.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.449-1835delA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197175 | ||||||
| chr12:7197184
|
TATATA | T | 4 | a0001c0001t0004g0037a0001c0001t0004g0216a0001c0001t0004g0224others(1): Show | 5 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1824_449-1820d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197184 | |||||
| chr12:7197187
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0004g0220a0002c0002t0001g0162 | 3 | HG02486.hp2 HG03471.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.449-1824A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197187 | ||||||
| chr12:7197188
|
T | C | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-1823T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197188 | ||||||
| chr12:7197189
|
A | C | 1 | a0001c0001t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.449-1822A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197189 | ||||||
| chr12:7197192
|
G | GTAA | 36 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0092others(33): Show | 39 | HG00621.hp2 HG01070.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.449-1817_449-1815d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197192 | |||||
| chr12:7197195
|
ATTATATA others(14): Show |
A | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.449-1814_449-1794d others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197195 | |||||
| chr12:7197195
|
ATTATATA others(33): Show |
A | 2 | a0001c0001t0001g0064a0001c0001t0001g0091 | 2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.449-1814_449-1775d others(42): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197195 | |||||
| chr12:7197196
|
TTA | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0150a0001c0001t0001g0153others(2): Show | 5 | HG01891.hp2 HG02148.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1809_449-1808d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197196 | |||||
| chr12:7197197
|
T | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(60): Show | 83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.449-1814T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197197 | ||||||
| chr12:7197199
|
TA | T | 62 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(59): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.449-1811delA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197199 | ||||||
| chr12:7197211
|
A | ATAATGTA others(89): Show |
1 | a0001c0001t0002g0261 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.449-1777_449-1776i others(98): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197211 | |||||
| chr12:7197211
|
A | G | 1 | a0002c0002t0004g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-1800A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197211 | ||||||
| chr12:7197212
|
T | C | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-1799T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197212 | ||||||
| chr12:7197213
|
A | AATGTAAT others(36): Show |
2 | a0001c0001t0004g0003a0001c0001t0004g0305 | 8 | HG02451.hp2 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-1777_449-1776i others(45): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197213 | |||||
| chr12:7197213
|
AATGTAAT others(12): Show |
A | 1 | a0001c0001t0008g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-1790_449-1772d others(21): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197213 | |||||
| chr12:7197213
|
AATGTAAT others(32): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.449-1790_449-1752d others(41): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197213 | |||||
| chr12:7197216
|
G | GTAA | 195 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.449-1793_449-1791d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197216 | |||||
| chr12:7197216
|
G | GTAATAAT others(19): Show |
1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-1791_449-1790i others(28): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197216 | |||||
| chr12:7197219
|
ATTATATA others(9): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.449-1790_449-1775d others(18): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197219 | |||||
| chr12:7197221
|
T | A | 18 | a0001c0001t0001g0109a0001c0001t0001g0153a0001c0001t0004g0212others(15): Show | 19 | HG00621.hp2 HG01070.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.449-1790T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197221 | ||||||
| chr12:7197222
|
A | AT | 3 | a0001c0001t0001g0109a0001c0001t0001g0153a0001c0001t0004g0212 | 3 | HG02080.hp2 HG03195.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.449-1788dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197222 | |||||
| chr12:7197222
|
A | ATATATGT others(61): Show |
2 | a0001c0001t0002g0040a0001c0001t0002g0275 | 3 | HG03516.hp1 NA18986.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.449-1777_449-1776i others(70): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197222 | |||||
| chr12:7197222
|
A | ATATATGT others(37): Show |
3 | a0001c0001t0002g0228a0001c0001t0002g0241a0001c0001t0002g0276 | 3 | NA18962.hp1 NA19059.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.449-1777_449-1776i others(46): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197222 | |||||
| chr12:7197223
|
TA | T | 8 | a0001c0001t0005g0205a0001c0001t0005g0206a0001c0001t0005g0208others(5): Show | 8 | HG00621.hp2 HG01070.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-1787delA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197223 | ||||||
| chr12:7197224
|
A | G | 1 | a0002c0002t0004g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-1787A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197224 | ||||||
| chr12:7197228
|
G | A | 1 | a0002c0002t0004g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-1783G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197228 | ||||||
| chr12:7197230
|
C | A | 1 | a0002c0002t0004g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-1781C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197230 | ||||||
| chr12:7197231
|
A | T | 1 | a0002c0002t0004g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-1780A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197231 | ||||||
| chr12:7197232
|
T | A | 1 | a0002c0002t0004g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-1779T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197232 | ||||||
| chr12:7197232
|
T | TATATA | 19 | a0001c0001t0004g0212a0001c0001t0004g0214a0001c0001t0004g0219others(16): Show | 20 | HG00621.hp2 HG01070.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.449-1777_449-1776i others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197232 | |||||
| chr12:7197232
|
T | TATATAAT others(39): Show |
1 | a0001c0001t0002g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.449-1777_449-1776i others(48): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197232 | |||||
| chr12:7197232
|
T | TATGTAAT others(16): Show |
1 | a0002c0002t0005g0323 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.449-1766_449-1765i others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197232 | |||||
| chr12:7197232
|
T | TGTAATAA others(14): Show |
1 | a0001c0001t0004g0037 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.449-1779_449-1778i others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197232 | ||||||
| chr12:7197232
|
T | TGTAATAA others(59): Show |
1 | a0001c0001t0004g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.449-1779_449-1778i others(68): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197232 | ||||||
| chr12:7197235
|
G | A | 12 | a0001c0001t0001g0153a0001c0001t0002g0168a0001c0001t0002g0169others(9): Show | 12 | HG01123.hp1 HG01175.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.449-1776G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197235 | ||||||
| chr12:7197237
|
AATAATTA others(8): Show |
A | 2 | a0001c0001t0001g0153a0002c0002t0001g0162 | 2 | HG02486.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.449-1771_449-1757d others(17): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197237 | |||||
| chr12:7197238
|
A | ATG | 8 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0173others(5): Show | 8 | HG01123.hp1 HG01175.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-1772_449-1771i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197238 | |||||
| chr12:7197238
|
A | ATGTAATT others(43): Show |
1 | a0001c0001t0002g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.449-1772_449-1771i others(52): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197238 | |||||
| chr12:7197238
|
A | ATGTAATT others(91): Show |
1 | a0001c0001t0002g0242 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.449-1772_449-1771i others(100): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197238 | |||||
| chr12:7197240
|
A | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0091others(2): Show | 5 | HG02055.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1771A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197240 | ||||||
| chr12:7197241
|
AT | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0091others(2): Show | 5 | HG02055.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1768delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197241 | |||||
| chr12:7197242
|
T | TTA | 26 | a0001c0001t0001g0128a0001c0001t0002g0168a0001c0001t0002g0169others(23): Show | 27 | HG00621.hp2 HG01070.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.449-1765_449-1764d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197242
|
T | TTATGTCA others(60): Show |
1 | a0001c0001t0005g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.449-1766_449-1765i others(69): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197242
|
T | TTATGTCA others(18): Show |
11 | a0001c0001t0004g0216a0001c0001t0004g0220a0001c0001t0004g0298others(8): Show | 13 | HG00735.hp2 HG01109.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.449-1766_449-1765i others(27): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197242
|
T | TTATGTCA others(63): Show |
7 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0213others(4): Show | 9 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-1766_449-1765i others(72): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197242
|
T | TTATGTCA others(61): Show |
2 | a0001c0001t0004g0211a0001c0001t0004g0217 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.449-1766_449-1765i others(70): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197242
|
TTA | T | 50 | a0001c0001t0001g0147a0001c0001t0003g0005a0001c0001t0003g0010others(47): Show | 67 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.449-1765_449-1764d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197242
|
TTATATGT others(15): Show |
T | 2 | a0001c0001t0001g0097a0001c0001t0001g0116 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.449-1756_449-1735d others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197242 | |||||
| chr12:7197244
|
A | ATATATGT others(13): Show |
1 | a0001c0001t0002g0251 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.449-1764_449-1763i others(22): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197244 | |||||
| chr12:7197252
|
T | TATATA | 193 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.449-1757_449-1756i others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197252 | |||||
| chr12:7197255
|
G | A | 8 | a0001c0001t0001g0115a0001c0001t0002g0168a0001c0001t0002g0169others(5): Show | 8 | HG01123.hp1 HG01175.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-1756G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197255 | ||||||
| chr12:7197257
|
A | AATAATTA others(41): Show |
1 | a0001c0001t0002g0272 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.449-1707_449-1706i others(50): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197257 | |||||
| chr12:7197258
|
A | ATG | 7 | a0001c0001t0001g0115a0001c0001t0002g0168a0001c0001t0002g0169others(4): Show | 7 | HG01123.hp1 HG01175.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1752_449-1751i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197258 | |||||
| chr12:7197262
|
T | G | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1749T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197262 | ||||||
| chr12:7197262
|
TTA | T | 43 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0091others(40): Show | 60 | HG00280.hp1 HG00735.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.449-1743_449-1742d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197262 | |||||
| chr12:7197263
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.449-1748T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197263 | ||||||
| chr12:7197264
|
A | ATATATGT others(15): Show |
1 | a0002c0002t0005g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.449-1746_449-1725d others(24): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197264 | |||||
| chr12:7197264
|
A | ATGTCATA others(41): Show |
7 | a0001c0001t0005g0205a0001c0001t0005g0208a0002c0002t0005g0313others(4): Show | 7 | HG00621.hp2 HG01070.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1746_449-1745i others(50): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197264 | |||||
| chr12:7197264
|
A | ATGTCATA others(86): Show |
1 | a0001c0001t0004g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.449-1746_449-1745i others(95): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197264 | |||||
| chr12:7197264
|
A | ATGTCATA others(41): Show |
1 | a0001c0001t0005g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.449-1746_449-1745i others(50): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197264 | |||||
| chr12:7197264
|
A | ATGTCATA others(83): Show |
1 | a0001c0001t0004g0219 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.449-1746_449-1745i others(92): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197264 | |||||
| chr12:7197265
|
T | A | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1746T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197265 | ||||||
| chr12:7197266
|
A | T | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1745A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197266 | ||||||
| chr12:7197267
|
T | C | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1744T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197267 | ||||||
| chr12:7197272
|
C | A | 2 | a0001c0001t0004g0302a0001c0001t0004g0303 | 2 | HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.449-1739C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197272 | ||||||
| chr12:7197274
|
TATATA | T | 4 | a0001c0001t0002g0247a0001c0001t0002g0286a0001c0001t0004g0003others(1): Show | 10 | HG02129.hp1 HG02451.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.449-1734_449-1730d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197274 | |||||
| chr12:7197277
|
A | G | 4 | a0001c0001t0002g0169a0001c0001t0002g0173a0001c0001t0002g0239others(1): Show | 4 | HG01123.hp1 HG01175.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1734A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197277 | ||||||
| chr12:7197278
|
T | C | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1733T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197278 | ||||||
| chr12:7197278
|
T | TAATGTAA others(65): Show |
4 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0310others(1): Show | 6 | HG00597.hp2 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-1717_449-1716i others(74): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197278 | |||||
| chr12:7197279
|
A | AATAATTA others(8): Show |
3 | a0001c0001t0002g0169a0001c0001t0002g0173a0001c0001t0002g0239 | 3 | HG01123.hp1 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.449-1730_449-1729i others(17): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197279 | |||||
| chr12:7197279
|
A | AATGTAAT others(32): Show |
2 | a0001c0001t0002g0168a0001c0001t0002g0235 | 2 | HG03017.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.449-1725_449-1724i others(41): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197279 | |||||
| chr12:7197291
|
A | ATATGTCA others(16): Show |
1 | a0001c0001t0004g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.449-1717_449-1716i others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197291 | |||||
| chr12:7197299
|
CAT | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-1706_449-1705d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197299 | |||||
| chr12:7197305
|
T | C | 8 | a0001c0001t0001g0141a0001c0001t0004g0212a0001c0001t0011g0021others(5): Show | 10 | HG00597.hp2 HG01978.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.449-1706T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197305 | ||||||
| chr12:7197306
|
A | G | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1705A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197306 | ||||||
| chr12:7197313
|
T | TAATTA | 19 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0173others(16): Show | 26 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.449-1698_449-1697i others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197313 | ||||||
| chr12:7197313
|
T | TTA | 4 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0310others(1): Show | 6 | HG00597.hp2 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-1698_449-1697i others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197313 | ||||||
| chr12:7197314
|
C | A | 40 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(37): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.449-1697C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197314 | ||||||
| chr12:7197314
|
C | CATATGTC others(20): Show |
1 | a0001c0001t0002g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.449-1638_449-1612d others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197314 | |||||
| chr12:7197314
|
C | T | 23 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0173others(20): Show | 32 | HG00597.hp2 HG01123.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.449-1697C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197314 | ||||||
| chr12:7197314
|
CAT | C | 41 | a0001c0001t0001g0079a0001c0001t0004g0035a0001c0001t0004g0036others(38): Show | 47 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.449-1694_449-1693d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197314 | |||||
| chr12:7197316
|
T | TTATATAT others(14): Show |
1 | a0001c0001t0003g0202 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.449-1695_449-1694i others(23): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197316 | ||||||
| chr12:7197316
|
T | TTATATAT others(16): Show |
36 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(33): Show | 49 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.449-1695_449-1694i others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197316 | ||||||
| chr12:7197316
|
T | TTATATAT others(43): Show |
3 | a0001c0001t0003g0030a0001c0001t0003g0182a0001c0001t0003g0210 | 4 | NA18747.hp2 NA18997.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1695_449-1694i others(52): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197316 | ||||||
| chr12:7197327
|
C | T | 18 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0173others(15): Show | 25 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.449-1684C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197327 | ||||||
| chr12:7197328
|
A | G | 1 | a0001c0001t0004g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.449-1683A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197328 | ||||||
| chr12:7197335
|
TAATTA | T | 18 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0173others(15): Show | 25 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.449-1675_449-1671d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197335 | ||||||
| chr12:7197341
|
T | C | 18 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0173others(15): Show | 25 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.449-1670T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197341 | ||||||
| chr12:7197355
|
A | G | 18 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(15): Show | 21 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.449-1656A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197355 | ||||||
| chr12:7197361
|
ATAAT | A | 5 | a0001c0001t0004g0212a0001c0001t0011g0021a0002c0002t0005g0045others(2): Show | 7 | HG00597.hp2 HG02083.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1647_449-1644d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197361 | |||||
| chr12:7197363
|
A | T | 1 | a0002c0002t0005g0322 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.449-1648A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197363 | ||||||
| chr12:7197364
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.449-1647A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197364 | ||||||
| chr12:7197365
|
T | TATATGTC others(40): Show |
1 | a0002c0002t0005g0322 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.449-1646_449-1645i others(49): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197365 | ||||||
| chr12:7197365
|
T | TTATATAT others(16): Show |
1 | a0002c0002t0005g0316 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.449-1643_449-1621d others(25): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197365 | |||||
| chr12:7197365
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.449-1612_449-1611i others(52): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197365 | |||||
| chr12:7197365
|
T | TTATATAT others(43): Show |
13 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(10): Show | 16 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.449-1630_449-1629i others(52): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197365 | |||||
| chr12:7197366
|
T | TATATATG others(41): Show |
4 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(1): Show | 4 | HG01243.hp1 HG02647.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1630_449-1629i others(50): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197366 | |||||
| chr12:7197382
|
A | G | 1 | a0001c0001t0004g0219 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.449-1629A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197382 | ||||||
| chr12:7197391
|
A | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.449-1620A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197391 | ||||||
| chr12:7197392
|
TTA | T | 21 | a0001c0001t0004g0219a0001c0001t0004g0273a0001c0001t0005g0205others(18): Show | 24 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.449-1611_449-1610d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197392 | |||||
| chr12:7197392
|
TTATA | T | 8 | a0001c0001t0001g0097a0001c0001t0003g0005a0001c0001t0003g0030others(5): Show | 13 | HG02132.hp2 HG02965.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.449-1613_449-1610d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197392 | |||||
| chr12:7197393
|
T | TATATGTC others(12): Show |
3 | a0001c0001t0003g0033a0001c0001t0003g0188a0001c0001t0003g0196 | 4 | HG02738.hp2 NA18952.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1614_449-1613i others(21): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197393 | |||||
| chr12:7197394
|
A | ATATGTCA others(39): Show |
29 | a0001c0001t0003g0010a0001c0001t0003g0016a0001c0001t0003g0031others(26): Show | 37 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.449-1614_449-1613i others(48): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197394 | |||||
| chr12:7197394
|
A | ATGTCATA others(37): Show |
1 | a0001c0001t0003g0202 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.449-1616_449-1615i others(46): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197394 | |||||
| chr12:7197417
|
AT | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.449-1592delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197417 | |||||
| chr12:7197418
|
T | TA | 27 | a0001c0001t0003g0005a0001c0001t0003g0030a0001c0001t0003g0180others(24): Show | 35 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.449-1593_449-1592i others(3): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197418 | ||||||
| chr12:7197418
|
T | TAATTA | 3 | a0001c0001t0003g0033a0001c0001t0003g0188a0001c0001t0003g0196 | 4 | HG02738.hp2 NA18952.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1593_449-1592i others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197418 | ||||||
| chr12:7197418
|
T | TTA | 66 | a0001c0001t0003g0010a0001c0001t0003g0016a0001c0001t0003g0031others(63): Show | 85 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.449-1589_449-1588d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197418 | |||||
| chr12:7197426
|
C | T | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.449-1585C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197426 | ||||||
| chr12:7197428
|
T | C | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.449-1583T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197428 | ||||||
| chr12:7197432
|
C | T | 30 | a0001c0001t0003g0010a0001c0001t0003g0016a0001c0001t0003g0031others(27): Show | 38 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.449-1579C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197432 | ||||||
| chr12:7197440
|
T | TAATTATA others(69): Show |
2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.449-1571_449-1570i others(78): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TAATTATA others(73): Show |
2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.449-1571_449-1570i others(82): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TAATTATA others(100): Show |
11 | a0001c0001t0005g0207a0001c0001t0005g0208a0002c0002t0005g0313others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.449-1571_449-1570i others(109): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TAATTATA others(127): Show |
2 | a0002c0002t0005g0312a0002c0002t0005g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.449-1571_449-1570i others(136): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TAATTATA others(97): Show |
1 | a0002c0002t0005g0020 | 3 | HG00735.hp2 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.449-1571_449-1570i others(106): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TAATTATA others(71): Show |
1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-1571_449-1570i others(80): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TAATTATA others(71): Show |
7 | a0001c0001t0003g0005a0001c0001t0003g0030a0001c0001t0003g0180others(4): Show | 12 | HG02132.hp2 NA18747.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.449-1571_449-1570i others(80): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197440 | ||||||
| chr12:7197440
|
T | TTATA | 3 | a0001c0001t0003g0033a0001c0001t0003g0188a0001c0001t0003g0196 | 4 | HG02738.hp2 NA18952.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1568_449-1567i others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197440 | |||||
| chr12:7197440
|
T | TTATGTTA others(20): Show |
1 | a0001c0001t0002g0259 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.449-1555_449-1529d others(29): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197440 | |||||
| chr12:7197446
|
T | C | 4 | a0001c0001t0003g0033a0001c0001t0003g0188a0001c0001t0003g0196others(1): Show | 5 | HG02738.hp2 HG06807.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1565T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197446 | ||||||
| chr12:7197452
|
T | C | 1 | a0001c0001t0004g0219 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.449-1559T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197452 | ||||||
| chr12:7197456
|
GTAA | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 148 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.449-1550_449-1548d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197456 | |||||
| chr12:7197460
|
TAATTA | T | 4 | a0002c0002t0009g0332a0002c0002t0009g0334a0002c0002t0009g0335others(1): Show | 4 | HG02056.hp2 NA19004.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-1550_449-1546d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197460 | ||||||
| chr12:7197460
|
TAATTATA | T | 3 | a0001c0001t0003g0033a0001c0001t0003g0188a0001c0001t0003g0196 | 4 | HG02738.hp2 NA18952.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1550_449-1544d others(9): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197460 | ||||||
| chr12:7197461
|
A | T | 1 | a0001c0001t0004g0219 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.449-1550A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197461 | ||||||
| chr12:7197475
|
TATATA | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0092others(6): Show | 9 | NA18941.hp1 NA18942.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-1527_449-1523d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197475 | |||||
| chr12:7197482
|
TATA | T | 6 | a0001c0001t0002g0278a0001c0001t0002g0285a0001c0001t0003g0031others(3): Show | 7 | HG02970.hp2 NA18946.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1523_449-1521d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197482 | |||||
| chr12:7197483
|
A | G | 80 | a0001c0001t0002g0274a0001c0001t0003g0005a0001c0001t0003g0010others(77): Show | 100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.449-1528A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197483 | ||||||
| chr12:7197486
|
A | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0181a0001c0001t0003g0184 | 4 | NA18954.hp2 NA18964.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1525A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197486 | ||||||
| chr12:7197490
|
TTA | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.449-1515_449-1514d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197490 | |||||
| chr12:7197517
|
T | TTA | 58 | a0001c0001t0001g0159a0001c0001t0003g0005a0001c0001t0003g0010others(55): Show | 74 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.449-1490_449-1489d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197517 | |||||
| chr12:7197517
|
T | TTATATAT others(49): Show |
5 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0310others(2): Show | 7 | HG00597.hp2 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1489_449-1488i others(58): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197517 | |||||
| chr12:7197517
|
T | TTATATAT others(76): Show |
1 | a0002c0002t0005g0316 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.449-1489_449-1488i others(85): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197517 | |||||
| chr12:7197517
|
TTA | T | 4 | a0001c0001t0001g0078a0001c0001t0008g0004a0001c0001t0008g0225others(1): Show | 9 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-1490_449-1489d others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197517 | |||||
| chr12:7197535
|
G | GTAA | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.449-1474_449-1472d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197535 | |||||
| chr12:7197540
|
T | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.449-1471T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197540 | ||||||
| chr12:7197541
|
A | AT | 83 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(80): Show | 105 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.449-1469dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197541 | |||||
| chr12:7197541
|
A | ATTATATG others(19): Show |
2 | a0001c0001t0004g0212a0001c0001t0004g0213 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.449-1469_449-1468i others(28): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197541 | |||||
| chr12:7197545
|
A | G | 40 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(37): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.449-1466A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197545 | ||||||
| chr12:7197558
|
TATA | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0272 | 3 | NA18988.hp1 NA19001.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.449-1448_449-1446d others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197558 | |||||
| chr12:7197559
|
A | G | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.449-1452A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197559 | ||||||
| chr12:7197567
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.449-1444T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197567 | ||||||
| chr12:7197614
|
T | TC | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-1396dupC | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7197614 | |||||
| chr12:7197659
|
T | A | 1 | a0001c0001t0004g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.449-1352T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197659 | ||||||
| chr12:7197659
|
T | G | 3 | a0002c0002t0005g0312a0002c0002t0005g0315a0002c0002t0005g0316 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.449-1352T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197659 | ||||||
| chr12:7197663
|
T | A | 3 | a0002c0002t0005g0312a0002c0002t0005g0315a0002c0002t0005g0316 | 3 | HG01109.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.449-1348T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197663 | ||||||
| chr12:7197684
|
A | T | 40 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(37): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.449-1327A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197684 | ||||||
| chr12:7197687
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-1324T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197687 | ||||||
| chr12:7197853
|
T | C | 1 | a0001c0001t0003g0195 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.449-1158T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197853 | ||||||
| chr12:7197888
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.449-1123C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7197888 | ||||||
| chr12:7198009
|
T | C | 1 | a0002c0002t0005g0314 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.449-1002T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198009 | ||||||
| chr12:7198012
|
TTG | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.449-995_449-994del others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7198012 | |||||
| chr12:7198046
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.449-965T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198046 | ||||||
| chr12:7198097
|
A | G | 1 | a0002c0002t0005g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.449-914A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198097 | ||||||
| chr12:7198140
|
A | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.449-871A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198140 | ||||||
| chr12:7198195
|
A | G | 338 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.449-816A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198195 | ||||||
| chr12:7198196
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.449-815A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198196 | ||||||
| chr12:7198303
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 4 | HG01256.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-708G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198303 | ||||||
| chr12:7198309
|
G | A | 8 | a0001c0001t0002g0039a0001c0001t0002g0227a0001c0001t0002g0245others(5): Show | 9 | HG00558.hp2 HG02027.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-702G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198309 | ||||||
| chr12:7198415
|
T | G | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.449-596T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198415 | ||||||
| chr12:7198418
|
T | TA | 20 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0049others(17): Show | 24 | HG00735.hp1 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.449-592dupA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 7198418 | |||||
| chr12:7198480
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-531G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198480 | ||||||
| chr12:7198569
|
G | A | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.449-442G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198569 | ||||||
| chr12:7198703
|
T | C | 1 | a0001c0001t0015g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.449-308T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198703 | ||||||
| chr12:7198717
|
A | G | 1 | a0001c0001t0004g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.449-294A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 5/15 | chr12 | 7198717 | ||||||
| chr12:7199136
|
G | A | 20 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(17): Show | 23 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.551+23G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199136 | ||||||
| chr12:7199140
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0288 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.551+27C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199140 | ||||||
| chr12:7199184
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0001g0131others(2): Show | 5 | HG00140.hp1 HG01081.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.551+71C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199184 | ||||||
| chr12:7199185
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.551+72G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199185 | ||||||
| chr12:7199209
|
C | CT | 23 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0093others(20): Show | 31 | HG00673.hp2 HG01496.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.551+114dupT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7199209 | |||||
| chr12:7199209
|
C | CTT | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 150 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.551+113_551+114dup others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7199209 | |||||
| chr12:7199209
|
CT | C | 11 | a0001c0001t0002g0006a0001c0001t0002g0041a0001c0001t0002g0248others(8): Show | 16 | HG00558.hp2 HG00609.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.551+114delT | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7199209 | |||||
| chr12:7199227
|
T | TA | 12 | a0001c0001t0003g0032a0001c0001t0003g0184a0001c0001t0003g0190others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.551+115dupA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7199227 | |||||
| chr12:7199227
|
T | TTA | 34 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(31): Show | 48 | HG00438.hp2 HG01099.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.551+114_551+115ins others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199227 | ||||||
| chr12:7199227
|
T | TTTA | 37 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(34): Show | 44 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.551+114_551+115ins others(3): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199227 | ||||||
| chr12:7199228
|
A | T | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.551+115A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199228 | ||||||
| chr12:7199247
|
T | C | 329 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(326): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.551+134T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199247 | ||||||
| chr12:7199357
|
C | T | 1 | a0001c0001t0002g0284 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.551+244C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199357 | ||||||
| chr12:7199409
|
A | T | 9 | a0001c0001t0002g0029a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 10 | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.551+296A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199409 | ||||||
| chr12:7199411
|
A | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.551+298A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199411 | ||||||
| chr12:7199457
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.551+344C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199457 | ||||||
| chr12:7199620
|
A | G | 20 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(17): Show | 24 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.551+507A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199620 | ||||||
| chr12:7199635
|
T | C | 1 | a0001c0001t0002g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.551+522T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199635 | ||||||
| chr12:7199640
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.551+527A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199640 | ||||||
| chr12:7199714
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.551+601A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199714 | ||||||
| chr12:7199806
|
TGGACGGG others(87): Show |
T | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.551+740_551+833del others(94): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7199806 | |||||
| chr12:7199853
|
C | CGGACGGG others(87): Show |
9 | a0001c0001t0002g0029a0001c0001t0002g0167a0001c0001t0002g0168others(6): Show | 10 | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.551+762_551+855dup others(94): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7199853 | |||||
| chr12:7199853
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.551+740C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199853 | ||||||
| chr12:7199875
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 166 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.551+762A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199875 | ||||||
| chr12:7199889
|
CACCTCCC others(134): Show |
C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.551+777_551+917del | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199889 | ||||||
| chr12:7199905
|
G | A | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.551+792G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7199905 | ||||||
| chr12:7200013
|
A | G | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.551+900A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200013 | ||||||
| chr12:7200032
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.551+919A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200032 | ||||||
| chr12:7200042
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.551+929C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200042 | ||||||
| chr12:7200052
|
G | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0280a0001c0001t0002g0281others(2): Show | 6 | HG00408.hp1 HG02015.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.551+939G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200052 | ||||||
| chr12:7200060
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.551+947G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200060 | ||||||
| chr12:7200090
|
G | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.551+977G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200090 | ||||||
| chr12:7200093
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.551+980C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200093 | ||||||
| chr12:7200105
|
C | T | 2 | a0001c0001t0004g0212a0001c0001t0004g0213 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.551+992C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200105 | ||||||
| chr12:7200106
|
G | A | 1 | a0001c0001t0002g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.551+993G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200106 | ||||||
| chr12:7200116
|
G | A | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.551+1003G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200116 | ||||||
| chr12:7200139
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.551+1026G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200139 | ||||||
| chr12:7200172
|
A | G | 2 | a0002c0002t0002g0047a0002c0002t0002g0329 | 3 | HG03209.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.551+1059A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200172 | ||||||
| chr12:7200182
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.551+1069C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200182 | ||||||
| chr12:7200210
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.551+1097C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200210 | ||||||
| chr12:7200217
|
G | A | 1 | a0008c0008t0002g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.551+1104G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200217 | ||||||
| chr12:7200218
|
C | T | 2 | a0001c0001t0002g0234a0001c0001t0002g0257 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.551+1105C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200218 | ||||||
| chr12:7200232
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.551+1119C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200232 | ||||||
| chr12:7200233
|
G | A | 3 | a0003c0003t0004g0044a0003c0003t0004g0293a0003c0003t0004g0299 | 4 | HG02486.hp1 HG02970.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.551+1120G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200233 | ||||||
| chr12:7200287
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.551+1174C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200287 | ||||||
| chr12:7200307
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.551+1194A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200307 | ||||||
| chr12:7200374
|
C | T | 5 | a0001c0001t0011g0021a0002c0002t0005g0045a0002c0002t0005g0310others(2): Show | 7 | HG00597.hp2 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.551+1261C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200374 | ||||||
| chr12:7200402
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.551+1289C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200402 | ||||||
| chr12:7200468
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.552-1283C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200468 | ||||||
| chr12:7200562
|
G | A | 4 | a0001c0001t0002g0242a0001c0001t0002g0253a0001c0001t0002g0254others(1): Show | 4 | HG01943.hp1 NA18955.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.552-1189G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200562 | ||||||
| chr12:7200585
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.552-1166T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200585 | ||||||
| chr12:7200625
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.552-1126C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200625 | ||||||
| chr12:7200671
|
C | T | 1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552-1080C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200671 | ||||||
| chr12:7200691
|
C | A | 1 | a0001c0001t0003g0183 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.552-1060C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200691 | ||||||
| chr12:7200696
|
C | T | 2 | a0002c0002t0002g0307a0002c0002t0002g0308 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.552-1055C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200696 | ||||||
| chr12:7200755
|
C | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.552-996C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200755 | ||||||
| chr12:7200855
|
G | A | 8 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(5): Show | 9 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.552-896G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200855 | ||||||
| chr12:7200882
|
AAG | A | 20 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(17): Show | 23 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.552-864_552-863del others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7200882 | |||||
| chr12:7200901
|
C | T | 1 | a0003c0003t0004g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552-850C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200901 | ||||||
| chr12:7200903
|
TAGGGAG | T | 48 | a0001c0001t0003g0193a0001c0001t0004g0003a0001c0001t0004g0035others(45): Show | 62 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.552-825_552-820del others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7200903 | |||||
| chr12:7200903
|
TAGGGAGA others(5): Show |
T | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552-831_552-820del others(12): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7200903 | |||||
| chr12:7200918
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.552-833G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7200918 | ||||||
| chr12:7201007
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.552-744A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201007 | ||||||
| chr12:7201111
|
C | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.552-640C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201111 | ||||||
| chr12:7201118
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.552-633C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201118 | ||||||
| chr12:7201120
|
C | T | 3 | a0001c0001t0004g0035a0001c0001t0004g0214a0001c0001t0004g0298 | 4 | HG02559.hp2 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.552-631C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201120 | ||||||
| chr12:7201133
|
G | A | 4 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-618G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201133 | ||||||
| chr12:7201135
|
G | GCA | 22 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(19): Show | 25 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.552-604_552-603dup others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201135 | |||||
| chr12:7201135
|
G | GCACA | 58 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(55): Show | 76 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.552-606_552-603dup others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201135 | |||||
| chr12:7201135
|
GCACACAC others(3): Show |
G | 1 | a0001c0001t0002g0263 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.552-612_552-603del others(10): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201135 | |||||
| chr12:7201148
|
CGCACACA others(21): Show |
C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.552-602_552-575del others(28): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201148 | ||||||
| chr12:7201149
|
G | A | 22 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(19): Show | 27 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.552-602G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201149 | ||||||
| chr12:7201151
|
A | ACG | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.552-599_552-598ins others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201151 | |||||
| chr12:7201158
|
T | C | 20 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(17): Show | 24 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.552-593T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201158 | ||||||
| chr12:7201160
|
T | C | 1 | a0002c0002t0005g0323 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.552-591T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201160 | ||||||
| chr12:7201178
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.552-573T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201178 | ||||||
| chr12:7201187
|
G | A | 1 | a0001c0001t0002g0242 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.552-564G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201187 | ||||||
| chr12:7201187
|
GCATA | G | 3 | a0001c0001t0003g0200a0003c0003t0004g0044a0003c0003t0004g0299 | 4 | HG00099.hp1 HG02486.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-557_552-554del others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201187 | |||||
| chr12:7201190
|
T | C | 1 | a0001c0001t0003g0032 | 2 | HG00642.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.552-561T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201190 | ||||||
| chr12:7201194
|
T | C | 82 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(79): Show | 103 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.552-557T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201194 | ||||||
| chr12:7201197
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.552-554A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201197 | ||||||
| chr12:7201200
|
T | C | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.552-551T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201200 | ||||||
| chr12:7201202
|
C | T | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552-549C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201202 | ||||||
| chr12:7201242
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.552-509A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201242 | ||||||
| chr12:7201243
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.552-508A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201243 | ||||||
| chr12:7201259
|
G | A | 1 | a0001c0001t0003g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.552-492G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201259 | ||||||
| chr12:7201270
|
TAC | T | 33 | a0001c0001t0005g0205a0001c0001t0005g0206a0001c0001t0005g0207others(30): Show | 43 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.552-473_552-472del others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201270 | |||||
| chr12:7201276
|
CACAT | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.552-473_552-470del others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201276 | |||||
| chr12:7201296
|
CACACAT | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 171 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.552-442_552-437del others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201296 | |||||
| chr12:7201298
|
CACAT | C | 38 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(35): Show | 52 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.552-449_552-446del others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201298 | |||||
| chr12:7201306
|
C | G | 38 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(35): Show | 52 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.552-445C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201306 | ||||||
| chr12:7201307
|
ATACACAT others(46): Show |
A | 1 | a0001c0001t0013g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.552-442_552-390del others(53): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201307 | |||||
| chr12:7201310
|
C | G | 1 | a0001c0001t0003g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.552-441C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201310 | ||||||
| chr12:7201312
|
C | T | 1 | a0001c0001t0003g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.552-439C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201312 | ||||||
| chr12:7201328
|
C | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.552-423C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201328 | ||||||
| chr12:7201330
|
C | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.552-421C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201330 | ||||||
| chr12:7201332
|
T | C | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.552-419T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201332 | ||||||
| chr12:7201332
|
T | TATAC | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 159 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.552-418_552-417ins others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201332 | |||||
| chr12:7201342
|
T | C | 1 | a0001c0001t0015g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.552-409T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201342 | ||||||
| chr12:7201342
|
T | TATAC | 327 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.552-405_552-402dup others(4): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 7201342 | |||||
| chr12:7201427
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.552-324A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201427 | ||||||
| chr12:7201605
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.552-146T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 6/15 | chr12 | 7201605 | ||||||
| chr12:7202019
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.642+178A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 7/15 | chr12 | 7202019 | ||||||
| chr12:7202048
|
A | G | 1 | a0002c0002t0005g0313 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.643-193A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 7/15 | chr12 | 7202048 | ||||||
| chr12:7202051
|
C | T | 2 | a0001c0001t0002g0168a0001c0001t0002g0169 | 2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.643-190C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 7/15 | chr12 | 7202051 | ||||||
| chr12:7202056
|
G | C | 1 | a0001c0001t0002g0228 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.643-185G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 7/15 | chr12 | 7202056 | ||||||
| chr12:7202210
|
C | G | 1 | a0001c0001t0007g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-31C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 7/15 | chr12 | 7202210 | ||||||
| chr12:7202387
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+36C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 8/15 | chr12 | 7202387 | ||||||
| chr12:7202443
|
T | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0091others(2): Show | 5 | HG02622.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+92T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 8/15 | chr12 | 7202443 | ||||||
| chr12:7202731
|
C | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0027others(53): Show | 66 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.846+27C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7202731 | ||||||
| chr12:7202892
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.846+188C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7202892 | ||||||
| chr12:7202987
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.846+283T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7202987 | ||||||
| chr12:7203022
|
T | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.846+318T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203022 | ||||||
| chr12:7203172
|
A | AACTGGAC others(280): Show |
1 | a0001c0001t0008g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.847-257_847-256ins others(287): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203172 | |||||
| chr12:7203172
|
A | AACTGGAC others(290): Show |
2 | a0001c0001t0008g0004a0001c0001t0008g0225 | 7 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.847-257_847-256ins others(297): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203172 | |||||
| chr12:7203176
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.847-256A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203176 | ||||||
| chr12:7203177
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.847-255A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203177 | ||||||
| chr12:7203179
|
CTA | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 156 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.847-251_847-250del others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203179 | |||||
| chr12:7203180
|
T | TGGA | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0160others(2): Show | 5 | HG02080.hp2 HG02818.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-252_847-251ins others(3): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203180 | ||||||
| chr12:7203181
|
A | ATGCAC | 5 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0167others(2): Show | 8 | HG01070.hp1 HG01261.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.847-214_847-210dup others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203181 | |||||
| chr12:7203181
|
A | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0160others(2): Show | 5 | HG02080.hp2 HG02818.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-251A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203181 | ||||||
| chr12:7203181
|
ATG | A | 3 | a0001c0001t0003g0034a0001c0001t0003g0191a0004c0004t0003g0309 | 4 | NA18962.hp2 NA18973.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-250_847-249del others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203181 | ||||||
| chr12:7203181
|
ATGCACTG | A | 29 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(26): Show | 41 | HG00438.hp2 HG01099.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.847-250_847-244del others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203181 | ||||||
| chr12:7203181
|
ATGCACTG others(5): Show |
A | 24 | a0001c0001t0003g0032a0001c0001t0003g0195a0001c0001t0003g0196others(21): Show | 28 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.847-250_847-239del others(12): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203181 | ||||||
| chr12:7203181
|
ATGCACTG others(8): Show |
A | 1 | a0001c0001t0002g0265 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.847-224_847-210del others(15): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203181 | |||||
| chr12:7203181
|
ATGCACTG others(10): Show |
A | 29 | a0001c0001t0003g0190a0001c0001t0003g0199a0001c0001t0004g0219others(26): Show | 34 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.847-250_847-234del others(17): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203181 | ||||||
| chr12:7203182
|
TGC | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.847-249_847-248del others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203182 | ||||||
| chr12:7203184
|
C | A | 3 | a0001c0001t0003g0034a0001c0001t0003g0191a0004c0004t0003g0309 | 4 | NA18962.hp2 NA18973.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-248C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203184 | ||||||
| chr12:7203184
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.847-248C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203184 | ||||||
| chr12:7203188
|
G | A | 6 | a0001c0001t0003g0034a0001c0001t0003g0191a0001c0001t0008g0004others(3): Show | 12 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-244G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203188 | ||||||
| chr12:7203189
|
C | A | 32 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(29): Show | 45 | HG00438.hp2 HG01099.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.847-243C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203189 | ||||||
| chr12:7203189
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.847-243C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203189 | ||||||
| chr12:7203193
|
G | A | 35 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(32): Show | 53 | HG00438.hp2 HG01099.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.847-239G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203193 | ||||||
| chr12:7203194
|
C | A | 56 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(53): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.847-238C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203194 | ||||||
| chr12:7203194
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.847-238C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203194 | ||||||
| chr12:7203198
|
G | A | 59 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(56): Show | 81 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.847-234G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203198 | ||||||
| chr12:7203198
|
G | GGACTAGA others(233): Show |
1 | a0001c0001t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.847-234_847-233ins others(240): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203198 | ||||||
| chr12:7203199
|
C | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.847-233C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203199 | ||||||
| chr12:7203199
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 160 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.847-233C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203199 | ||||||
| chr12:7203203
|
G | A | 89 | a0001c0001t0001g0160a0001c0001t0003g0005a0001c0001t0003g0010others(86): Show | 116 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.847-229G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203203 | ||||||
| chr12:7203204
|
C | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.847-228C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203204 | ||||||
| chr12:7203204
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 160 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.847-228C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203204 | ||||||
| chr12:7203208
|
G | A | 89 | a0001c0001t0001g0160a0001c0001t0003g0005a0001c0001t0003g0010others(86): Show | 116 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.847-224G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203208 | ||||||
| chr12:7203209
|
C | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.847-223C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203209 | ||||||
| chr12:7203209
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 160 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.847-223C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203209 | ||||||
| chr12:7203212
|
T | TAGACTAG others(278): Show |
1 | a0002c0002t0001g0162 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.847-220_847-219ins others(285): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203212 | ||||||
| chr12:7203213
|
G | A | 99 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0113others(96): Show | 126 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.847-219G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203213 | ||||||
| chr12:7203214
|
C | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.847-218C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203214 | ||||||
| chr12:7203214
|
C | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 159 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.847-218C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203214 | ||||||
| chr12:7203217
|
T | A | 1 | a0002c0002t0001g0162 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.847-215T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203217 | ||||||
| chr12:7203218
|
G | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(151): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.847-214G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203218 | ||||||
| chr12:7203219
|
C | A | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.847-213C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203219 | ||||||
| chr12:7203219
|
C | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 159 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.847-213C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203219 | ||||||
| chr12:7203222
|
T | TAGACGAC others(285): Show |
1 | a0001c0001t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.847-209_847-208ins others(292): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACGAC others(285): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0120 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.847-209_847-208ins others(292): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACGAC others(290): Show |
2 | a0001c0001t0001g0084a0006c0009t0001g0102 | 2 | NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.847-209_847-208ins others(297): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(326): Show |
1 | a0001c0001t0001g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.847-209_847-208ins others(333): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(331): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG01106.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.847-209_847-208ins others(338): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(300): Show |
1 | a0001c0001t0001g0157 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(307): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(285): Show |
1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.847-209_847-208ins others(292): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(290): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0095 | 2 | HG00609.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.847-209_847-208ins others(297): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(295): Show |
40 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(37): Show | 48 | HG00099.hp2 HG00738.hp2 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(302): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(300): Show |
7 | a0001c0001t0001g0043a0001c0001t0001g0094a0001c0001t0001g0110others(4): Show | 8 | HG01361.hp1 HG01978.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(307): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(295): Show |
1 | a0001c0001t0001g0093 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(302): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(278): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0159 | 2 | HG03130.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.847-209_847-208ins others(285): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(283): Show |
4 | a0002c0002t0009g0332a0002c0002t0009g0334a0002c0002t0009g0335others(1): Show | 4 | HG02056.hp2 NA19004.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(290): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(271): Show |
1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(278): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(295): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056 | 5 | HG00642.hp2 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(302): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(317): Show |
1 | a0001c0001t0001g0025 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.847-209_847-208ins others(324): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(290): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0115others(2): Show | 5 | HG02056.hp1 NA18952.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(297): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(300): Show |
44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0026others(41): Show | 55 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(307): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(305): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0150 | 2 | HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.847-209_847-208ins others(312): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(288): Show |
1 | a0001c0001t0001g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.847-209_847-208ins others(295): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(278): Show |
1 | a0001c0001t0001g0107 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(285): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(283): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0097 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.847-209_847-208ins others(290): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(288): Show |
1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(295): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(271): Show |
1 | a0001c0001t0007g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(278): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(276): Show |
5 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0165others(2): Show | 6 | HG02818.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.847-209_847-208ins others(283): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(271): Show |
1 | a0001c0001t0007g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(278): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203222
|
T | TAGACTAG others(254): Show |
1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.847-209_847-208ins others(261): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203222 | |||||
| chr12:7203224
|
C | A | 1 | a0001c0001t0003g0191 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.847-208C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203224 | ||||||
| chr12:7203224
|
CATT | C | 84 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(81): Show | 106 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.847-206_847-204del others(3): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203224 | |||||
| chr12:7203226
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(138): Show | 170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.847-206T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203226 | ||||||
| chr12:7203229
|
C | CACTAACT others(25): Show |
4 | a0001c0001t0001g0160a0001c0001t0008g0004a0001c0001t0008g0225others(1): Show | 9 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.847-202_847-201ins others(32): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203229 | |||||
| chr12:7203229
|
C | CAG | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 161 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.847-202_847-201ins others(2): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 7203229 | |||||
| chr12:7203229
|
C | G | 84 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(81): Show | 106 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.847-203C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203229 | ||||||
| chr12:7203263
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.847-169T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203263 | ||||||
| chr12:7203302
|
C | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.847-130C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 9/15 | chr12 | 7203302 | ||||||
| chr12:7203666
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 11 | NA18940.hp1 NA18942.hp2 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.966+115G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7203666 | ||||||
| chr12:7203767
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.966+216C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7203767 | ||||||
| chr12:7203883
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.966+332G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7203883 | ||||||
| chr12:7203898
|
G | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.966+347G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7203898 | ||||||
| chr12:7203978
|
TTCTTA | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0025others(19): Show | 28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.966+432_966+436del others(5): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 7203978 | |||||
| chr12:7204026
|
A | T | 20 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0011g0021others(17): Show | 24 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.966+475A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204026 | ||||||
| chr12:7204145
|
T | C | 1 | a0001c0001t0004g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.966+594T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204145 | ||||||
| chr12:7204226
|
G | C | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+675G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204226 | ||||||
| chr12:7204228
|
G | C | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+677G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204228 | ||||||
| chr12:7204229
|
G | T | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+678G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204229 | ||||||
| chr12:7204230
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+679G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204230 | ||||||
| chr12:7204233
|
A | T | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+682A>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204233 | ||||||
| chr12:7204234
|
A | C | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+683A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204234 | ||||||
| chr12:7204236
|
A | C | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+685A>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204236 | ||||||
| chr12:7204237
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+686A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204237 | ||||||
| chr12:7204240
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+689A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204240 | ||||||
| chr12:7204241
|
C | T | 1 | a0001c0001t0002g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.966+690C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204241 | ||||||
| chr12:7204447
|
C | A | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.966+896C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204447 | ||||||
| chr12:7204457
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.966+906C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204457 | ||||||
| chr12:7204588
|
A | G | 1 | a0001c0001t0010g0233 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.966+1037A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204588 | ||||||
| chr12:7204601
|
A | G | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.966+1050A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204601 | ||||||
| chr12:7204676
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.966+1125C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204676 | ||||||
| chr12:7204679
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.966+1128A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204679 | ||||||
| chr12:7204719
|
G | A | 3 | a0001c0001t0004g0003a0001c0001t0004g0302a0001c0001t0004g0305 | 9 | HG02055.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+1168G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204719 | ||||||
| chr12:7204767
|
G | A | 1 | a0001c0001t0004g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.966+1216G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7204767 | ||||||
| chr12:7205063
|
C | T | 1 | a0001c0001t0005g0205 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.966+1512C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205063 | ||||||
| chr12:7205076
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.966+1525G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205076 | ||||||
| chr12:7205150
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.966+1599T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205150 | ||||||
| chr12:7205181
|
T | A | 1 | a0001c0001t0002g0269 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.966+1630T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205181 | ||||||
| chr12:7205181
|
TA | T | 4 | a0001c0001t0004g0003a0001c0001t0004g0302a0001c0001t0004g0303others(1): Show | 10 | HG02055.hp2 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.966+1634delA | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 7205181 | |||||
| chr12:7205233
|
G | T | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.966+1682G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205233 | ||||||
| chr12:7205301
|
TAGAC | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.966+1753_966+1756d others(6): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 7205301 | |||||
| chr12:7205556
|
G | A | 1 | a0001c0001t0002g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.966+2005G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205556 | ||||||
| chr12:7205680
|
G | A | 1 | a0001c0001t0019g0175 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.967-1979G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205680 | ||||||
| chr12:7205873
|
T | C | 40 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(37): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.967-1786T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205873 | ||||||
| chr12:7205895
|
A | G | 4 | a0001c0001t0004g0003a0001c0001t0004g0302a0001c0001t0004g0303others(1): Show | 10 | HG02055.hp2 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.967-1764A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205895 | ||||||
| chr12:7205913
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(223): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.967-1746T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7205913 | ||||||
| chr12:7206050
|
G | A | 85 | a0001c0001t0002g0242a0001c0001t0003g0005a0001c0001t0003g0010others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.967-1609G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206050 | ||||||
| chr12:7206088
|
C | T | 85 | a0001c0001t0002g0242a0001c0001t0003g0005a0001c0001t0003g0010others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.967-1571C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206088 | ||||||
| chr12:7206172
|
C | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.967-1487C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206172 | ||||||
| chr12:7206291
|
T | C | 21 | a0001c0001t0002g0242a0001c0001t0005g0207a0001c0001t0005g0208others(18): Show | 25 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.967-1368T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206291 | ||||||
| chr12:7206343
|
G | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0257 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.967-1316G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206343 | ||||||
| chr12:7206362
|
T | C | 2 | a0003c0003t0004g0044a0003c0003t0004g0299 | 3 | HG02486.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.967-1297T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206362 | ||||||
| chr12:7206407
|
G | C | 8 | a0001c0001t0002g0039a0001c0001t0002g0227a0001c0001t0002g0245others(5): Show | 9 | HG00558.hp2 HG02027.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.967-1252G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206407 | ||||||
| chr12:7206462
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.967-1197C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206462 | ||||||
| chr12:7206496
|
T | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(223): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.967-1163T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206496 | ||||||
| chr12:7206556
|
TC | T | 3 | a0001c0001t0003g0030a0001c0001t0003g0182a0001c0001t0003g0210 | 4 | NA18747.hp2 NA18997.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1102delC | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206556 | ||||||
| chr12:7206579
|
CTATAA | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.967-1076_967-1072d others(7): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 7206579 | |||||
| chr12:7206604
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.967-1055C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206604 | ||||||
| chr12:7206606
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.967-1053C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206606 | ||||||
| chr12:7206713
|
CAAT | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.967-939_967-937del others(3): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 7206713 | |||||
| chr12:7206783
|
T | A | 1 | a0001c0001t0002g0280 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.967-876T>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206783 | ||||||
| chr12:7206802
|
T | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(223): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.967-857T>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206802 | ||||||
| chr12:7206888
|
G | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.967-771G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7206888 | ||||||
| chr12:7207522
|
T | C | 4 | a0001c0001t0002g0017a0001c0001t0002g0048a0001c0001t0002g0238others(1): Show | 7 | HG00673.hp2 NA18970.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.967-137T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7207522 | ||||||
| chr12:7207533
|
C | T | 1 | a0001c0001t0017g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.967-126C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7207533 | ||||||
| chr12:7207547
|
C | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.967-112C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7207547 | ||||||
| chr12:7207553
|
C | G | 1 | a0001c0001t0003g0183 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.967-106C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7207553 | ||||||
| chr12:7207633
|
C | G | 85 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0016others(82): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.967-26C>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 10/15 | chr12 | 7207633 | ||||||
| chr12:7207926
|
C | T | 8 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(5): Show | 9 | HG01891.hp2 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111-84C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 11/15 | chr12 | 7207926 | ||||||
| chr12:7208245
|
G | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | NA18612.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1181+165G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 12/15 | chr12 | 7208245 | ||||||
| chr12:7208296
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0172 | 2 | HG00140.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1182-161T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 12/15 | chr12 | 7208296 | ||||||
| chr12:7208687
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1394+18C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 13/15 | chr12 | 7208687 | ||||||
| chr12:7208691
|
G | A | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG01099.hp2 HG01243.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394+22G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 13/15 | chr12 | 7208691 | ||||||
| chr12:7208875
|
G | A | 3 | a0001c0001t0002g0227a0001c0001t0002g0249a0001c0001t0002g0290 | 3 | NA18965.hp1 NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1395-130G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 13/15 | chr12 | 7208875 | ||||||
| chr12:7208920
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1395-85G>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 13/15 | chr12 | 7208920 | ||||||
| chr12:7209217
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0078 | 2 | HG03831.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1560+47T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | chr12 | 7209217 | ||||||
| chr12:7209233
|
T | C | 3 | a0003c0003t0004g0044a0003c0003t0004g0293a0003c0003t0004g0299 | 4 | HG02486.hp1 HG02970.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1560+63T>C | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | chr12 | 7209233 | ||||||
| chr12:7209437
|
G | A | 1 | a0001c0001t0018g0052 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1561-246G>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | chr12 | 7209437 | ||||||
| chr12:7209438
|
A | G | 1 | a0001c0001t0018g0052 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1561-245A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | chr12 | 7209438 | ||||||
| chr12:7209585
|
C | CTGGAGTA others(24): Show |
1 | a0001c0001t0018g0052 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1561-79_1561-78ins others(31): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 7209585 | |||||
| chr12:7209608
|
G | GCTGAGTC others(25): Show |
330 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(327): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.1561-44_1561-43ins others(32): Show |
PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 7209608 | |||||
| chr12:7209608
|
G | T | 2 | a0001c0001t0017g0204a0001c0001t0018g0052 | 2 | HG03579.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1561-75G>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 14/15 | chr12 | 7209608 | ||||||
| chr12:7209853
|
A | G | 1 | a0002c0002t0001g0162 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1718+13A>G | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 15/15 | chr12 | 7209853 | ||||||
| chr12:7209883
|
C | T | 5 | a0001c0001t0002g0042a0001c0001t0002g0280a0001c0001t0002g0281others(2): Show | 6 | HG00408.hp1 HG02015.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1718+43C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 15/15 | chr12 | 7209883 | ||||||
| chr12:7209894
|
C | A | 3 | a0001c0001t0008g0004a0001c0001t0008g0225a0001c0001t0008g0226 | 8 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1718+54C>A | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 15/15 | chr12 | 7209894 | ||||||
| chr12:7209933
|
C | T | 7 | a0001c0001t0007g0028a0001c0001t0007g0163a0001c0001t0007g0164others(4): Show | 8 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1719-89C>T | PEX5 | ENSG00000139197.11 | transcript | ENST00000675855.1 | protein_coding | 15/15 | chr12 | 7209933 |