Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 196463 |
| ensemblid | ENSG00000151176.8 |
| hgncid | 27283 |
| symbol | PLBD2 |
| name | phospholipase B domain containing 2 |
| refseq_nuc | NM_173542.4 |
| refseq_prot | NP_775813.2 |
| ensembl_nuc | ENST00000280800.5 |
| ensembl_prot | ENSP00000280800.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 113358587 |
| end | 113391629 |
| strand | + |
| ver | v1.2 |
| region | chr12:113358587-113391629 |
| region5000 | chr12:113353587-113396629 |
| regionname0 | PLBD2_chr12_113358587_113391629 |
| regionname5000 | PLBD2_chr12_113353587_113396629 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 589 | 173 | 67 | 19 | 65 | 5 | 16 | 49 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0002 | 1/0 | 589 | 88 | 5 | 39 | 32 | 2 | 9 | 18 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0003 | 0/0 | 589 | 11 | 4 | 3 | 0 | 1 | 3 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0004 | 0/0 | 589 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0005 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0006 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0007 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0008 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| a0009 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | MVGQM others(584): Show |
chr12 | 113353587 | 113396629 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1767 | 161 | 58 | 17 | 64 | 5 | 16 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0001c0004 | 0/0 | 1767 | 6 | 5 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0001c0005 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0001c0006 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0001c0010 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0001c0013 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0001c0014 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0002c0002 | 1/0 | 1767 | 87 | 5 | 38 | 32 | 2 | 9 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0002c0007 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0003c0003 | 0/0 | 1767 | 11 | 4 | 3 | 0 | 1 | 3 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0004c0011 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0005c0012 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0006c0009 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0007c0016 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0008c0015 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 | ||
| a0009c0008 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | ATGGT others(1762): Show |
chr12 | 113353587 | 113396629 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4787 | 88 | 39 | 12 | 23 | 5 | 9 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0002 | 0/0 | 4787 | 22 | 0 | 0 | 20 | 0 | 2 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0003 | 0/0 | 4787 | 21 | 1 | 3 | 16 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0008 | 0/0 | 4787 | 4 | 4 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0009 | 0/0 | 4787 | 2 | 0 | 0 | 1 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0010 | 0/0 | 4791 | 3 | 3 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4786): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0012 | 0/0 | 4787 | 2 | 0 | 0 | 0 | 0 | 2 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0013 | 0/0 | 4788 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0014 | 0/0 | 4788 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0016 | 0/0 | 4787 | 2 | 0 | 0 | 2 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0017 | 0/0 | 4788 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0021 | 0/0 | 4787 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0022 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0024 | 0/0 | 4787 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0025 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0027 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0028 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0030 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4770): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0031 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0033 | 0/0 | 4792 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4787): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0034 | 0/0 | 4788 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0001t0035 | 0/1 | 4787 | 1 | 0 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0004t0015 | 0/0 | 4788 | 2 | 1 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0004t0018 | 0/0 | 4788 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0004t0020 | 0/0 | 4788 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0005t0001 | 0/0 | 4787 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0006t0013 | 0/0 | 4788 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4783): Show |
chr12 | 113353587 | 113396629 |
| a0001c0010t0002 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0013t0001 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0001c0014t0029 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0001 | 1/0 | 4787 | 54 | 3 | 22 | 21 | 0 | 7 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0002 | 0/0 | 4787 | 3 | 0 | 0 | 3 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0004 | 0/0 | 4787 | 8 | 0 | 8 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0005 | 0/0 | 4787 | 7 | 1 | 4 | 0 | 2 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0006 | 0/0 | 4787 | 7 | 0 | 0 | 7 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0009 | 0/0 | 4787 | 2 | 0 | 1 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0011 | 0/0 | 4787 | 2 | 1 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0019 | 0/0 | 4787 | 2 | 0 | 0 | 0 | 0 | 2 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0023 | 0/0 | 4777 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4772): Show |
chr12 | 113353587 | 113396629 |
| a0002c0002t0032 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0002c0007t0011 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0003c0003t0001 | 0/0 | 4787 | 4 | 4 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0003c0003t0007 | 0/0 | 4787 | 7 | 0 | 3 | 0 | 1 | 3 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0004c0011t0001 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0005c0012t0001 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0006c0009t0001 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0007c0016t0026 | 0/0 | 4787 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0008c0015t0002 | 0/0 | 4787 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| a0009c0008t0001 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | AGCAT others(4782): Show |
chr12 | 113353587 | 113396629 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 2 | 0 | 2 | 2 | 2 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0002 | 0/0 | 9 | 1 | 2 | 6 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0008g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0016g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0017g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0021g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0021g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0022g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0024g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0025g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0027g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0028g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0030g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0031g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0033g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0034g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0001t0035g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0004t0015g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0004t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0004t0018g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0004t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0004t0020g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0004t0020g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0006t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0010t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0013t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0001c0014t0029g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0001 | 0/0 | 13 | 1 | 2 | 10 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0005g0003 | 0/0 | 6 | 1 | 3 | 0 | 2 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0006g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0009g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0011g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0019g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0023g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0002t0032g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0002c0007t0011g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0007g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0007g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0007g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0003c0003t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0004c0011t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0005c0012t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0006c0009t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0007c0016t0026g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0008c0015t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| a0009c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00099 | hp2 | a0003 | c0003 | t0007 | g0065 | EUR | GBR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00408 | hp2 | a0002 | c0002 | t0006 | g0001 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00438 | hp1 | a0001 | c0001 | t0030 | g0107 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00438 | hp2 | a0002 | c0002 | t0006 | g0001 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00642 | hp1 | a0001 | c0013 | t0001 | g0047 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00642 | hp2 | a0002 | c0002 | t0032 | g0140 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00741 | hp1 | a0003 | c0003 | t0007 | g0005 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01069 | hp2 | a0002 | c0002 | t0023 | g0003 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01081 | hp2 | a0002 | c0002 | t0004 | g0001 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01099 | hp2 | a0001 | c0001 | t0025 | g0139 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01243 | hp1 | a0001 | c0001 | t0034 | g0128 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01255 | hp1 | a0002 | c0002 | t0004 | g0001 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01257 | hp1 | a0002 | c0002 | t0005 | g0003 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01261 | hp1 | a0003 | c0003 | t0007 | g0005 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01346 | hp1 | a0002 | c0002 | t0005 | g0061 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01358 | hp1 | a0002 | c0002 | t0005 | g0003 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01358 | hp2 | a0003 | c0003 | t0007 | g0030 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01361 | hp1 | a0002 | c0002 | t0005 | g0003 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01361 | hp2 | a0002 | c0002 | t0009 | g0080 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01433 | hp1 | a0002 | c0002 | t0004 | g0013 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01433 | hp2 | a0002 | c0007 | t0011 | g0074 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01891 | hp2 | a0001 | c0001 | t0033 | g0040 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0079 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01943 | hp1 | a0001 | c0004 | t0015 | g0159 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01952 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01975 | hp2 | a0002 | c0002 | t0004 | g0042 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01978 | hp1 | a0002 | c0002 | t0004 | g0116 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02015 | hp1 | a0002 | c0002 | t0006 | g0001 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02027 | hp2 | a0002 | c0002 | t0006 | g0052 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02055 | hp1 | a0001 | c0004 | t0018 | g0146 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02080 | hp1 | a0002 | c0002 | t0006 | g0056 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02148 | hp2 | a0002 | c0002 | t0011 | g0007 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | CDX | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | CDX | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0193 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02258 | hp2 | a0002 | c0002 | t0005 | g0003 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02293 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02293 | hp2 | a0004 | c0011 | t0001 | g0034 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02572 | hp1 | a0001 | c0006 | t0013 | g0186 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02615 | hp1 | a0001 | c0001 | t0027 | g0168 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02630 | hp2 | a0006 | c0009 | t0001 | g0121 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0187 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02647 | hp2 | a0001 | c0004 | t0018 | g0147 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02683 | hp2 | a0001 | c0001 | t0012 | g0171 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0099 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0191 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02896 | hp1 | a0001 | c0001 | t0021 | g0038 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03139 | hp2 | a0001 | c0004 | t0020 | g0160 | AFR | ESN | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03225 | hp1 | a0001 | c0004 | t0020 | g0161 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03225 | hp2 | a0001 | c0004 | t0015 | g0166 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03492 | hp1 | a0002 | c0002 | t0019 | g0088 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0188 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03654 | hp1 | a0007 | c0016 | t0026 | g0005 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03688 | hp1 | a0003 | c0003 | t0007 | g0026 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03704 | hp1 | a0002 | c0002 | t0019 | g0001 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0031 | SAS | BEB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | BEB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0170 | SAS | BEB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03834 | hp2 | a0001 | c0001 | t0024 | g0169 | SAS | BEB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | BEB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG04115 | hp1 | a0008 | c0015 | t0002 | g0162 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG04115 | hp2 | a0003 | c0003 | t0007 | g0026 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | STU | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18747 | hp1 | a0002 | c0002 | t0006 | g0076 | EAS | CHB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18961 | hp2 | a0009 | c0008 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18974 | hp2 | a0002 | c0002 | t0009 | g0071 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18979 | hp1 | a0001 | c0010 | t0002 | g0006 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18991 | hp2 | a0001 | c0001 | t0031 | g0133 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19009 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19011 | hp1 | a0001 | c0001 | t0016 | g0175 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0109 | AFR | LWK | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19043 | hp1 | a0001 | c0014 | t0029 | g0158 | AFR | LWK | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19043 | hp2 | a0001 | c0001 | t0017 | g0148 | AFR | LWK | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19068 | hp2 | a0002 | c0002 | t0006 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | ASW | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20129 | hp2 | a0001 | c0001 | t0028 | g0173 | AFR | ASW | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20752 | hp1 | a0002 | c0002 | t0005 | g0003 | EUR | TSI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20805 | hp2 | a0002 | c0002 | t0005 | g0003 | EUR | TSI | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | GIH | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20905 | hp2 | a0003 | c0003 | t0007 | g0192 | SAS | GIH | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02559 | hp1 | a0005 | c0012 | t0001 | g0010 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0190 | AFR | ACB | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | USA | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | USA | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0189 | AFR | USA | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA20300 | hp2 | a0002 | c0002 | t0011 | g0081 | AFR | USA | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | LWK | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| NA21309 | hp2 | a0001 | c0001 | t0021 | g0084 | AFR | LWK | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0035 | g0103 | REF | REF | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0093 | REF | REF | PLBD2_chr12_113353587_113396629 | PLBD2 | chr12 | 113353587 | 113396629 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113358755 | A | G | 1 | a0007 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.155A>G | p.Asp52Gly | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/12 | 169/4787 | 155/1770 | 52/589 | chr12 | 113358755 | |||
| chr12:113358761 | A | C | 8 | a0001 a0003 a0004 others(5): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
missense_variant | MODERATE | c.161A>C | p.Gln54Pro | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/12 | 175/4787 | 161/1770 | 54/589 | chr12 | 113358761 | |||
| chr12:113372656 | A | G | 1 | a0008 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.392A>G | p.Tyr131Cys | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/12 | 406/4787 | 392/1770 | 131/589 | chr12 | 113372656 | |||
| chr12:113380783 | T | G | 1 | a0009 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.898T>G | p.Ser300Ala | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/12 | 912/4787 | 898/1770 | 300/589 | chr12 | 113380783 | |||
| chr12:113384207 | C | T | 1 | a0005 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1060C>T | p.Arg354Cys | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/12 | 1074/4787 | 1060/1770 | 354/589 | chr12 | 113384207 | |||
| chr12:113384225 | G | A | 1 | a0006 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1078G>A | p.Ala360Thr | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/12 | 1092/4787 | 1078/1770 | 360/589 | chr12 | 113384225 | |||
| chr12:113387826 | C | T | 1 | a0004 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1522C>T | p.Arg508Cys | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/12 | 1536/4787 | 1522/1770 | 508/589 | chr12 | 113387826 | |||
| chr12:113387874 | C | T | 2 | a0003 a0007 |
12 | HG00099.hp2 HG00741.hp1 HG01261.hp1 others(9): Show |
missense_variant | MODERATE | c.1570C>T | p.Arg524Cys | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/12 | 1584/4787 | 1570/1770 | 524/589 | chr12 | 113387874 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113358609 | C | A | 1 | a0001c0006 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.9C>A | p.Gly3Gly | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/12 | 23/4787 | 9/1770 | 3/589 | chr12 | 113358609 | |||
| chr12:113358723 | G | T | 1 | a0001c0005 | 2 | HG03209.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.123G>T | p.Ala41Ala | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/12 | 137/4787 | 123/1770 | 41/589 | chr12 | 113358723 | |||
| chr12:113372711 | C | T | 2 | a0001c0014 a0002c0007 |
2 | HG01433.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.447C>T | p.Val149Val | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/12 | 461/4787 | 447/1770 | 149/589 | chr12 | 113372711 | |||
| chr12:113374841 | C | T | 1 | a0001c0013 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.693C>T | p.Asn231Asn | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/12 | 707/4787 | 693/1770 | 231/589 | chr12 | 113374841 | |||
| chr12:113380794 | C | T | 1 | a0001c0004 | 6 | HG01943.hp1 HG02055.hp1 HG02647.hp2 others(3): Show |
synonymous_variant | LOW | c.909C>T | p.Pro303Pro | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/12 | 923/4787 | 909/1770 | 303/589 | chr12 | 113380794 | |||
| chr12:113388533 | G | A | 1 | a0001c0010 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1677G>A | p.Pro559Pro | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1691/4787 | 1677/1770 | 559/589 | chr12 | 113388533 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113358594 | T | C | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(19): Show |
77 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-7T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/12 | 7 | chr12 | 113358594 | ||||||
| chr12:113388637 | C | G | 7 | a0001c0001t0017 a0001c0001t0027 a0001c0001t0028 others(4): Show |
15 | HG00099.hp2 HG00741.hp1 HG01261.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 11 | chr12 | 113388637 | ||||||
| chr12:113388695 | A | G | 2 | a0001c0001t0021 a0001c0001t0025 |
3 | HG01099.hp2 HG02896.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*69A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 69 | chr12 | 113388695 | ||||||
| chr12:113388730 | C | T | 10 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(7): Show |
37 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*104C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 104 | chr12 | 113388730 | ||||||
| chr12:113388904 | A | C | 1 | a0001c0004t0018 | 2 | HG02055.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*278A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 278 | chr12 | 113388904 | ||||||
| chr12:113388935 | G | A | 2 | a0001c0004t0015 a0001c0004t0020 |
4 | HG01943.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 309 | chr12 | 113388935 | ||||||
| chr12:113389025 | C | CCAGCTGC others(22): Show |
1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401_*429dupAGCTGC others(23): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 430 | INFO_REALIGN_3_PRIME | chr12 | 113389025 | |||||
| chr12:113389084 | G | A | 1 | a0001c0004t0018 | 2 | HG02055.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 458 | chr12 | 113389084 | ||||||
| chr12:113389339 | C | T | 1 | a0001c0001t0024 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 713 | chr12 | 113389339 | ||||||
| chr12:113389357 | A | G | 1 | a0002c0002t0006 | 7 | HG00408.hp2 HG00438.hp2 HG02015.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*731A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 731 | chr12 | 113389357 | ||||||
| chr12:113389385 | A | G | 1 | a0001c0001t0014 | 2 | HG02559.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*759A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 759 | chr12 | 113389385 | ||||||
| chr12:113389439 | A | G | 1 | a0001c0001t0016 | 2 | NA19009.hp2 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*813A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 813 | chr12 | 113389439 | ||||||
| chr12:113389501 | C | G | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(1): Show |
27 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*875C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 875 | chr12 | 113389501 | ||||||
| chr12:113389593 | T | TC | 3 | a0001c0001t0017 a0001c0004t0015 a0001c0004t0020 |
6 | HG01943.hp1 HG02647.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*968dupC | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 969 | INFO_REALIGN_3_PRIME | chr12 | 113389593 | |||||
| chr12:113389699 | C | CT | 6 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0033 others(3): Show |
8 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1083dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1084 | INFO_REALIGN_3_PRIME | chr12 | 113389699 | |||||
| chr12:113389810 | G | A | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(1): Show |
27 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1184G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1184 | chr12 | 113389810 | ||||||
| chr12:113389989 | A | C | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(1): Show |
27 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1363A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1363 | chr12 | 113389989 | ||||||
| chr12:113389996 | G | A | 1 | a0001c0001t0031 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1370 | chr12 | 113389996 | ||||||
| chr12:113390007 | C | G | 1 | a0002c0002t0032 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1381C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1381 | chr12 | 113390007 | ||||||
| chr12:113390089 | A | G | 8 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0017 others(5): Show |
12 | HG01243.hp1 HG01943.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1463A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1463 | chr12 | 113390089 | ||||||
| chr12:113390132 | T | C | 2 | a0001c0001t0008 a0001c0001t0022 |
5 | HG02257.hp2 HG02897.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1506T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1506 | chr12 | 113390132 | ||||||
| chr12:113390176 | A | G | 8 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0017 others(5): Show |
12 | HG01243.hp1 HG01943.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1550A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1550 | chr12 | 113390176 | ||||||
| chr12:113390218 | C | A | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1592 | chr12 | 113390218 | ||||||
| chr12:113390219 | TATCCATT others(24): Show |
T | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1594_*1624delATCC others(27): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1594 | chr12 | 113390219 | ||||||
| chr12:113390257 | T | A | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1631T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1631 | chr12 | 113390257 | ||||||
| chr12:113390265 | C | T | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1639 | chr12 | 113390265 | ||||||
| chr12:113390284 | A | C | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1658 | chr12 | 113390284 | ||||||
| chr12:113390287 | C | G | 7 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(4): Show |
33 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1661C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1661 | chr12 | 113390287 | ||||||
| chr12:113390307 | T | A | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1681 | chr12 | 113390307 | ||||||
| chr12:113390313 | T | C | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1687T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1687 | chr12 | 113390313 | ||||||
| chr12:113390319 | ACCCATCC others(3): Show |
A | 1 | a0002c0002t0023 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1695_*1704delCCAT others(6): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1695 | INFO_REALIGN_3_PRIME | chr12 | 113390319 | |||||
| chr12:113390350 | C | A | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1724C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1724 | chr12 | 113390350 | ||||||
| chr12:113390360 | TCAATCCA others(3): Show |
T | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1735_*1744delCAAT others(6): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1735 | chr12 | 113390360 | ||||||
| chr12:113390373 | T | C | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1747T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1747 | chr12 | 113390373 | ||||||
| chr12:113390436 | A | G | 3 | a0001c0001t0017 a0001c0004t0015 a0001c0004t0020 |
6 | HG01943.hp1 HG02647.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1810A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1810 | chr12 | 113390436 | ||||||
| chr12:113390551 | C | G | 2 | a0002c0002t0005 a0002c0002t0023 |
8 | HG01069.hp2 HG01257.hp1 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1925C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1925 | chr12 | 113390551 | ||||||
| chr12:113390603 | C | T | 1 | a0002c0002t0004 | 8 | HG01081.hp2 HG01255.hp1 HG01433.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1977C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 1977 | chr12 | 113390603 | ||||||
| chr12:113390729 | C | CCCAT | 2 | a0001c0001t0010 a0001c0001t0033 |
4 | HG01891.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2114_*2117dupATCC | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2118 | INFO_REALIGN_3_PRIME | chr12 | 113390729 | |||||
| chr12:113390823 | C | T | 1 | a0001c0001t0022 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2197C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2197 | chr12 | 113390823 | ||||||
| chr12:113390886 | C | T | 1 | a0001c0014t0029 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2260C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2260 | chr12 | 113390886 | ||||||
| chr12:113390903 | G | A | 1 | a0001c0001t0028 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2277G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2277 | chr12 | 113390903 | ||||||
| chr12:113391043 | T | C | 4 | a0001c0001t0012 a0001c0001t0024 a0001c0001t0028 others(1): Show |
5 | HG02683.hp2 HG03834.hp1 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2417T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2417 | chr12 | 113391043 | ||||||
| chr12:113391099 | T | C | 2 | a0001c0004t0015 a0001c0004t0020 |
4 | HG01943.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2473T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2473 | chr12 | 113391099 | ||||||
| chr12:113391309 | C | T | 1 | a0001c0001t0028 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2683C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2683 | chr12 | 113391309 | ||||||
| chr12:113391494 | G | A | 2 | a0001c0001t0012 a0001c0001t0024 |
3 | HG02683.hp2 HG03834.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2868G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2868 | chr12 | 113391494 | ||||||
| chr12:113391560 | T | G | 1 | a0002c0002t0019 | 2 | HG03492.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2934T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2934 | chr12 | 113391560 | ||||||
| chr12:113391577 | G | A | 2 | a0002c0002t0011 a0002c0007t0011 |
3 | HG01433.hp2 HG02148.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2951G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 12/12 | 2951 | chr12 | 113391577 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113358895 | G | C | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
splice_region_variant&intron_variant | LOW | c.290+5G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113358895 | |||||||
| chr12:113359042 | G | T | 1 | a0001c0001t0008g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+152G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359042 | |||||||
| chr12:113359051 | A | C | 56 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(53): Show |
71 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(68): Show |
intron_variant | MODIFIER | c.290+161A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359051 | |||||||
| chr12:113359066 | T | G | 52 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(49): Show |
66 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(63): Show |
intron_variant | MODIFIER | c.290+176T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359066 | |||||||
| chr12:113359102 | C | G | 5 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(2): Show |
5 | HG02572.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+212C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359102 | |||||||
| chr12:113359190 | G | C | 1 | a0001c0001t0010g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290+300G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359190 | |||||||
| chr12:113359436 | C | T | 6 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(3): Show |
6 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+546C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359436 | |||||||
| chr12:113359589 | T | C | 1 | a0002c0002t0001g0011 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.290+699T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359589 | |||||||
| chr12:113359796 | C | T | 1 | a0001c0001t0025g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.290+906C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113359796 | |||||||
| chr12:113359811 | CAG | C | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.290+924_290+925del others(2): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113359811 | ||||||
| chr12:113360036 | C | T | 17 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(14): Show |
17 | HG01109.hp2 HG01167.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.290+1146C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360036 | |||||||
| chr12:113360049 | C | T | 1 | a0006c0009t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.290+1159C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360049 | |||||||
| chr12:113360142 | G | A | 25 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(22): Show |
30 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.290+1252G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360142 | |||||||
| chr12:113360381 | G | A | 1 | a0001c0001t0027g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.290+1491G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360381 | |||||||
| chr12:113360428 | C | T | 17 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(14): Show |
26 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.290+1538C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360428 | |||||||
| chr12:113360459 | G | T | 1 | a0001c0001t0003g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.290+1569G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360459 | |||||||
| chr12:113360534 | C | G | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.290+1644C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360534 | |||||||
| chr12:113360600 | A | G | 52 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(49): Show |
66 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(63): Show |
intron_variant | MODIFIER | c.290+1710A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360600 | |||||||
| chr12:113360658 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.290+1768T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360658 | |||||||
| chr12:113360677 | G | A | 2 | a0001c0004t0018g0146 a0001c0004t0018g0147 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.290+1787G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360677 | |||||||
| chr12:113360718 | C | T | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.290+1828C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360718 | |||||||
| chr12:113360834 | T | G | 5 | a0001c0001t0002g0172 a0001c0001t0012g0170 a0001c0001t0012g0171 others(2): Show |
5 | HG02683.hp2 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1944T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360834 | |||||||
| chr12:113360862 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.290+1972G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360862 | |||||||
| chr12:113360907 | T | C | 54 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(51): Show |
68 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(65): Show |
intron_variant | MODIFIER | c.290+2017T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360907 | |||||||
| chr12:113360955 | C | T | 1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.290+2065C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113360955 | |||||||
| chr12:113361218 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.290+2328C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361218 | |||||||
| chr12:113361220 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02280.hp1 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.290+2330C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361220 | |||||||
| chr12:113361245 | T | A | 1 | a0002c0002t0001g0029 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.290+2355T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361245 | |||||||
| chr12:113361303 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.290+2413C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361303 | |||||||
| chr12:113361327 | G | GT | 11 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.290+2450dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113361327 | ||||||
| chr12:113361337 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290+2447T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361337 | |||||||
| chr12:113361341 | G | GT | 14 | a0001c0001t0001g0028 a0001c0001t0001g0104 a0001c0001t0001g0105 others(11): Show |
15 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+2467dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113361341 | ||||||
| chr12:113361341 | G | T | 21 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0185 others(18): Show |
21 | HG00423.hp2 HG01943.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.290+2451G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361341 | |||||||
| chr12:113361341 | GT | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0025 others(26): Show |
43 | HG00544.hp1 HG01168.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.290+2467delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113361341 | ||||||
| chr12:113361342 | T | G | 14 | a0001c0001t0001g0185 a0001c0001t0002g0163 a0001c0001t0002g0164 others(11): Show |
14 | HG00423.hp2 HG01943.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.290+2452T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361342 | |||||||
| chr12:113361346 | T | G | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(24): Show |
32 | HG00423.hp2 HG00544.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.290+2456T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361346 | |||||||
| chr12:113361348 | T | G | 3 | a0003c0003t0007g0026 a0003c0003t0007g0030 a0003c0003t0007g0192 |
4 | HG01358.hp2 HG03688.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+2458T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361348 | |||||||
| chr12:113361487 | G | T | 1 | a0001c0001t0027g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.290+2597G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361487 | |||||||
| chr12:113361855 | C | T | 1 | a0001c0001t0027g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.290+2965C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113361855 | |||||||
| chr12:113362112 | G | A | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.290+3222G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362112 | |||||||
| chr12:113362312 | G | C | 2 | a0001c0004t0018g0146 a0001c0004t0018g0147 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.290+3422G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362312 | |||||||
| chr12:113362330 | T | TA | 6 | a0001c0001t0001g0185 a0001c0001t0009g0031 a0001c0001t0013g0188 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+3453dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113362330 | ||||||
| chr12:113362399 | C | T | 1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.290+3509C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362399 | |||||||
| chr12:113362404 | A | G | 1 | a0002c0002t0001g0102 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.290+3514A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362404 | |||||||
| chr12:113362431 | G | T | 1 | a0001c0001t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290+3541G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362431 | |||||||
| chr12:113362490 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.290+3600C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362490 | |||||||
| chr12:113362791 | A | AT | 9 | a0001c0001t0001g0100 a0002c0002t0004g0116 a0003c0003t0001g0005 others(6): Show |
13 | HG00741.hp1 HG01261.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+3913dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113362791 | ||||||
| chr12:113362791 | AT | A | 54 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(51): Show |
68 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(65): Show |
intron_variant | MODIFIER | c.290+3913delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113362791 | ||||||
| chr12:113362818 | T | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0035 others(4): Show |
8 | HG00280.hp1 HG01106.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+3928T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362818 | |||||||
| chr12:113362951 | AT | A | 24 | a0001c0001t0001g0185 a0001c0001t0002g0025 a0001c0001t0003g0002 others(21): Show |
34 | HG01168.hp2 HG01358.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.290+4077delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113362951 | ||||||
| chr12:113362951 | ATT | A | 24 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.290+4076_290+4077d others(4): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113362951 | ||||||
| chr12:113362997 | T | C | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.290+4107T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113362997 | |||||||
| chr12:113363023 | T | C | 51 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(48): Show |
65 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(62): Show |
intron_variant | MODIFIER | c.290+4133T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363023 | |||||||
| chr12:113363136 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290+4246C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363136 | |||||||
| chr12:113363136 | C | T | 1 | a0001c0001t0010g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.290+4246C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363136 | |||||||
| chr12:113363285 | A | G | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.290+4395A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363285 | |||||||
| chr12:113363382 | G | C | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.290+4492G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363382 | |||||||
| chr12:113363537 | C | CT | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0096 others(9): Show |
12 | HG00423.hp2 HG00544.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.290+4666dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113363537 | ||||||
| chr12:113363738 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.290+4848C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363738 | |||||||
| chr12:113363759 | G | C | 1 | a0001c0001t0009g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.290+4869G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363759 | |||||||
| chr12:113363780 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290+4890A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113363780 | |||||||
| chr12:113364075 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(2): Show |
5 | HG02572.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-5041C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113364075 | |||||||
| chr12:113364215 | G | A | 1 | a0002c0002t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.291-4901G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113364215 | |||||||
| chr12:113364250 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(203): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.291-4866T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113364250 | |||||||
| chr12:113364289 | G | A | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.291-4827G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113364289 | |||||||
| chr12:113364383 | G | A | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.291-4733G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113364383 | |||||||
| chr12:113364470 | CT | C | 47 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0002g0006 others(44): Show |
61 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.291-4633delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113364470 | ||||||
| chr12:113364722 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.291-4394A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113364722 | |||||||
| chr12:113365033 | T | C | 6 | a0001c0001t0002g0172 a0001c0001t0012g0170 a0001c0001t0012g0171 others(3): Show |
6 | HG02615.hp1 HG02683.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-4083T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365033 | |||||||
| chr12:113365087 | T | C | 4 | a0001c0001t0010g0027 a0001c0001t0010g0041 a0001c0001t0010g0099 others(1): Show |
4 | HG01891.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-4029T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365087 | |||||||
| chr12:113365127 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.291-3989C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365127 | |||||||
| chr12:113365184 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.291-3932A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365184 | |||||||
| chr12:113365229 | C | A | 4 | a0001c0001t0002g0172 a0001c0001t0012g0170 a0001c0001t0012g0171 others(1): Show |
4 | HG02683.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-3887C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365229 | |||||||
| chr12:113365262 | C | T | 1 | a0002c0002t0019g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.291-3854C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365262 | |||||||
| chr12:113365325 | AT | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0014t0029g0158 others(2): Show |
5 | HG01167.hp2 HG01975.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-3775delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113365325 | ||||||
| chr12:113365533 | CA | C | 5 | a0001c0001t0002g0172 a0001c0001t0012g0170 a0001c0001t0012g0171 others(2): Show |
5 | HG02683.hp2 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-3580delA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113365533 | ||||||
| chr12:113365588 | C | T | 5 | a0001c0001t0002g0172 a0001c0001t0012g0170 a0001c0001t0012g0171 others(2): Show |
5 | HG02683.hp2 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-3528C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365588 | |||||||
| chr12:113365898 | T | A | 1 | a0001c0006t0013g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.291-3218T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113365898 | |||||||
| chr12:113366385 | C | T | 17 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(14): Show |
22 | HG00423.hp2 HG00544.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-2731C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113366385 | |||||||
| chr12:113366411 | C | CACAAAAC others(26): Show |
16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.291-2699_291-2698i others(35): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113366411 | ||||||
| chr12:113366432 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.291-2684A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113366432 | |||||||
| chr12:113366805 | C | A | 1 | a0002c0002t0001g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.291-2311C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113366805 | |||||||
| chr12:113367028 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.291-2088C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367028 | |||||||
| chr12:113367049 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.291-2067C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367049 | |||||||
| chr12:113367214 | G | A | 1 | a0006c0009t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.291-1902G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367214 | |||||||
| chr12:113367284 | T | C | 1 | a0001c0001t0027g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-1832T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367284 | |||||||
| chr12:113367372 | CAG | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0048 others(1): Show |
4 | HG00642.hp1 HG01943.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1742_291-1741d others(4): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113367372 | ||||||
| chr12:113367376 | A | G | 24 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.291-1740A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367376 | |||||||
| chr12:113367521 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.291-1595A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367521 | |||||||
| chr12:113367579 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.291-1537G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367579 | |||||||
| chr12:113367695 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291-1421G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367695 | |||||||
| chr12:113367748 | C | CA | 17 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
17 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-1351dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113367748 | ||||||
| chr12:113367759 | A | AAAAAAAA others(3): Show |
2 | a0001c0004t0018g0146 a0008c0015t0002g0162 |
2 | HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.291-1351_291-1350i others(12): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113367759 | ||||||
| chr12:113367759 | A | AAAAAAAA others(2): Show |
22 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(19): Show |
27 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.291-1351_291-1350i others(11): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113367759 | ||||||
| chr12:113367759 | A | AAAAAAAG | 25 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(22): Show |
34 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.291-1349_291-1343d others(9): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113367759 | ||||||
| chr12:113367774 | C | G | 2 | a0001c0001t0021g0038 a0001c0001t0021g0084 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.291-1342C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367774 | |||||||
| chr12:113367808 | T | G | 54 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0053 others(51): Show |
71 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(68): Show |
intron_variant | MODIFIER | c.291-1308T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367808 | |||||||
| chr12:113367872 | A | C | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.291-1244A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367872 | |||||||
| chr12:113367957 | C | A | 5 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(2): Show |
5 | HG02572.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-1159C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113367957 | |||||||
| chr12:113368082 | G | GA | 6 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(3): Show |
6 | HG02080.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1022dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113368082 | ||||||
| chr12:113368082 | GA | G | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.291-1022delA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 113368082 | ||||||
| chr12:113368288 | G | A | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.291-828G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368288 | |||||||
| chr12:113368448 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | NA18612.hp2 NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.291-668G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368448 | |||||||
| chr12:113368469 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.291-647G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368469 | |||||||
| chr12:113368505 | G | A | 24 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.291-611G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368505 | |||||||
| chr12:113368567 | C | T | 1 | a0001c0004t0020g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291-549C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368567 | |||||||
| chr12:113368577 | C | T | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.291-539C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368577 | |||||||
| chr12:113368827 | A | G | 1 | a0001c0001t0014g0190 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.291-289A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368827 | |||||||
| chr12:113368890 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0100 |
2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.291-226G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368890 | |||||||
| chr12:113368928 | G | A | 1 | a0001c0001t0034g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.291-188G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113368928 | |||||||
| chr12:113369007 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.291-109G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113369007 | |||||||
| chr12:113369109 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp2 | splice_region_variant&intron_variant | LOW | c.291-7C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 1/11 | chr12 | 113369109 | |||||||
| chr12:113369234 | G | A | 3 | a0002c0002t0005g0003 a0002c0002t0005g0061 a0002c0002t0023g0003 |
8 | HG01069.hp2 HG01257.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+25G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369234 | |||||||
| chr12:113369310 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.384+101T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369310 | |||||||
| chr12:113369553 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.384+344G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369553 | |||||||
| chr12:113369670 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.384+461C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369670 | |||||||
| chr12:113369693 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.384+484G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369693 | |||||||
| chr12:113369700 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.384+491T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369700 | |||||||
| chr12:113369817 | T | C | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384+608T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369817 | |||||||
| chr12:113369877 | T | G | 5 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+668T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369877 | |||||||
| chr12:113369887 | A | G | 1 | a0001c0001t0002g0025 | 2 | NA19004.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.384+678A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369887 | |||||||
| chr12:113369946 | C | T | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.384+737C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113369946 | |||||||
| chr12:113370100 | C | T | 46 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(43): Show |
60 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.384+891C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370100 | |||||||
| chr12:113370229 | T | A | 1 | a0001c0001t0014g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.384+1020T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370229 | |||||||
| chr12:113370262 | G | A | 1 | a0001c0001t0017g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+1053G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370262 | |||||||
| chr12:113370472 | C | CT | 5 | a0001c0001t0001g0059 a0001c0001t0001g0110 a0001c0001t0014g0191 others(2): Show |
5 | HG01106.hp2 HG02027.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+1285dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 113370472 | ||||||
| chr12:113370472 | CT | C | 28 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0085 others(25): Show |
37 | HG01070.hp1 HG01167.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.384+1285delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 113370472 | ||||||
| chr12:113370472 | CTT | C | 26 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(23): Show |
31 | HG00423.hp2 HG00544.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+1284_384+1285d others(4): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 113370472 | ||||||
| chr12:113370472 | CTTT | C | 5 | a0001c0001t0028g0173 a0001c0004t0015g0159 a0001c0004t0015g0166 others(2): Show |
5 | HG01943.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+1283_384+1285d others(5): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 113370472 | ||||||
| chr12:113370477 | T | C | 5 | a0001c0001t0010g0027 a0001c0001t0010g0041 a0001c0001t0010g0099 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+1268T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370477 | |||||||
| chr12:113370479 | T | C | 20 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(17): Show |
25 | HG00423.hp2 HG00544.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.384+1270T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370479 | |||||||
| chr12:113370534 | T | C | 1 | a0002c0002t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.384+1325T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370534 | |||||||
| chr12:113370679 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0100 |
2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.384+1470T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370679 | |||||||
| chr12:113370706 | G | C | 1 | a0003c0003t0007g0065 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.384+1497G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113370706 | |||||||
| chr12:113371312 | C | G | 1 | a0002c0002t0001g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.385-1337C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371312 | |||||||
| chr12:113371312 | C | T | 17 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(14): Show |
22 | HG00423.hp2 HG00544.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.385-1337C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371312 | |||||||
| chr12:113371424 | A | G | 22 | a0001c0001t0001g0185 a0001c0001t0002g0025 a0001c0001t0003g0002 others(19): Show |
31 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.385-1225A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371424 | |||||||
| chr12:113371457 | A | G | 48 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(45): Show |
62 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(59): Show |
intron_variant | MODIFIER | c.385-1192A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371457 | |||||||
| chr12:113371480 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.385-1169G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371480 | |||||||
| chr12:113371657 | C | T | 22 | a0001c0001t0001g0185 a0001c0001t0002g0025 a0001c0001t0003g0002 others(19): Show |
31 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.385-992C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371657 | |||||||
| chr12:113371879 | C | G | 5 | a0002c0002t0001g0021 a0002c0002t0001g0043 a0002c0002t0001g0063 others(2): Show |
6 | HG01070.hp1 HG02300.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-770C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113371879 | |||||||
| chr12:113372203 | G | A | 2 | a0001c0004t0018g0146 a0001c0004t0018g0147 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.385-446G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113372203 | |||||||
| chr12:113372303 | A | G | 52 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(49): Show |
66 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(63): Show |
intron_variant | MODIFIER | c.385-346A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113372303 | |||||||
| chr12:113372350 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.385-299A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113372350 | |||||||
| chr12:113372579 | G | T | 4 | a0001c0004t0015g0159 a0001c0004t0015g0166 a0001c0004t0020g0160 others(1): Show |
4 | HG01943.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-70G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113372579 | |||||||
| chr12:113372621 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-28C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113372621 | |||||||
| chr12:113372629 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.385-20G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 2/11 | chr12 | 113372629 | |||||||
| chr12:113372956 | A | G | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.543+149A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113372956 | |||||||
| chr12:113373008 | C | T | 24 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.543+201C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373008 | |||||||
| chr12:113373028 | T | C | 22 | a0001c0001t0001g0185 a0001c0001t0002g0025 a0001c0001t0003g0002 others(19): Show |
31 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.543+221T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373028 | |||||||
| chr12:113373065 | A | G | 1 | a0001c0004t0020g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.543+258A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373065 | |||||||
| chr12:113373497 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+690C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373497 | |||||||
| chr12:113373550 | C | A | 4 | a0002c0002t0001g0022 a0002c0002t0001g0091 a0002c0002t0001g0092 others(1): Show |
5 | HG01192.hp1 HG01255.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+743C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373550 | |||||||
| chr12:113373550 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.543+743C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373550 | |||||||
| chr12:113373585 | C | T | 1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+778C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373585 | |||||||
| chr12:113373653 | C | T | 1 | a0001c0001t0003g0177 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.544-821C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373653 | |||||||
| chr12:113373698 | A | G | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-776A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373698 | |||||||
| chr12:113373760 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-714C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113373760 | |||||||
| chr12:113374189 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-285G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113374189 | |||||||
| chr12:113374193 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.544-281C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113374193 | |||||||
| chr12:113374279 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0066 a0001c0001t0001g0067 |
4 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-195T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113374279 | |||||||
| chr12:113374450 | C | T | 1 | a0001c0001t0034g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.544-24C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 3/11 | chr12 | 113374450 | |||||||
| chr12:113374614 | G | C | 1 | a0002c0002t0001g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.644+40G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 4/11 | chr12 | 113374614 | |||||||
| chr12:113374752 | C | G | 1 | a0002c0002t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.645-41C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 4/11 | chr12 | 113374752 | |||||||
| chr12:113375046 | G | T | 1 | a0001c0006t0013g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.859+39G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375046 | |||||||
| chr12:113375078 | G | A | 23 | a0001c0001t0001g0185 a0001c0001t0002g0025 a0001c0001t0003g0002 others(20): Show |
32 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.859+71G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375078 | |||||||
| chr12:113375107 | A | T | 2 | a0002c0002t0001g0141 a0002c0002t0001g0144 |
2 | HG01167.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.859+100A>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375107 | |||||||
| chr12:113375108 | C | T | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.859+101C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375108 | |||||||
| chr12:113375210 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.859+203G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375210 | |||||||
| chr12:113375259 | C | T | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.859+252C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375259 | |||||||
| chr12:113375320 | A | AT | 24 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.859+320dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113375320 | ||||||
| chr12:113375553 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.859+546A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375553 | |||||||
| chr12:113375648 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.859+641G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375648 | |||||||
| chr12:113375911 | T | C | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.859+904T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113375911 | |||||||
| chr12:113376069 | G | A | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.859+1062G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376069 | |||||||
| chr12:113376144 | G | A | 5 | a0001c0001t0001g0085 a0001c0001t0010g0027 a0001c0001t0010g0041 others(2): Show |
5 | HG01891.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+1137G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376144 | |||||||
| chr12:113376163 | A | AT | 13 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0112 others(10): Show |
13 | HG01346.hp2 HG02055.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.859+1174dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113376163 | ||||||
| chr12:113376163 | AT | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0048 others(5): Show |
8 | HG00642.hp1 HG01943.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.859+1174delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113376163 | ||||||
| chr12:113376208 | A | G | 47 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(44): Show |
61 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.859+1201A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376208 | |||||||
| chr12:113376415 | C | T | 3 | a0001c0001t0012g0170 a0001c0001t0012g0171 a0001c0001t0024g0169 |
3 | HG02683.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.859+1408C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376415 | |||||||
| chr12:113376433 | G | A | 1 | a0001c0001t0014g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.859+1426G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376433 | |||||||
| chr12:113376679 | C | T | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.859+1672C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376679 | |||||||
| chr12:113376729 | A | G | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.859+1722A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376729 | |||||||
| chr12:113376914 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.859+1907G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113376914 | |||||||
| chr12:113377294 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0014g0190 a0001c0001t0014g0191 |
3 | HG02559.hp2 HG02818.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.859+2287C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113377294 | |||||||
| chr12:113377587 | A | G | 3 | a0001c0001t0012g0170 a0001c0001t0012g0171 a0001c0001t0024g0169 |
3 | HG02683.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.859+2580A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113377587 | |||||||
| chr12:113377588 | G | C | 3 | a0001c0001t0012g0170 a0001c0001t0012g0171 a0001c0001t0024g0169 |
3 | HG02683.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.859+2581G>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113377588 | |||||||
| chr12:113377673 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0004c0011t0001g0034 |
4 | HG00280.hp1 HG01106.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+2666G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113377673 | |||||||
| chr12:113377712 | G | T | 16 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(13): Show |
25 | HG01168.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.859+2705G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113377712 | |||||||
| chr12:113377728 | T | A | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.859+2721T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113377728 | |||||||
| chr12:113378149 | G | T | 1 | a0001c0001t0017g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.860-2596G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378149 | |||||||
| chr12:113378161 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.860-2584G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378161 | |||||||
| chr12:113378170 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.860-2575T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378170 | |||||||
| chr12:113378291 | C | CA | 53 | a0001c0001t0001g0185 a0001c0001t0002g0006 a0001c0001t0002g0023 others(50): Show |
67 | HG00423.hp2 HG00544.hp1 HG01168.hp2 others(64): Show |
intron_variant | MODIFIER | c.860-2439dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113378291 | ||||||
| chr12:113378515 | T | C | 5 | a0001c0001t0001g0185 a0001c0001t0013g0188 a0001c0001t0017g0187 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.860-2230T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378515 | |||||||
| chr12:113378560 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.860-2185C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378560 | |||||||
| chr12:113378651 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0070 |
2 | HG01081.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.860-2094T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378651 | |||||||
| chr12:113378667 | G | A | 24 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0149 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.860-2078G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378667 | |||||||
| chr12:113378683 | CT | C | 27 | a0001c0001t0001g0072 a0001c0001t0002g0006 a0001c0001t0002g0023 others(24): Show |
32 | HG00423.hp2 HG00544.hp1 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.860-2046delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113378683 | ||||||
| chr12:113378970 | G | A | 1 | a0002c0002t0005g0061 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.860-1775G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113378970 | |||||||
| chr12:113379038 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.860-1707G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113379038 | |||||||
| chr12:113379067 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.860-1678G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113379067 | |||||||
| chr12:113379153 | C | G | 1 | a0002c0002t0011g0081 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.860-1592C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113379153 | |||||||
| chr12:113379307 | C | CA | 16 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0185 others(13): Show |
17 | HG00597.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.860-1415dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113379307 | ||||||
| chr12:113379307 | CA | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0058 a0001c0001t0001g0131 others(23): Show |
31 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.860-1415delA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 113379307 | ||||||
| chr12:113379762 | AGATCGCC others(15): Show |
A | 1 | a0002c0002t0009g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.860-982_860-961del others(22): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113379762 | |||||||
| chr12:113379901 | G | A | 8 | a0001c0001t0001g0053 a0001c0001t0001g0123 a0002c0002t0001g0007 others(5): Show |
10 | HG00558.hp1 HG00673.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-844G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113379901 | |||||||
| chr12:113379918 | C | G | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.860-827C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113379918 | |||||||
| chr12:113380058 | A | G | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.860-687A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380058 | |||||||
| chr12:113380147 | A | T | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.860-598A>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380147 | |||||||
| chr12:113380151 | T | A | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.860-594T>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380151 | |||||||
| chr12:113380238 | G | A | 3 | a0001c0001t0027g0168 a0001c0001t0034g0128 a0001c0006t0013g0186 |
3 | HG01243.hp1 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.860-507G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380238 | |||||||
| chr12:113380326 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.860-419C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380326 | |||||||
| chr12:113380415 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.860-330G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380415 | |||||||
| chr12:113380519 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0110 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.860-226T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380519 | |||||||
| chr12:113380633 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.860-112G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380633 | |||||||
| chr12:113380644 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.860-101G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380644 | |||||||
| chr12:113380652 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.860-93T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380652 | |||||||
| chr12:113380684 | G | A | 1 | a0001c0001t0017g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.860-61G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380684 | |||||||
| chr12:113380692 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.860-53G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380692 | |||||||
| chr12:113380733 | C | G | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.860-12C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380733 | |||||||
| chr12:113380740 | C | T | 2 | a0001c0004t0015g0159 a0001c0004t0015g0166 |
2 | HG01943.hp1 HG03225.hp2 |
splice_region_variant&intron_variant | LOW | c.860-5C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 5/11 | chr12 | 113380740 | |||||||
| chr12:113380923 | G | A | 46 | a0001c0001t0001g0085 a0001c0001t0001g0117 a0001c0001t0001g0118 others(43): Show |
55 | HG01168.hp2 HG01243.hp1 HG01496.hp2 others(52): Show |
intron_variant | MODIFIER | c.957+81G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113380923 | |||||||
| chr12:113380990 | T | C | 37 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(34): Show |
46 | HG01168.hp2 HG01243.hp1 HG01496.hp2 others(43): Show |
intron_variant | MODIFIER | c.957+148T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113380990 | |||||||
| chr12:113381062 | C | T | 4 | a0001c0001t0013g0188 a0001c0001t0027g0168 a0001c0001t0034g0128 others(1): Show |
4 | HG01243.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+220C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381062 | |||||||
| chr12:113381087 | C | G | 1 | a0002c0002t0001g0102 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.957+245C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381087 | |||||||
| chr12:113381109 | T | C | 1 | a0002c0002t0009g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.957+267T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381109 | |||||||
| chr12:113381110 | C | T | 1 | a0002c0002t0009g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.957+268C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381110 | |||||||
| chr12:113381264 | C | T | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.957+422C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381264 | |||||||
| chr12:113381636 | G | A | 19 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(16): Show |
28 | HG01168.hp2 HG01496.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.957+794G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381636 | |||||||
| chr12:113381744 | T | TTTTGTGC others(30): Show |
1 | a0001c0001t0001g0097 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.957+905_957+941dup others(37): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113381744 | ||||||
| chr12:113381925 | C | T | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+1083C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113381925 | |||||||
| chr12:113382180 | A | T | 19 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(16): Show |
28 | HG01168.hp2 HG01496.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.957+1338A>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382180 | |||||||
| chr12:113382239 | T | C | 19 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(16): Show |
28 | HG01168.hp2 HG01496.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.957+1397T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382239 | |||||||
| chr12:113382307 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.957+1465A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382307 | |||||||
| chr12:113382383 | C | T | 1 | a0002c0002t0001g0082 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.957+1541C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382383 | |||||||
| chr12:113382403 | G | A | 3 | a0001c0001t0014g0190 a0001c0001t0014g0191 a0001c0001t0017g0187 |
3 | HG02559.hp2 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.957+1561G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382403 | |||||||
| chr12:113382447 | A | AT | 6 | a0001c0001t0014g0190 a0001c0001t0014g0191 a0001c0001t0017g0187 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+1616dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382447 | ||||||
| chr12:113382490 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.958-1615C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382490 | |||||||
| chr12:113382664 | A | T | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.958-1441A>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382664 | |||||||
| chr12:113382755 | A | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0008g0004 others(2): Show |
8 | HG02145.hp2 HG02257.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-1350A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382755 | |||||||
| chr12:113382816 | T | G | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.958-1289T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382816 | |||||||
| chr12:113382833 | TTTTGTGT others(5): Show |
T | 1 | a0001c0014t0029g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.958-1270_958-1259d others(14): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382833 | ||||||
| chr12:113382835 | T | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG01433.hp2 NA18612.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-1270T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382835 | |||||||
| chr12:113382835 | T | TTG | 46 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
52 | HG00423.hp1 HG00423.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.958-1238_958-1237d others(4): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTGTG | 13 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0062 others(10): Show |
14 | HG00544.hp2 HG00673.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.958-1240_958-1237d others(6): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTGTG others(4): Show |
1 | a0001c0004t0018g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.958-1269_958-1268i others(13): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTTGT others(3): Show |
1 | a0001c0001t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.958-1269_958-1268i others(12): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTTGT others(9): Show |
1 | a0001c0013t0001g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.958-1269_958-1268i others(18): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTTTT others(3): Show |
1 | a0001c0001t0012g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.958-1269_958-1268i others(12): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTTTT others(7): Show |
2 | a0001c0001t0014g0190 a0001c0001t0017g0187 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.958-1269_958-1268i others(16): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTTTT others(4): Show |
1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.958-1269_958-1268i others(13): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | T | TTTTTTTT others(13): Show |
1 | a0001c0001t0014g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.958-1269_958-1268i others(22): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | TTG | T | 4 | a0001c0001t0003g0176 a0001c0001t0016g0002 a0001c0001t0016g0175 others(1): Show |
4 | NA19009.hp2 NA19011.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-1238_958-1237d others(4): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382835 | TTGTG | T | 6 | a0003c0003t0001g0005 a0003c0003t0001g0109 a0003c0003t0007g0026 others(3): Show |
8 | HG00099.hp2 HG01358.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-1240_958-1237d others(6): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382835 | ||||||
| chr12:113382837 | G | T | 21 | a0001c0001t0001g0046 a0001c0001t0002g0025 a0001c0001t0003g0002 others(18): Show |
30 | HG01168.hp2 HG01496.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.958-1268G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382837 | |||||||
| chr12:113382839 | G | T | 23 | a0001c0001t0001g0046 a0001c0001t0002g0025 a0001c0001t0003g0002 others(20): Show |
29 | HG01496.hp2 HG02015.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.958-1266G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382839 | |||||||
| chr12:113382841 | G | T | 3 | a0001c0001t0003g0176 a0001c0001t0016g0002 a0001c0001t0016g0175 |
3 | NA19009.hp2 NA19011.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.958-1264G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382841 | |||||||
| chr12:113382854 | TGTGTGTG others(6): Show |
T | 1 | a0001c0001t0001g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.958-1250_958-1238d others(15): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382854 | |||||||
| chr12:113382855 | GTGTGTGT others(6): Show |
G | 3 | a0001c0001t0027g0168 a0001c0001t0034g0128 a0001c0006t0013g0186 |
3 | HG01243.hp1 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.958-1248_958-1236d others(15): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382855 | ||||||
| chr12:113382857 | GTGTGTGT others(4): Show |
G | 1 | a0001c0001t0013g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-1246_958-1236d others(13): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382857 | ||||||
| chr12:113382857 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0017g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.958-1246_958-1235d others(14): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382857 | ||||||
| chr12:113382865 | GTGT | G | 13 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0024 others(10): Show |
21 | HG01168.hp2 HG01496.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.958-1238_958-1236d others(5): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382865 | ||||||
| chr12:113382867 | G | GT | 3 | a0001c0001t0001g0020 a0002c0002t0001g0001 a0002c0002t0005g0061 |
5 | HG01346.hp1 HG02074.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-1215dupT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382867 | ||||||
| chr12:113382867 | G | GTGT | 4 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0112 others(1): Show |
5 | HG02572.hp2 NA18906.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-1237_958-1236i others(5): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382867 | ||||||
| chr12:113382867 | G | T | 1 | a0001c0001t0001g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-1238G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382867 | |||||||
| chr12:113382867 | GT | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0095 a0001c0001t0025g0139 others(3): Show |
7 | HG01099.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-1215delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113382867 | ||||||
| chr12:113382868 | T | TG | 11 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0048 others(8): Show |
11 | HG00280.hp1 HG00642.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.958-1237_958-1236i others(3): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382868 | |||||||
| chr12:113382868 | T | TGTG | 7 | a0001c0001t0001g0075 a0001c0001t0001g0132 a0001c0001t0002g0023 others(4): Show |
8 | HG00544.hp1 NA18747.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-1237_958-1236i others(5): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382868 | |||||||
| chr12:113382869 | T | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0057 others(24): Show |
29 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.958-1236T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382869 | |||||||
| chr12:113382870 | T | G | 10 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0075 others(7): Show |
10 | HG00642.hp1 HG01943.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.958-1235T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382870 | |||||||
| chr12:113382871 | T | G | 9 | a0001c0001t0012g0170 a0001c0001t0012g0171 a0001c0001t0024g0169 others(6): Show |
9 | HG01943.hp1 HG02055.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-1234T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382871 | |||||||
| chr12:113382872 | T | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0013t0001g0047 |
3 | HG00642.hp1 HG01943.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.958-1233T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382872 | |||||||
| chr12:113382873 | T | G | 8 | a0001c0001t0012g0170 a0001c0001t0024g0169 a0001c0004t0015g0159 others(5): Show |
8 | HG01943.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-1232T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382873 | |||||||
| chr12:113382874 | T | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0013t0001g0047 |
3 | HG00642.hp1 HG01943.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.958-1231T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382874 | |||||||
| chr12:113382875 | T | G | 8 | a0001c0001t0001g0046 a0001c0001t0024g0169 a0001c0004t0015g0159 others(5): Show |
8 | HG01943.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-1230T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382875 | |||||||
| chr12:113382877 | T | G | 2 | a0001c0004t0018g0146 a0001c0004t0018g0147 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.958-1228T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382877 | |||||||
| chr12:113382879 | T | G | 1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.958-1226T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382879 | |||||||
| chr12:113382881 | T | G | 1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.958-1224T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382881 | |||||||
| chr12:113382961 | T | C | 1 | a0001c0001t0013g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-1144T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382961 | |||||||
| chr12:113382996 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.958-1109G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113382996 | |||||||
| chr12:113383293 | C | T | 1 | a0002c0002t0001g0017 | 2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.958-812C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383293 | |||||||
| chr12:113383322 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.958-783G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383322 | |||||||
| chr12:113383424 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.958-681G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383424 | |||||||
| chr12:113383538 | C | G | 40 | a0001c0001t0002g0153 a0001c0001t0002g0155 a0001c0001t0003g0002 others(37): Show |
48 | HG00642.hp1 HG01168.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.958-567C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383538 | |||||||
| chr12:113383827 | T | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0053 others(8): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.958-278T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383827 | |||||||
| chr12:113383828 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.958-277G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383828 | |||||||
| chr12:113383846 | A | C | 20 | a0001c0001t0002g0155 a0001c0001t0003g0002 a0001c0001t0003g0024 others(17): Show |
28 | HG00642.hp1 HG01168.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.958-259A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383846 | |||||||
| chr12:113383931 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.958-174G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | chr12 | 113383931 | |||||||
| chr12:113383996 | C | CA | 9 | a0001c0001t0001g0072 a0001c0001t0001g0134 a0001c0001t0009g0031 others(6): Show |
9 | HG01168.hp1 HG01358.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-85dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113383996 | ||||||
| chr12:113383996 | CA | C | 15 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0003g0024 others(12): Show |
15 | HG01934.hp2 HG02155.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-85delA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113383996 | ||||||
| chr12:113383996 | CAAAAAAA others(4): Show |
C | 2 | a0001c0004t0015g0159 a0001c0004t0015g0166 |
2 | HG01943.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.958-95_958-85delAA others(9): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 113383996 | ||||||
| chr12:113384362 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1118+97G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/11 | chr12 | 113384362 | |||||||
| chr12:113384484 | A | G | 1 | a0002c0002t0001g0017 | 2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1118+219A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/11 | chr12 | 113384484 | |||||||
| chr12:113384598 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1119-253G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/11 | chr12 | 113384598 | |||||||
| chr12:113384620 | C | G | 1 | a0001c0004t0018g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1119-231C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/11 | chr12 | 113384620 | |||||||
| chr12:113384845 | C | T | 1 | a0001c0001t0028g0173 | 1 | NA20129.hp2 | splice_region_variant&intron_variant | LOW | c.1119-6C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 7/11 | chr12 | 113384845 | |||||||
| chr12:113384992 | C | T | 5 | a0001c0001t0014g0190 a0001c0001t0014g0191 a0001c0001t0027g0168 others(2): Show |
5 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214+46C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 8/11 | chr12 | 113384992 | |||||||
| chr12:113385207 | C | G | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | splice_region_variant&intron_variant | LOW | c.1215-5C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 8/11 | chr12 | 113385207 | |||||||
| chr12:113385291 | C | T | 1 | a0001c0001t0017g0187 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1286+8C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385291 | |||||||
| chr12:113385310 | G | A | 1 | a0001c0001t0022g0189 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1286+27G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385310 | |||||||
| chr12:113385412 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+129C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385412 | |||||||
| chr12:113385576 | G | A | 1 | a0004c0011t0001g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1286+293G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385576 | |||||||
| chr12:113385655 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1286+372C>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385655 | |||||||
| chr12:113385688 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1286+405C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385688 | |||||||
| chr12:113385750 | G | A | 4 | a0001c0004t0015g0159 a0001c0004t0015g0166 a0001c0004t0020g0160 others(1): Show |
4 | HG01943.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+467G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385750 | |||||||
| chr12:113385772 | A | G | 2 | a0001c0004t0018g0146 a0001c0004t0018g0147 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1286+489A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113385772 | |||||||
| chr12:113386073 | GCCTTTTG others(3): Show |
G | 1 | a0001c0001t0001g0015 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1286+793_1286+802d others(12): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386073 | ||||||
| chr12:113386074 | C | T | 2 | a0002c0002t0001g0020 a0002c0002t0001g0069 |
2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1286+791C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386074 | |||||||
| chr12:113386170 | TTTG | T | 7 | a0001c0001t0017g0187 a0001c0004t0015g0159 a0001c0004t0015g0166 others(4): Show |
7 | HG01943.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-749_1287-747d others(5): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386170 | ||||||
| chr12:113386228 | A | ACCCAGGC others(323): Show |
1 | a0001c0001t0001g0097 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1287-482_1287-481i others(332): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386228 | ||||||
| chr12:113386291 | CGATTCTT others(158): Show |
C | 13 | a0001c0001t0012g0170 a0001c0001t0012g0171 a0001c0001t0013g0188 others(10): Show |
13 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1287-565_1287-401d others(2): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386291 | ||||||
| chr12:113386354 | AT | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0117 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-566delT | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386354 | ||||||
| chr12:113386355 | TTTTTTTT others(157): Show |
T | 5 | a0001c0004t0015g0159 a0001c0004t0015g0166 a0001c0004t0018g0147 others(2): Show |
5 | HG01943.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-565_1287-402d others(2): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386355 | ||||||
| chr12:113386356 | TTTTTTTT others(156): Show |
T | 1 | a0001c0004t0018g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287-565_1287-403d others(2): Show |
PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 113386356 | ||||||
| chr12:113386377 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | NA18612.hp2 NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1287-560G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386377 | |||||||
| chr12:113386447 | G | A | 1 | a0001c0001t0002g0164 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1287-490G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386447 | |||||||
| chr12:113386531 | T | G | 2 | a0001c0001t0001g0138 a0001c0001t0031g0133 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1287-406T>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386531 | |||||||
| chr12:113386576 | A | G | 1 | a0001c0001t0021g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1287-361A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386576 | |||||||
| chr12:113386667 | C | A | 1 | a0006c0009t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1287-270C>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386667 | |||||||
| chr12:113386771 | G | A | 18 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0150 others(15): Show |
26 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1287-166G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 9/11 | chr12 | 113386771 | |||||||
| chr12:113387297 | G | A | 1 | a0002c0002t0006g0052 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1439+208G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387297 | |||||||
| chr12:113387374 | C | T | 9 | a0001c0001t0013g0188 a0001c0001t0014g0190 a0001c0001t0014g0191 others(6): Show |
9 | HG01243.hp1 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1439+285C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387374 | |||||||
| chr12:113387464 | A | C | 19 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0150 others(16): Show |
27 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1440-280A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387464 | |||||||
| chr12:113387506 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1440-238A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387506 | |||||||
| chr12:113387587 | C | T | 19 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0150 others(16): Show |
27 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1440-157C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387587 | |||||||
| chr12:113387607 | G | T | 7 | a0001c0001t0013g0188 a0001c0001t0014g0190 a0001c0001t0014g0191 others(4): Show |
7 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440-137G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387607 | |||||||
| chr12:113387624 | G | T | 9 | a0001c0001t0013g0188 a0001c0001t0014g0190 a0001c0001t0014g0191 others(6): Show |
9 | HG01243.hp1 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1440-120G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387624 | |||||||
| chr12:113387634 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1440-110A>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387634 | |||||||
| chr12:113387690 | G | A | 1 | a0001c0001t0017g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1440-54G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 10/11 | chr12 | 113387690 | |||||||
| chr12:113387998 | C | T | 6 | a0001c0001t0013g0188 a0001c0001t0014g0190 a0001c0001t0014g0191 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+92C>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/11 | chr12 | 113387998 | |||||||
| chr12:113388017 | G | A | 3 | a0001c0001t0012g0170 a0001c0001t0012g0171 a0001c0001t0024g0169 |
3 | HG02683.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1602+111G>A | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/11 | chr12 | 113388017 | |||||||
| chr12:113388198 | T | C | 29 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0150 others(26): Show |
37 | HG01168.hp2 HG01361.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.1603-261T>C | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/11 | chr12 | 113388198 | |||||||
| chr12:113388199 | A | G | 7 | a0001c0001t0017g0148 a0001c0001t0017g0187 a0001c0004t0015g0159 others(4): Show |
7 | HG01943.hp1 HG02647.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-260A>G | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/11 | chr12 | 113388199 | |||||||
| chr12:113388213 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1603-246G>T | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/11 | chr12 | 113388213 | |||||||
| chr12:113388336 | C | CA | 15 | a0001c0001t0002g0163 a0001c0001t0003g0183 a0001c0001t0012g0170 others(12): Show |
15 | HG01243.hp1 HG02055.hp1 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.1603-110dupA | PLBD2 | ENSG00000151176.8 | transcript | ENST00000280800.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 113388336 |