Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10954 |
|---|---|
| ensemblid | ENSG00000065485.20 |
| hgncid | 24811 |
| symbol | PDIA5 |
| name | protein disulfide isomerase family A member 5 |
| refseq_nuc | NM_006810.4 |
| refseq_prot | NP_006801.1 |
| ensembl_nuc | ENST00000316218.12 |
| ensembl_prot | ENSP00000323313.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 123067025 |
| end | 123162104 |
| strand | + |
| ver | v1.2 |
| region | chr3:123067025-123162104 |
| region5000 | chr3:123062025-123167104 |
| regionname0 | PDIA5_chr3_123067025_123162104 |
| regionname5000 | PDIA5_chr3_123062025_123167104 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 519 | 314 | 74 | 66 | 117 | 14 | 41 | 92 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0002 | 0/0 | 519 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0003 | 0/0 | 519 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0004 | 0/0 | 519 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0005 | 0/0 | 519 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0006 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0007 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0008 | 0/0 | 519 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0009 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0010 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| 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 | 0/1 | 1560 | 147 | 46 | 27 | 44 | 6 | 23 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0002 | 0/0 | 1560 | 73 | 5 | 15 | 43 | 3 | 7 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0003 | 1/0 | 1560 | 50 | 16 | 18 | 4 | 3 | 8 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0004 | 0/0 | 1560 | 22 | 1 | 5 | 13 | 1 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0005 | 0/0 | 1560 | 11 | 1 | 1 | 8 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0006 | 0/0 | 1560 | 6 | 0 | 0 | 5 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0007 | 0/0 | 1560 | 4 | 3 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0008 | 0/0 | 1560 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0009 | 0/0 | 1560 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0010 | 0/0 | 1560 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0011 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0012 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0013 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0014 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0015 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0016 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0017 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0018 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0019 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| c0020 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 285 | 332 | 82 | 68 | 124 | 14 | 42 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| 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 | 0/1 | 1560 | 147 | 46 | 27 | 44 | 6 | 23 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0002 | 0/0 | 1560 | 73 | 5 | 15 | 43 | 3 | 7 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0003 | 1/0 | 1560 | 50 | 16 | 18 | 4 | 3 | 8 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0004 | 0/0 | 1560 | 22 | 1 | 5 | 13 | 1 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0005 | 0/0 | 1560 | 11 | 1 | 1 | 8 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0006 | 0/0 | 1560 | 6 | 0 | 0 | 5 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0011 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0014 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0016 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0018 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0002c0007 | 0/0 | 1560 | 4 | 3 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0002c0008 | 0/0 | 1560 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0003c0010 | 0/0 | 1560 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0004c0009 | 0/0 | 1560 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0005c0012 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0006c0017 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0007c0013 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0008c0015 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0009c0019 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0010c0020 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1844 | 147 | 46 | 27 | 44 | 6 | 23 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0002t0001 | 0/0 | 1844 | 73 | 5 | 15 | 43 | 3 | 7 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0003t0001 | 1/0 | 1844 | 50 | 16 | 18 | 4 | 3 | 8 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0004t0001 | 0/0 | 1844 | 22 | 1 | 5 | 13 | 1 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0005t0001 | 0/0 | 1844 | 11 | 1 | 1 | 8 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0006t0001 | 0/0 | 1844 | 6 | 0 | 0 | 5 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0011t0001 | 0/0 | 1844 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0014t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0016t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0001c0018t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0002c0007t0001 | 0/0 | 1844 | 4 | 3 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0002c0008t0001 | 0/0 | 1844 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0003c0010t0001 | 0/0 | 1844 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0004c0009t0001 | 0/0 | 1844 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0005c0012t0001 | 0/0 | 1844 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0006c0017t0001 | 0/0 | 1844 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0007c0013t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0008c0015t0001 | 0/0 | 1844 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0009c0019t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| a0010c0020t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | copy fasta | chr3 | 123062025 | 123167104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0006t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0011t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0014t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0016t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0001c0018t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0007t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0007t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0007t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0007t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0008t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0002c0008t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0003c0010t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0003c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0004c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0004c0009t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0005c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0005c0012t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0006c0017t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0007c0013t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0008c0015t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0009c0019t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| a0010c0020t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | GBR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0304 | EUR | GBR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0088 | EUR | FIN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00280 | hp2 | a0001 | c0006 | t0001 | g0120 | EUR | FIN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00408 | hp1 | a0001 | c0005 | t0001 | g0014 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0112 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0065 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0118 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01109 | hp2 | a0002 | c0007 | t0001 | g0287 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01167 | hp1 | a0008 | c0015 | t0001 | g0220 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0318 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01346 | hp1 | a0001 | c0005 | t0001 | g0180 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0160 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0314 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0084 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0119 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0099 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0306 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0137 | EUR | IBS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0309 | EUR | IBS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0146 | EUR | IBS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0071 | EUR | IBS | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0285 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0265 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0114 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0234 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0315 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0319 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0316 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02056 | hp2 | a0001 | c0005 | t0001 | g0216 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02071 | hp2 | a0001 | c0005 | t0001 | g0145 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02080 | hp2 | a0001 | c0005 | t0001 | g0163 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02129 | hp2 | a0010 | c0020 | t0001 | g0217 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02135 | hp2 | a0001 | c0005 | t0001 | g0107 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | CDX | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0177 | EAS | CDX | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0278 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02572 | hp2 | a0001 | c0014 | t0001 | g0272 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0028 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02630 | hp1 | a0002 | c0007 | t0001 | g0286 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02683 | hp1 | a0001 | c0004 | t0001 | g0261 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0037 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02717 | hp1 | a0002 | c0008 | t0001 | g0288 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02723 | hp2 | a0002 | c0008 | t0001 | g0047 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02886 | hp2 | a0005 | c0012 | t0001 | g0050 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02895 | hp2 | a0002 | c0007 | t0001 | g0267 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0224 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02976 | hp2 | a0005 | c0012 | t0001 | g0049 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03098 | hp1 | a0001 | c0011 | t0001 | g0058 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03098 | hp2 | a0001 | c0018 | t0001 | g0241 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03139 | hp2 | a0001 | c0011 | t0001 | g0283 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0258 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0257 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03225 | hp2 | a0001 | c0016 | t0001 | g0284 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03453 | hp1 | a0002 | c0008 | t0001 | g0046 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0270 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0208 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0086 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0098 | SAS | PJL | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03831 | hp1 | a0001 | c0005 | t0001 | g0156 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0113 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0260 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04184 | hp1 | a0006 | c0017 | t0001 | g0223 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0072 | SAS | BEB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0202 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0101 | AFR | YRI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18945 | hp2 | a0003 | c0010 | t0001 | g0245 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18946 | hp2 | a0003 | c0010 | t0001 | g0244 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18947 | hp1 | a0001 | c0006 | t0001 | g0248 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18950 | hp1 | a0009 | c0019 | t0001 | g0263 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18978 | hp1 | a0001 | c0006 | t0001 | g0179 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18978 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0188 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0100 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18981 | hp2 | a0001 | c0005 | t0001 | g0155 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18986 | hp2 | a0007 | c0013 | t0001 | g0198 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0189 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18990 | hp2 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18995 | hp2 | a0001 | c0004 | t0001 | g0142 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19030 | hp1 | a0002 | c0007 | t0001 | g0289 | AFR | LWK | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0322 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19058 | hp2 | a0001 | c0005 | t0001 | g0182 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19062 | hp2 | a0001 | c0006 | t0001 | g0239 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0079 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19066 | hp2 | a0001 | c0006 | t0001 | g0172 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19074 | hp1 | a0001 | c0005 | t0001 | g0173 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19085 | hp2 | a0004 | c0009 | t0001 | g0195 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19090 | hp1 | a0004 | c0009 | t0001 | g0196 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ASW | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0126 | AFR | ASW | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0307 | EUR | TSI | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0074 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0320 | AMR | CLM | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0038 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | USA | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0115 | REF | REF | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0056 | REF | REF | PDIA5_chr3_123062025_123167104 | PDIA5 | chr3 | 123062025 | 123167104 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123092361
|
C | G | 1 | a0010 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.176C>G | p.Ala59Gly | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/17 | 316/1844 | 176/1560 | 59/519 | chr3 | 123092361 | ||
| chr3:123092403
|
C | T | 2 | a0002a0005 | 9 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
missense_variant | MODERATE | c.218C>T | p.Ala73Val | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/17 | 358/1844 | 218/1560 | 73/519 | chr3 | 123092403 | ||
| chr3:123102442
|
A | G | 1 | a0009 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.289A>G | p.Met97Val | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 4/17 | 429/1844 | 289/1560 | 97/519 | chr3 | 123102442 | ||
| chr3:123130542
|
A | G | 1 | a0006 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.836A>G | p.Tyr279Cys | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/17 | 976/1844 | 836/1560 | 279/519 | chr3 | 123130542 | ||
| chr3:123146254
|
G | A | 1 | a0007 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.1137G>A | p.Met379Ile | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/17 | 1277/1844 | 1137/1560 | 379/519 | chr3 | 123146254 | ||
| chr3:123150263
|
C | T | 1 | a0003 | 2 | NA18945.hp2 NA18946.hp2 |
missense_variant | MODERATE | c.1172C>T | p.Thr391Met | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/17 | 1312/1844 | 1172/1560 | 391/519 | chr3 | 123150263 | ||
| chr3:123150358
|
G | A | 1 | a0004 | 2 | NA19085.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.1267G>A | p.Ala423Thr | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/17 | 1407/1844 | 1267/1560 | 423/519 | chr3 | 123150358 | ||
| chr3:123161381
|
G | A | 2 | a0005a0008 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.1405G>A | p.Ala469Thr | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/17 | 1545/1844 | 1405/1560 | 469/519 | chr3 | 123161381 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123130537
|
C | T | 1 | a0001c0018 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.831C>T | p.Ser277Ser | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/17 | 971/1844 | 831/1560 | 277/519 | chr3 | 123130537 | ||
| chr3:123145589
|
G | A | 13 | a0001c0001a0001c0002a0001c0005others(10): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
synonymous_variant | LOW | c.978G>A | p.Ala326Ala | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/17 | 1118/1844 | 978/1560 | 326/519 | chr3 | 123145589 | ||
| chr3:123150285
|
C | T | 2 | a0001c0011a0001c0016 | 3 | HG03098.hp1 HG03139.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.1194C>T | p.Ser398Ser | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/17 | 1334/1844 | 1194/1560 | 398/519 | chr3 | 123150285 | ||
| chr3:123150300
|
G | C | 3 | a0001c0005a0001c0006a0001c0014 | 18 | HG00280.hp2 HG00408.hp1 HG01346.hp1 others(15): Show |
synonymous_variant | LOW | c.1209G>C | p.Val403Val | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/17 | 1349/1844 | 1209/1560 | 403/519 | chr3 | 123150300 | ||
| chr3:123161344
|
T | C | 7 | a0001c0002a0001c0004a0001c0006others(4): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
synonymous_variant | LOW | c.1368T>C | p.Cys456Cys | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/17 | 1508/1844 | 1368/1560 | 456/519 | chr3 | 123161344 |
| 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 |
|---|
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123067390
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.42+184C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123067390 | ||||||
| chr3:123067403
|
C | A | 1 | a0001c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.42+197C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123067403 | ||||||
| chr3:123067409
|
C | T | 1 | a0001c0004t0001g0322 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.42+203C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123067409 | ||||||
| chr3:123067761
|
T | C | 1 | a0001c0002t0001g0010 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.42+555T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123067761 | ||||||
| chr3:123067860
|
T | C | 2 | a0001c0001t0001g0011a0001c0003t0001g0012 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.42+654T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123067860 | ||||||
| chr3:123067999
|
G | T | 18 | a0001c0001t0001g0305a0001c0001t0001g0308a0001c0001t0001g0310others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.42+793G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123067999 | ||||||
| chr3:123068138
|
G | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+932G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123068138 | ||||||
| chr3:123068202
|
G | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0002t0001g0041others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+996G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123068202 | ||||||
| chr3:123068398
|
T | G | 2 | a0001c0002t0001g0009a0001c0002t0001g0042 | 2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.42+1192T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123068398 | ||||||
| chr3:123068666
|
A | T | 28 | a0001c0001t0001g0011a0001c0001t0001g0280a0001c0001t0001g0281others(25): Show | 28 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.42+1460A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123068666 | ||||||
| chr3:123069113
|
A | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0003t0001g0278 | 3 | HG02109.hp1 HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.42+1907A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069113 | ||||||
| chr3:123069159
|
C | G | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.42+1953C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069159 | ||||||
| chr3:123069207
|
C | T | 10 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0273others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+2001C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069207 | ||||||
| chr3:123069300
|
A | T | 8 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0273others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+2094A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069300 | ||||||
| chr3:123069489
|
C | G | 2 | a0001c0001t0001g0264a0009c0019t0001g0263 | 2 | NA18943.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.42+2283C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069489 | ||||||
| chr3:123069512
|
T | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.42+2306T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069512 | ||||||
| chr3:123069533
|
G | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.42+2327G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069533 | ||||||
| chr3:123069535
|
C | T | 14 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(11): Show | 14 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.42+2329C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069535 | ||||||
| chr3:123069575
|
A | G | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.42+2369A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069575 | ||||||
| chr3:123069583
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.42+2377C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069583 | ||||||
| chr3:123069622
|
A | G | 14 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(11): Show | 14 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.42+2416A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069622 | ||||||
| chr3:123069775
|
A | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.42+2569A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069775 | ||||||
| chr3:123069776
|
T | TTTTCATT others(3): Show |
1 | a0001c0001t0001g0262 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.42+2575_42+2576ins others(10): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123069776 | |||||
| chr3:123069860
|
C | T | 1 | a0001c0004t0001g0261 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.42+2654C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069860 | ||||||
| chr3:123069861
|
G | A | 3 | a0001c0001t0001g0305a0001c0003t0001g0306a0001c0004t0001g0304 | 3 | HG00099.hp2 HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.42+2655G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069861 | ||||||
| chr3:123069918
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.42+2712C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123069918 | ||||||
| chr3:123070044
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0282a0001c0001t0001g0323others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+2838C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070044 | ||||||
| chr3:123070045
|
G | A | 7 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(4): Show | 7 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+2839G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070045 | ||||||
| chr3:123070046
|
C | T | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.42+2840C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070046 | ||||||
| chr3:123070089
|
C | CA | 30 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0280others(27): Show | 30 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.42+2898dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123070089 | |||||
| chr3:123070191
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.42+2985A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070191 | ||||||
| chr3:123070282
|
T | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.42+3076T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070282 | ||||||
| chr3:123070423
|
A | G | 24 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 24 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3217A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070423 | ||||||
| chr3:123070589
|
G | A | 24 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 24 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3383G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070589 | ||||||
| chr3:123070655
|
C | T | 24 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 24 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3449C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070655 | ||||||
| chr3:123070703
|
C | T | 3 | a0001c0001t0001g0035a0001c0003t0001g0036a0001c0003t0001g0037 | 3 | HG00642.hp2 HG02698.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.42+3497C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070703 | ||||||
| chr3:123070917
|
G | A | 1 | a0001c0011t0001g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.42+3711G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123070917 | ||||||
| chr3:123070917
|
G | GA | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0053others(8): Show | 11 | HG01981.hp1 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+3721dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123070917 | |||||
| chr3:123071143
|
A | T | 1 | a0001c0003t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.42+3937A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123071143 | ||||||
| chr3:123071687
|
C | T | 3 | a0001c0001t0001g0259a0001c0003t0001g0258a0001c0004t0001g0257 | 3 | HG02895.hp1 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.42+4481C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123071687 | ||||||
| chr3:123071736
|
G | T | 24 | a0001c0001t0001g0011a0001c0001t0001g0282a0001c0001t0001g0293others(21): Show | 24 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.42+4530G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123071736 | ||||||
| chr3:123071894
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.42+4688G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123071894 | ||||||
| chr3:123071958
|
G | C | 20 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0178others(17): Show | 20 | HG01106.hp1 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.42+4752G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123071958 | ||||||
| chr3:123072109
|
T | A | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.42+4903T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072109 | ||||||
| chr3:123072201
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.42+4995G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072201 | ||||||
| chr3:123072240
|
A | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+5034A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072240 | ||||||
| chr3:123072344
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0282a0001c0001t0001g0323others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.42+5138C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072344 | ||||||
| chr3:123072540
|
C | T | 2 | a0001c0004t0001g0013a0001c0005t0001g0014 | 2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.42+5334C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072540 | ||||||
| chr3:123072595
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.42+5389C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072595 | ||||||
| chr3:123072777
|
T | G | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0178others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.42+5571T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072777 | ||||||
| chr3:123072853
|
C | T | 5 | a0002c0007t0001g0267a0002c0007t0001g0286a0002c0007t0001g0287others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+5647C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072853 | ||||||
| chr3:123072912
|
C | CTG | 5 | a0001c0002t0001g0010a0001c0003t0001g0038a0001c0003t0001g0051others(2): Show | 5 | HG02109.hp2 HG02886.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+5736_42+5737dup others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTG | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0053others(6): Show | 9 | HG01934.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+5734_42+5737dup others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(3): Show |
19 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(16): Show | 19 | HG00673.hp2 HG01099.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.42+5728_42+5737dup others(10): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(5): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0168others(3): Show | 7 | HG00140.hp1 HG00642.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+5726_42+5737dup others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(7): Show |
2 | a0001c0002t0001g0307a0001c0003t0001g0037 | 2 | HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.42+5724_42+5737dup others(14): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(9): Show |
7 | a0001c0001t0001g0184a0001c0001t0001g0308a0001c0001t0001g0310others(4): Show | 7 | HG00099.hp1 HG00735.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+5722_42+5737dup others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(11): Show |
17 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(14): Show | 17 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.42+5720_42+5737dup others(18): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(13): Show |
4 | a0001c0001t0001g0254a0001c0001t0001g0298a0001c0002t0001g0255others(1): Show | 4 | HG00609.hp1 HG01123.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+5718_42+5737dup others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(15): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0282a0001c0001t0001g0299others(6): Show | 9 | HG01109.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+5716_42+5737dup others(22): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(17): Show |
2 | a0001c0001t0001g0300a0001c0003t0001g0258 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.42+5714_42+5737dup others(24): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(19): Show |
5 | a0001c0001t0001g0256a0001c0001t0001g0324a0001c0003t0001g0012others(2): Show | 5 | HG02451.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+5712_42+5737dup others(26): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(21): Show |
3 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0003t0001g0285 | 3 | HG01515.hp2 HG01884.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.42+5710_42+5737dup others(28): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
C | CTGTGTGT others(23): Show |
2 | a0001c0001t0001g0259a0001c0001t0001g0303 | 2 | HG02735.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.42+5708_42+5737dup others(30): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
CTG | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0043others(129): Show | 136 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.42+5736_42+5737del others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072912
|
CTGTG | C | 14 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0068others(11): Show | 14 | HG00741.hp1 HG01175.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+5734_42+5737del others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123072912 | |||||
| chr3:123072996
|
G | A | 2 | a0001c0001t0001g0108a0001c0005t0001g0107 | 2 | HG02135.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.42+5790G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123072996 | ||||||
| chr3:123073112
|
C | T | 5 | a0002c0007t0001g0267a0002c0007t0001g0286a0002c0007t0001g0287others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+5906C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073112 | ||||||
| chr3:123073393
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.42+6187G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073393 | ||||||
| chr3:123073440
|
G | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.42+6234G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073440 | ||||||
| chr3:123073734
|
T | G | 26 | a0001c0001t0001g0011a0001c0001t0001g0254a0001c0001t0001g0256others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.42+6528T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073734 | ||||||
| chr3:123073763
|
G | A | 3 | a0001c0001t0001g0259a0001c0003t0001g0258a0001c0004t0001g0257 | 3 | HG02895.hp1 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.42+6557G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073763 | ||||||
| chr3:123073765
|
G | T | 26 | a0001c0001t0001g0011a0001c0001t0001g0254a0001c0001t0001g0256others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.42+6559G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073765 | ||||||
| chr3:123073839
|
G | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(20): Show | 24 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.42+6633G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123073839 | ||||||
| chr3:123074185
|
C | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(1): Show | 4 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+6979C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123074185 | ||||||
| chr3:123074501
|
TAAC | T | 24 | a0001c0001t0001g0259a0001c0001t0001g0305a0001c0001t0001g0308others(21): Show | 24 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+7301_42+7303del others(3): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123074501 | |||||
| chr3:123074756
|
T | C | 2 | a0002c0008t0001g0046a0002c0008t0001g0047 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.42+7550T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123074756 | ||||||
| chr3:123074773
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.42+7567G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123074773 | ||||||
| chr3:123074837
|
C | T | 1 | a0001c0003t0001g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42+7631C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123074837 | ||||||
| chr3:123074996
|
G | GTTAA | 3 | a0001c0001t0001g0016a0001c0002t0001g0030a0001c0002t0001g0031 | 3 | NA18948.hp2 NA18983.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.42+7791_42+7794dup others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123074996 | |||||
| chr3:123075208
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+8002C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075208 | ||||||
| chr3:123075247
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.42+8041G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075247 | ||||||
| chr3:123075277
|
G | C | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0273others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+8071G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075277 | ||||||
| chr3:123075389
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+8183T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075389 | ||||||
| chr3:123075637
|
G | A | 1 | a0001c0002t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.42+8431G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075637 | ||||||
| chr3:123075716
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA18999.hp1 NA19068.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.42+8510G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075716 | ||||||
| chr3:123075822
|
A | AG | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+8617dupG | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123075822 | |||||
| chr3:123075829
|
C | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+8623C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075829 | ||||||
| chr3:123075830
|
G | GGAATCTG others(1): Show |
26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+8624_42+8625ins others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075830 | ||||||
| chr3:123075843
|
A | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+8637A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123075843 | ||||||
| chr3:123076443
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.42+9237T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123076443 | ||||||
| chr3:123076795
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 5 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+9589G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123076795 | ||||||
| chr3:123076954
|
C | T | 6 | a0001c0002t0001g0246a0001c0002t0001g0247a0001c0002t0001g0249others(3): Show | 6 | NA18947.hp1 NA18972.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+9748C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123076954 | ||||||
| chr3:123077076
|
G | A | 1 | a0001c0004t0001g0189 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.42+9870G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077076 | ||||||
| chr3:123077501
|
C | G | 1 | a0001c0003t0001g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42+10295C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077501 | ||||||
| chr3:123077502
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0003t0001g0051others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+10296G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077502 | ||||||
| chr3:123077542
|
A | T | 1 | a0001c0002t0001g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.42+10336A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077542 | ||||||
| chr3:123077544
|
A | G | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.42+10338A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077544 | ||||||
| chr3:123077549
|
T | TAC | 30 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0164others(27): Show | 30 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.42+10377_42+10378d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077549 | |||||
| chr3:123077549
|
T | TACAC | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0002t0001g0103 | 3 | HG01099.hp2 NA18971.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.42+10375_42+10378d others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077549 | |||||
| chr3:123077549
|
TAC | T | 5 | a0001c0001t0001g0256a0001c0001t0001g0279a0001c0003t0001g0076others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+10377_42+10378d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077549 | |||||
| chr3:123077549
|
TACAC | T | 27 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(24): Show | 27 | HG00099.hp2 HG00733.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.42+10375_42+10378d others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077549 | |||||
| chr3:123077549
|
TACACAC | T | 21 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0034others(18): Show | 21 | HG00099.hp1 HG00609.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.42+10373_42+10378d others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077549 | |||||
| chr3:123077549
|
TACACACA others(1): Show |
T | 20 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 21 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.42+10371_42+10378d others(10): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077549 | |||||
| chr3:123077589
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.42+10383T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077589 | ||||||
| chr3:123077614
|
T | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.42+10408T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077614 | ||||||
| chr3:123077665
|
A | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+10459A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077665 | ||||||
| chr3:123077717
|
A | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+10511A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077717 | ||||||
| chr3:123077775
|
A | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.42+10569A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077775 | ||||||
| chr3:123077812
|
C | CT | 10 | a0001c0001t0001g0029a0001c0001t0001g0106a0001c0001t0001g0290others(7): Show | 10 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+10621dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077812 | |||||
| chr3:123077812
|
CT | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0001t0001g0190others(18): Show | 21 | HG01071.hp1 HG01074.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.42+10621delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123077812 | |||||
| chr3:123077842
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0002t0001g0041 | 3 | HG02559.hp2 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.42+10636C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077842 | ||||||
| chr3:123077946
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+10740A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077946 | ||||||
| chr3:123077952
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02922.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+10746G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077952 | ||||||
| chr3:123077956
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.42+10750C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077956 | ||||||
| chr3:123077998
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.42+10792C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123077998 | ||||||
| chr3:123078071
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.42+10865G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123078071 | ||||||
| chr3:123078144
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.42+10938C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123078144 | ||||||
| chr3:123078193
|
A | G | 27 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 28 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.43-10975A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123078193 | ||||||
| chr3:123078319
|
C | T | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0273others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10849C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123078319 | ||||||
| chr3:123078435
|
T | C | 24 | a0001c0001t0001g0259a0001c0001t0001g0305a0001c0001t0001g0308others(21): Show | 24 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-10733T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123078435 | ||||||
| chr3:123078469
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(2): Show | 5 | HG01884.hp1 HG02486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-10699G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123078469 | ||||||
| chr3:123079097
|
G | A | 1 | a0001c0004t0001g0065 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.43-10071G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079097 | ||||||
| chr3:123079175
|
C | CT | 35 | a0001c0001t0001g0034a0001c0001t0001g0161a0001c0001t0001g0178others(32): Show | 35 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.43-9970dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123079175 | |||||
| chr3:123079175
|
C | CTT | 25 | a0001c0001t0001g0259a0001c0001t0001g0299a0001c0001t0001g0300others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.43-9971_43-9970dup others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123079175 | |||||
| chr3:123079240
|
G | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.43-9928G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079240 | ||||||
| chr3:123079370
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.43-9798C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079370 | ||||||
| chr3:123079409
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43-9759T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079409 | ||||||
| chr3:123079488
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.43-9680C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079488 | ||||||
| chr3:123079617
|
T | C | 3 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0002t0001g0292 | 3 | HG01934.hp2 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.43-9551T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079617 | ||||||
| chr3:123079641
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-9527C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079641 | ||||||
| chr3:123079826
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.43-9342C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123079826 | ||||||
| chr3:123080028
|
G | A | 1 | a0001c0002t0001g0117 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.43-9140G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080028 | ||||||
| chr3:123080155
|
T | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 26 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.43-9013T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080155 | ||||||
| chr3:123080157
|
T | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(35): Show | 39 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.43-9011T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080157 | ||||||
| chr3:123080158
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.43-9010G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080158 | ||||||
| chr3:123080283
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-8885G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080283 | ||||||
| chr3:123080331
|
G | A | 1 | a0001c0003t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43-8837G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080331 | ||||||
| chr3:123080337
|
G | A | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43-8831G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080337 | ||||||
| chr3:123080588
|
C | A | 6 | a0001c0002t0001g0121a0001c0003t0001g0112a0001c0003t0001g0118others(3): Show | 6 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-8580C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080588 | ||||||
| chr3:123080631
|
A | G | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0178others(13): Show | 16 | HG01106.hp1 HG01257.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-8537A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080631 | ||||||
| chr3:123080865
|
T | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0002t0001g0022others(4): Show | 7 | HG00673.hp2 NA18948.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-8303T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080865 | ||||||
| chr3:123080874
|
C | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.43-8294C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080874 | ||||||
| chr3:123080973
|
A | T | 1 | a0001c0001t0001g0008 | 2 | NA18970.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.43-8195A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123080973 | ||||||
| chr3:123081106
|
A | G | 1 | a0001c0002t0001g0159 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.43-8062A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123081106 | ||||||
| chr3:123081209
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.43-7959G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123081209 | ||||||
| chr3:123081440
|
A | G | 1 | a0001c0003t0001g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.43-7728A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123081440 | ||||||
| chr3:123081594
|
G | T | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43-7574G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123081594 | ||||||
| chr3:123081624
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.43-7544G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123081624 | ||||||
| chr3:123081778
|
T | TA | 5 | a0001c0001t0001g0048a0002c0008t0001g0046a0002c0008t0001g0047others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-7389dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123081778 | |||||
| chr3:123081891
|
C | G | 2 | a0005c0012t0001g0049a0005c0012t0001g0050 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.43-7277C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123081891 | ||||||
| chr3:123082182
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0122 | 3 | HG02809.hp1 HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.43-6986G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082182 | ||||||
| chr3:123082199
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.43-6969C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082199 | ||||||
| chr3:123082314
|
C | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0256a0001c0001t0001g0282others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.43-6854C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082314 | ||||||
| chr3:123082443
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-6725G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082443 | ||||||
| chr3:123082482
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-6686G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082482 | ||||||
| chr3:123082522
|
G | A | 2 | a0001c0001t0001g0169a0001c0003t0001g0064 | 2 | HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.43-6646G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082522 | ||||||
| chr3:123082626
|
C | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0002t0001g0041 | 3 | HG02559.hp2 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.43-6542C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082626 | ||||||
| chr3:123082651
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-6517G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082651 | ||||||
| chr3:123082825
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0282a0001c0001t0001g0323others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-6343G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082825 | ||||||
| chr3:123082970
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.43-6198G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123082970 | ||||||
| chr3:123083020
|
G | C | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43-6148G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083020 | ||||||
| chr3:123083107
|
G | A | 2 | a0001c0001t0001g0169a0001c0003t0001g0064 | 2 | HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.43-6061G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083107 | ||||||
| chr3:123083134
|
C | T | 76 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0108others(73): Show | 78 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.43-6034C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083134 | ||||||
| chr3:123083188
|
G | T | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43-5980G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083188 | ||||||
| chr3:123083222
|
G | T | 1 | a0001c0006t0001g0248 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.43-5946G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083222 | ||||||
| chr3:123083326
|
C | T | 2 | a0003c0010t0001g0244a0003c0010t0001g0245 | 2 | NA18945.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.43-5842C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083326 | ||||||
| chr3:123083534
|
C | A | 5 | a0002c0007t0001g0267a0002c0007t0001g0286a0002c0007t0001g0287others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-5634C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083534 | ||||||
| chr3:123083546
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-5622C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083546 | ||||||
| chr3:123083571
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.43-5597G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083571 | ||||||
| chr3:123083767
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.43-5401A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083767 | ||||||
| chr3:123083844
|
A | G | 1 | a0001c0004t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.43-5324A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123083844 | ||||||
| chr3:123084024
|
C | T | 22 | a0001c0001t0001g0305a0001c0001t0001g0308a0001c0001t0001g0310others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.43-5144C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084024 | ||||||
| chr3:123084163
|
A | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 26 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.43-5005A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084163 | ||||||
| chr3:123084251
|
C | T | 1 | a0006c0017t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43-4917C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084251 | ||||||
| chr3:123084526
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0016others(44): Show | 48 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.43-4642G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084526 | ||||||
| chr3:123084566
|
G | A | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43-4602G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084566 | ||||||
| chr3:123084827
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43-4341G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084827 | ||||||
| chr3:123084887
|
G | T | 1 | a0001c0002t0001g0271 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.43-4281G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084887 | ||||||
| chr3:123084892
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 23 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-4276C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084892 | ||||||
| chr3:123084904
|
T | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0190a0001c0001t0001g0192others(72): Show | 77 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-4264T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123084904 | ||||||
| chr3:123085234
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-3934C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085234 | ||||||
| chr3:123085400
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0254others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.43-3768A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085400 | ||||||
| chr3:123085458
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0254others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.43-3710A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085458 | ||||||
| chr3:123085532
|
C | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 26 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.43-3636C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085532 | ||||||
| chr3:123085721
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43-3447C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085721 | ||||||
| chr3:123085756
|
A | G | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43-3412A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085756 | ||||||
| chr3:123085772
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-3396A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085772 | ||||||
| chr3:123085930
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-3238T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123085930 | ||||||
| chr3:123086022
|
A | G | 2 | a0001c0001t0001g0282a0001c0016t0001g0284 | 2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.43-3146A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123086022 | ||||||
| chr3:123086321
|
C | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0190a0001c0001t0001g0192others(70): Show | 75 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.43-2847C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123086321 | ||||||
| chr3:123086330
|
C | G | 1 | a0001c0001t0001g0111 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.43-2838C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123086330 | ||||||
| chr3:123086849
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-2319T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123086849 | ||||||
| chr3:123087126
|
G | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0053others(8): Show | 11 | HG01934.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-2042G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087126 | ||||||
| chr3:123087128
|
C | G | 2 | a0001c0002t0001g0097a0001c0002t0001g0132 | 2 | NA18944.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.43-2040C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087128 | ||||||
| chr3:123087345
|
C | CT | 24 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0184others(21): Show | 24 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-1813dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123087345 | |||||
| chr3:123087470
|
A | ATT | 19 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0254others(16): Show | 19 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-1688_43-1687dup others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123087470 | |||||
| chr3:123087470
|
AT | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 23 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-1687delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 123087470 | |||||
| chr3:123087548
|
C | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0053others(8): Show | 11 | HG01934.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-1620C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087548 | ||||||
| chr3:123087578
|
A | G | 21 | a0001c0001t0001g0305a0001c0001t0001g0308a0001c0001t0001g0310others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.43-1590A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087578 | ||||||
| chr3:123087700
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.43-1468T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087700 | ||||||
| chr3:123087713
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.43-1455C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087713 | ||||||
| chr3:123087910
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.43-1258A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123087910 | ||||||
| chr3:123088013
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.43-1155G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088013 | ||||||
| chr3:123088116
|
C | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.43-1052C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088116 | ||||||
| chr3:123088239
|
T | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0293others(4): Show | 7 | HG01934.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-929T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088239 | ||||||
| chr3:123088316
|
G | C | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43-852G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088316 | ||||||
| chr3:123088428
|
T | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0016others(89): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.43-740T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088428 | ||||||
| chr3:123088544
|
T | C | 1 | a0001c0002t0001g0059 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.43-624T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088544 | ||||||
| chr3:123088641
|
A | G | 1 | a0001c0002t0001g0103 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.43-527A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088641 | ||||||
| chr3:123088712
|
G | T | 10 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0235others(7): Show | 10 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.43-456G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088712 | ||||||
| chr3:123088827
|
C | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0254others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.43-341C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123088827 | ||||||
| chr3:123089045
|
T | C | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43-123T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123089045 | ||||||
| chr3:123089148
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.43-20G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 1/16 | chr3 | 123089148 | ||||||
| chr3:123089353
|
A | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0243 | 3 | NA18947.hp2 NA18981.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.169+59A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123089353 | ||||||
| chr3:123089387
|
C | T | 4 | a0001c0002t0001g0078a0001c0004t0001g0060a0001c0004t0001g0079others(1): Show | 4 | NA18970.hp2 NA18978.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+93C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123089387 | ||||||
| chr3:123089520
|
G | T | 1 | a0008c0015t0001g0220 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.169+226G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123089520 | ||||||
| chr3:123089653
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 5 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+359C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123089653 | ||||||
| chr3:123089695
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169+401C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123089695 | ||||||
| chr3:123089848
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0053others(8): Show | 11 | HG01934.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+554G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123089848 | ||||||
| chr3:123090177
|
A | G | 2 | a0001c0001t0001g0219a0001c0002t0001g0218 | 2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.169+883A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090177 | ||||||
| chr3:123090369
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0002t0001g0041 | 3 | HG02559.hp2 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.169+1075C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090369 | ||||||
| chr3:123090406
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169+1112G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090406 | ||||||
| chr3:123090435
|
T | C | 1 | a0001c0004t0001g0304 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.169+1141T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090435 | ||||||
| chr3:123090448
|
T | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0254a0001c0001t0001g0256others(18): Show | 21 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.169+1154T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090448 | ||||||
| chr3:123090553
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0254others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.169+1259T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090553 | ||||||
| chr3:123090667
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169+1373T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090667 | ||||||
| chr3:123090678
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0254a0001c0001t0001g0282others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+1384T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090678 | ||||||
| chr3:123090691
|
G | A | 2 | a0001c0001t0001g0134a0001c0003t0001g0133 | 2 | HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.169+1397G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090691 | ||||||
| chr3:123090736
|
T | C | 25 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 26 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+1442T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090736 | ||||||
| chr3:123090922
|
G | A | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.170-1433G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123090922 | ||||||
| chr3:123091129
|
A | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0254others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.170-1226A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091129 | ||||||
| chr3:123091344
|
T | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.170-1011T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091344 | ||||||
| chr3:123091364
|
G | A | 2 | a0001c0002t0001g0193a0001c0002t0001g0194 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.170-991G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091364 | ||||||
| chr3:123091454
|
C | G | 2 | a0001c0002t0001g0255a0001c0003t0001g0252 | 2 | HG00609.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.170-901C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091454 | ||||||
| chr3:123091673
|
G | C | 1 | a0001c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.170-682G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091673 | ||||||
| chr3:123091683
|
C | T | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.170-672C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091683 | ||||||
| chr3:123091709
|
G | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.170-646G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123091709 | ||||||
| chr3:123092193
|
C | A | 1 | a0001c0002t0001g0255 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.170-162C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123092193 | ||||||
| chr3:123092251
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.170-104C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123092251 | ||||||
| chr3:123092327
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-28T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 2/16 | chr3 | 123092327 | ||||||
| chr3:123092504
|
T | G | 20 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0254others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.257+62T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123092504 | ||||||
| chr3:123092511
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.257+69G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123092511 | ||||||
| chr3:123092777
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+335G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123092777 | ||||||
| chr3:123092827
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.257+385T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123092827 | ||||||
| chr3:123093045
|
G | A | 1 | a0001c0003t0001g0234 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.257+603G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093045 | ||||||
| chr3:123093137
|
G | A | 2 | a0001c0001t0001g0021a0001c0002t0001g0022 | 2 | HG00673.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.257+695G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093137 | ||||||
| chr3:123093208
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.257+766T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093208 | ||||||
| chr3:123093258
|
G | GGT | 55 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0040others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.257+838_257+839dup others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123093258 | |||||
| chr3:123093258
|
GGT | G | 12 | a0001c0001t0001g0256a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+838_257+839del others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123093258 | |||||
| chr3:123093258
|
GGTGT | G | 5 | a0002c0007t0001g0267a0002c0007t0001g0286a0002c0007t0001g0287others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+836_257+839del others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123093258 | |||||
| chr3:123093493
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.257+1051A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093493 | ||||||
| chr3:123093502
|
G | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02451.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.257+1060G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093502 | ||||||
| chr3:123093537
|
A | G | 2 | a0001c0004t0001g0177a0001c0004t0001g0322 | 2 | HG02155.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.257+1095A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093537 | ||||||
| chr3:123093649
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0016others(66): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.257+1207G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093649 | ||||||
| chr3:123093683
|
G | A | 2 | a0001c0001t0001g0240a0001c0018t0001g0241 | 2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.257+1241G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093683 | ||||||
| chr3:123093714
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0020others(14): Show | 18 | HG00140.hp1 HG00673.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.257+1272G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093714 | ||||||
| chr3:123093728
|
G | A | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.257+1286G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093728 | ||||||
| chr3:123093784
|
C | T | 4 | a0001c0001t0001g0254a0001c0001t0001g0282a0001c0011t0001g0283others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+1342C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093784 | ||||||
| chr3:123093960
|
G | A | 45 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0043others(42): Show | 45 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.257+1518G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093960 | ||||||
| chr3:123093978
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+1536C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123093978 | ||||||
| chr3:123094086
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+1644G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094086 | ||||||
| chr3:123094203
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA18999.hp1 NA19068.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.257+1761T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094203 | ||||||
| chr3:123094241
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.257+1799T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094241 | ||||||
| chr3:123094376
|
A | C | 15 | a0001c0001t0001g0240a0001c0001t0001g0256a0001c0001t0001g0290others(12): Show | 15 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+1934A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094376 | ||||||
| chr3:123094406
|
G | A | 4 | a0001c0001t0001g0254a0001c0001t0001g0282a0001c0011t0001g0283others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+1964G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094406 | ||||||
| chr3:123094589
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.257+2147C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094589 | ||||||
| chr3:123094956
|
G | C | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.257+2514G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123094956 | ||||||
| chr3:123095007
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.257+2565G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123095007 | ||||||
| chr3:123095090
|
C | T | 21 | a0001c0001t0001g0305a0001c0001t0001g0308a0001c0001t0001g0310others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.257+2648C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123095090 | ||||||
| chr3:123095206
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0073others(9): Show | 14 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.257+2764C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123095206 | ||||||
| chr3:123095429
|
T | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+2987T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123095429 | ||||||
| chr3:123095673
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+3231C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123095673 | ||||||
| chr3:123095749
|
C | CA | 30 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0280others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.257+3326dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123095749 | |||||
| chr3:123095749
|
C | CAAA | 14 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0282others(11): Show | 14 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.257+3324_257+3326d others(5): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123095749 | |||||
| chr3:123095749
|
CA | C | 17 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0053others(14): Show | 17 | HG01070.hp1 HG01884.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.257+3326delA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123095749 | |||||
| chr3:123095857
|
G | A | 2 | a0004c0009t0001g0195a0004c0009t0001g0196 | 2 | NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.257+3415G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123095857 | ||||||
| chr3:123096002
|
C | T | 1 | a0001c0002t0001g0247 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.257+3560C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096002 | ||||||
| chr3:123096068
|
C | T | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(1): Show | 4 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+3626C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096068 | ||||||
| chr3:123096081
|
G | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 23 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.257+3639G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096081 | ||||||
| chr3:123096329
|
GGCGCGTA others(7): Show |
G | 12 | a0001c0001t0001g0256a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+3890_257+3903d others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123096329 | |||||
| chr3:123096365
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0002t0001g0221 | 3 | HG00423.hp1 HG00609.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.257+3923T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096365 | ||||||
| chr3:123096370
|
A | G | 6 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+3928A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096370 | ||||||
| chr3:123096395
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.257+3953C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096395 | ||||||
| chr3:123096552
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+4110T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096552 | ||||||
| chr3:123096644
|
C | T | 1 | a0001c0006t0001g0239 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.257+4202C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096644 | ||||||
| chr3:123096668
|
C | T | 4 | a0001c0001t0001g0297a0001c0001t0001g0301a0001c0001t0001g0302others(1): Show | 4 | HG01099.hp1 HG01515.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+4226C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096668 | ||||||
| chr3:123096687
|
C | T | 12 | a0001c0001t0001g0256a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+4245C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096687 | ||||||
| chr3:123096688
|
A | G | 17 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0256others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.257+4246A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096688 | ||||||
| chr3:123096699
|
G | A | 2 | a0001c0001t0001g0048a0001c0003t0001g0052 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.257+4257G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096699 | ||||||
| chr3:123096850
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.257+4408C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096850 | ||||||
| chr3:123096893
|
C | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.257+4451C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096893 | ||||||
| chr3:123096955
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+4513G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096955 | ||||||
| chr3:123096955
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.257+4513G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096955 | ||||||
| chr3:123096957
|
G | A | 1 | a0001c0002t0001g0247 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.257+4515G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123096957 | ||||||
| chr3:123097025
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 33 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.257+4583A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097025 | ||||||
| chr3:123097374
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.257+4932A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097374 | ||||||
| chr3:123097691
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0282a0001c0011t0001g0283 | 3 | HG01891.hp1 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.258-4720C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097691 | ||||||
| chr3:123097694
|
CT | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-4716delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097694 | ||||||
| chr3:123097857
|
A | G | 1 | a0001c0003t0001g0319 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.258-4554A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097857 | ||||||
| chr3:123097955
|
G | A | 12 | a0001c0001t0001g0305a0001c0001t0001g0313a0001c0002t0001g0253others(9): Show | 12 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.258-4456G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097955 | ||||||
| chr3:123097975
|
C | G | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-4436C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123097975 | ||||||
| chr3:123098050
|
T | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-4361T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098050 | ||||||
| chr3:123098199
|
G | A | 2 | a0001c0001t0001g0240a0001c0018t0001g0241 | 2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.258-4212G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098199 | ||||||
| chr3:123098215
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.258-4196G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098215 | ||||||
| chr3:123098240
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-4171G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098240 | ||||||
| chr3:123098260
|
T | C | 12 | a0001c0001t0001g0305a0001c0001t0001g0313a0001c0002t0001g0253others(9): Show | 12 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.258-4151T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098260 | ||||||
| chr3:123098265
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-4146G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098265 | ||||||
| chr3:123098281
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258-4130G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098281 | ||||||
| chr3:123098328
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.258-4083T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098328 | ||||||
| chr3:123098702
|
GAAC | G | 30 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 30 | HG00673.hp2 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.258-3707_258-3705d others(5): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123098702 | |||||
| chr3:123098706
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.258-3705A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098706 | ||||||
| chr3:123098910
|
G | C | 1 | a0001c0002t0001g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.258-3501G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098910 | ||||||
| chr3:123098993
|
A | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.258-3418A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123098993 | ||||||
| chr3:123099057
|
G | GCA | 5 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0323others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-3336_258-3335d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123099057 | |||||
| chr3:123099057
|
G | GCACA | 15 | a0001c0001t0001g0066a0001c0001t0001g0256a0001c0001t0001g0280others(12): Show | 15 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.258-3338_258-3335d others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123099057 | |||||
| chr3:123099057
|
GCA | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(28): Show | 31 | HG00673.hp2 HG00738.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.258-3336_258-3335d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123099057 | |||||
| chr3:123099057
|
GCACACA | G | 12 | a0001c0001t0001g0305a0001c0001t0001g0313a0001c0002t0001g0253others(9): Show | 12 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.258-3340_258-3335d others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123099057 | |||||
| chr3:123099059
|
A | G | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-3352A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099059 | ||||||
| chr3:123099060
|
C | T | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.258-3351C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099060 | ||||||
| chr3:123099072
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.258-3339C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099072 | ||||||
| chr3:123099378
|
G | A | 1 | a0001c0004t0001g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.258-3033G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099378 | ||||||
| chr3:123099413
|
G | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-2998G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099413 | ||||||
| chr3:123099426
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.258-2985G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099426 | ||||||
| chr3:123099475
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258-2936G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099475 | ||||||
| chr3:123099509
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-2902C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099509 | ||||||
| chr3:123099610
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-2801C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099610 | ||||||
| chr3:123099928
|
G | A | 43 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(40): Show | 43 | HG00673.hp2 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.258-2483G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123099928 | ||||||
| chr3:123100322
|
A | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.258-2089A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100322 | ||||||
| chr3:123100400
|
C | T | 3 | a0001c0003t0001g0278a0002c0007t0001g0287a0002c0007t0001g0289 | 3 | HG01109.hp2 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.258-2011C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100400 | ||||||
| chr3:123100419
|
T | A | 1 | a0001c0004t0001g0100 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.258-1992T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100419 | ||||||
| chr3:123100506
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258-1905C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100506 | ||||||
| chr3:123100595
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258-1816G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100595 | ||||||
| chr3:123100740
|
T | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.258-1671T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100740 | ||||||
| chr3:123100741
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-1670C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100741 | ||||||
| chr3:123100888
|
G | A | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-1523G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123100888 | ||||||
| chr3:123101049
|
G | C | 1 | a0001c0004t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.258-1362G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101049 | ||||||
| chr3:123101071
|
T | A | 1 | a0001c0002t0001g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.258-1340T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101071 | ||||||
| chr3:123101256
|
A | G | 1 | a0001c0002t0001g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.258-1155A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101256 | ||||||
| chr3:123101385
|
G | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.258-1026G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101385 | ||||||
| chr3:123101414
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.258-997C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101414 | ||||||
| chr3:123101549
|
C | G | 1 | a0001c0002t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.258-862C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101549 | ||||||
| chr3:123101608
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.258-803G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101608 | ||||||
| chr3:123101666
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.258-745C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101666 | ||||||
| chr3:123101667
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-744C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101667 | ||||||
| chr3:123101885
|
C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.258-526C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123101885 | ||||||
| chr3:123101906
|
C | CT | 11 | a0001c0001t0001g0130a0001c0001t0001g0230a0001c0001t0001g0233others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-484dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123101906
|
C | CTTTTTT | 8 | a0001c0001t0001g0170a0001c0001t0001g0192a0001c0001t0001g0197others(5): Show | 9 | HG01256.hp2 HG01258.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-489_258-484dup others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123101906
|
C | CTTTTTTT | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.258-490_258-484dup others(7): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123101906
|
C | CTTTTTTT others(1): Show |
46 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(43): Show | 46 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.258-491_258-484dup others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123101906
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0183others(3): Show | 6 | HG01106.hp1 HG02293.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-492_258-484dup others(9): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123101906
|
C | CTTTTTTT others(3): Show |
7 | a0001c0002t0001g0317a0001c0003t0001g0314a0001c0003t0001g0316others(4): Show | 7 | HG01123.hp2 HG01255.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-493_258-484dup others(10): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123101906
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258-495_258-484dup others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 123101906 | |||||
| chr3:123102012
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-399C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123102012 | ||||||
| chr3:123102050
|
C | T | 1 | a0001c0002t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.258-361C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123102050 | ||||||
| chr3:123102056
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258-355C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123102056 | ||||||
| chr3:123102261
|
C | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.258-150C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123102261 | ||||||
| chr3:123102374
|
C | T | 4 | a0001c0001t0001g0115a0001c0002t0001g0116a0001c0003t0001g0113others(1): Show | 4 | HG01943.hp1 HG02300.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-37C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 3/16 | chr3 | 123102374 | ||||||
| chr3:123102538
|
T | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.341+44T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 4/16 | chr3 | 123102538 | ||||||
| chr3:123102559
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0282others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+65C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 4/16 | chr3 | 123102559 | ||||||
| chr3:123102564
|
A | G | 1 | a0001c0003t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.341+70A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 4/16 | chr3 | 123102564 | ||||||
| chr3:123102630
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02922.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-121T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 4/16 | chr3 | 123102630 | ||||||
| chr3:123102631
|
T | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.342-120T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 4/16 | chr3 | 123102631 | ||||||
| chr3:123102824
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.387+28A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123102824 | ||||||
| chr3:123102825
|
T | A | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.387+29T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123102825 | ||||||
| chr3:123102829
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.387+33G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123102829 | ||||||
| chr3:123102898
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.387+102T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123102898 | ||||||
| chr3:123103042
|
C | T | 1 | a0001c0003t0001g0234 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.387+246C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103042 | ||||||
| chr3:123103269
|
A | G | 3 | a0001c0001t0001g0152a0001c0004t0001g0001a0001c0004t0001g0261 | 4 | HG01256.hp2 HG01258.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+473A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103269 | ||||||
| chr3:123103424
|
G | C | 37 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00673.hp2 HG00738.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+628G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103424 | ||||||
| chr3:123103432
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(209): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.387+636C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103432 | ||||||
| chr3:123103447
|
C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.387+651C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103447 | ||||||
| chr3:123103478
|
A | G | 231 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.387+682A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103478 | ||||||
| chr3:123103603
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.387+807A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103603 | ||||||
| chr3:123103794
|
T | G | 1 | a0001c0003t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.387+998T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103794 | ||||||
| chr3:123103835
|
G | C | 3 | a0001c0001t0001g0256a0002c0008t0001g0046a0002c0008t0001g0047 | 3 | HG02451.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.387+1039G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103835 | ||||||
| chr3:123103838
|
C | G | 227 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.387+1042C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103838 | ||||||
| chr3:123103983
|
A | G | 1 | a0001c0002t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.387+1187A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123103983 | ||||||
| chr3:123104210
|
A | G | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(238): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.387+1414A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104210 | ||||||
| chr3:123104466
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.387+1670G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104466 | ||||||
| chr3:123104522
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(183): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.387+1726C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104522 | ||||||
| chr3:123104523
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.387+1727G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104523 | ||||||
| chr3:123104531
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.387+1735G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104531 | ||||||
| chr3:123104591
|
A | G | 12 | a0001c0001t0001g0305a0001c0001t0001g0313a0001c0002t0001g0253others(9): Show | 12 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.387+1795A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104591 | ||||||
| chr3:123104810
|
T | C | 17 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0178others(14): Show | 17 | HG01106.hp1 HG01257.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.388-1939T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104810 | ||||||
| chr3:123104956
|
C | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(238): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.388-1793C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123104956 | ||||||
| chr3:123105030
|
C | T | 272 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(269): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.388-1719C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105030 | ||||||
| chr3:123105207
|
G | A | 2 | a0001c0003t0001g0076a0001c0011t0001g0283 | 2 | HG01074.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.388-1542G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105207 | ||||||
| chr3:123105310
|
A | G | 1 | a0001c0011t0001g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388-1439A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105310 | ||||||
| chr3:123105389
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0293others(4): Show | 7 | HG01934.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-1360G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105389 | ||||||
| chr3:123105525
|
G | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(238): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.388-1224G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105525 | ||||||
| chr3:123105666
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.388-1083A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105666 | ||||||
| chr3:123105739
|
GCA | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(223): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.388-987_388-986del others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 123105739 | |||||
| chr3:123105739
|
GCACA | G | 37 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0066others(34): Show | 37 | HG00099.hp2 HG00609.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-989_388-986del others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 123105739 | |||||
| chr3:123105747
|
A | G | 14 | a0001c0001t0001g0066a0001c0001t0001g0280a0001c0001t0001g0281others(11): Show | 14 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.388-1002A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105747 | ||||||
| chr3:123105829
|
G | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0280others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.388-920G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105829 | ||||||
| chr3:123105927
|
A | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0053others(16): Show | 19 | HG00735.hp1 HG01884.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.388-822A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105927 | ||||||
| chr3:123105966
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.388-783A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123105966 | ||||||
| chr3:123106193
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.388-556T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123106193 | ||||||
| chr3:123106290
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.388-459G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123106290 | ||||||
| chr3:123106445
|
A | G | 2 | a0001c0003t0001g0037a0001c0003t0001g0112 | 2 | HG00738.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.388-304A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123106445 | ||||||
| chr3:123106464
|
T | A | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.388-285T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123106464 | ||||||
| chr3:123106743
|
C | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0256a0002c0008t0001g0046others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.388-6C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 5/16 | chr3 | 123106743 | ||||||
| chr3:123107007
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(189): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.480+166C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107007 | ||||||
| chr3:123107081
|
T | C | 4 | a0001c0001t0001g0034a0001c0002t0001g0032a0001c0002t0001g0033others(1): Show | 4 | HG01070.hp1 HG01081.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+240T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107081 | ||||||
| chr3:123107207
|
T | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.480+366T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107207 | ||||||
| chr3:123107411
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.480+570C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107411 | ||||||
| chr3:123107424
|
G | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.480+583G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107424 | ||||||
| chr3:123107435
|
A | G | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.480+594A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107435 | ||||||
| chr3:123107485
|
T | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0004t0001g0257others(1): Show | 4 | HG01433.hp1 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+644T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107485 | ||||||
| chr3:123107719
|
G | A | 2 | a0001c0001t0001g0235a0007c0013t0001g0198 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.480+878G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107719 | ||||||
| chr3:123107883
|
C | T | 3 | a0001c0001t0001g0240a0001c0004t0001g0257a0001c0018t0001g0241 | 3 | HG01433.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.480+1042C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123107883 | ||||||
| chr3:123108022
|
T | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.480+1181T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123108022 | ||||||
| chr3:123108234
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0279 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.480+1393A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123108234 | ||||||
| chr3:123108281
|
C | CT | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 41 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.480+1457dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 123108281 | |||||
| chr3:123108613
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480+1772G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123108613 | ||||||
| chr3:123108617
|
C | CGG | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.480+1776_480+1777i others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123108617 | ||||||
| chr3:123109479
|
AATTTTGT others(64): Show |
A | 1 | a0001c0003t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.481-1463_481-1393d others(73): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 123109479 | |||||
| chr3:123109902
|
T | C | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(208): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.481-1042T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123109902 | ||||||
| chr3:123110143
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(183): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.481-801C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110143 | ||||||
| chr3:123110182
|
C | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG00673.hp2 HG01070.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.481-762C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110182 | ||||||
| chr3:123110326
|
G | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.481-618G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110326 | ||||||
| chr3:123110568
|
C | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0002t0001g0204 | 3 | NA18953.hp2 NA19068.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.481-376C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110568 | ||||||
| chr3:123110608
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.481-336G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110608 | ||||||
| chr3:123110713
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0282a0001c0011t0001g0283 | 3 | HG01891.hp1 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.481-231G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110713 | ||||||
| chr3:123110912
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.481-32C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110912 | ||||||
| chr3:123110918
|
G | A | 2 | a0001c0002t0001g0193a0001c0002t0001g0194 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481-26G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 6/16 | chr3 | 123110918 | ||||||
| chr3:123111271
|
A | G | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.541+267A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123111271 | ||||||
| chr3:123111329
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.541+325G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123111329 | ||||||
| chr3:123111367
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.541+363C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123111367 | ||||||
| chr3:123111390
|
G | A | 1 | a0001c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.541+386G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123111390 | ||||||
| chr3:123111947
|
C | T | 2 | a0001c0001t0001g0254a0001c0006t0001g0120 | 2 | HG00280.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.541+943C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123111947 | ||||||
| chr3:123112015
|
C | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.541+1011C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112015 | ||||||
| chr3:123112241
|
G | T | 2 | a0001c0001t0001g0240a0001c0018t0001g0241 | 2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.541+1237G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112241 | ||||||
| chr3:123112355
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.541+1351T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112355 | ||||||
| chr3:123112366
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.541+1362C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112366 | ||||||
| chr3:123112441
|
C | T | 13 | a0001c0001t0001g0170a0001c0001t0001g0178a0001c0001t0001g0181others(10): Show | 13 | HG02080.hp1 HG02155.hp2 NA18978.hp1 others(10): Show |
intron_variant | MODIFIER | c.541+1437C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112441 | ||||||
| chr3:123112534
|
C | CT | 26 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(23): Show | 26 | HG00673.hp2 HG00738.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.541+1556dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 123112534 | |||||
| chr3:123112534
|
C | CTT | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0275others(13): Show | 16 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.541+1555_541+1556d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 123112534 | |||||
| chr3:123112534
|
CT | C | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.541+1556delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 123112534 | |||||
| chr3:123112534
|
CTT | C | 13 | a0001c0001t0001g0106a0001c0001t0001g0136a0001c0001t0001g0152others(10): Show | 13 | HG01081.hp1 HG01515.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.541+1555_541+1556d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 123112534 | |||||
| chr3:123112585
|
G | C | 3 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0002t0001g0292 | 3 | HG01934.hp2 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.541+1581G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112585 | ||||||
| chr3:123112642
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.541+1638G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112642 | ||||||
| chr3:123112644
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.541+1640G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123112644 | ||||||
| chr3:123113227
|
A | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(252): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.541+2223A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113227 | ||||||
| chr3:123113257
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(1): Show | 4 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2253G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113257 | ||||||
| chr3:123113392
|
G | A | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.541+2388G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113392 | ||||||
| chr3:123113457
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+2453C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113457 | ||||||
| chr3:123113596
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.541+2592C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113596 | ||||||
| chr3:123113597
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.541+2593G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113597 | ||||||
| chr3:123113656
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.542-2575A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113656 | ||||||
| chr3:123113719
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.542-2512G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113719 | ||||||
| chr3:123113756
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0281a0001c0001t0001g0323others(2): Show | 5 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-2475G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123113756 | ||||||
| chr3:123114156
|
C | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(129): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.542-2075C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114156 | ||||||
| chr3:123114174
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0021others(17): Show | 21 | HG00099.hp1 HG00673.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.542-2057G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114174 | ||||||
| chr3:123114224
|
G | A | 15 | a0001c0001t0001g0130a0001c0001t0001g0259a0001c0001t0001g0268others(12): Show | 15 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.542-2007G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114224 | ||||||
| chr3:123114234
|
G | T | 59 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0017others(56): Show | 59 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.542-1997G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114234 | ||||||
| chr3:123114243
|
G | C | 199 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(196): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.542-1988G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114243 | ||||||
| chr3:123114334
|
G | A | 27 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0069others(24): Show | 27 | HG00597.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.542-1897G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114334 | ||||||
| chr3:123114366
|
A | AC | 54 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0053others(51): Show | 54 | HG00597.hp1 HG00642.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.542-1858dupC | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 123114366 | |||||
| chr3:123114437
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.542-1794C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114437 | ||||||
| chr3:123114549
|
G | A | 1 | a0001c0004t0001g0315 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.542-1682G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114549 | ||||||
| chr3:123114620
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.542-1611G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114620 | ||||||
| chr3:123114630
|
C | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0105a0001c0001t0001g0127others(4): Show | 7 | HG00735.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.542-1601C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114630 | ||||||
| chr3:123114672
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.542-1559C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114672 | ||||||
| chr3:123114699
|
A | T | 2 | a0001c0003t0001g0270a0001c0005t0001g0126 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.542-1532A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114699 | ||||||
| chr3:123114738
|
G | A | 2 | a0001c0001t0001g0108a0001c0005t0001g0107 | 2 | HG02135.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.542-1493G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114738 | ||||||
| chr3:123114851
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.542-1380A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114851 | ||||||
| chr3:123114878
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0087 | 3 | HG01255.hp1 HG01261.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.542-1353G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114878 | ||||||
| chr3:123114992
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.542-1239T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123114992 | ||||||
| chr3:123115194
|
T | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.542-1037T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115194 | ||||||
| chr3:123115417
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.542-814G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115417 | ||||||
| chr3:123115489
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.542-742C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115489 | ||||||
| chr3:123115532
|
G | A | 2 | a0001c0001t0001g0256a0001c0003t0001g0051 | 2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.542-699G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115532 | ||||||
| chr3:123115547
|
C | G | 2 | a0001c0001t0001g0125a0001c0011t0001g0283 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.542-684C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115547 | ||||||
| chr3:123115746
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.542-485G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115746 | ||||||
| chr3:123115771
|
C | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0053others(35): Show | 38 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.542-460C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115771 | ||||||
| chr3:123115772
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-459G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115772 | ||||||
| chr3:123115899
|
G | A | 42 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(39): Show | 42 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.542-332G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115899 | ||||||
| chr3:123115963
|
A | G | 42 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(39): Show | 42 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.542-268A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123115963 | ||||||
| chr3:123116040
|
A | T | 197 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.542-191A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123116040 | ||||||
| chr3:123116156
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0243 | 3 | NA18947.hp2 NA18981.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.542-75T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123116156 | ||||||
| chr3:123116200
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.542-31C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 7/16 | chr3 | 123116200 | ||||||
| chr3:123116309
|
C | T | 1 | a0001c0002t0001g0057 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.609+11C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116309 | ||||||
| chr3:123116363
|
A | G | 199 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(196): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.609+65A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116363 | ||||||
| chr3:123116385
|
T | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(128): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.609+87T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116385 | ||||||
| chr3:123116433
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.609+135C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116433 | ||||||
| chr3:123116691
|
T | C | 1 | a0001c0002t0001g0124 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.609+393T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116691 | ||||||
| chr3:123116693
|
A | T | 1 | a0001c0002t0001g0124 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.609+395A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116693 | ||||||
| chr3:123116694
|
G | A | 1 | a0001c0002t0001g0124 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.609+396G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116694 | ||||||
| chr3:123116731
|
A | G | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.609+433A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116731 | ||||||
| chr3:123116775
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+477G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116775 | ||||||
| chr3:123116784
|
G | A | 1 | a0001c0011t0001g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.609+486G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123116784 | ||||||
| chr3:123117017
|
G | C | 2 | a0001c0002t0001g0097a0001c0002t0001g0132 | 2 | NA18944.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.609+719G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117017 | ||||||
| chr3:123117043
|
A | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.609+745A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117043 | ||||||
| chr3:123117108
|
C | T | 7 | a0001c0001t0001g0170a0001c0005t0001g0155a0001c0005t0001g0156others(4): Show | 7 | HG02080.hp2 HG03831.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+810C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117108 | ||||||
| chr3:123117145
|
A | G | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+847A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117145 | ||||||
| chr3:123117153
|
T | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(127): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.609+855T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117153 | ||||||
| chr3:123117157
|
A | T | 197 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.609+859A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117157 | ||||||
| chr3:123117329
|
T | C | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.609+1031T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117329 | ||||||
| chr3:123117372
|
T | TATTATAT others(5): Show |
1 | a0001c0001t0001g0297 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.609+1074_609+1075i others(14): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117372 | ||||||
| chr3:123117372
|
T | TTATATAT others(23): Show |
2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.609+1075_609+1076i others(32): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117372 | |||||
| chr3:123117372
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.609+1075_609+1076i others(34): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117372 | |||||
| chr3:123117374
|
T | A | 4 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(1): Show | 4 | HG01099.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+1076T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117374 | ||||||
| chr3:123117374
|
T | TATATATA others(12): Show |
1 | a0001c0002t0001g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.609+1076_609+1077i others(21): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117374 | ||||||
| chr3:123117374
|
T | TATATATA others(16): Show |
1 | a0001c0001t0001g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.609+1076_609+1077i others(25): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117374 | ||||||
| chr3:123117374
|
T | TATATATA others(18): Show |
1 | a0001c0001t0001g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.609+1076_609+1077i others(27): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117374 | ||||||
| chr3:123117374
|
T | TATATATA others(28): Show |
1 | a0001c0001t0001g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.609+1076_609+1077i others(37): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117374 | ||||||
| chr3:123117374
|
T | TTA | 9 | a0001c0001t0001g0130a0001c0001t0001g0259a0001c0001t0001g0268others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.609+1100_609+1101d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATA | 15 | a0001c0001t0001g0170a0001c0001t0001g0273a0001c0002t0001g0059others(12): Show | 15 | HG00738.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.609+1098_609+1101d others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATA | 4 | a0001c0001t0001g0019a0001c0002t0001g0124a0001c0002t0001g0246others(1): Show | 4 | HG01106.hp2 HG03486.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+1096_609+1101d others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(1): Show |
63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.609+1094_609+1101d others(10): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(3): Show |
34 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0040others(31): Show | 35 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+1092_609+1101d others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(8): Show |
1 | a0001c0001t0001g0290 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.609+1086_609+1087i others(17): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(5): Show |
34 | a0001c0001t0001g0020a0001c0001t0001g0066a0001c0001t0001g0108others(31): Show | 34 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.609+1090_609+1101d others(14): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(7): Show |
20 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0063others(17): Show | 22 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.609+1088_609+1101d others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(9): Show |
19 | a0001c0001t0001g0045a0001c0001t0001g0090a0001c0001t0001g0161others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.609+1086_609+1101d others(18): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(11): Show |
19 | a0001c0001t0001g0115a0001c0001t0001g0185a0001c0001t0001g0197others(16): Show | 19 | HG00642.hp2 HG00673.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.609+1084_609+1101d others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(13): Show |
11 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0089others(8): Show | 12 | HG00140.hp2 HG01943.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.609+1082_609+1101d others(22): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(15): Show |
6 | a0001c0001t0001g0069a0001c0001t0001g0225a0001c0002t0001g0296others(3): Show | 6 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.609+1080_609+1101d others(24): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(17): Show |
8 | a0001c0001t0001g0095a0001c0001t0001g0301a0001c0002t0001g0236others(5): Show | 8 | HG01515.hp2 NA18957.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.609+1078_609+1101d others(26): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(19): Show |
8 | a0001c0001t0001g0073a0001c0001t0001g0181a0001c0001t0001g0212others(5): Show | 8 | HG02155.hp2 HG02630.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(28): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(21): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0082others(10): Show | 13 | HG02280.hp1 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(30): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(23): Show |
4 | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0003t0001g0258others(1): Show | 4 | HG00639.hp2 HG01123.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(32): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(25): Show |
7 | a0001c0001t0001g0169a0001c0001t0001g0275a0001c0002t0001g0030others(4): Show | 7 | HG01106.hp1 HG01167.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(34): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(27): Show |
4 | a0001c0001t0001g0083a0001c0001t0001g0282a0001c0003t0001g0270others(1): Show | 4 | HG02723.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(36): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(29): Show |
6 | a0001c0001t0001g0295a0001c0001t0001g0321a0001c0002t0001g0121others(3): Show | 6 | HG00642.hp1 HG00741.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(38): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(31): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0081a0001c0003t0001g0084others(1): Show | 4 | HG01361.hp1 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+1101_609+1102i others(40): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(33): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0206 | 2 | HG00597.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.609+1101_609+1102i others(42): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(35): Show |
1 | a0001c0003t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.609+1101_609+1102i others(44): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTATATAT others(39): Show |
1 | a0001c0002t0001g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.609+1101_609+1102i others(48): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
T | TTTTATAT others(23): Show |
2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01934.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.609+1077_609+1078i others(32): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
TTA | T | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1100_609+1101d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117374
|
TTATA | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0128a0001c0002t0001g0104 | 3 | HG02055.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.609+1098_609+1101d others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123117374 | |||||
| chr3:123117399
|
T | TATATATA others(38): Show |
1 | a0001c0001t0001g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.609+1101_609+1102i others(47): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117399 | ||||||
| chr3:123117498
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1200T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117498 | ||||||
| chr3:123117627
|
T | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.609+1329T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117627 | ||||||
| chr3:123117714
|
T | C | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+1416T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117714 | ||||||
| chr3:123117874
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1576T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117874 | ||||||
| chr3:123117939
|
T | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.609+1641T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117939 | ||||||
| chr3:123117951
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0017others(64): Show | 67 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.609+1653A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123117951 | ||||||
| chr3:123118097
|
G | A | 14 | a0001c0001t0001g0152a0001c0001t0001g0305a0001c0001t0001g0313others(11): Show | 15 | HG00099.hp2 HG00733.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.609+1799G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118097 | ||||||
| chr3:123118402
|
C | G | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+2104C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118402 | ||||||
| chr3:123118517
|
G | T | 1 | a0001c0002t0001g0159 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.609+2219G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118517 | ||||||
| chr3:123118669
|
A | G | 3 | a0001c0001t0001g0073a0001c0002t0001g0075a0001c0004t0001g0074 | 3 | HG01123.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.609+2371A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118669 | ||||||
| chr3:123118720
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.609+2422C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118720 | ||||||
| chr3:123118801
|
C | T | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(136): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.609+2503C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118801 | ||||||
| chr3:123118926
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.609+2628A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123118926 | ||||||
| chr3:123119136
|
A | G | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02451.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.609+2838A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123119136 | ||||||
| chr3:123119138
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.609+2840G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123119138 | ||||||
| chr3:123119437
|
T | C | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+3139T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123119437 | ||||||
| chr3:123119563
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.609+3265G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123119563 | ||||||
| chr3:123119611
|
C | T | 15 | a0001c0001t0001g0170a0001c0002t0001g0059a0001c0002t0001g0096others(12): Show | 15 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.609+3313C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123119611 | ||||||
| chr3:123119900
|
AT | A | 52 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0035others(49): Show | 52 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.609+3604delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123119900 | |||||
| chr3:123120010
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.609+3712G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120010 | ||||||
| chr3:123120152
|
T | G | 52 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0035others(49): Show | 52 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.609+3854T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120152 | ||||||
| chr3:123120174
|
G | A | 2 | a0004c0009t0001g0195a0004c0009t0001g0196 | 2 | NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.609+3876G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120174 | ||||||
| chr3:123120243
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(35): Show | 38 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.610-3823G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120243 | ||||||
| chr3:123120366
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01934.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.610-3700A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120366 | ||||||
| chr3:123120393
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0200 | 2 | NA19056.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.610-3673G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120393 | ||||||
| chr3:123120494
|
G | A | 1 | a0001c0003t0001g0036 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.610-3572G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120494 | ||||||
| chr3:123120521
|
C | T | 1 | a0001c0018t0001g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.610-3545C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120521 | ||||||
| chr3:123120605
|
C | T | 2 | a0001c0001t0001g0128a0001c0002t0001g0104 | 2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.610-3461C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120605 | ||||||
| chr3:123120631
|
T | TC | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-3433dupC | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 123120631 | |||||
| chr3:123120678
|
G | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(183): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.610-3388G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120678 | ||||||
| chr3:123120717
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-3349T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120717 | ||||||
| chr3:123120759
|
T | C | 2 | a0005c0012t0001g0049a0005c0012t0001g0050 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.610-3307T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120759 | ||||||
| chr3:123120783
|
C | G | 1 | a0001c0002t0001g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.610-3283C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120783 | ||||||
| chr3:123120896
|
T | C | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-3170T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120896 | ||||||
| chr3:123120938
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-3128C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123120938 | ||||||
| chr3:123121029
|
G | A | 145 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(142): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.610-3037G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121029 | ||||||
| chr3:123121051
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-3015G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121051 | ||||||
| chr3:123121178
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-2888G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121178 | ||||||
| chr3:123121332
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-2734C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121332 | ||||||
| chr3:123121466
|
A | G | 186 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(183): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.610-2600A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121466 | ||||||
| chr3:123121641
|
G | A | 2 | a0001c0002t0001g0124a0001c0002t0001g0143 | 2 | NA18953.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.610-2425G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121641 | ||||||
| chr3:123121650
|
C | T | 2 | a0001c0003t0001g0224a0008c0015t0001g0220 | 2 | HG01167.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.610-2416C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121650 | ||||||
| chr3:123121670
|
T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.610-2396T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121670 | ||||||
| chr3:123121773
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(6): Show | 9 | HG01109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.610-2293C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121773 | ||||||
| chr3:123121884
|
A | G | 145 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(142): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.610-2182A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121884 | ||||||
| chr3:123121898
|
G | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.610-2168G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121898 | ||||||
| chr3:123121900
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0039others(19): Show | 23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.610-2166G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121900 | ||||||
| chr3:123121909
|
G | A | 32 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(29): Show | 32 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.610-2157G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123121909 | ||||||
| chr3:123122215
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(140): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.610-1851G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122215 | ||||||
| chr3:123122224
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.610-1842G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122224 | ||||||
| chr3:123122252
|
A | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.610-1814A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122252 | ||||||
| chr3:123122299
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.610-1767A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122299 | ||||||
| chr3:123122325
|
C | T | 10 | a0001c0001t0001g0070a0001c0001t0001g0295a0001c0001t0001g0308others(7): Show | 10 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.610-1741C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122325 | ||||||
| chr3:123122439
|
G | T | 1 | a0001c0003t0001g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.610-1627G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122439 | ||||||
| chr3:123122481
|
G | A | 1 | a0001c0003t0001g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610-1585G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122481 | ||||||
| chr3:123122513
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.610-1553A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122513 | ||||||
| chr3:123122523
|
A | G | 2 | a0001c0001t0001g0015a0001c0003t0001g0076 | 2 | HG01074.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.610-1543A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122523 | ||||||
| chr3:123122547
|
T | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-1519T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122547 | ||||||
| chr3:123122806
|
C | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0221a0001c0003t0001g0231 | 4 | HG02155.hp1 NA18944.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-1260C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122806 | ||||||
| chr3:123122947
|
G | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(187): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.610-1119G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123122947 | ||||||
| chr3:123123296
|
C | T | 1 | a0001c0004t0001g0189 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.610-770C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123123296 | ||||||
| chr3:123123409
|
G | A | 2 | a0001c0001t0001g0115a0001c0003t0001g0113 | 2 | HG03834.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.610-657G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123123409 | ||||||
| chr3:123123561
|
C | T | 1 | a0001c0003t0001g0318 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.610-505C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123123561 | ||||||
| chr3:123123610
|
A | G | 1 | a0001c0002t0001g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.610-456A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123123610 | ||||||
| chr3:123123691
|
C | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(6): Show | 9 | HG01109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.610-375C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123123691 | ||||||
| chr3:123123764
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(137): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.610-302G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 8/16 | chr3 | 123123764 | ||||||
| chr3:123124162
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18945.hp1 | splice_region_variant&intron_variant | LOW | c.701+5G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 9/16 | chr3 | 123124162 | ||||||
| chr3:123124173
|
T | C | 36 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0055others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.701+16T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 9/16 | chr3 | 123124173 | ||||||
| chr3:123124262
|
C | T | 1 | a0001c0003t0001g0067 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.702-10C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 9/16 | chr3 | 123124262 | ||||||
| chr3:123124263
|
G | T | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.702-9G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 9/16 | chr3 | 123124263 | ||||||
| chr3:123124357
|
G | A | 10 | a0001c0001t0001g0130a0001c0001t0001g0259a0001c0001t0001g0268others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+14G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123124357 | ||||||
| chr3:123124365
|
C | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(142): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.773+22C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123124365 | ||||||
| chr3:123124400
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.773+57G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123124400 | ||||||
| chr3:123124413
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.773+70G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123124413 | ||||||
| chr3:123124657
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+314T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123124657 | ||||||
| chr3:123124830
|
A | G | 1 | a0001c0002t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.773+487A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123124830 | ||||||
| chr3:123125121
|
T | A | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.773+778T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125121 | ||||||
| chr3:123125223
|
G | A | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.773+880G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125223 | ||||||
| chr3:123125563
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.773+1220C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125563 | ||||||
| chr3:123125797
|
T | C | 1 | a0001c0003t0001g0234 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.773+1454T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125797 | ||||||
| chr3:123125836
|
C | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(30): Show | 33 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.773+1493C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125836 | ||||||
| chr3:123125908
|
T | C | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.773+1565T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125908 | ||||||
| chr3:123125994
|
A | G | 3 | a0001c0001t0001g0095a0001c0002t0001g0078a0001c0003t0001g0091 | 3 | NA18970.hp2 NA18972.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.773+1651A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123125994 | ||||||
| chr3:123126025
|
C | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0186a0001c0002t0001g0030others(4): Show | 7 | HG00597.hp2 NA18939.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.773+1682C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126025 | ||||||
| chr3:123126104
|
T | G | 150 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(147): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.773+1761T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126104 | ||||||
| chr3:123126126
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(181): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.773+1783A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126126 | ||||||
| chr3:123126230
|
G | A | 135 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(132): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.773+1887G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126230 | ||||||
| chr3:123126267
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.773+1924C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126267 | ||||||
| chr3:123126318
|
A | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.773+1975A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126318 | ||||||
| chr3:123126567
|
C | T | 2 | a0001c0001t0001g0264a0009c0019t0001g0263 | 2 | NA18943.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.773+2224C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126567 | ||||||
| chr3:123126575
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(181): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.773+2232T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126575 | ||||||
| chr3:123126615
|
G | A | 2 | a0001c0003t0001g0036a0001c0003t0001g0077 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.773+2272G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126615 | ||||||
| chr3:123126645
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.773+2302G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126645 | ||||||
| chr3:123126824
|
C | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(141): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.773+2481C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123126824 | ||||||
| chr3:123127228
|
C | G | 1 | a0002c0008t0001g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.773+2885C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127228 | ||||||
| chr3:123127440
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.774-3040A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127440 | ||||||
| chr3:123127441
|
A | C | 2 | a0001c0002t0001g0097a0001c0002t0001g0132 | 2 | NA18944.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.774-3039A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127441 | ||||||
| chr3:123127459
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.774-3021C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127459 | ||||||
| chr3:123127469
|
C | T | 5 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG00673.hp1 NA18945.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.774-3011C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127469 | ||||||
| chr3:123127492
|
A | G | 187 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(184): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.774-2988A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127492 | ||||||
| chr3:123127511
|
A | G | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-2969A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127511 | ||||||
| chr3:123127707
|
A | G | 1 | a0001c0004t0001g0100 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.774-2773A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127707 | ||||||
| chr3:123127713
|
T | C | 1 | a0001c0002t0001g0227 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.774-2767T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127713 | ||||||
| chr3:123127760
|
G | A | 1 | a0001c0004t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.774-2720G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123127760 | ||||||
| chr3:123128034
|
C | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(141): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.774-2446C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128034 | ||||||
| chr3:123128177
|
A | G | 186 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(183): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.774-2303A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128177 | ||||||
| chr3:123128374
|
G | A | 2 | a0001c0002t0001g0103a0001c0002t0001g0191 | 2 | HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.774-2106G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128374 | ||||||
| chr3:123128414
|
CT | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(3): Show | 6 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-2064delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 123128414 | |||||
| chr3:123128491
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.774-1989A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128491 | ||||||
| chr3:123128629
|
T | G | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.774-1851T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128629 | ||||||
| chr3:123128773
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.774-1707G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128773 | ||||||
| chr3:123128924
|
A | T | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.774-1556A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123128924 | ||||||
| chr3:123129059
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0308a0001c0001t0001g0321 | 3 | HG01261.hp1 HG01516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.774-1421G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129059 | ||||||
| chr3:123129066
|
C | CAAAT | 197 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.774-1412_774-1411i others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 123129066 | |||||
| chr3:123129367
|
G | A | 3 | a0001c0005t0001g0155a0001c0005t0001g0156a0001c0005t0001g0163 | 3 | HG02080.hp2 HG03831.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.774-1113G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129367 | ||||||
| chr3:123129402
|
C | A | 7 | a0001c0001t0001g0170a0001c0005t0001g0155a0001c0005t0001g0156others(4): Show | 7 | HG02080.hp2 HG03831.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.774-1078C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129402 | ||||||
| chr3:123129402
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.774-1078C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129402 | ||||||
| chr3:123129430
|
T | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(187): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.774-1050T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129430 | ||||||
| chr3:123129467
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG02135.hp2 NA18943.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.774-1013C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129467 | ||||||
| chr3:123129519
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.774-961A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129519 | ||||||
| chr3:123129621
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.774-859C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129621 | ||||||
| chr3:123129775
|
C | A | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.774-705C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129775 | ||||||
| chr3:123129799
|
A | T | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.774-681A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129799 | ||||||
| chr3:123129899
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.774-581G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123129899 | ||||||
| chr3:123130030
|
C | T | 2 | a0001c0001t0001g0219a0001c0002t0001g0218 | 2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.774-450C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123130030 | ||||||
| chr3:123130109
|
C | T | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0123others(3): Show | 6 | NA18997.hp2 NA19058.hp1 NA19068.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-371C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123130109 | ||||||
| chr3:123130287
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0282 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.774-193G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123130287 | ||||||
| chr3:123130322
|
G | A | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-158G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123130322 | ||||||
| chr3:123130442
|
G | C | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.774-38G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 10/16 | chr3 | 123130442 | ||||||
| chr3:123130778
|
G | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+162G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123130778 | ||||||
| chr3:123130983
|
G | A | 1 | a0001c0003t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.910+367G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123130983 | ||||||
| chr3:123131000
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.910+384G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131000 | ||||||
| chr3:123131059
|
G | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.910+443G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131059 | ||||||
| chr3:123131281
|
G | A | 3 | a0001c0001t0001g0161a0001c0002t0001g0141a0001c0002t0001g0207 | 3 | HG01346.hp2 HG01993.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.910+665G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131281 | ||||||
| chr3:123131397
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.910+781G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131397 | ||||||
| chr3:123131459
|
T | A | 3 | a0001c0001t0001g0134a0001c0003t0001g0027a0001c0003t0001g0133 | 3 | HG02145.hp2 HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.910+843T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131459 | ||||||
| chr3:123131509
|
T | G | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+893T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131509 | ||||||
| chr3:123131514
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0105a0001c0001t0001g0127others(3): Show | 6 | HG00735.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+898G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131514 | ||||||
| chr3:123131527
|
C | G | 1 | a0001c0002t0001g0228 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.910+911C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131527 | ||||||
| chr3:123131595
|
C | T | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.910+979C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131595 | ||||||
| chr3:123131729
|
C | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+1113C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131729 | ||||||
| chr3:123131741
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0282 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.910+1125T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131741 | ||||||
| chr3:123131839
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0144 | 2 | HG02280.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.910+1223G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123131839 | ||||||
| chr3:123132091
|
T | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(137): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.910+1475T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132091 | ||||||
| chr3:123132098
|
A | G | 3 | a0001c0005t0001g0155a0001c0005t0001g0156a0001c0005t0001g0163 | 3 | HG02080.hp2 HG03831.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.910+1482A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132098 | ||||||
| chr3:123132105
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(3): Show | 6 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+1489G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132105 | ||||||
| chr3:123132176
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.910+1560C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132176 | ||||||
| chr3:123132187
|
G | C | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+1571G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132187 | ||||||
| chr3:123132253
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.910+1637G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132253 | ||||||
| chr3:123132414
|
T | C | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+1798T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132414 | ||||||
| chr3:123132446
|
T | C | 1 | a0001c0003t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.910+1830T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132446 | ||||||
| chr3:123132594
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+1978C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132594 | ||||||
| chr3:123132753
|
A | C | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+2137A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132753 | ||||||
| chr3:123132756
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.910+2140C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132756 | ||||||
| chr3:123132993
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(136): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.910+2377A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132993 | ||||||
| chr3:123132995
|
G | A | 27 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0069others(24): Show | 27 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.910+2379G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123132995 | ||||||
| chr3:123133077
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(3): Show | 6 | HG00639.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+2461G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133077 | ||||||
| chr3:123133482
|
G | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.910+2866G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133482 | ||||||
| chr3:123133499
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01934.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.910+2883G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133499 | ||||||
| chr3:123133628
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.910+3012G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133628 | ||||||
| chr3:123133967
|
G | GTTTTC | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.910+3367_910+3371d others(7): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123133967 | |||||
| chr3:123133973
|
T | A | 2 | a0001c0002t0001g0097a0001c0002t0001g0132 | 2 | NA18944.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.910+3357T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133973 | ||||||
| chr3:123133976
|
TCTTTTCT others(4): Show |
T | 5 | a0001c0001t0001g0063a0001c0001t0001g0139a0001c0001t0001g0297others(2): Show | 6 | HG01099.hp1 HG03486.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+3372_910+3382d others(13): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123133976 | |||||
| chr3:123133988
|
C | T | 147 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.910+3372C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133988 | ||||||
| chr3:123133992
|
T | C | 147 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.910+3376T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133992 | ||||||
| chr3:123133999
|
T | C | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.910+3383T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123133999 | ||||||
| chr3:123134003
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.910+3387C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134003 | ||||||
| chr3:123134003
|
CCTTTT | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0139a0001c0001t0001g0297others(2): Show | 6 | HG01099.hp1 HG03486.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+3399_910+3403d others(7): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123134003 | |||||
| chr3:123134175
|
C | T | 2 | a0001c0003t0001g0101a0001c0003t0001g0318 | 2 | HG01255.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.910+3559C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134175 | ||||||
| chr3:123134275
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.910+3659C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134275 | ||||||
| chr3:123134295
|
C | T | 1 | a0001c0003t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.910+3679C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134295 | ||||||
| chr3:123134478
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0105a0001c0001t0001g0127others(3): Show | 6 | HG00735.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+3862G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134478 | ||||||
| chr3:123134507
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0105a0001c0001t0001g0127others(3): Show | 6 | HG00735.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+3891C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134507 | ||||||
| chr3:123134833
|
G | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(139): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.910+4217G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134833 | ||||||
| chr3:123134958
|
A | G | 199 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(196): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.910+4342A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123134958 | ||||||
| chr3:123135020
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.910+4404C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135020 | ||||||
| chr3:123135068
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.910+4452G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135068 | ||||||
| chr3:123135118
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0039others(44): Show | 48 | HG00597.hp2 HG00642.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.910+4502T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135118 | ||||||
| chr3:123135210
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0039others(19): Show | 23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.910+4594G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135210 | ||||||
| chr3:123135328
|
C | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0055others(13): Show | 16 | HG00735.hp1 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.910+4712C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135328 | ||||||
| chr3:123135329
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.910+4713G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135329 | ||||||
| chr3:123135335
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.910+4719C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135335 | ||||||
| chr3:123135354
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.910+4738A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135354 | ||||||
| chr3:123135422
|
G | A | 47 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(44): Show | 47 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.910+4806G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135422 | ||||||
| chr3:123135425
|
A | G | 16 | a0001c0001t0001g0170a0001c0002t0001g0059a0001c0002t0001g0096others(13): Show | 16 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.910+4809A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135425 | ||||||
| chr3:123135526
|
G | A | 2 | a0005c0012t0001g0049a0005c0012t0001g0050 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.910+4910G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135526 | ||||||
| chr3:123135647
|
GC | G | 14 | a0001c0001t0001g0170a0001c0002t0001g0059a0001c0002t0001g0096others(11): Show | 14 | HG00738.hp1 HG01346.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.910+5032delC | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135647 | ||||||
| chr3:123135707
|
A | C | 4 | a0001c0001t0001g0020a0001c0004t0001g0025a0001c0004t0001g0061others(1): Show | 4 | HG00408.hp2 HG03669.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+5091A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135707 | ||||||
| chr3:123135745
|
C | CT | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.910+5152dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123135745 | |||||
| chr3:123135745
|
C | CTTT | 7 | a0001c0001t0001g0295a0001c0002t0001g0296a0001c0003t0001g0278others(4): Show | 7 | HG00733.hp1 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.910+5150_910+5152d others(5): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123135745 | |||||
| chr3:123135745
|
C | CTTTT | 38 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0068others(35): Show | 38 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.910+5149_910+5152d others(6): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123135745 | |||||
| chr3:123135745
|
CTT | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0308a0001c0001t0001g0321others(4): Show | 7 | HG00642.hp1 HG00741.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.910+5151_910+5152d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123135745 | |||||
| chr3:123135859
|
C | CT | 35 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.910+5257dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123135859 | |||||
| chr3:123135859
|
CT | C | 18 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0001g0152others(15): Show | 18 | HG01070.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.910+5257delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123135859 | |||||
| chr3:123135910
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.910+5294G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135910 | ||||||
| chr3:123135974
|
T | G | 8 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(5): Show | 8 | HG00639.hp2 HG00733.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+5358T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123135974 | ||||||
| chr3:123136052
|
T | C | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(155): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.910+5436T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136052 | ||||||
| chr3:123136066
|
G | A | 2 | a0001c0004t0001g0025a0001c0004t0001g0135 | 2 | HG00408.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.910+5450G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136066 | ||||||
| chr3:123136088
|
A | G | 36 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.910+5472A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136088 | ||||||
| chr3:123136363
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.910+5747C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136363 | ||||||
| chr3:123136580
|
A | C | 1 | a0006c0017t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.910+5964A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136580 | ||||||
| chr3:123136725
|
C | CA | 15 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0140others(12): Show | 15 | HG00597.hp2 HG01934.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.910+6133dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123136725 | |||||
| chr3:123136725
|
CA | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(137): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.910+6133delA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123136725 | |||||
| chr3:123136725
|
CAA | C | 15 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0181others(12): Show | 15 | HG00597.hp1 HG01175.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.910+6132_910+6133d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123136725 | |||||
| chr3:123136725
|
CAAA | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(25): Show | 28 | HG00423.hp1 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.910+6131_910+6133d others(5): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123136725 | |||||
| chr3:123136741
|
A | T | 2 | a0001c0003t0001g0038a0001c0003t0001g0285 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.910+6125A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136741 | ||||||
| chr3:123136745
|
A | T | 2 | a0001c0003t0001g0038a0001c0003t0001g0285 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.910+6129A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136745 | ||||||
| chr3:123136748
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.910+6132A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136748 | ||||||
| chr3:123136749
|
A | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0081others(15): Show | 18 | HG00639.hp2 HG00733.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.910+6133A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136749 | ||||||
| chr3:123136781
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+6165C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136781 | ||||||
| chr3:123136782
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02486.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+6166A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136782 | ||||||
| chr3:123136795
|
C | T | 8 | a0001c0001t0001g0070a0001c0001t0001g0308a0001c0001t0001g0321others(5): Show | 8 | HG00642.hp1 HG00741.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+6179C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136795 | ||||||
| chr3:123136847
|
G | A | 1 | a0001c0004t0001g0065 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.910+6231G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136847 | ||||||
| chr3:123136847
|
G | C | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.910+6231G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136847 | ||||||
| chr3:123136877
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.910+6261G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136877 | ||||||
| chr3:123136920
|
T | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0068others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.910+6304T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123136920 | ||||||
| chr3:123137069
|
A | G | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.910+6453A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123137069 | ||||||
| chr3:123137123
|
A | G | 1 | a0001c0002t0001g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.910+6507A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123137123 | ||||||
| chr3:123137161
|
G | A | 4 | a0001c0001t0001g0170a0001c0005t0001g0173a0001c0006t0001g0172others(1): Show | 4 | NA18978.hp1 NA19066.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+6545G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123137161 | ||||||
| chr3:123137698
|
C | T | 1 | a0001c0002t0001g0162 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.910+7082C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123137698 | ||||||
| chr3:123138246
|
C | A | 3 | a0001c0001t0001g0305a0001c0003t0001g0114a0001c0004t0001g0304 | 3 | HG00099.hp2 HG00733.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.911-7276C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123138246 | ||||||
| chr3:123138655
|
G | A | 3 | a0001c0003t0001g0278a0002c0007t0001g0287a0002c0007t0001g0289 | 3 | HG01109.hp2 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.911-6867G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123138655 | ||||||
| chr3:123138979
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(6): Show | 9 | HG00639.hp2 HG00733.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.911-6543A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123138979 | ||||||
| chr3:123139002
|
C | T | 128 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(125): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.911-6520C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139002 | ||||||
| chr3:123139210
|
C | T | 1 | a0001c0003t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.911-6312C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139210 | ||||||
| chr3:123139299
|
C | G | 1 | a0001c0003t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.911-6223C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139299 | ||||||
| chr3:123139317
|
A | G | 1 | a0001c0003t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.911-6205A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139317 | ||||||
| chr3:123139328
|
A | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.911-6194A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139328 | ||||||
| chr3:123139329
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.911-6193C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139329 | ||||||
| chr3:123139386
|
C | T | 1 | a0001c0002t0001g0154 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.911-6136C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139386 | ||||||
| chr3:123139610
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.911-5912C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139610 | ||||||
| chr3:123139824
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.911-5698C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139824 | ||||||
| chr3:123139972
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0125a0001c0001t0001g0184others(8): Show | 11 | HG01167.hp1 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.911-5550A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139972 | ||||||
| chr3:123139984
|
A | G | 14 | a0001c0001t0001g0048a0001c0001t0001g0106a0001c0001t0001g0130others(11): Show | 14 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.911-5538A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123139984 | ||||||
| chr3:123140020
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.911-5502C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140020 | ||||||
| chr3:123140021
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.911-5501G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140021 | ||||||
| chr3:123140037
|
G | A | 1 | a0001c0003t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.911-5485G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140037 | ||||||
| chr3:123140113
|
C | T | 25 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0108others(22): Show | 25 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.911-5409C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140113 | ||||||
| chr3:123140379
|
GA | G | 43 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0039others(40): Show | 43 | HG00735.hp1 HG01109.hp2 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.911-5139delA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123140379 | |||||
| chr3:123140474
|
G | A | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.911-5048G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140474 | ||||||
| chr3:123140570
|
G | A | 1 | a0001c0018t0001g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.911-4952G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140570 | ||||||
| chr3:123140594
|
G | GCCTGTGG others(6): Show |
113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(110): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.911-4925_911-4924i others(15): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123140594 | |||||
| chr3:123140732
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.911-4790G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140732 | ||||||
| chr3:123140842
|
G | A | 1 | a0001c0006t0001g0188 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.911-4680G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140842 | ||||||
| chr3:123140849
|
G | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(249): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.911-4673G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140849 | ||||||
| chr3:123140976
|
C | T | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.911-4546C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123140976 | ||||||
| chr3:123141021
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.911-4501G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141021 | ||||||
| chr3:123141126
|
A | T | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.911-4396A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141126 | ||||||
| chr3:123141148
|
G | A | 2 | a0001c0001t0001g0055a0001c0018t0001g0241 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.911-4374G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141148 | ||||||
| chr3:123141234
|
T | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.911-4288T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141234 | ||||||
| chr3:123141237
|
G | C | 1 | a0001c0002t0001g0187 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.911-4285G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141237 | ||||||
| chr3:123141304
|
AGCCTCTC others(6): Show |
A | 5 | a0001c0003t0001g0278a0002c0007t0001g0267a0002c0007t0001g0286others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.911-4210_911-4198d others(15): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123141304 | |||||
| chr3:123141309
|
C | G | 3 | a0001c0002t0001g0174a0001c0002t0001g0175a0001c0002t0001g0176 | 3 | NA18999.hp2 NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.911-4213C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141309 | ||||||
| chr3:123141451
|
A | G | 3 | a0001c0003t0001g0278a0002c0007t0001g0287a0002c0007t0001g0289 | 3 | HG01109.hp2 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.911-4071A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141451 | ||||||
| chr3:123141451
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-4071A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141451 | ||||||
| chr3:123141509
|
A | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.911-4013A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141509 | ||||||
| chr3:123141550
|
T | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.911-3972T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141550 | ||||||
| chr3:123141754
|
CA | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0081others(4): Show | 7 | HG00639.hp2 HG01934.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.911-3761delA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123141754 | |||||
| chr3:123141841
|
G | C | 29 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0039others(26): Show | 29 | HG00735.hp1 HG01433.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.911-3681G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141841 | ||||||
| chr3:123141847
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.911-3675G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141847 | ||||||
| chr3:123141913
|
T | C | 2 | a0005c0012t0001g0049a0005c0012t0001g0050 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.911-3609T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141913 | ||||||
| chr3:123141918
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(142): Show | 150 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.911-3604C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141918 | ||||||
| chr3:123141967
|
C | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0111others(29): Show | 33 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.911-3555C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123141967 | ||||||
| chr3:123142232
|
T | C | 7 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0079others(4): Show | 7 | HG02155.hp2 NA18950.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.911-3290T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142232 | ||||||
| chr3:123142241
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(106): Show | 111 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.911-3281G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142241 | ||||||
| chr3:123142358
|
A | T | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.911-3164A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142358 | ||||||
| chr3:123142487
|
T | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0122a0001c0014t0001g0272 | 3 | HG02572.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.911-3035T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142487 | ||||||
| chr3:123142658
|
G | A | 6 | a0001c0005t0001g0107a0001c0005t0001g0155a0001c0005t0001g0156others(3): Show | 6 | HG02080.hp2 HG02135.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.911-2864G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142658 | ||||||
| chr3:123142670
|
G | A | 2 | a0001c0001t0001g0313a0001c0002t0001g0317 | 2 | HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.911-2852G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142670 | ||||||
| chr3:123142678
|
C | G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(135): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.911-2844C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142678 | ||||||
| chr3:123142715
|
G | C | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.911-2807G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142715 | ||||||
| chr3:123142720
|
G | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0048others(15): Show | 19 | HG01175.hp1 HG01261.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.911-2802G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142720 | ||||||
| chr3:123142761
|
T | G | 1 | a0001c0002t0001g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.911-2761T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142761 | ||||||
| chr3:123142934
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.911-2588T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142934 | ||||||
| chr3:123142983
|
C | T | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.911-2539C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123142983 | ||||||
| chr3:123143014
|
T | C | 1 | a0001c0002t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.911-2508T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143014 | ||||||
| chr3:123143041
|
C | T | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.911-2481C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143041 | ||||||
| chr3:123143091
|
G | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0282a0001c0018t0001g0241 | 3 | HG02280.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.911-2431G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143091 | ||||||
| chr3:123143092
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.911-2430A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143092 | ||||||
| chr3:123143168
|
C | CA | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.911-2353dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123143168 | |||||
| chr3:123143241
|
T | C | 8 | a0001c0002t0001g0010a0001c0002t0001g0030a0001c0002t0001g0031others(5): Show | 8 | HG00609.hp1 HG01346.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.911-2281T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143241 | ||||||
| chr3:123143242
|
G | A | 7 | a0001c0002t0001g0010a0001c0002t0001g0030a0001c0002t0001g0031others(4): Show | 7 | HG00609.hp1 HG01346.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.911-2280G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143242 | ||||||
| chr3:123143386
|
C | CA | 208 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.911-2118dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123143386 | |||||
| chr3:123143386
|
C | CAA | 7 | a0001c0003t0001g0270a0001c0003t0001g0278a0001c0006t0001g0179others(4): Show | 7 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.911-2119_911-2118d others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 123143386 | |||||
| chr3:123143392
|
A | AG | 17 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0053others(14): Show | 18 | HG01175.hp1 HG01261.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.911-2130_911-2129i others(3): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143392 | ||||||
| chr3:123143467
|
A | T | 1 | a0001c0001t0001g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.911-2055A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143467 | ||||||
| chr3:123143469
|
T | A | 1 | a0001c0001t0001g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.911-2053T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143469 | ||||||
| chr3:123143567
|
A | G | 2 | a0001c0001t0001g0055a0001c0018t0001g0241 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.911-1955A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143567 | ||||||
| chr3:123143592
|
G | T | 1 | a0001c0001t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.911-1930G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143592 | ||||||
| chr3:123143759
|
G | A | 1 | a0001c0004t0001g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.911-1763G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143759 | ||||||
| chr3:123143823
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.911-1699C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143823 | ||||||
| chr3:123143871
|
C | T | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.911-1651C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143871 | ||||||
| chr3:123143932
|
A | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(95): Show | 102 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.911-1590A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143932 | ||||||
| chr3:123143980
|
C | T | 1 | a0001c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.911-1542C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143980 | ||||||
| chr3:123143981
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-1541G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123143981 | ||||||
| chr3:123144013
|
G | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(59): Show | 63 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.911-1509G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144013 | ||||||
| chr3:123144146
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(85): Show | 92 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.911-1376C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144146 | ||||||
| chr3:123144173
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0139a0001c0001t0001g0148others(2): Show | 5 | HG02738.hp2 HG03017.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.911-1349C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144173 | ||||||
| chr3:123144180
|
G | A | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.911-1342G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144180 | ||||||
| chr3:123144379
|
T | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.911-1143T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144379 | ||||||
| chr3:123144623
|
G | A | 1 | a0001c0003t0001g0147 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.911-899G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144623 | ||||||
| chr3:123144662
|
A | G | 1 | a0001c0003t0001g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.911-860A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144662 | ||||||
| chr3:123144776
|
T | A | 3 | a0001c0003t0001g0052a0001c0003t0001g0101a0001c0003t0001g0258 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.911-746T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144776 | ||||||
| chr3:123144779
|
G | A | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.911-743G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144779 | ||||||
| chr3:123144779
|
G | C | 7 | a0001c0001t0001g0181a0001c0002t0001g0007a0001c0002t0001g0093others(4): Show | 8 | HG02129.hp1 NA18948.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.911-743G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144779 | ||||||
| chr3:123144864
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-658G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144864 | ||||||
| chr3:123144877
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0039others(16): Show | 19 | HG00735.hp1 HG01433.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.911-645G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144877 | ||||||
| chr3:123144921
|
A | G | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.911-601A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144921 | ||||||
| chr3:123144994
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-528T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123144994 | ||||||
| chr3:123145142
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-380G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123145142 | ||||||
| chr3:123145200
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.911-322G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123145200 | ||||||
| chr3:123145251
|
A | T | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.911-271A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123145251 | ||||||
| chr3:123145480
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.911-42C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 11/16 | chr3 | 123145480 | ||||||
| chr3:123145628
|
T | C | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981+36T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145628 | ||||||
| chr3:123145644
|
A | G | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.981+52A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145644 | ||||||
| chr3:123145708
|
G | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0111others(29): Show | 33 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.981+116G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145708 | ||||||
| chr3:123145740
|
TAGAC | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 119 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.981+152_981+155del others(4): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 123145740 | |||||
| chr3:123145748
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02451.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.981+156T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145748 | ||||||
| chr3:123145780
|
C | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.981+188C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145780 | ||||||
| chr3:123145839
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.981+247T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145839 | ||||||
| chr3:123145884
|
G | A | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.982-215G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145884 | ||||||
| chr3:123145924
|
G | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 156 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.982-175G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145924 | ||||||
| chr3:123145960
|
T | TG | 115 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 120 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.982-136dupG | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 123145960 | |||||
| chr3:123145970
|
C | T | 1 | a0001c0003t0001g0234 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.982-129C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145970 | ||||||
| chr3:123145971
|
T | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.982-128T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 12/16 | chr3 | 123145971 | ||||||
| chr3:123146289
|
T | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1142+30T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146289 | ||||||
| chr3:123146369
|
G | A | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1142+110G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146369 | ||||||
| chr3:123146413
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 118 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.1142+154G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146413 | ||||||
| chr3:123146416
|
C | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1142+157C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146416 | ||||||
| chr3:123146491
|
C | T | 1 | a0001c0003t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1142+232C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146491 | ||||||
| chr3:123146516
|
G | A | 2 | a0001c0011t0001g0058a0001c0016t0001g0284 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1142+257G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146516 | ||||||
| chr3:123146788
|
A | G | 1 | a0001c0001t0001g0006 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1142+529A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146788 | ||||||
| chr3:123146817
|
GT | G | 86 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(83): Show | 90 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.1142+562delT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 123146817 | |||||
| chr3:123146919
|
C | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01175.hp1 HG01261.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1142+660C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123146919 | ||||||
| chr3:123147414
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1142+1155T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147414 | ||||||
| chr3:123147426
|
G | A | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1142+1167G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147426 | ||||||
| chr3:123147452
|
A | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(219): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1142+1193A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147452 | ||||||
| chr3:123147612
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1142+1353T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147612 | ||||||
| chr3:123147619
|
A | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02451.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1142+1360A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147619 | ||||||
| chr3:123147716
|
T | C | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1142+1457T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147716 | ||||||
| chr3:123147757
|
C | T | 2 | a0005c0012t0001g0049a0005c0012t0001g0050 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1142+1498C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147757 | ||||||
| chr3:123147858
|
C | T | 2 | a0001c0003t0001g0062a0001c0003t0001g0270 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1142+1599C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147858 | ||||||
| chr3:123147930
|
C | T | 3 | a0001c0003t0001g0052a0001c0003t0001g0101a0001c0003t0001g0258 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1142+1671C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147930 | ||||||
| chr3:123147969
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1142+1710C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123147969 | ||||||
| chr3:123148064
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0111others(13): Show | 17 | HG00423.hp2 HG00609.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1142+1805C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148064 | ||||||
| chr3:123148098
|
G | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01175.hp1 HG01261.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1142+1839G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148098 | ||||||
| chr3:123148290
|
G | T | 1 | a0001c0001t0001g0281 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1143-1944G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148290 | ||||||
| chr3:123148304
|
A | G | 1 | a0001c0002t0001g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1143-1930A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148304 | ||||||
| chr3:123148322
|
C | T | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1143-1912C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148322 | ||||||
| chr3:123148406
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1143-1828G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148406 | ||||||
| chr3:123148493
|
C | T | 1 | a0001c0003t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1143-1741C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148493 | ||||||
| chr3:123148568
|
T | TA | 70 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(67): Show | 71 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1143-1652dupA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 123148568 | |||||
| chr3:123148568
|
TA | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0211others(32): Show | 36 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1143-1652delA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 123148568 | |||||
| chr3:123148626
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1143-1608G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148626 | ||||||
| chr3:123148780
|
T | C | 2 | a0005c0012t0001g0049a0005c0012t0001g0050 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1143-1454T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148780 | ||||||
| chr3:123148973
|
G | A | 6 | a0001c0003t0001g0098a0001c0004t0001g0065a0001c0004t0001g0257others(3): Show | 6 | HG00741.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-1261G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123148973 | ||||||
| chr3:123149102
|
C | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG00673.hp2 NA18971.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1143-1132C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149102 | ||||||
| chr3:123149151
|
T | C | 1 | a0001c0014t0001g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1143-1083T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149151 | ||||||
| chr3:123149254
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1143-980G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149254 | ||||||
| chr3:123149288
|
A | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1143-946A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149288 | ||||||
| chr3:123149336
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1143-898T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149336 | ||||||
| chr3:123149439
|
G | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0039others(16): Show | 19 | HG00735.hp1 HG01433.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1143-795G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149439 | ||||||
| chr3:123149583
|
GC | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1143-650delC | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149583 | ||||||
| chr3:123149591
|
A | G | 174 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1143-643A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149591 | ||||||
| chr3:123149650
|
TG | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1143-583delG | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149650 | ||||||
| chr3:123149821
|
C | G | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1143-413C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149821 | ||||||
| chr3:123149838
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 118 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.1143-396A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149838 | ||||||
| chr3:123149960
|
G | T | 2 | a0001c0001t0001g0055a0001c0018t0001g0241 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1143-274G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149960 | ||||||
| chr3:123149965
|
G | T | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1143-269G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149965 | ||||||
| chr3:123149979
|
G | A | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(219): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1143-255G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123149979 | ||||||
| chr3:123150043
|
A | G | 1 | a0001c0003t0001g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1143-191A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123150043 | ||||||
| chr3:123150146
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0313 | 2 | HG02293.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1143-88G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123150146 | ||||||
| chr3:123150194
|
C | T | 9 | a0001c0003t0001g0076a0001c0003t0001g0114a0001c0003t0001g0160others(6): Show | 9 | HG01074.hp1 HG01123.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-40C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123150194 | ||||||
| chr3:123150206
|
G | A | 9 | a0001c0003t0001g0076a0001c0003t0001g0114a0001c0003t0001g0160others(6): Show | 9 | HG01074.hp1 HG01123.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-28G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 13/16 | chr3 | 123150206 | ||||||
| chr3:123150463
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1273+99G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123150463 | ||||||
| chr3:123150479
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1273+115G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123150479 | ||||||
| chr3:123150630
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0044others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273+266G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123150630 | ||||||
| chr3:123150874
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1273+510C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123150874 | ||||||
| chr3:123151097
|
C | T | 2 | a0004c0009t0001g0195a0004c0009t0001g0196 | 2 | NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1273+733C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151097 | ||||||
| chr3:123151098
|
C | T | 2 | a0004c0009t0001g0195a0004c0009t0001g0196 | 2 | NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1273+734C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151098 | ||||||
| chr3:123151181
|
C | T | 1 | a0001c0004t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1273+817C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151181 | ||||||
| chr3:123151305
|
A | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(56): Show | 60 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1273+941A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151305 | ||||||
| chr3:123151419
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0105others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273+1055C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151419 | ||||||
| chr3:123151420
|
G | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0243 | 3 | NA18947.hp2 NA18981.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1273+1056G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151420 | ||||||
| chr3:123151656
|
G | A | 1 | a0001c0002t0001g0236 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1273+1292G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151656 | ||||||
| chr3:123151698
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(38): Show | 43 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1273+1334C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151698 | ||||||
| chr3:123151734
|
T | TCCTG | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(102): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1273+1415_1273+141 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
T | TCCTGCCT others(1): Show |
50 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0026others(47): Show | 51 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1273+1411_1273+141 others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
T | TCCTGCCT others(5): Show |
14 | a0001c0001t0001g0044a0001c0001t0001g0148a0001c0001t0001g0232others(11): Show | 14 | HG00733.hp2 HG01109.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1273+1407_1273+141 others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
TCCTG | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0039others(22): Show | 25 | HG00735.hp1 HG01109.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1273+1415_1273+141 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
TCCTGCCT others(1): Show |
T | 5 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0240others(2): Show | 5 | HG01433.hp1 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+1411_1273+141 others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
TCCTGCCT others(5): Show |
T | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(41): Show | 46 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1273+1407_1273+141 others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
TCCTGCCT others(9): Show |
T | 18 | a0001c0001t0001g0045a0001c0001t0001g0068a0001c0001t0001g0069others(15): Show | 18 | HG01169.hp2 HG01175.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1273+1403_1273+141 others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151734
|
TCCTGCCT others(13): Show |
T | 3 | a0001c0001t0001g0081a0001c0001t0001g0106a0002c0007t0001g0289 | 3 | HG02809.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1273+1399_1273+141 others(24): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151734 | |||||
| chr3:123151746
|
G | GCCTGCCT others(190): Show |
1 | a0001c0002t0001g0250 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1273+1406_1273+140 others(201): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151746 | |||||
| chr3:123151746
|
G | GCCTT | 3 | a0001c0001t0001g0087a0001c0001t0001g0152a0001c0003t0001g0036 | 3 | HG00642.hp2 HG02300.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1273+1385_1273+138 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151746 | |||||
| chr3:123151782
|
G | GGCCTGCC others(9): Show |
4 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280others(1): Show | 4 | HG02559.hp2 HG02615.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1443_1273+145 others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151782 | |||||
| chr3:123151782
|
G | GGCCTGCC others(33): Show |
1 | a0001c0016t0001g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1273+1447_1273+148 others(44): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151782 | |||||
| chr3:123151795
|
G | GCCTGCCT others(241): Show |
1 | a0001c0004t0001g0072 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1273+1509_1273+151 others(252): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151795 | |||||
| chr3:123151843
|
GCCTTCCT others(57): Show |
G | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1273+1487_1273+155 others(68): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151843 | |||||
| chr3:123151874
|
C | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1273+1510C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151874 | ||||||
| chr3:123151875
|
G | GCCTTCCT others(9): Show |
2 | a0001c0002t0001g0174a0001c0002t0001g0175 | 2 | NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1273+1539_1273+155 others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151875 | |||||
| chr3:123151883
|
G | GCCTGCCT others(317): Show |
1 | a0003c0010t0001g0244 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1273+1538_1273+153 others(328): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151883 | |||||
| chr3:123151883
|
G | GCCTGCCT others(329): Show |
1 | a0001c0003t0001g0091 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1273+1538_1273+153 others(340): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151883 | |||||
| chr3:123151883
|
G | GCCTGCCT others(229): Show |
1 | a0001c0003t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1273+1538_1273+153 others(240): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151883 | |||||
| chr3:123151883
|
G | GCCTGCCT others(333): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0149others(3): Show | 7 | HG00597.hp2 NA18962.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273+1538_1273+153 others(344): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151883 | |||||
| chr3:123151883
|
G | GCCTGCCT others(333): Show |
28 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0083others(25): Show | 29 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1273+1538_1273+153 others(344): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151883 | |||||
| chr3:123151883
|
G | GCCTGCCT others(317): Show |
1 | a0001c0003t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1273+1538_1273+153 others(328): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151883 | |||||
| chr3:123151887
|
GCCTT | G | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(4): Show | 7 | HG01175.hp1 HG02293.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273+1531_1273+153 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151887 | |||||
| chr3:123151888
|
C | A | 1 | a0001c0003t0001g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1273+1524C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151888 | ||||||
| chr3:123151891
|
T | G | 11 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(8): Show | 11 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+1527T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151891 | ||||||
| chr3:123151895
|
T | G | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0081others(15): Show | 18 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.1273+1531T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151895 | ||||||
| chr3:123151899
|
G | A | 2 | a0001c0003t0001g0062a0001c0018t0001g0241 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1273+1535G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151899 | ||||||
| chr3:123151903
|
G | T | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(48): Show | 53 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1273+1539G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151903 | ||||||
| chr3:123151907
|
T | G | 11 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(8): Show | 11 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+1543T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151907 | ||||||
| chr3:123151911
|
T | G | 14 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(11): Show | 14 | HG01167.hp1 HG01346.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1273+1547T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151911 | ||||||
| chr3:123151918
|
T | C | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(4): Show | 7 | HG01175.hp1 HG02293.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273+1554T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151918 | ||||||
| chr3:123151919
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0259a0001c0001t0001g0269 | 3 | HG01884.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1273+1555T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151919 | ||||||
| chr3:123151923
|
T | G | 6 | a0001c0001t0001g0295a0001c0003t0001g0265a0001c0003t0001g0266others(3): Show | 6 | HG01167.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273+1559T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151923 | ||||||
| chr3:123151927
|
T | G | 15 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0295others(12): Show | 15 | HG01167.hp1 HG01346.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1273+1563T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151927 | ||||||
| chr3:123151927
|
TCCTGCCT others(9): Show |
T | 3 | a0001c0001t0001g0152a0001c0001t0001g0212a0001c0003t0001g0036 | 3 | HG00642.hp2 HG03491.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1273+1599_1273+161 others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151927 | |||||
| chr3:123151930
|
T | C | 11 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(8): Show | 11 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+1566T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151930 | ||||||
| chr3:123151931
|
G | T | 11 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(8): Show | 11 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+1567G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151931 | ||||||
| chr3:123151934
|
T | A | 1 | a0001c0001t0001g0008 | 2 | NA18970.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1273+1570T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151934 | ||||||
| chr3:123151935
|
T | G | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(4): Show | 7 | HG01175.hp1 HG02293.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273+1571T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151935 | ||||||
| chr3:123151943
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1273+1579G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151943 | ||||||
| chr3:123151946
|
T | C | 4 | a0001c0001t0001g0295a0005c0012t0001g0049a0005c0012t0001g0050others(1): Show | 4 | HG01167.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1582T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151946 | ||||||
| chr3:123151947
|
G | T | 4 | a0001c0001t0001g0295a0005c0012t0001g0049a0005c0012t0001g0050others(1): Show | 4 | HG01167.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1583G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151947 | ||||||
| chr3:123151955
|
T | G | 11 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(8): Show | 11 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+1591T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151955 | ||||||
| chr3:123151955
|
T | TCCTGCCT others(305): Show |
1 | a0001c0001t0001g0139 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1273+1598_1273+159 others(316): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151955 | |||||
| chr3:123151963
|
G | T | 14 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0139others(11): Show | 14 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1273+1599G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151963 | ||||||
| chr3:123151971
|
T | G | 15 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0295others(12): Show | 15 | HG01167.hp1 HG01346.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1273+1607T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151971 | ||||||
| chr3:123151975
|
GCCTTCCT others(21): Show |
G | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(4): Show | 7 | HG01175.hp1 HG02293.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273+1623_1273+165 others(32): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151975 | |||||
| chr3:123151987
|
G | GCCTTCCT others(5): Show |
1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1273+1631_1273+164 others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151987 | |||||
| chr3:123151991
|
T | G | 7 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0295others(4): Show | 7 | HG01167.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273+1627T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151991 | ||||||
| chr3:123151995
|
G | T | 12 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0295others(9): Show | 12 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273+1631G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123151995 | ||||||
| chr3:123151995
|
GCCTT | G | 4 | a0001c0001t0001g0089a0001c0001t0001g0183a0001c0001t0001g0268others(1): Show | 4 | HG00140.hp2 HG00609.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+1651_1273+165 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151995 | |||||
| chr3:123151999
|
T | TCCTGCCT others(109): Show |
1 | a0002c0007t0001g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1273+1638_1273+163 others(120): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151999 | |||||
| chr3:123151999
|
T | TCCTTCCT others(73): Show |
2 | a0001c0003t0001g0062a0001c0018t0001g0241 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1273+1658_1273+165 others(84): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123151999 | |||||
| chr3:123152003
|
T | G | 16 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0295others(13): Show | 16 | HG01167.hp1 HG01346.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1273+1639T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152003 | ||||||
| chr3:123152003
|
T | TCCTGCCT others(97): Show |
1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1273+1642_1273+164 others(108): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152003 | |||||
| chr3:123152003
|
T | TCCTGCCT others(209): Show |
1 | a0001c0001t0001g0273 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1273+1642_1273+164 others(220): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152003 | |||||
| chr3:123152003
|
T | TCCTGCCT others(77): Show |
4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+1642_1273+164 others(88): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152003 | |||||
| chr3:123152003
|
TCCTTCCT others(9): Show |
T | 1 | a0001c0004t0001g0189 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1273+1651_1273+166 others(20): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152003 | |||||
| chr3:123152007
|
T | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1273+1643T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152007 | ||||||
| chr3:123152015
|
T | G | 17 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0128others(14): Show | 17 | HG00735.hp1 HG01346.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+1651T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152015 | ||||||
| chr3:123152015
|
T | TCCTGCCT others(189): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0259others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1658_1273+165 others(200): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152015 | |||||
| chr3:123152015
|
T | TCCTGCCT others(93): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0054others(10): Show | 13 | HG01109.hp2 HG01433.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1273+1658_1273+165 others(104): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152015 | |||||
| chr3:123152024
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+1660C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152024 | ||||||
| chr3:123152056
|
C | T | 11 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0299others(8): Show | 11 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+1692C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152056 | ||||||
| chr3:123152059
|
TCCTG | T | 9 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273+1703_1273+170 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152059 | |||||
| chr3:123152072
|
T | C | 32 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(29): Show | 32 | HG00735.hp1 HG01109.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1273+1708T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152072 | ||||||
| chr3:123152080
|
C | CCTGCCTT others(97): Show |
1 | a0002c0008t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1273+1718_1273+171 others(108): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152080 | |||||
| chr3:123152080
|
C | CCTGCCTT others(1): Show |
17 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 17 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1273+1718_1273+171 others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152080 | |||||
| chr3:123152083
|
T | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+1719T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152083 | ||||||
| chr3:123152087
|
T | G | 27 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 27 | HG01109.hp2 HG01346.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.1273+1723T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152087 | ||||||
| chr3:123152091
|
G | T | 31 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(28): Show | 31 | HG00735.hp1 HG01109.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.1273+1727G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152091 | ||||||
| chr3:123152092
|
C | CCTGCCTT others(81): Show |
1 | a0002c0007t0001g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1273+1730_1273+173 others(92): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152092 | |||||
| chr3:123152095
|
T | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+1731T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152095 | ||||||
| chr3:123152099
|
G | T | 13 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(10): Show | 13 | HG00735.hp1 HG01346.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1273+1735G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152099 | ||||||
| chr3:123152099
|
GCCTT | G | 111 | a0001c0001t0001g0055a0001c0001t0001g0212a0001c0001t0001g0254others(108): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1273+1759_1273+176 others(8): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152099 | |||||
| chr3:123152099
|
GCCTTCCT others(1): Show |
G | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(101): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1273+1755_1273+176 others(12): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152099 | |||||
| chr3:123152103
|
T | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+1739T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152103 | ||||||
| chr3:123152107
|
T | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 18 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1273+1743T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152107 | ||||||
| chr3:123152111
|
T | G | 10 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0299others(7): Show | 10 | HG01346.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1273+1747T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152111 | ||||||
| chr3:123152111
|
T | TCCTTCCT others(5): Show |
13 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0081others(10): Show | 13 | HG01167.hp1 HG01175.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.1273+1758_1273+175 others(16): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152111 | |||||
| chr3:123152111
|
T | TCCTTCCT others(21): Show |
39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(36): Show | 41 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1273+1758_1273+175 others(32): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152111 | |||||
| chr3:123152119
|
T | G | 1 | a0002c0007t0001g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1273+1755T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152119 | ||||||
| chr3:123152123
|
T | G | 38 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0068others(35): Show | 39 | HG00609.hp2 HG01167.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.1273+1759T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152123 | ||||||
| chr3:123152127
|
G | T | 1 | a0002c0007t0001g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1273+1763G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152127 | ||||||
| chr3:123152143
|
G | T | 1 | a0002c0007t0001g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1273+1779G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152143 | ||||||
| chr3:123152190
|
C | T | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(7): Show | 10 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1273+1826C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152190 | ||||||
| chr3:123152270
|
T | C | 19 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0081others(16): Show | 19 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.1273+1906T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152270 | ||||||
| chr3:123152425
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0003t0001g0208 | 3 | HG00140.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1273+2061C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152425 | ||||||
| chr3:123152443
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0268 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1273+2079C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152443 | ||||||
| chr3:123152497
|
T | C | 1 | a0002c0007t0001g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1273+2133T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152497 | ||||||
| chr3:123152585
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1273+2221C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152585 | ||||||
| chr3:123152679
|
G | C | 2 | a0001c0003t0001g0062a0001c0018t0001g0241 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1274-2292G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152679 | ||||||
| chr3:123152913
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1274-2058C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152913 | ||||||
| chr3:123152933
|
G | A | 5 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0024others(2): Show | 5 | HG00673.hp1 NA18946.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1274-2038G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123152933 | ||||||
| chr3:123152965
|
C | CT | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1274-1992dupT | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123152965 | |||||
| chr3:123153068
|
C | T | 1 | a0001c0011t0001g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1274-1903C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153068 | ||||||
| chr3:123153079
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1274-1892C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153079 | ||||||
| chr3:123153102
|
C | T | 6 | a0001c0003t0001g0160a0001c0003t0001g0234a0001c0003t0001g0316others(3): Show | 6 | HG01123.hp2 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-1869C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153102 | ||||||
| chr3:123153104
|
G | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0268 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1274-1867G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153104 | ||||||
| chr3:123153228
|
TA | T | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1274-1738delA | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123153228 | |||||
| chr3:123153306
|
G | A | 22 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0081others(19): Show | 22 | HG01167.hp1 HG01175.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1274-1665G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153306 | ||||||
| chr3:123153325
|
GGCCTGCA others(3): Show |
G | 1 | a0001c0004t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1274-1637_1274-162 others(14): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 123153325 | |||||
| chr3:123153358
|
A | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1274-1613A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153358 | ||||||
| chr3:123153429
|
T | C | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1274-1542T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153429 | ||||||
| chr3:123153464
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1274-1507G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153464 | ||||||
| chr3:123153469
|
G | A | 1 | a0001c0002t0001g0187 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1274-1502G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153469 | ||||||
| chr3:123153507
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1274-1464G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153507 | ||||||
| chr3:123153544
|
G | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02451.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1274-1427G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153544 | ||||||
| chr3:123153597
|
A | G | 3 | a0001c0003t0001g0052a0001c0003t0001g0101a0001c0003t0001g0258 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1274-1374A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153597 | ||||||
| chr3:123153612
|
C | T | 2 | a0001c0001t0001g0125a0001c0014t0001g0272 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1274-1359C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153612 | ||||||
| chr3:123153676
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1274-1295C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153676 | ||||||
| chr3:123153731
|
G | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0293 | 2 | HG01934.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1274-1240G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153731 | ||||||
| chr3:123153801
|
A | G | 1 | a0001c0011t0001g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1274-1170A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153801 | ||||||
| chr3:123153867
|
G | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0105others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1274-1104G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153867 | ||||||
| chr3:123153901
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1274-1070G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153901 | ||||||
| chr3:123153916
|
T | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1274-1055T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123153916 | ||||||
| chr3:123154045
|
G | T | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1274-926G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154045 | ||||||
| chr3:123154079
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1274-892A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154079 | ||||||
| chr3:123154215
|
G | A | 3 | a0001c0001t0001g0295a0001c0005t0001g0126a0001c0005t0001g0180 | 3 | HG01346.hp1 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1274-756G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154215 | ||||||
| chr3:123154436
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1274-535C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154436 | ||||||
| chr3:123154516
|
A | C | 1 | a0001c0002t0001g0191 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1274-455A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154516 | ||||||
| chr3:123154544
|
G | A | 12 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(9): Show | 12 | HG01167.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1274-427G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154544 | ||||||
| chr3:123154568
|
G | A | 1 | a0001c0002t0001g0022 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1274-403G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154568 | ||||||
| chr3:123154626
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0273 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1274-345G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154626 | ||||||
| chr3:123154662
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1274-309C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154662 | ||||||
| chr3:123154766
|
C | A | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1274-205C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154766 | ||||||
| chr3:123154800
|
T | C | 2 | a0001c0003t0001g0062a0001c0018t0001g0241 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1274-171T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 14/16 | chr3 | 123154800 | ||||||
| chr3:123155052
|
C | T | 1 | a0001c0003t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1344+11C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155052 | ||||||
| chr3:123155076
|
G | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1344+35G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155076 | ||||||
| chr3:123155125
|
C | T | 2 | a0001c0002t0001g0124a0001c0002t0001g0143 | 2 | NA18953.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1344+84C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155125 | ||||||
| chr3:123155128
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1344+87G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155128 | ||||||
| chr3:123155483
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1344+442T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155483 | ||||||
| chr3:123155531
|
G | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0213 | 2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1344+490G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155531 | ||||||
| chr3:123155554
|
G | T | 2 | a0001c0001t0001g0152a0001c0003t0001g0036 | 2 | HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1344+513G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155554 | ||||||
| chr3:123155565
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1344+524A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155565 | ||||||
| chr3:123155593
|
T | G | 9 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1344+552T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155593 | ||||||
| chr3:123155632
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1344+591C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155632 | ||||||
| chr3:123155633
|
G | A | 2 | a0001c0003t0001g0062a0001c0018t0001g0241 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1344+592G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155633 | ||||||
| chr3:123155782
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+741C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155782 | ||||||
| chr3:123155951
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1344+910A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123155951 | ||||||
| chr3:123156030
|
C | G | 1 | a0001c0003t0001g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1344+989C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156030 | ||||||
| chr3:123156111
|
A | G | 22 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0081others(19): Show | 22 | HG01167.hp1 HG01175.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1344+1070A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156111 | ||||||
| chr3:123156331
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0184a0001c0001t0001g0280 | 3 | HG02559.hp2 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1344+1290G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156331 | ||||||
| chr3:123156403
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0280 | 2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1344+1362C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156403 | ||||||
| chr3:123156703
|
G | T | 1 | a0001c0011t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1344+1662G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156703 | ||||||
| chr3:123156726
|
C | G | 1 | a0001c0002t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1344+1685C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156726 | ||||||
| chr3:123156798
|
G | T | 39 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(36): Show | 39 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1344+1757G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156798 | ||||||
| chr3:123156800
|
G | T | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(7): Show | 10 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+1759G>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156800 | ||||||
| chr3:123156826
|
A | AG | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1344+1786dupG | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 123156826 | |||||
| chr3:123156837
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1344+1796C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156837 | ||||||
| chr3:123156965
|
T | C | 1 | a0001c0002t0001g0030 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1344+1924T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123156965 | ||||||
| chr3:123157100
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2059C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157100 | ||||||
| chr3:123157181
|
C | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(1): Show | 4 | HG01175.hp1 HG03927.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2140C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157181 | ||||||
| chr3:123157480
|
G | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(34): Show | 39 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1344+2439G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157480 | ||||||
| chr3:123157600
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1344+2559G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157600 | ||||||
| chr3:123157619
|
T | C | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(7): Show | 10 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+2578T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157619 | ||||||
| chr3:123157772
|
C | T | 1 | a0002c0007t0001g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1344+2731C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157772 | ||||||
| chr3:123157854
|
A | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0105others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+2813A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157854 | ||||||
| chr3:123157923
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1344+2882G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123157923 | ||||||
| chr3:123158159
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1344+3118G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158159 | ||||||
| chr3:123158236
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1345-3085C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158236 | ||||||
| chr3:123158282
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1345-3039G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158282 | ||||||
| chr3:123158316
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1345-3005T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158316 | ||||||
| chr3:123158344
|
A | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1345-2977A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158344 | ||||||
| chr3:123158353
|
C | T | 5 | a0001c0003t0001g0062a0001c0018t0001g0241a0005c0012t0001g0049others(2): Show | 5 | HG01167.hp1 HG02886.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-2968C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158353 | ||||||
| chr3:123158543
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(34): Show | 39 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1345-2778C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158543 | ||||||
| chr3:123158758
|
T | C | 1 | a0001c0003t0001g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1345-2563T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158758 | ||||||
| chr3:123158936
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1345-2385C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158936 | ||||||
| chr3:123158949
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1345-2372T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158949 | ||||||
| chr3:123158985
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1345-2336G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123158985 | ||||||
| chr3:123159002
|
A | T | 2 | a0001c0003t0001g0062a0001c0018t0001g0241 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1345-2319A>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159002 | ||||||
| chr3:123159058
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1345-2263T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159058 | ||||||
| chr3:123159172
|
A | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1345-2149A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159172 | ||||||
| chr3:123159217
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0105others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-2104G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159217 | ||||||
| chr3:123159266
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1345-2055C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159266 | ||||||
| chr3:123159307
|
T | G | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1345-2014T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159307 | ||||||
| chr3:123159325
|
C | G | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1345-1996C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159325 | ||||||
| chr3:123159381
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1345-1940C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159381 | ||||||
| chr3:123159440
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1345-1881G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159440 | ||||||
| chr3:123159507
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1345-1814G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159507 | ||||||
| chr3:123159727
|
C | T | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345-1594C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159727 | ||||||
| chr3:123159731
|
G | A | 5 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0024others(2): Show | 5 | HG00673.hp1 NA18946.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-1590G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159731 | ||||||
| chr3:123159774
|
G | A | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(7): Show | 10 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1345-1547G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159774 | ||||||
| chr3:123159775
|
G | A | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(7): Show | 10 | HG01175.hp1 HG01346.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1345-1546G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159775 | ||||||
| chr3:123159816
|
G | A | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345-1505G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159816 | ||||||
| chr3:123159857
|
C | G | 1 | a0001c0003t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345-1464C>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159857 | ||||||
| chr3:123159889
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1345-1432C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159889 | ||||||
| chr3:123159953
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1345-1368A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123159953 | ||||||
| chr3:123160017
|
T | C | 4 | a0001c0003t0001g0265a0001c0003t0001g0266a0001c0003t0001g0270others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-1304T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160017 | ||||||
| chr3:123160050
|
C | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0003t0001g0052others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-1271C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160050 | ||||||
| chr3:123160093
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1345-1228G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160093 | ||||||
| chr3:123160110
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1345-1211C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160110 | ||||||
| chr3:123160161
|
T | C | 13 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1345-1160T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160161 | ||||||
| chr3:123160168
|
C | T | 1 | a0001c0003t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1345-1153C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160168 | ||||||
| chr3:123160185
|
T | C | 13 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(10): Show | 13 | HG01167.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1345-1136T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160185 | ||||||
| chr3:123160203
|
C | T | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1345-1118C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160203 | ||||||
| chr3:123160250
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1345-1071T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160250 | ||||||
| chr3:123160293
|
T | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 22 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1345-1028T>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160293 | ||||||
| chr3:123160302
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1345-1019C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160302 | ||||||
| chr3:123160448
|
C | CG | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(107): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1345-869dupG | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 123160448 | |||||
| chr3:123160529
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1345-792G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160529 | ||||||
| chr3:123160692
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-629A>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160692 | ||||||
| chr3:123160770
|
T | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0127a0001c0001t0001g0164others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-551T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160770 | ||||||
| chr3:123160771
|
C | A | 1 | a0001c0002t0001g0187 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1345-550C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123160771 | ||||||
| chr3:123161013
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1345-308C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123161013 | ||||||
| chr3:123161013
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(34): Show | 39 | HG00140.hp1 HG00597.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1345-308C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123161013 | ||||||
| chr3:123161142
|
A | C | 1 | a0001c0003t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1345-179A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123161142 | ||||||
| chr3:123161205
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1345-116T>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123161205 | ||||||
| chr3:123161271
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(107): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1345-50G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 15/16 | chr3 | 123161271 | ||||||
| chr3:123161581
|
G | A | 1 | a0001c0003t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1479+126G>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161581 | ||||||
| chr3:123161664
|
A | C | 9 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0298others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1479+209A>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161664 | ||||||
| chr3:123161688
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1480-192C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161688 | ||||||
| chr3:123161705
|
G | C | 2 | a0001c0003t0001g0265a0001c0003t0001g0266 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1480-175G>C | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161705 | ||||||
| chr3:123161711
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1480-169C>T | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161711 | ||||||
| chr3:123161735
|
C | A | 4 | a0001c0003t0001g0265a0001c0003t0001g0266a0001c0003t0001g0270others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-145C>A | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161735 | ||||||
| chr3:123161849
|
T | TTC | 3 | a0005c0012t0001g0049a0005c0012t0001g0050a0008c0015t0001g0220 | 3 | HG01167.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1480-16_1480-15dup others(2): Show |
PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 123161849 | |||||
| chr3:123161856
|
T | G | 3 | a0001c0001t0001g0003a0001c0003t0001g0038a0001c0003t0001g0285 | 4 | HG01884.hp1 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-24T>G | PDIA5 | ENSG00000065485.20 | transcript | ENST00000316218.12 | protein_coding | 16/16 | chr3 | 123161856 |