Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 59339 |
| ensemblid | ENSG00000169499.15 |
| hgncid | 14336 |
| symbol | PLEKHA2 |
| name | pleckstrin homology domain containing A2 |
| refseq_nuc | NM_021623.2 |
| refseq_prot | NP_067636.1 |
| ensembl_nuc | ENST00000617275.5 |
| ensembl_prot | ENSP00000482228.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 38901346 |
| end | 38973912 |
| strand | + |
| ver | v1.2 |
| region | chr8:38901346-38973912 |
| region5000 | chr8:38896346-38978912 |
| regionname0 | PLEKHA2_chr8_38901346_38973912 |
| regionname5000 | PLEKHA2_chr8_38896346_38978912 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 425 | 368 | 88 | 69 | 154 | 16 | 39 | 116 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | MPYVD others(420): Show |
chr8 | 38896346 | 38978912 |
| a0002 | 0/0 | 425 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | MPYVD others(420): Show |
chr8 | 38896346 | 38978912 |
| a0003 | 0/0 | 425 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | MPYVD others(420): Show |
chr8 | 38896346 | 38978912 |
| a0004 | 0/0 | 425 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | MPYVD others(420): Show |
chr8 | 38896346 | 38978912 |
| a0005 | 0/0 | 425 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | MPYVD others(420): Show |
chr8 | 38896346 | 38978912 |
| a0006 | 0/0 | 425 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | MPYVD others(420): Show |
chr8 | 38896346 | 38978912 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1275 | 365 | 87 | 68 | 153 | 16 | 39 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0001c0003 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0001c0007 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0001c0008 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0002c0002 | 0/0 | 1275 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0003c0005 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0004c0006 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0005c0004 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 | ||
| a0006c0009 | 0/0 | 1275 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | ATGCC others(1270): Show |
chr8 | 38896346 | 38978912 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5536 | 120 | 7 | 31 | 64 | 6 | 12 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0002 | 0/0 | 5531 | 65 | 11 | 13 | 29 | 6 | 6 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0003 | 0/1 | 5531 | 36 | 5 | 9 | 8 | 2 | 11 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0004 | 0/0 | 5532 | 15 | 0 | 1 | 13 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0005 | 0/0 | 5538 | 12 | 0 | 3 | 8 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5533): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0006 | 0/0 | 5530 | 9 | 0 | 3 | 6 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0007 | 0/0 | 5535 | 9 | 8 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5530): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0008 | 0/0 | 5534 | 6 | 1 | 1 | 4 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5529): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0009 | 0/0 | 5539 | 7 | 7 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5534): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0010 | 0/0 | 5536 | 6 | 0 | 0 | 6 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0011 | 1/0 | 5530 | 6 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0012 | 0/0 | 5530 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0013 | 0/0 | 5530 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0014 | 0/0 | 5530 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0015 | 0/0 | 5533 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5528): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0016 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5534): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0017 | 0/0 | 5529 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5524): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0018 | 0/0 | 5540 | 3 | 1 | 0 | 2 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5535): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0019 | 0/0 | 5518 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5513): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0020 | 0/0 | 5519 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5514): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0021 | 0/0 | 5530 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0022 | 0/0 | 5533 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5528): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0023 | 0/0 | 5538 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5533): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0024 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5532): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0025 | 0/0 | 5539 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5534): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0026 | 0/0 | 5541 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5536): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0027 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5524): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0028 | 0/0 | 5534 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5529): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0029 | 0/0 | 5537 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5532): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0030 | 0/0 | 5530 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0032 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0033 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0034 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0035 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0036 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0037 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0038 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0039 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5528): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0040 | 0/0 | 5536 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0041 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0042 | 0/0 | 5535 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5530): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0043 | 0/0 | 5536 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0044 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0045 | 0/0 | 5535 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5530): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0046 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5530): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0047 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5530): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0048 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5532): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0049 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0050 | 0/0 | 5518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5513): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0052 | 0/0 | 5531 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0053 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0054 | 0/0 | 5535 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5530): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0055 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0056 | 0/0 | 5531 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0001t0057 | 0/0 | 5531 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0001c0003t0001 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0001c0007t0016 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5534): Show |
chr8 | 38896346 | 38978912 |
| a0001c0008t0017 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5524): Show |
chr8 | 38896346 | 38978912 |
| a0002c0002t0001 | 0/0 | 5536 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0002c0002t0004 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5527): Show |
chr8 | 38896346 | 38978912 |
| a0002c0002t0031 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0002c0002t0051 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5525): Show |
chr8 | 38896346 | 38978912 |
| a0003c0005t0002 | 0/0 | 5531 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5526): Show |
chr8 | 38896346 | 38978912 |
| a0004c0006t0001 | 0/0 | 5536 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5531): Show |
chr8 | 38896346 | 38978912 |
| a0005c0004t0005 | 0/0 | 5538 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5533): Show |
chr8 | 38896346 | 38978912 |
| a0006c0009t0008 | 0/0 | 5534 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | AGACC others(5529): Show |
chr8 | 38896346 | 38978912 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0007g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0008g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0010g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0010g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0010g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0010g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0011g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0012g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0013g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0014g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0014g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0015g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0015g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0015g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0015g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0016g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0017g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0017g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0018g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0018g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0018g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0019g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0020g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0021g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0021g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0022g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0022g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0023g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0023g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0024g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0024g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0025g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0025g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0026g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0026g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0027g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0027g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0028g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0028g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0029g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0029g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0030g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0032g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0033g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0034g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0035g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0036g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0037g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0038g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0039g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0040g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0041g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0042g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0043g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0044g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0045g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0046g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0047g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0048g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0049g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0050g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0052g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0053g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0054g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0055g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0056g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0001t0057g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0007t0016g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0001c0008t0017g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0002c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0002c0002t0031g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0002c0002t0051g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0003c0005t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0004c0006t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0005c0004t0005g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| a0006c0009t0008g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0104 | EUR | GBR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00280 | hp2 | a0001 | c0001 | t0022 | g0185 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0060 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0341 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00609 | hp2 | a0001 | c0001 | t0010 | g0314 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00621 | hp2 | a0001 | c0001 | t0015 | g0239 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00673 | hp1 | a0001 | c0001 | t0052 | g0269 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00733 | hp1 | a0001 | c0001 | t0017 | g0223 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0300 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00735 | hp1 | a0001 | c0001 | t0056 | g0187 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01070 | hp1 | a0001 | c0001 | t0023 | g0356 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01071 | hp2 | a0001 | c0001 | t0023 | g0357 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0353 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01099 | hp2 | a0003 | c0005 | t0002 | g0332 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01168 | hp2 | a0005 | c0004 | t0005 | g0351 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01192 | hp1 | a0001 | c0001 | t0029 | g0004 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0186 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01255 | hp1 | a0001 | c0001 | t0053 | g0006 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0363 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0335 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0362 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0369 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01515 | hp1 | a0001 | c0001 | t0042 | g0241 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0144 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0150 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0303 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0291 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0346 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0331 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01993 | hp1 | a0001 | c0008 | t0017 | g0371 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02027 | hp1 | a0001 | c0001 | t0015 | g0179 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0108 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02055 | hp2 | a0001 | c0001 | t0020 | g0009 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02083 | hp2 | a0001 | c0001 | t0057 | g0189 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02132 | hp1 | a0001 | c0001 | t0010 | g0307 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02132 | hp2 | a0001 | c0001 | t0015 | g0322 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02135 | hp1 | a0001 | c0001 | t0046 | g0197 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0319 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02145 | hp2 | a0001 | c0001 | t0029 | g0160 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0079 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0091 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02258 | hp1 | a0001 | c0001 | t0025 | g0072 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02258 | hp2 | a0001 | c0001 | t0035 | g0212 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0337 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0208 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0092 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0148 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0224 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02647 | hp1 | a0001 | c0001 | t0027 | g0152 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02647 | hp2 | a0001 | c0001 | t0037 | g0180 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02683 | hp1 | a0001 | c0001 | t0040 | g0265 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02717 | hp1 | a0001 | c0001 | t0024 | g0083 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02723 | hp1 | a0001 | c0001 | t0020 | g0073 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02723 | hp2 | a0002 | c0002 | t0031 | g0034 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02738 | hp1 | a0001 | c0001 | t0036 | g0306 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02738 | hp2 | a0006 | c0009 | t0008 | g0174 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02809 | hp1 | a0001 | c0001 | t0033 | g0170 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0075 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02818 | hp2 | a0001 | c0001 | t0050 | g0166 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02886 | hp1 | a0001 | c0001 | t0028 | g0154 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0086 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02895 | hp1 | a0002 | c0002 | t0051 | g0078 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02895 | hp2 | a0001 | c0001 | t0026 | g0084 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02896 | hp2 | a0001 | c0001 | t0018 | g0243 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02897 | hp1 | a0001 | c0001 | t0026 | g0082 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0249 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03041 | hp1 | a0001 | c0001 | t0027 | g0163 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0211 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0248 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03130 | hp1 | a0001 | c0007 | t0016 | g0156 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0155 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0213 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0010 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0093 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03239 | hp1 | a0001 | c0001 | t0038 | g0234 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0146 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03453 | hp2 | a0001 | c0001 | t0054 | g0158 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0193 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0145 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03491 | hp2 | a0001 | c0001 | t0021 | g0215 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0071 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03516 | hp2 | a0001 | c0001 | t0016 | g0005 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03579 | hp1 | a0001 | c0001 | t0028 | g0153 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0070 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0292 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03688 | hp1 | a0001 | c0001 | t0030 | g0037 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03688 | hp2 | a0001 | c0001 | t0039 | g0273 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0320 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0064 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03710 | hp2 | a0001 | c0001 | t0017 | g0061 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0354 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04204 | hp1 | a0001 | c0001 | t0043 | g0059 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0090 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0142 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0195 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18906 | hp1 | a0001 | c0001 | t0034 | g0210 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18944 | hp1 | a0001 | c0001 | t0018 | g0373 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0333 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18948 | hp2 | a0001 | c0001 | t0021 | g0277 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18949 | hp1 | a0001 | c0001 | t0008 | g0287 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0358 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18953 | hp1 | a0001 | c0001 | t0047 | g0182 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18957 | hp2 | a0001 | c0001 | t0010 | g0259 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18964 | hp1 | a0001 | c0001 | t0041 | g0304 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18964 | hp2 | a0001 | c0001 | t0015 | g0286 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0367 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18985 | hp2 | a0001 | c0001 | t0048 | g0366 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0348 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0278 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0247 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0260 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19075 | hp1 | a0001 | c0001 | t0007 | g0299 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19085 | hp2 | a0001 | c0001 | t0044 | g0289 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19088 | hp2 | a0001 | c0001 | t0018 | g0130 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA19240 | hp2 | a0001 | c0001 | t0032 | g0094 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20129 | hp1 | a0001 | c0001 | t0055 | g0190 | AFR | ASW | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20129 | hp2 | a0001 | c0001 | t0049 | g0143 | AFR | ASW | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | GIH | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | GIH | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG01123 | hp2 | a0004 | c0006 | t0001 | g0044 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0162 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG02559 | hp2 | a0001 | c0001 | t0045 | g0301 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0151 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0165 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0298 | REF | REF | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0164 | REF | REF | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38901443 | G | GT | 1 | a0001 | 3 | HG00735.hp1 HG02083.hp2 NA20129.hp1 |
splice_region_variant | LOW | c.-26_-25insT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/12 | chr8 | 38901443 | |||||||
| chr8:38936025 | C | T | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.173C>T | p.Ala58Val | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/12 | 296/5530 | 173/1278 | 58/425 | chr8 | 38936025 | |||
| chr8:38952236 | T | A | 1 | a0002 | 4 | HG02723.hp2 HG02895.hp1 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.557T>A | p.Ile186Asn | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/12 | 680/5530 | 557/1278 | 186/425 | chr8 | 38952236 | |||
| chr8:38952651 | C | T | 1 | a0004 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.649C>T | p.Arg217Cys | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/12 | 772/5530 | 649/1278 | 217/425 | chr8 | 38952651 | |||
| chr8:38957365 | C | A | 1 | a0005 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.816C>A | p.Ser272Arg | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/12 | 939/5530 | 816/1278 | 272/425 | chr8 | 38957365 | |||
| chr8:38969650 | G | A | 1 | a0003 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1145G>A | p.Arg382His | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1268/5530 | 1145/1278 | 382/425 | chr8 | 38969650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38950918 | G | T | 1 | a0001c0008 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.414G>T | p.Leu138Leu | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/12 | 537/5530 | 414/1278 | 138/425 | chr8 | 38950918 | |||
| chr8:38950981 | C | G | 1 | a0001c0007 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.477C>G | p.Pro159Pro | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/12 | 600/5530 | 477/1278 | 159/425 | chr8 | 38950981 | |||
| chr8:38952174 | G | A | 1 | a0001c0003 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.495G>A | p.Gly165Gly | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/12 | 618/5530 | 495/1278 | 165/425 | chr8 | 38952174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38969826 | G | C | 1 | a0001c0001t0010 | 6 | HG00609.hp2 HG02132.hp1 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 43 | chr8 | 38969826 | ||||||
| chr8:38969834 | G | A | 1 | a0001c0001t0049 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 51 | chr8 | 38969834 | ||||||
| chr8:38969941 | C | CTG | 7 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0022 others(4): Show |
16 | HG00280.hp2 HG00621.hp2 HG01243.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*194_*195dupGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38969941 | C | CTGTG | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(13): Show |
149 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*192_*195dupGTGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38969941 | C | CTGTGTG | 6 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0024 others(3): Show |
20 | HG00423.hp1 HG00733.hp2 HG01070.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*190_*195dupGTGTGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38969941 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0018 others(2): Show |
16 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*195dupGTGTGT others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38969941 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0026 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186_*195dupGTGTGT others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38969941 | CTG | C | 6 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0017 others(3): Show |
15 | HG00733.hp1 HG01993.hp1 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*194_*195delGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 194 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38969941 | CTGTGTGT others(5): Show |
C | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0050 |
5 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*184_*195delGTGTGT others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 184 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | |||||
| chr8:38970407 | A | T | 4 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0025 others(1): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*624A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 624 | chr8 | 38970407 | ||||||
| chr8:38970466 | T | A | 2 | a0002c0002t0031 a0002c0002t0051 |
2 | HG02723.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 683 | chr8 | 38970466 | ||||||
| chr8:38970570 | G | T | 1 | a0001c0001t0014 | 4 | HG02451.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*787G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 787 | chr8 | 38970570 | ||||||
| chr8:38970595 | G | A | 1 | a0001c0001t0040 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 812 | chr8 | 38970595 | ||||||
| chr8:38970615 | G | A | 2 | a0001c0001t0032 a0001c0001t0049 |
2 | NA19240.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*832G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 832 | chr8 | 38970615 | ||||||
| chr8:38970742 | G | C | 1 | a0001c0001t0055 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 959 | chr8 | 38970742 | ||||||
| chr8:38970842 | G | A | 1 | a0001c0001t0041 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1059 | chr8 | 38970842 | ||||||
| chr8:38971331 | G | A | 1 | a0001c0001t0023 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1548G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1548 | chr8 | 38971331 | ||||||
| chr8:38971390 | C | T | 1 | a0001c0001t0037 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1607 | chr8 | 38971390 | ||||||
| chr8:38971737 | C | T | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0050 |
5 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1954C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1954 | chr8 | 38971737 | ||||||
| chr8:38971759 | C | T | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0050 |
5 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1976 | chr8 | 38971759 | ||||||
| chr8:38971844 | G | A | 1 | a0001c0001t0033 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2061G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2061 | chr8 | 38971844 | ||||||
| chr8:38971850 | G | C | 1 | a0001c0001t0037 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2067G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2067 | chr8 | 38971850 | ||||||
| chr8:38971878 | C | T | 1 | a0001c0001t0036 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2095 | chr8 | 38971878 | ||||||
| chr8:38971879 | G | A | 1 | a0001c0001t0054 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2096 | chr8 | 38971879 | ||||||
| chr8:38971946 | C | CA | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(23): Show |
194 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2173dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2174 | INFO_REALIGN_3_PRIME | chr8 | 38971946 | |||||
| chr8:38972183 | A | AT | 6 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0027 others(3): Show |
14 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2412dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2413 | INFO_REALIGN_3_PRIME | chr8 | 38972183 | |||||
| chr8:38972183 | AT | A | 4 | a0001c0001t0019 a0001c0001t0021 a0001c0001t0038 others(1): Show |
6 | HG01515.hp1 HG03239.hp1 HG03491.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2412delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2412 | INFO_REALIGN_3_PRIME | chr8 | 38972183 | |||||
| chr8:38972349 | G | T | 2 | a0001c0001t0028 a0001c0001t0034 |
3 | HG02886.hp1 HG03579.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2566G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2566 | chr8 | 38972349 | ||||||
| chr8:38972422 | T | C | 1 | a0001c0001t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2639 | chr8 | 38972422 | ||||||
| chr8:38972486 | GA | G | 1 | a0001c0001t0006 | 9 | HG01928.hp2 HG01981.hp1 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2705delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2705 | INFO_REALIGN_3_PRIME | chr8 | 38972486 | |||||
| chr8:38972530 | A | G | 27 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(24): Show |
195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2747A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2747 | chr8 | 38972530 | ||||||
| chr8:38972531 | A | G | 27 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(24): Show |
195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2748A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2748 | chr8 | 38972531 | ||||||
| chr8:38972565 | T | C | 1 | a0001c0001t0043 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2782T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2782 | chr8 | 38972565 | ||||||
| chr8:38972772 | T | G | 2 | a0001c0001t0039 a0001c0001t0049 |
2 | HG03688.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2989T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2989 | chr8 | 38972772 | ||||||
| chr8:38972814 | T | G | 1 | a0001c0001t0025 | 2 | HG02258.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3031T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3031 | chr8 | 38972814 | ||||||
| chr8:38972887 | A | T | 1 | a0001c0001t0044 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3104A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3104 | chr8 | 38972887 | ||||||
| chr8:38973540 | A | G | 47 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(44): Show |
266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3757A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3757 | chr8 | 38973540 | ||||||
| chr8:38973615 | T | C | 4 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0025 others(1): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3832T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3832 | chr8 | 38973615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38901439 | C | CG | 333 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(330): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
splice_donor_variant&intron_variant | HIGH | c.-24+1dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38901439 | ||||||
| chr8:38901499 | GGGGGCTG others(17): Show |
G | 1 | a0001c0001t0018g0373 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-24+59_-24+82delCT others(22): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38901499 | ||||||
| chr8:38901524 | G | A | 3 | a0001c0001t0016g0005 a0001c0001t0029g0004 a0001c0001t0053g0006 |
3 | HG01192.hp1 HG01255.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+79G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901524 | |||||||
| chr8:38901710 | C | T | 72 | a0001c0001t0001g0302 a0001c0001t0001g0310 a0001c0001t0001g0311 others(69): Show |
73 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-24+265C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901710 | |||||||
| chr8:38901730 | C | CG | 9 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0002g0008 others(6): Show |
10 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+291dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38901730 | ||||||
| chr8:38901745 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0176 a0001c0001t0001g0177 others(203): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.-24+300C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901745 | |||||||
| chr8:38901890 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-24+445C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901890 | |||||||
| chr8:38901951 | C | T | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-24+506C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901951 | |||||||
| chr8:38902074 | G | C | 55 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(52): Show |
55 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-24+629G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902074 | |||||||
| chr8:38902092 | C | A | 72 | a0001c0001t0001g0302 a0001c0001t0001g0310 a0001c0001t0001g0311 others(69): Show |
73 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-24+647C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902092 | |||||||
| chr8:38902130 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18982.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-24+685C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902130 | |||||||
| chr8:38902145 | C | T | 1 | a0001c0001t0005g0300 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24+700C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902145 | |||||||
| chr8:38902203 | A | C | 1 | a0001c0001t0007g0299 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-24+758A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902203 | |||||||
| chr8:38902216 | GGT | G | 16 | a0001c0001t0002g0085 a0001c0001t0002g0087 a0001c0001t0002g0192 others(13): Show |
16 | HG02257.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24+775_-24+776del others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902216 | ||||||
| chr8:38902218 | T | TG | 49 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0041 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.-24+774dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | ||||||
| chr8:38902218 | T | TGG | 33 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(30): Show |
33 | HG00280.hp1 HG00639.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-24+774_-24+775ins others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | ||||||
| chr8:38902218 | T | TGGG | 24 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0038 others(21): Show |
24 | HG01358.hp1 HG01516.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24+774_-24+775ins others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | ||||||
| chr8:38902218 | T | TGGGG | 11 | a0001c0001t0001g0107 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG00423.hp2 HG03540.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+774_-24+775ins others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | ||||||
| chr8:38902219 | GT | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(44): Show |
48 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-24+775delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902219 | |||||||
| chr8:38902220 | T | G | 218 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-24+775T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902220 | |||||||
| chr8:38902221 | G | C | 4 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0010g0195 others(1): Show |
4 | HG02135.hp1 NA18612.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+776G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902221 | |||||||
| chr8:38902222 | G | C | 28 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0217 others(25): Show |
28 | HG00733.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-24+777G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902222 | |||||||
| chr8:38902233 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0008g0225 a0001c0001t0032g0094 |
3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+788T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902233 | |||||||
| chr8:38902387 | G | A | 47 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0100 others(44): Show |
47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-24+942G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902387 | |||||||
| chr8:38902406 | A | G | 1 | a0001c0001t0001g0372 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-24+961A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902406 | |||||||
| chr8:38902501 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-24+1056G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902501 | |||||||
| chr8:38902507 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-24+1062G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902507 | |||||||
| chr8:38902516 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0002g0191 a0001c0001t0012g0224 others(1): Show |
4 | HG00733.hp1 HG02630.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+1071C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902516 | |||||||
| chr8:38902529 | A | G | 61 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(58): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-24+1084A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902529 | |||||||
| chr8:38902614 | C | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(219): Show |
224 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.-24+1169C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902614 | |||||||
| chr8:38902731 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0003g0296 |
2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-24+1286A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902731 | |||||||
| chr8:38902933 | C | T | 3 | a0001c0001t0001g0293 a0001c0001t0001g0295 a0001c0001t0004g0294 |
3 | HG02015.hp2 HG02083.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-24+1488C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902933 | |||||||
| chr8:38903076 | A | G | 25 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0181 others(22): Show |
25 | HG00280.hp2 HG00735.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-24+1631A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903076 | |||||||
| chr8:38903216 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-24+1771A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903216 | |||||||
| chr8:38903494 | G | A | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0002g0175 others(5): Show |
8 | HG01123.hp1 HG01168.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2049G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903494 | |||||||
| chr8:38903577 | A | G | 1 | a0001c0001t0003g0292 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-24+2132A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903577 | |||||||
| chr8:38903617 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0008g0225 a0001c0001t0032g0094 |
3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+2172A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903617 | |||||||
| chr8:38903665 | C | G | 49 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0138 others(46): Show |
49 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-24+2220C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903665 | |||||||
| chr8:38903708 | G | A | 3 | a0001c0001t0016g0005 a0001c0001t0029g0004 a0001c0001t0053g0006 |
3 | HG01192.hp1 HG01255.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+2263G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903708 | |||||||
| chr8:38904098 | G | C | 11 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0146 others(8): Show |
11 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+2653G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904098 | |||||||
| chr8:38904133 | C | T | 1 | a0001c0001t0011g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+2688C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904133 | |||||||
| chr8:38904287 | G | T | 144 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0176 others(141): Show |
145 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.-24+2842G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904287 | |||||||
| chr8:38904323 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-24+2878G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904323 | |||||||
| chr8:38904334 | G | T | 100 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-24+2889G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904334 | |||||||
| chr8:38904425 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-24+2980T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904425 | |||||||
| chr8:38904538 | A | G | 100 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-24+3093A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904538 | |||||||
| chr8:38904671 | T | C | 47 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0107 others(44): Show |
47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-24+3226T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904671 | |||||||
| chr8:38904728 | G | A | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-24+3283G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904728 | |||||||
| chr8:38904791 | C | G | 2 | a0001c0001t0049g0143 a0001c0001t0050g0166 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+3346C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904791 | |||||||
| chr8:38904837 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-24+3392A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904837 | |||||||
| chr8:38904966 | T | C | 1 | a0001c0001t0005g0015 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-24+3521T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904966 | |||||||
| chr8:38905017 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-24+3572C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905017 | |||||||
| chr8:38905228 | G | T | 1 | a0001c0001t0002g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-24+3783G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905228 | |||||||
| chr8:38905352 | G | A | 2 | a0001c0001t0002g0229 a0001c0001t0009g0228 |
2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-24+3907G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905352 | |||||||
| chr8:38905412 | C | T | 1 | a0001c0001t0002g0370 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-24+3967C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905412 | |||||||
| chr8:38905458 | TA | T | 283 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(280): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-24+4025delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38905458 | ||||||
| chr8:38905599 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-24+4154G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905599 | |||||||
| chr8:38905661 | G | C | 1 | a0001c0001t0036g0306 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-24+4216G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905661 | |||||||
| chr8:38905685 | C | CT | 239 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-24+4257dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38905685 | ||||||
| chr8:38905685 | C | CTT | 9 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0368 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-24+4256_-24+4257d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38905685 | ||||||
| chr8:38905715 | C | T | 1 | a0001c0001t0012g0224 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-24+4270C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905715 | |||||||
| chr8:38905729 | T | G | 288 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-24+4284T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905729 | |||||||
| chr8:38905753 | C | T | 3 | a0001c0001t0016g0005 a0001c0001t0029g0004 a0001c0001t0053g0006 |
3 | HG01192.hp1 HG01255.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+4308C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905753 | |||||||
| chr8:38905789 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-24+4344A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905789 | |||||||
| chr8:38905802 | A | G | 1 | a0001c0001t0017g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-24+4357A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905802 | |||||||
| chr8:38905882 | C | T | 9 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0365 others(6): Show |
9 | HG01257.hp1 HG01258.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24+4437C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905882 | |||||||
| chr8:38906089 | G | A | 53 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
53 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-24+4644G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906089 | |||||||
| chr8:38906150 | G | T | 11 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0146 others(8): Show |
11 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+4705G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906150 | |||||||
| chr8:38906198 | C | T | 143 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0176 others(140): Show |
144 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.-24+4753C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906198 | |||||||
| chr8:38906207 | A | C | 1 | a0001c0001t0008g0287 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-24+4762A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906207 | |||||||
| chr8:38906261 | T | C | 46 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0107 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.-24+4816T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906261 | |||||||
| chr8:38906465 | C | A | 3 | a0001c0001t0001g0095 a0001c0001t0008g0225 a0001c0001t0032g0094 |
3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+5020C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906465 | |||||||
| chr8:38906853 | G | A | 1 | a0001c0001t0011g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-24+5408G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906853 | |||||||
| chr8:38906857 | A | G | 1 | a0001c0001t0005g0300 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24+5412A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906857 | |||||||
| chr8:38906974 | C | G | 3 | a0001c0001t0012g0211 a0001c0001t0012g0213 a0001c0001t0035g0212 |
3 | HG02258.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-24+5529C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906974 | |||||||
| chr8:38907206 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0002g0175 a0001c0001t0003g0173 others(1): Show |
4 | HG01168.hp1 HG01256.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+5761A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907206 | |||||||
| chr8:38907211 | T | C | 1 | a0001c0001t0038g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-24+5766T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907211 | |||||||
| chr8:38907322 | ATTAT | A | 3 | a0001c0001t0001g0240 a0001c0001t0002g0242 a0001c0001t0042g0241 |
3 | HG00735.hp2 HG01069.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-24+5882_-24+5885d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907322 | ||||||
| chr8:38907424 | G | A | 26 | a0001c0001t0001g0018 a0001c0001t0001g0176 a0001c0001t0001g0177 others(23): Show |
26 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-24+5979G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907424 | |||||||
| chr8:38907608 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(23): Show |
27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-24+6163A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907608 | |||||||
| chr8:38907675 | C | A | 11 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0146 others(8): Show |
11 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+6230C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907675 | |||||||
| chr8:38907760 | C | CA | 241 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-24+6330dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907760 | ||||||
| chr8:38907760 | C | CAA | 113 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0099 others(110): Show |
114 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-24+6329_-24+6330d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907760 | ||||||
| chr8:38907780 | T | A | 8 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0146 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+6335T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907780 | |||||||
| chr8:38907796 | C | T | 6 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0013 others(3): Show |
7 | HG02055.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24+6351C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907796 | |||||||
| chr8:38907818 | T | TTATG | 143 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0095 others(140): Show |
144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-24+6417_-24+6420d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | ||||||
| chr8:38907818 | T | TTATGTAT others(1): Show |
4 | a0001c0001t0002g0136 a0001c0001t0002g0308 a0001c0001t0002g0309 others(1): Show |
4 | HG00673.hp2 HG03831.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+6413_-24+6420d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | ||||||
| chr8:38907818 | TTATG | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0235 a0001c0001t0001g0240 others(8): Show |
12 | HG00735.hp2 HG01069.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24+6417_-24+6420d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | ||||||
| chr8:38907818 | TTATGTAT others(1): Show |
T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0290 a0001c0001t0002g0022 others(2): Show |
5 | HG02056.hp1 HG02486.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+6413_-24+6420d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | ||||||
| chr8:38907818 | TTATGTAT others(5): Show |
T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0025 others(43): Show |
46 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-24+6409_-24+6420d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | ||||||
| chr8:38908114 | C | A | 6 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0013g0150 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+6669C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908114 | |||||||
| chr8:38908237 | C | A | 6 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG02027.hp1 HG02165.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+6792C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908237 | |||||||
| chr8:38908388 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0003g0023 |
2 | HG02486.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-24+6943G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908388 | |||||||
| chr8:38908556 | A | G | 48 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0206 others(45): Show |
48 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.-24+7111A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908556 | |||||||
| chr8:38908929 | T | G | 279 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(276): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-24+7484T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908929 | |||||||
| chr8:38909073 | G | A | 118 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0206 others(115): Show |
119 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.-24+7628G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909073 | |||||||
| chr8:38909142 | C | CA | 7 | a0001c0001t0001g0100 a0001c0001t0001g0250 a0001c0001t0001g0251 others(4): Show |
7 | NA18973.hp2 NA18985.hp1 NA19030.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+7711dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909142 | ||||||
| chr8:38909142 | CA | C | 78 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-24+7711delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909142 | ||||||
| chr8:38909335 | G | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(23): Show |
27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-24+7890G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909335 | |||||||
| chr8:38909393 | A | G | 1 | a0001c0001t0002g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-24+7948A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909393 | |||||||
| chr8:38909453 | C | T | 1 | a0001c0001t0005g0353 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-24+8008C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909453 | |||||||
| chr8:38909467 | A | AG | 280 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-24+8022_-24+8023i others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909467 | |||||||
| chr8:38909493 | G | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0133 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-24+8048G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909493 | |||||||
| chr8:38909532 | T | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0360 a0001c0001t0002g0098 others(2): Show |
5 | NA18951.hp1 NA18957.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+8087T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909532 | |||||||
| chr8:38909586 | T | C | 1 | a0001c0001t0037g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-24+8141T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909586 | |||||||
| chr8:38909925 | C | T | 4 | a0001c0001t0001g0343 a0001c0001t0002g0344 a0001c0001t0002g0369 others(1): Show |
4 | HG01361.hp2 HG01496.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-7982C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909925 | |||||||
| chr8:38909959 | C | CT | 121 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0099 others(118): Show |
122 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(119): Show |
intron_variant | MODIFIER | c.-23-7933dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909959 | ||||||
| chr8:38909959 | C | CTT | 6 | a0001c0001t0001g0339 a0001c0001t0001g0342 a0001c0001t0002g0340 others(3): Show |
6 | HG00423.hp1 HG02132.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-7934_-23-7933d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909959 | ||||||
| chr8:38910216 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0018g0130 |
2 | NA18982.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-23-7691C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910216 | |||||||
| chr8:38910266 | G | T | 284 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-23-7641G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910266 | |||||||
| chr8:38910561 | G | A | 4 | a0001c0001t0001g0343 a0001c0001t0002g0344 a0001c0001t0002g0369 others(1): Show |
4 | HG01361.hp2 HG01496.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-7346G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910561 | |||||||
| chr8:38910916 | G | A | 40 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0110 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-6991G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910916 | |||||||
| chr8:38911049 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23-6858G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911049 | |||||||
| chr8:38911170 | C | T | 1 | a0001c0001t0003g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-23-6737C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911170 | |||||||
| chr8:38911171 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-23-6736G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911171 | |||||||
| chr8:38911244 | C | CT | 220 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(217): Show |
222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-23-6653dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38911244 | ||||||
| chr8:38911298 | A | G | 223 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(220): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-23-6609A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911298 | |||||||
| chr8:38911636 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-23-6271G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911636 | |||||||
| chr8:38912038 | C | T | 1 | a0001c0001t0021g0277 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-23-5869C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912038 | |||||||
| chr8:38912475 | C | T | 1 | a0001c0001t0002g0338 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-23-5432C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912475 | |||||||
| chr8:38912534 | C | T | 1 | a0001c0001t0019g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-23-5373C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912534 | |||||||
| chr8:38912606 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-23-5301A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912606 | |||||||
| chr8:38912690 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-23-5217G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912690 | |||||||
| chr8:38913295 | C | T | 39 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0110 others(36): Show |
39 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.-23-4612C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913295 | |||||||
| chr8:38913370 | G | GA | 282 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-23-4521dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38913370 | ||||||
| chr8:38913370 | G | GAA | 6 | a0001c0001t0001g0025 a0001c0001t0001g0131 a0001c0001t0007g0077 others(3): Show |
6 | HG02129.hp2 HG02897.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-4522_-23-4521d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38913370 | ||||||
| chr8:38913379 | A | AG | 3 | a0001c0001t0003g0060 a0001c0001t0005g0064 a0001c0001t0043g0059 |
3 | HG00323.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-23-4528_-23-4527i others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913379 | |||||||
| chr8:38913396 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-23-4511A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913396 | |||||||
| chr8:38913469 | A | G | 290 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-23-4438A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913469 | |||||||
| chr8:38913497 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(23): Show |
27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-23-4410A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913497 | |||||||
| chr8:38913742 | TC | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0002g0055 others(5): Show |
8 | HG02015.hp1 HG02155.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23-4160delC | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38913742 | ||||||
| chr8:38913748 | G | A | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-23-4159G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913748 | |||||||
| chr8:38913890 | A | G | 290 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-23-4017A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913890 | |||||||
| chr8:38913968 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(23): Show |
27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-23-3939T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913968 | |||||||
| chr8:38913985 | G | T | 1 | a0001c0001t0003g0345 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-23-3922G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913985 | |||||||
| chr8:38914063 | G | A | 290 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-23-3844G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914063 | |||||||
| chr8:38914247 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-23-3660G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914247 | |||||||
| chr8:38914644 | A | C | 288 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-3263A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914644 | |||||||
| chr8:38914731 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0008g0225 a0001c0001t0032g0094 |
3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-23-3176T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914731 | |||||||
| chr8:38914883 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23-3024C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914883 | |||||||
| chr8:38914953 | A | C | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0003g0137 others(1): Show |
4 | HG00423.hp2 NA19005.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-2954A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914953 | |||||||
| chr8:38914957 | CTCT | C | 81 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0095 others(78): Show |
81 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-23-2943_-23-2941d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38914957 | ||||||
| chr8:38915038 | T | C | 288 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2869T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915038 | |||||||
| chr8:38915100 | G | A | 288 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2807G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915100 | |||||||
| chr8:38915168 | A | G | 7 | a0001c0001t0001g0226 a0001c0001t0002g0191 a0001c0001t0014g0247 others(4): Show |
7 | HG00733.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-2739A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915168 | |||||||
| chr8:38915183 | C | T | 51 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0206 others(48): Show |
51 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-23-2724C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915183 | |||||||
| chr8:38915202 | C | T | 288 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2705C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915202 | |||||||
| chr8:38915370 | G | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(22): Show |
26 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-2537G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915370 | |||||||
| chr8:38915462 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0074 others(22): Show |
26 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-2445C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915462 | |||||||
| chr8:38915695 | T | G | 1 | a0001c0001t0002g0244 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-23-2212T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915695 | |||||||
| chr8:38915709 | C | A | 59 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(56): Show |
59 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-23-2198C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915709 | |||||||
| chr8:38915711 | G | A | 6 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0146 others(3): Show |
6 | HG02257.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-2196G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915711 | |||||||
| chr8:38915746 | T | C | 288 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2161T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915746 | |||||||
| chr8:38915830 | T | G | 2 | a0001c0001t0001g0311 a0001c0001t0002g0312 |
2 | NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-23-2077T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915830 | |||||||
| chr8:38915873 | T | G | 56 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(53): Show |
56 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-23-2034T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915873 | |||||||
| chr8:38915922 | T | C | 5 | a0001c0001t0001g0107 a0001c0001t0002g0105 a0001c0001t0002g0106 others(2): Show |
5 | NA18941.hp1 NA18944.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-1985T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915922 | |||||||
| chr8:38915937 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0020g0073 a0002c0002t0004g0070 |
3 | HG02055.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-23-1970C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915937 | |||||||
| chr8:38916034 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-23-1873G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916034 | |||||||
| chr8:38916138 | G | A | 1 | a0001c0001t0037g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-23-1769G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916138 | |||||||
| chr8:38916255 | G | T | 5 | a0001c0001t0001g0107 a0001c0001t0002g0105 a0001c0001t0002g0106 others(2): Show |
5 | NA18941.hp1 NA18944.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-1652G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916255 | |||||||
| chr8:38916376 | T | C | 16 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0126 others(13): Show |
16 | HG00423.hp2 HG02040.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23-1531T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916376 | |||||||
| chr8:38916482 | A | G | 1 | a0001c0001t0006g0337 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-23-1425A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916482 | |||||||
| chr8:38916554 | C | T | 1 | a0001c0001t0050g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-23-1353C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916554 | |||||||
| chr8:38916841 | T | C | 295 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-23-1066T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916841 | |||||||
| chr8:38916934 | G | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02080.hp2 HG02129.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-973G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916934 | |||||||
| chr8:38917178 | C | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG00280.hp2 HG00639.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23-729C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917178 | |||||||
| chr8:38917178 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-23-729C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917178 | |||||||
| chr8:38917288 | C | T | 65 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(62): Show |
65 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23-619C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917288 | |||||||
| chr8:38917423 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23-484C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917423 | |||||||
| chr8:38917675 | A | G | 1 | a0001c0001t0001g0336 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23-232A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917675 | |||||||
| chr8:38918282 | C | T | 1 | a0001c0001t0016g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.141+212C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918282 | |||||||
| chr8:38918312 | C | G | 40 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0110 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.141+242C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918312 | |||||||
| chr8:38918474 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+404C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918474 | |||||||
| chr8:38918553 | C | CACACAAA others(190): Show |
1 | a0001c0001t0013g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918553 | C | CACACAAA others(190): Show |
1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918553 | C | CACACAAA others(179): Show |
2 | a0001c0001t0005g0346 a0001c0001t0028g0153 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+488_141+489ins others(186): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918553 | C | CACACAAA others(190): Show |
322 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(319): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918553 | C | CACACAAA others(190): Show |
1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918553 | C | CACACAAA others(190): Show |
40 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0110 others(37): Show |
40 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918553 | C | CACACAAA others(190): Show |
1 | a0001c0001t0017g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | ||||||
| chr8:38918556 | A | ACAAACAC others(190): Show |
3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0013g0150 |
3 | HG01891.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918556 | ||||||
| chr8:38918561 | T | C | 2 | a0001c0001t0005g0346 a0001c0001t0028g0153 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+491T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918561 | |||||||
| chr8:38918562 | T | C | 2 | a0001c0001t0005g0346 a0001c0001t0028g0153 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+492T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918562 | |||||||
| chr8:38918564 | T | G | 2 | a0001c0001t0005g0346 a0001c0001t0028g0153 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+494T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918564 | |||||||
| chr8:38918572 | C | T | 2 | a0001c0001t0005g0346 a0001c0001t0028g0153 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+502C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918572 | |||||||
| chr8:38918575 | G | A | 2 | a0001c0001t0005g0346 a0001c0001t0028g0153 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+505G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918575 | |||||||
| chr8:38918646 | A | G | 4 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(1): Show |
4 | NA18946.hp1 NA18946.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+576A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918646 | |||||||
| chr8:38918679 | C | A | 6 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG02027.hp1 HG02165.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+609C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918679 | |||||||
| chr8:38918681 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0008g0225 a0001c0001t0032g0094 |
3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.141+611C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918681 | |||||||
| chr8:38918685 | G | A | 8 | a0001c0001t0001g0206 a0001c0001t0001g0230 a0001c0001t0001g0231 others(5): Show |
8 | HG00733.hp2 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+615G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918685 | |||||||
| chr8:38918707 | G | A | 1 | a0001c0001t0053g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+637G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918707 | |||||||
| chr8:38918738 | G | A | 2 | a0001c0001t0019g0071 a0001c0001t0025g0072 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.141+668G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918738 | |||||||
| chr8:38918743 | C | T | 3 | a0001c0001t0012g0211 a0001c0001t0012g0213 a0001c0001t0035g0212 |
3 | HG02258.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.141+673C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918743 | |||||||
| chr8:38918744 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141+674G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918744 | |||||||
| chr8:38918746 | A | G | 1 | a0001c0001t0008g0287 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.141+676A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918746 | |||||||
| chr8:38918892 | T | C | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+822T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918892 | |||||||
| chr8:38918905 | C | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(289): Show |
294 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.141+835C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918905 | |||||||
| chr8:38918957 | C | T | 1 | a0001c0001t0001g0365 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.141+887C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918957 | |||||||
| chr8:38919090 | T | G | 1 | a0001c0001t0033g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+1020T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919090 | |||||||
| chr8:38919120 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.141+1050G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919120 | |||||||
| chr8:38919395 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(158): Show |
163 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.141+1325T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919395 | |||||||
| chr8:38919628 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(156): Show |
161 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.141+1558G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919628 | |||||||
| chr8:38919831 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.141+1761A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919831 | |||||||
| chr8:38919942 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.141+1872G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919942 | |||||||
| chr8:38920118 | T | A | 1 | a0001c0001t0053g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+2048T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920118 | |||||||
| chr8:38920133 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.141+2063G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920133 | |||||||
| chr8:38920182 | T | G | 1 | a0001c0001t0021g0277 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.141+2112T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920182 | |||||||
| chr8:38920199 | A | G | 4 | a0001c0001t0003g0081 a0001c0001t0003g0088 a0001c0001t0009g0089 others(1): Show |
4 | HG02451.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+2129A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920199 | |||||||
| chr8:38920211 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.141+2141C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920211 | |||||||
| chr8:38920225 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0025 others(177): Show |
182 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.141+2155G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920225 | |||||||
| chr8:38920236 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.141+2166T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920236 | |||||||
| chr8:38920296 | A | G | 46 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0110 others(43): Show |
46 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.141+2226A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920296 | |||||||
| chr8:38920308 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.141+2238G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920308 | |||||||
| chr8:38920355 | T | C | 28 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0051 others(25): Show |
28 | HG00408.hp2 HG01175.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.141+2285T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920355 | |||||||
| chr8:38920358 | G | T | 25 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0051 others(22): Show |
25 | HG00408.hp2 HG01175.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+2288G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920358 | |||||||
| chr8:38920360 | T | G | 4 | a0001c0001t0001g0100 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | NA18977.hp2 NA18982.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2290T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920360 | |||||||
| chr8:38920361 | A | T | 4 | a0001c0001t0001g0100 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | NA18977.hp2 NA18982.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2291A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920361 | |||||||
| chr8:38920374 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.141+2304T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920374 | |||||||
| chr8:38920376 | A | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(281): Show |
286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.141+2306A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920376 | |||||||
| chr8:38920378 | G | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(281): Show |
286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.141+2308G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920378 | |||||||
| chr8:38920405 | T | C | 1 | a0001c0001t0003g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.141+2335T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920405 | |||||||
| chr8:38920434 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0003g0123 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.141+2364A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920434 | |||||||
| chr8:38920459 | G | C | 1 | a0001c0001t0005g0300 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.141+2389G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920459 | |||||||
| chr8:38920575 | G | GT | 14 | a0001c0001t0001g0048 a0001c0001t0001g0099 a0001c0001t0001g0246 others(11): Show |
14 | HG00408.hp1 HG00673.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+2518dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38920575 | ||||||
| chr8:38920607 | C | T | 1 | a0001c0001t0055g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.141+2537C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920607 | |||||||
| chr8:38920743 | G | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.141+2673G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920743 | |||||||
| chr8:38920847 | C | A | 1 | a0001c0001t0003g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+2777C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920847 | |||||||
| chr8:38920863 | C | T | 45 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.141+2793C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920863 | |||||||
| chr8:38921021 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.141+2951G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921021 | |||||||
| chr8:38921197 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.141+3127G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921197 | |||||||
| chr8:38921204 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141+3134A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921204 | |||||||
| chr8:38921640 | C | T | 5 | a0001c0001t0007g0146 a0001c0001t0013g0145 a0001c0001t0016g0079 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+3570C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921640 | |||||||
| chr8:38921700 | C | A | 1 | a0001c0001t0003g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141+3630C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921700 | |||||||
| chr8:38922129 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(267): Show |
272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.141+4059G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922129 | |||||||
| chr8:38922168 | T | G | 15 | a0001c0001t0001g0074 a0001c0001t0002g0085 a0001c0001t0003g0081 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+4098T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922168 | |||||||
| chr8:38922248 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+4178C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922248 | |||||||
| chr8:38922308 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0013g0145 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.141+4238G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922308 | |||||||
| chr8:38922533 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.141+4463C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922533 | |||||||
| chr8:38922611 | A | G | 48 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(45): Show |
48 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.141+4541A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922611 | |||||||
| chr8:38923088 | A | C | 144 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(141): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.141+5018A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923088 | |||||||
| chr8:38923134 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+5064C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923134 | |||||||
| chr8:38923394 | A | G | 3 | a0001c0001t0016g0079 a0001c0001t0037g0180 a0001c0007t0016g0156 |
3 | HG02257.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.141+5324A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923394 | |||||||
| chr8:38923500 | C | T | 6 | a0001c0001t0002g0192 a0001c0001t0007g0146 a0001c0001t0011g0157 others(3): Show |
6 | HG01884.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+5430C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923500 | |||||||
| chr8:38923515 | A | T | 5 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(2): Show |
5 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+5445A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923515 | |||||||
| chr8:38923522 | C | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(197): Show |
202 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.141+5452C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923522 | |||||||
| chr8:38923578 | C | T | 1 | a0001c0001t0017g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.141+5508C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923578 | |||||||
| chr8:38923611 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0017g0223 |
2 | HG00733.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.141+5541C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923611 | |||||||
| chr8:38923702 | ACAATTGG others(18): Show |
A | 3 | a0001c0001t0003g0292 a0001c0001t0036g0306 a0001c0001t0040g0265 |
3 | HG02683.hp1 HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.141+5634_141+5658d others(27): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38923702 | ||||||
| chr8:38923970 | G | C | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141+5900G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923970 | |||||||
| chr8:38924002 | C | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+5932C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924002 | |||||||
| chr8:38924141 | C | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+6071C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924141 | |||||||
| chr8:38924143 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.141+6073C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924143 | |||||||
| chr8:38924151 | G | A | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+6081G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924151 | |||||||
| chr8:38924178 | T | C | 57 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.141+6108T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924178 | |||||||
| chr8:38924190 | C | T | 2 | a0001c0001t0011g0157 a0001c0001t0012g0224 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.141+6120C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924190 | |||||||
| chr8:38924332 | G | A | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+6262G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924332 | |||||||
| chr8:38924369 | C | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+6299C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924369 | |||||||
| chr8:38924393 | T | C | 1 | a0002c0002t0031g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141+6323T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924393 | |||||||
| chr8:38924406 | C | T | 84 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0025 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.141+6336C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924406 | |||||||
| chr8:38924497 | G | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0261 a0001c0001t0001g0350 others(5): Show |
8 | HG00408.hp1 NA18952.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+6427G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924497 | |||||||
| chr8:38924573 | G | A | 58 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(55): Show |
58 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.141+6503G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924573 | |||||||
| chr8:38924757 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0095 others(53): Show |
57 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.141+6687C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924757 | |||||||
| chr8:38924800 | G | A | 6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
6 | HG01106.hp2 HG01358.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+6730G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924800 | |||||||
| chr8:38925109 | T | C | 78 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.141+7039T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925109 | |||||||
| chr8:38925265 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141+7195C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925265 | |||||||
| chr8:38925295 | C | T | 1 | a0001c0001t0044g0289 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.141+7225C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925295 | |||||||
| chr8:38925296 | G | A | 1 | a0001c0001t0013g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.141+7226G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925296 | |||||||
| chr8:38925502 | C | T | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.141+7432C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925502 | |||||||
| chr8:38925550 | G | A | 1 | a0001c0001t0013g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141+7480G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925550 | |||||||
| chr8:38925911 | C | A | 1 | a0001c0001t0052g0269 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.141+7841C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925911 | |||||||
| chr8:38925935 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.141+7865A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925935 | |||||||
| chr8:38926066 | G | A | 57 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.141+7996G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926066 | |||||||
| chr8:38926081 | T | A | 2 | a0001c0001t0001g0361 a0001c0001t0048g0366 |
2 | NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.141+8011T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926081 | |||||||
| chr8:38926230 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.141+8160A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926230 | |||||||
| chr8:38926381 | C | CT | 55 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.141+8328dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38926381 | ||||||
| chr8:38926381 | CT | C | 56 | a0001c0001t0001g0025 a0001c0001t0001g0074 a0001c0001t0001g0110 others(53): Show |
56 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.141+8328delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38926381 | ||||||
| chr8:38926418 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.141+8348C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926418 | |||||||
| chr8:38926615 | G | A | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.141+8545G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926615 | |||||||
| chr8:38926659 | G | T | 1 | a0001c0001t0003g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.141+8589G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926659 | |||||||
| chr8:38926782 | T | G | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+8712T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926782 | |||||||
| chr8:38926899 | G | C | 22 | a0001c0001t0001g0074 a0001c0001t0001g0226 a0001c0001t0001g0227 others(19): Show |
22 | HG00733.hp1 HG02055.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.141+8829G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926899 | |||||||
| chr8:38926932 | C | A | 4 | a0001c0001t0001g0095 a0001c0001t0028g0153 a0001c0001t0028g0154 others(1): Show |
4 | HG01891.hp2 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+8862C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926932 | |||||||
| chr8:38927006 | G | A | 1 | a0001c0001t0001g0365 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.141+8936G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927006 | |||||||
| chr8:38927027 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+8957G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927027 | |||||||
| chr8:38927162 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0095 others(53): Show |
57 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.142-8832A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927162 | |||||||
| chr8:38927606 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.142-8388T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927606 | |||||||
| chr8:38927678 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0095 others(54): Show |
58 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-8316A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927678 | |||||||
| chr8:38927893 | G | A | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-8101G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927893 | |||||||
| chr8:38927976 | A | C | 1 | a0001c0007t0016g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142-8018A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927976 | |||||||
| chr8:38928085 | A | G | 1 | a0001c0001t0007g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.142-7909A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928085 | |||||||
| chr8:38928172 | GCAGT | G | 16 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(13): Show |
16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-7818_142-7815d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928172 | ||||||
| chr8:38928236 | C | CT | 134 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0025 others(131): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.142-7738dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928236 | ||||||
| chr8:38928236 | C | CTT | 56 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(53): Show |
56 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.142-7739_142-7738d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928236 | ||||||
| chr8:38928236 | CT | C | 9 | a0001c0001t0001g0181 a0001c0001t0001g0226 a0001c0001t0001g0339 others(6): Show |
9 | HG00733.hp1 HG02055.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-7738delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928236 | ||||||
| chr8:38928397 | C | T | 1 | a0001c0001t0002g0364 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.142-7597C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928397 | |||||||
| chr8:38928406 | A | T | 80 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.142-7588A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928406 | |||||||
| chr8:38928474 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7520C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928474 | |||||||
| chr8:38928538 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-7456C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928538 | |||||||
| chr8:38928549 | C | T | 135 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0069 others(132): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.142-7445C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928549 | |||||||
| chr8:38928680 | A | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0133 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.142-7314A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928680 | |||||||
| chr8:38928862 | G | A | 2 | a0001c0001t0014g0208 a0001c0001t0019g0090 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-7132G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928862 | |||||||
| chr8:38928909 | G | A | 1 | a0001c0001t0012g0224 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-7085G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928909 | |||||||
| chr8:38928913 | C | G | 2 | a0001c0001t0011g0157 a0001c0001t0012g0224 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.142-7081C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928913 | |||||||
| chr8:38928919 | G | A | 12 | a0001c0001t0001g0206 a0001c0001t0001g0230 a0001c0001t0001g0231 others(9): Show |
12 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-7075G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928919 | |||||||
| chr8:38928968 | G | A | 25 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(22): Show |
25 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.142-7026G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928968 | |||||||
| chr8:38929016 | C | G | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0334 others(1): Show |
4 | HG00423.hp2 NA18961.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6978C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929016 | |||||||
| chr8:38929209 | G | A | 2 | a0001c0001t0002g0344 a0001c0001t0002g0369 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.142-6785G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929209 | |||||||
| chr8:38929248 | A | T | 8 | a0001c0001t0001g0330 a0001c0001t0001g0336 a0001c0001t0002g0335 others(5): Show |
8 | HG01099.hp2 HG01257.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-6746A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929248 | |||||||
| chr8:38929299 | C | A | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-6695C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929299 | |||||||
| chr8:38929881 | AT | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(49): Show |
53 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-6112delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929881 | |||||||
| chr8:38929952 | C | T | 14 | a0001c0001t0001g0253 a0001c0001t0001g0275 a0001c0001t0001g0329 others(11): Show |
14 | HG01168.hp2 HG01934.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6042C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929952 | |||||||
| chr8:38929954 | C | T | 1 | a0001c0001t0005g0300 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.142-6040C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929954 | |||||||
| chr8:38929995 | G | A | 2 | a0001c0001t0005g0064 a0001c0001t0043g0059 |
2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.142-5999G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929995 | |||||||
| chr8:38930090 | C | G | 80 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.142-5904C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930090 | |||||||
| chr8:38930160 | G | A | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5834G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930160 | |||||||
| chr8:38930161 | G | C | 2 | a0001c0001t0020g0009 a0002c0002t0004g0070 |
2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.142-5833G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930161 | |||||||
| chr8:38930186 | C | CTTTA | 10 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG01106.hp2 HG01358.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-5780_142-5777d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | ||||||
| chr8:38930186 | C | CTTTATTT others(1): Show |
53 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(50): Show |
53 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.142-5784_142-5777d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | ||||||
| chr8:38930186 | C | CTTTATTT others(5): Show |
3 | a0001c0001t0001g0051 a0001c0001t0002g0021 a0001c0001t0002g0191 |
3 | HG02080.hp2 HG03017.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.142-5788_142-5777d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | ||||||
| chr8:38930186 | C | CTTTATTT others(9): Show |
1 | a0001c0001t0001g0050 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.142-5792_142-5777d others(18): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | ||||||
| chr8:38930186 | CTTTATTT others(1): Show |
C | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5784_142-5777d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | ||||||
| chr8:38930245 | G | A | 1 | a0001c0001t0042g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.142-5749G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930245 | |||||||
| chr8:38930346 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0002g0242 a0001c0001t0042g0241 |
3 | HG00639.hp2 HG01069.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.142-5648C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930346 | |||||||
| chr8:38930445 | C | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0024 others(114): Show |
118 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.142-5549C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930445 | |||||||
| chr8:38930447 | C | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0024 others(114): Show |
118 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.142-5547C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930447 | |||||||
| chr8:38930496 | G | A | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-5498G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930496 | |||||||
| chr8:38930510 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.142-5484C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930510 | |||||||
| chr8:38930637 | G | A | 6 | a0001c0001t0001g0330 a0001c0001t0002g0335 a0001c0001t0006g0303 others(3): Show |
6 | HG01099.hp2 HG01257.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-5357G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930637 | |||||||
| chr8:38930646 | CGGCAT | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(169): Show |
173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.142-5333_142-5329d others(7): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930646 | ||||||
| chr8:38930914 | A | G | 3 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 |
3 | HG02922.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.142-5080A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930914 | |||||||
| chr8:38931064 | T | G | 4 | a0001c0001t0001g0343 a0001c0001t0002g0344 a0001c0001t0002g0369 others(1): Show |
4 | HG01361.hp2 HG01496.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-4930T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931064 | |||||||
| chr8:38931135 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-4859G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931135 | |||||||
| chr8:38931304 | C | T | 1 | a0001c0001t0011g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-4690C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931304 | |||||||
| chr8:38931310 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-4684G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931310 | |||||||
| chr8:38931356 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.142-4638C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931356 | |||||||
| chr8:38931593 | G | C | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-4401G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931593 | |||||||
| chr8:38931809 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-4185C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931809 | |||||||
| chr8:38931980 | A | T | 2 | a0001c0001t0002g0362 a0001c0001t0002g0363 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.142-4014A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931980 | |||||||
| chr8:38931995 | C | A | 1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.142-3999C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931995 | |||||||
| chr8:38932021 | C | T | 3 | a0001c0001t0002g0305 a0001c0001t0003g0328 a0001c0001t0004g0367 |
3 | NA18970.hp1 NA18980.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.142-3973C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932021 | |||||||
| chr8:38932055 | A | C | 2 | a0001c0001t0014g0208 a0001c0001t0019g0090 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-3939A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932055 | |||||||
| chr8:38932145 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.142-3849T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932145 | |||||||
| chr8:38932173 | T | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0011g0157 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-3821T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932173 | |||||||
| chr8:38932279 | C | T | 82 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0095 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.142-3715C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932279 | |||||||
| chr8:38932497 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142-3497G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932497 | |||||||
| chr8:38932675 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.142-3319G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932675 | |||||||
| chr8:38932969 | C | G | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-3025C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932969 | |||||||
| chr8:38933080 | G | A | 16 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(13): Show |
16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-2914G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933080 | |||||||
| chr8:38933089 | T | C | 16 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(13): Show |
16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-2905T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933089 | |||||||
| chr8:38933117 | C | T | 20 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-2877C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933117 | |||||||
| chr8:38933218 | A | G | 2 | a0001c0001t0016g0079 a0001c0007t0016g0156 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142-2776A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933218 | |||||||
| chr8:38933248 | C | T | 16 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(13): Show |
16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-2746C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933248 | |||||||
| chr8:38933268 | T | G | 194 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(191): Show |
195 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.142-2726T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933268 | |||||||
| chr8:38933432 | G | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(278): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.142-2562G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933432 | |||||||
| chr8:38933586 | C | CCG | 3 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0002g0087 |
3 | HG02109.hp1 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142-2408_142-2407i others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933586 | |||||||
| chr8:38933778 | T | TAAAAAAA others(3): Show |
6 | a0001c0001t0001g0095 a0001c0001t0001g0368 a0001c0001t0003g0029 others(3): Show |
6 | HG00733.hp1 HG01891.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2209_142-2200d others(12): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | ||||||
| chr8:38933778 | T | TAAAAAAA others(4): Show |
48 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(45): Show |
48 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-2210_142-2200d others(13): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | ||||||
| chr8:38933778 | T | TAAAAAAA others(5): Show |
6 | a0001c0001t0001g0240 a0001c0001t0002g0030 a0001c0001t0002g0036 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2211_142-2200d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | ||||||
| chr8:38933778 | T | TAAAAAAA others(6): Show |
5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0021 others(2): Show |
5 | HG01243.hp2 HG02080.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-2212_142-2200d others(15): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | ||||||
| chr8:38933778 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0003g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.142-2213_142-2200d others(16): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | ||||||
| chr8:38933790 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0037g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.142-2200_142-2199i others(44): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0274 a0001c0001t0016g0148 |
2 | HG01070.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(31): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0262 a0001c0001t0002g0199 a0001c0001t0002g0369 |
3 | HG01175.hp2 HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(30): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(20): Show |
12 | a0001c0001t0001g0206 a0001c0001t0001g0263 a0001c0001t0002g0022 others(9): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(29): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(19): Show |
16 | a0001c0001t0001g0043 a0001c0001t0001g0100 a0001c0001t0001g0230 others(13): Show |
16 | HG00642.hp2 HG00733.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(28): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(18): Show |
22 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0138 others(19): Show |
23 | HG00280.hp2 HG01106.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(27): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(17): Show |
14 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0219 others(11): Show |
14 | HG01516.hp1 HG01517.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(26): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(16): Show |
4 | a0001c0001t0003g0134 a0001c0001t0003g0296 a0001c0001t0005g0353 others(1): Show |
4 | HG01081.hp2 HG01099.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(25): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(13): Show |
4 | a0001c0001t0001g0232 a0001c0001t0003g0204 a0001c0001t0056g0187 others(1): Show |
4 | HG00735.hp1 HG02572.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(22): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(12): Show |
22 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(19): Show |
22 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(21): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0233 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-2200_142-2199i others(20): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0013g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142-2200_142-2199i others(19): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0014g0208 a0001c0001t0019g0090 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0008g0225 a0001c0001t0009g0093 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(13): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933790 | A | AAAAGAAA others(1): Show |
14 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(11): Show |
14 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-2201_142-2200i others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | ||||||
| chr8:38933830 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0015g0179 |
2 | HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.142-2164A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933830 | |||||||
| chr8:38933911 | A | T | 1 | a0001c0001t0002g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-2083A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933911 | |||||||
| chr8:38933985 | C | G | 4 | a0001c0001t0001g0293 a0001c0001t0001g0295 a0001c0001t0002g0057 others(1): Show |
4 | HG02015.hp2 HG02083.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-2009C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933985 | |||||||
| chr8:38934157 | A | AAT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0002g0087 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-1823_142-1822d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38934157 | ||||||
| chr8:38934191 | C | T | 108 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(105): Show |
108 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-1803C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934191 | |||||||
| chr8:38934197 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.142-1797A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934197 | |||||||
| chr8:38934234 | A | G | 42 | a0001c0001t0001g0100 a0001c0001t0001g0206 a0001c0001t0001g0214 others(39): Show |
43 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-1760A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934234 | |||||||
| chr8:38934285 | C | T | 20 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0085 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-1709C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934285 | |||||||
| chr8:38934374 | C | T | 3 | a0001c0001t0002g0102 a0001c0001t0002g0133 a0001c0001t0003g0121 |
3 | HG01361.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.142-1620C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934374 | |||||||
| chr8:38934410 | C | T | 23 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-1584C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934410 | |||||||
| chr8:38934515 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.142-1479C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934515 | |||||||
| chr8:38934518 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.142-1476G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934518 | |||||||
| chr8:38934597 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.142-1397G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934597 | |||||||
| chr8:38934614 | C | T | 1 | a0001c0001t0011g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-1380C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934614 | |||||||
| chr8:38934622 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-1372G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934622 | |||||||
| chr8:38934644 | C | A | 75 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(72): Show |
76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-1350C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934644 | |||||||
| chr8:38934694 | T | G | 1 | a0001c0001t0013g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142-1300T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934694 | |||||||
| chr8:38934816 | GTA | G | 110 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(107): Show |
110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.142-1164_142-1163d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38934816 | ||||||
| chr8:38934848 | C | T | 75 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(72): Show |
76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-1146C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934848 | |||||||
| chr8:38934872 | TA | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(35): Show |
38 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.142-1112delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38934872 | ||||||
| chr8:38934873 | A | T | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-1121A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934873 | |||||||
| chr8:38935040 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-954G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935040 | |||||||
| chr8:38935256 | G | A | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-738G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935256 | |||||||
| chr8:38935353 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(49): Show |
53 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-641G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935353 | |||||||
| chr8:38935368 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0002g0087 |
3 | HG02109.hp1 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142-626A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935368 | |||||||
| chr8:38935381 | A | C | 1 | a0002c0002t0031g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142-613A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935381 | |||||||
| chr8:38935430 | C | CT | 16 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0013 others(13): Show |
16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-548dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38935430 | ||||||
| chr8:38935457 | G | T | 59 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.142-537G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935457 | |||||||
| chr8:38935606 | A | T | 9 | a0001c0001t0001g0095 a0001c0001t0001g0226 a0001c0001t0003g0200 others(6): Show |
9 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-388A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935606 | |||||||
| chr8:38935637 | T | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(279): Show |
284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.142-357T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935637 | |||||||
| chr8:38935816 | A | G | 1 | a0001c0001t0025g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.142-178A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935816 | |||||||
| chr8:38936115 | G | A | 1 | a0001c0001t0013g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198+65G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936115 | |||||||
| chr8:38936150 | A | C | 1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+100A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936150 | |||||||
| chr8:38936164 | T | G | 48 | a0001c0001t0001g0100 a0001c0001t0001g0118 a0001c0001t0001g0119 others(45): Show |
49 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.198+114T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936164 | |||||||
| chr8:38936181 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.198+131C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936181 | |||||||
| chr8:38936312 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0062 |
2 | HG02523.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.198+262C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936312 | |||||||
| chr8:38936318 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(52): Show |
56 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.198+268A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936318 | |||||||
| chr8:38936320 | G | A | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+270G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936320 | |||||||
| chr8:38936357 | A | G | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+307A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936357 | |||||||
| chr8:38936408 | T | C | 1 | a0001c0001t0005g0358 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.198+358T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936408 | |||||||
| chr8:38936558 | C | T | 1 | a0001c0001t0008g0287 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.198+508C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936558 | |||||||
| chr8:38936580 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+530A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936580 | |||||||
| chr8:38936858 | G | C | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+808G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936858 | |||||||
| chr8:38936939 | A | G | 112 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(109): Show |
112 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.198+889A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936939 | |||||||
| chr8:38936946 | T | C | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+896T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936946 | |||||||
| chr8:38937128 | A | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1078A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937128 | |||||||
| chr8:38937268 | C | T | 1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+1218C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937268 | |||||||
| chr8:38937313 | C | G | 1 | a0001c0001t0009g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+1263C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937313 | |||||||
| chr8:38937431 | G | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0002g0055 others(2): Show |
5 | HG02015.hp1 HG02155.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+1381G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937431 | |||||||
| chr8:38937481 | G | A | 3 | a0001c0001t0013g0145 a0001c0001t0013g0151 a0001c0001t0027g0152 |
3 | HG02647.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.198+1431G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937481 | |||||||
| chr8:38937485 | G | C | 74 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(71): Show |
75 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.198+1435G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937485 | |||||||
| chr8:38937521 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.198+1471G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937521 | |||||||
| chr8:38937684 | A | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1634A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937684 | |||||||
| chr8:38937709 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.198+1659C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937709 | |||||||
| chr8:38937844 | C | T | 4 | a0001c0001t0002g0209 a0001c0001t0013g0142 a0001c0001t0045g0301 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1794C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937844 | |||||||
| chr8:38937870 | C | T | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198+1820C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937870 | |||||||
| chr8:38937871 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.198+1821G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937871 | |||||||
| chr8:38937898 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0006g0097 |
2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.198+1848C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937898 | |||||||
| chr8:38937900 | T | G | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1850T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937900 | |||||||
| chr8:38937901 | G | C | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1851G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937901 | |||||||
| chr8:38937909 | G | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1859G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937909 | |||||||
| chr8:38937950 | A | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1900A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937950 | |||||||
| chr8:38937951 | G | C | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1901G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937951 | |||||||
| chr8:38937952 | T | TGTGTTCT others(10): Show |
1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1903_198+1904i others(19): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38937952 | ||||||
| chr8:38937956 | G | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1906G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937956 | |||||||
| chr8:38937971 | G | C | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1921G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937971 | |||||||
| chr8:38937973 | C | A | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1923C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937973 | |||||||
| chr8:38937973 | C | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1923C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937973 | |||||||
| chr8:38938091 | T | G | 22 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(19): Show |
22 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+2041T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938091 | |||||||
| chr8:38938129 | C | A | 31 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(28): Show |
31 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.198+2079C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938129 | |||||||
| chr8:38938129 | C | T | 9 | a0001c0001t0001g0095 a0001c0001t0001g0226 a0001c0001t0003g0200 others(6): Show |
9 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+2079C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938129 | |||||||
| chr8:38938177 | G | A | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2127G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938177 | |||||||
| chr8:38938383 | A | T | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2333A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938383 | |||||||
| chr8:38938452 | G | GCTGCCAC others(5): Show |
8 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0311 others(5): Show |
8 | HG00621.hp1 HG00621.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+2409_198+2420d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938452 | ||||||
| chr8:38938667 | A | C | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2617A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938667 | |||||||
| chr8:38938671 | C | A | 1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2621C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938671 | |||||||
| chr8:38938758 | G | GTGGATGG others(84): Show |
1 | a0001c0001t0002g0359 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2731_198+2732i others(93): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938758 | ||||||
| chr8:38938857 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0005g0221 |
2 | NA19009.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.198+2807C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938857 | |||||||
| chr8:38938900 | C | CT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(104): Show |
108 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.198+2865dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938900 | ||||||
| chr8:38938900 | CT | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0250 a0001c0001t0003g0200 others(6): Show |
9 | HG01168.hp2 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+2865delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938900 | ||||||
| chr8:38939013 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(258): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.198+2963T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939013 | |||||||
| chr8:38939368 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(52): Show |
56 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.198+3318A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939368 | |||||||
| chr8:38939420 | A | T | 19 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(16): Show |
19 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+3370A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939420 | |||||||
| chr8:38939637 | G | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0031 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.198+3587G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939637 | |||||||
| chr8:38939679 | C | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+3629C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939679 | |||||||
| chr8:38939698 | A | G | 1 | a0006c0009t0008g0174 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.198+3648A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939698 | |||||||
| chr8:38939774 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(283): Show |
288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.198+3724T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939774 | |||||||
| chr8:38939818 | A | G | 287 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(284): Show |
289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.198+3768A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939818 | |||||||
| chr8:38939996 | G | T | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-3793G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939996 | |||||||
| chr8:38940045 | G | T | 1 | a0001c0001t0007g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-3744G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940045 | |||||||
| chr8:38940073 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(237): Show |
242 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.199-3716C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940073 | |||||||
| chr8:38940093 | T | TA | 22 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0113 others(19): Show |
22 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-3675dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | ||||||
| chr8:38940093 | TA | T | 90 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(87): Show |
90 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.199-3675delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | ||||||
| chr8:38940093 | TAA | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0043 others(105): Show |
110 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.199-3676_199-3675d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | ||||||
| chr8:38940093 | TAAA | T | 6 | a0001c0001t0002g0192 a0001c0001t0003g0254 a0001c0001t0007g0146 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-3677_199-3675d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | ||||||
| chr8:38940124 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-3665G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940124 | |||||||
| chr8:38940142 | A | G | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-3647A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940142 | |||||||
| chr8:38940315 | CT | C | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3472delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940315 | ||||||
| chr8:38940322 | C | T | 94 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0074 others(91): Show |
95 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.199-3467C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940322 | |||||||
| chr8:38940398 | C | T | 1 | a0001c0001t0013g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-3391C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940398 | |||||||
| chr8:38940485 | G | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3304G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940485 | |||||||
| chr8:38940486 | G | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3303G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940486 | |||||||
| chr8:38940494 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-3295T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940494 | |||||||
| chr8:38940539 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.199-3250G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940539 | |||||||
| chr8:38940548 | A | T | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-3241A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940548 | |||||||
| chr8:38940630 | C | G | 23 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-3159C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940630 | |||||||
| chr8:38940631 | G | A | 59 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.199-3158G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940631 | |||||||
| chr8:38940650 | C | CG | 99 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0041 others(96): Show |
100 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.199-3127dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | ||||||
| chr8:38940650 | C | CGG | 73 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0050 others(70): Show |
74 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.199-3128_199-3127d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | ||||||
| chr8:38940650 | C | CGGG | 19 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0227 others(16): Show |
19 | HG00621.hp1 HG00621.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.199-3129_199-3127d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | ||||||
| chr8:38940650 | CG | C | 52 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0045 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.199-3127delG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | ||||||
| chr8:38940656 | G | C | 3 | a0001c0001t0003g0060 a0001c0001t0005g0064 a0001c0001t0043g0059 |
3 | HG00323.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.199-3133G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940656 | |||||||
| chr8:38940657 | G | GT | 4 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0013g0150 others(1): Show |
4 | HG01891.hp1 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3132_199-3131i others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940657 | |||||||
| chr8:38940696 | T | C | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-3093T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940696 | |||||||
| chr8:38940893 | A | ATT | 59 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.199-2895_199-2894d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940893 | ||||||
| chr8:38940894 | T | TTA | 36 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(33): Show |
36 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.199-2882_199-2881d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940894 | ||||||
| chr8:38941030 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.199-2759T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941030 | |||||||
| chr8:38941055 | CT | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(241): Show |
246 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.199-2716delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38941055 | ||||||
| chr8:38941055 | CTT | C | 9 | a0001c0001t0001g0316 a0001c0001t0003g0023 a0001c0001t0003g0029 others(6): Show |
9 | HG01069.hp2 HG02451.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-2717_199-2716d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38941055 | ||||||
| chr8:38941110 | G | A | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-2679G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941110 | |||||||
| chr8:38941117 | C | T | 2 | a0001c0001t0016g0079 a0001c0007t0016g0156 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-2672C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941117 | |||||||
| chr8:38941149 | C | T | 1 | a0001c0001t0002g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.199-2640C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941149 | |||||||
| chr8:38941159 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0007g0159 a0001c0001t0017g0223 |
3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-2630C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941159 | |||||||
| chr8:38941218 | G | C | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-2571G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941218 | |||||||
| chr8:38941256 | A | C | 3 | a0001c0001t0001g0226 a0001c0001t0007g0159 a0001c0001t0017g0223 |
3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-2533A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941256 | |||||||
| chr8:38941301 | C | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-2488C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941301 | |||||||
| chr8:38941335 | C | T | 23 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-2454C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941335 | |||||||
| chr8:38941382 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.199-2407A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941382 | |||||||
| chr8:38941539 | G | A | 75 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(72): Show |
76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.199-2250G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941539 | |||||||
| chr8:38941601 | A | T | 1 | a0001c0001t0037g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.199-2188A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941601 | |||||||
| chr8:38941687 | T | C | 1 | a0001c0001t0003g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-2102T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941687 | |||||||
| chr8:38941794 | A | T | 23 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-1995A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941794 | |||||||
| chr8:38942124 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(158): Show |
162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.199-1665G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942124 | |||||||
| chr8:38942359 | C | T | 1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.199-1430C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942359 | |||||||
| chr8:38942360 | G | T | 74 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(71): Show |
75 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.199-1429G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942360 | |||||||
| chr8:38942453 | C | CA | 5 | a0001c0001t0001g0168 a0001c0001t0001g0365 a0001c0001t0002g0062 others(2): Show |
5 | HG01515.hp1 HG02523.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-1329dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38942453 | ||||||
| chr8:38942454 | A | C | 23 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-1335A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942454 | |||||||
| chr8:38942466 | C | T | 7 | a0001c0001t0001g0107 a0001c0001t0001g0279 a0001c0001t0002g0105 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-1323C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942466 | |||||||
| chr8:38942546 | G | C | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-1243G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942546 | |||||||
| chr8:38942610 | C | A | 5 | a0001c0001t0002g0192 a0001c0001t0007g0146 a0001c0001t0011g0157 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-1179C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942610 | |||||||
| chr8:38942777 | G | A | 3 | a0001c0001t0014g0208 a0001c0001t0019g0090 a0001c0001t0037g0180 |
3 | HG02451.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199-1012G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942777 | |||||||
| chr8:38942842 | G | A | 1 | a0001c0001t0003g0137 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.199-947G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942842 | |||||||
| chr8:38942899 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.199-890C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942899 | |||||||
| chr8:38942947 | G | A | 1 | a0001c0001t0011g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-842G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942947 | |||||||
| chr8:38943083 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(48): Show |
52 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.199-706C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943083 | |||||||
| chr8:38943153 | A | G | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-636A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943153 | |||||||
| chr8:38943246 | T | A | 1 | a0001c0001t0002g0340 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.199-543T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943246 | |||||||
| chr8:38943281 | G | T | 24 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0002g0192 others(21): Show |
24 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-508G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943281 | |||||||
| chr8:38943425 | G | A | 74 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(71): Show |
75 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.199-364G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943425 | |||||||
| chr8:38943446 | A | G | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-343A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943446 | |||||||
| chr8:38943542 | A | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-247A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943542 | |||||||
| chr8:38943561 | C | T | 3 | a0001c0001t0001g0329 a0001c0001t0001g0342 a0001c0001t0010g0278 |
3 | NA18612.hp2 NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.199-228C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943561 | |||||||
| chr8:38943767 | T | C | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-22T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943767 | |||||||
| chr8:38944024 | A | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(48): Show |
52 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.247+187A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944024 | |||||||
| chr8:38944041 | G | A | 2 | a0001c0001t0012g0213 a0001c0001t0035g0212 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.247+204G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944041 | |||||||
| chr8:38944107 | A | C | 23 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0117 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.247+270A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944107 | |||||||
| chr8:38944121 | A | G | 103 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0074 others(100): Show |
104 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.247+284A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944121 | |||||||
| chr8:38944163 | A | G | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.247+326A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944163 | |||||||
| chr8:38944168 | A | C | 3 | a0001c0001t0002g0192 a0001c0001t0007g0146 a0002c0002t0051g0078 |
3 | HG02895.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.247+331A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944168 | |||||||
| chr8:38944221 | G | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0024 others(107): Show |
111 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.247+384G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944221 | |||||||
| chr8:38944236 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0002g0087 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+399C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944236 | |||||||
| chr8:38944237 | G | A | 2 | a0001c0001t0016g0079 a0001c0007t0016g0156 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.247+400G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944237 | |||||||
| chr8:38944369 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.247+532T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944369 | |||||||
| chr8:38944409 | C | T | 1 | a0001c0001t0012g0211 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.247+572C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944409 | |||||||
| chr8:38944504 | G | GA | 109 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0074 others(106): Show |
110 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.247+677dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 38944504 | ||||||
| chr8:38944693 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0045g0301 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.247+856A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944693 | |||||||
| chr8:38944738 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(27): Show |
30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.247+901C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944738 | |||||||
| chr8:38944777 | T | C | 2 | a0001c0001t0011g0157 a0001c0001t0012g0224 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.247+940T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944777 | |||||||
| chr8:38944931 | ATGT | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(27): Show |
30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.247+1098_247+1100d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 38944931 | ||||||
| chr8:38944964 | G | C | 2 | a0001c0001t0016g0079 a0001c0007t0016g0156 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.247+1127G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944964 | |||||||
| chr8:38944968 | C | T | 1 | a0001c0001t0008g0287 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.247+1131C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944968 | |||||||
| chr8:38944973 | A | G | 1 | a0001c0001t0035g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247+1136A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944973 | |||||||
| chr8:38945052 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0007g0159 a0001c0001t0017g0223 |
3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.248-1072G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945052 | |||||||
| chr8:38945069 | C | T | 2 | a0001c0001t0028g0153 a0001c0001t0028g0154 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.248-1055C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945069 | |||||||
| chr8:38945147 | G | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-977G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945147 | |||||||
| chr8:38945167 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0007g0159 a0001c0001t0017g0223 |
3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.248-957G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945167 | |||||||
| chr8:38945180 | C | G | 3 | a0001c0001t0013g0145 a0001c0001t0013g0151 a0001c0001t0027g0152 |
3 | HG02647.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.248-944C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945180 | |||||||
| chr8:38945208 | T | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0181 others(50): Show |
54 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.248-916T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945208 | |||||||
| chr8:38945369 | A | T | 2 | a0001c0001t0014g0208 a0001c0001t0019g0090 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.248-755A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945369 | |||||||
| chr8:38945374 | C | G | 2 | a0001c0001t0014g0208 a0001c0001t0019g0090 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.248-750C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945374 | |||||||
| chr8:38945437 | G | A | 15 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.248-687G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945437 | |||||||
| chr8:38945441 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0006g0097 |
2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.248-683C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945441 | |||||||
| chr8:38945639 | G | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0274 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-485G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945639 | |||||||
| chr8:38945672 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.248-452A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945672 | |||||||
| chr8:38945814 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0032g0094 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.248-310G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945814 | |||||||
| chr8:38945850 | G | A | 1 | a0001c0001t0007g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.248-274G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945850 | |||||||
| chr8:38945883 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.248-241G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945883 | |||||||
| chr8:38945894 | T | C | 1 | a0001c0001t0013g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.248-230T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945894 | |||||||
| chr8:38946033 | T | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(29): Show |
32 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.248-91T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38946033 | |||||||
| chr8:38946362 | G | A | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.345+141G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946362 | |||||||
| chr8:38946375 | G | T | 74 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(71): Show |
75 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.345+154G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946375 | |||||||
| chr8:38946487 | G | A | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.345+266G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946487 | |||||||
| chr8:38946551 | A | G | 110 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0069 others(107): Show |
111 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.345+330A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946551 | |||||||
| chr8:38946708 | C | A | 256 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(253): Show |
257 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.345+487C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946708 | |||||||
| chr8:38946779 | T | C | 1 | a0001c0001t0009g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.345+558T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946779 | |||||||
| chr8:38947069 | T | G | 1 | a0001c0001t0001g0355 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.345+848T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947069 | |||||||
| chr8:38947111 | C | G | 279 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(276): Show |
280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.345+890C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947111 | |||||||
| chr8:38947160 | AAG | A | 163 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(160): Show |
163 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.345+946_345+947del others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38947160 | ||||||
| chr8:38947239 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.345+1018C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947239 | |||||||
| chr8:38947398 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+1177C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947398 | |||||||
| chr8:38947404 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0006g0097 |
2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.345+1183C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947404 | |||||||
| chr8:38947428 | C | T | 4 | a0001c0001t0014g0247 a0001c0001t0014g0248 a0001c0001t0014g0249 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+1207C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947428 | |||||||
| chr8:38947443 | T | G | 1 | a0001c0001t0002g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.345+1222T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947443 | |||||||
| chr8:38947531 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(27): Show |
30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.345+1310G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947531 | |||||||
| chr8:38947552 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.345+1331G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947552 | |||||||
| chr8:38947560 | C | G | 2 | a0001c0001t0016g0079 a0001c0007t0016g0156 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.345+1339C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947560 | |||||||
| chr8:38947577 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345+1356C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947577 | |||||||
| chr8:38947596 | C | G | 1 | a0001c0001t0001g0280 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.345+1375C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947596 | |||||||
| chr8:38947614 | G | A | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.345+1393G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947614 | |||||||
| chr8:38947881 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.345+1660G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947881 | |||||||
| chr8:38947918 | C | T | 59 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+1697C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947918 | |||||||
| chr8:38947963 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(27): Show |
30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.345+1742G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947963 | |||||||
| chr8:38948010 | C | G | 59 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0038 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+1789C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948010 | |||||||
| chr8:38948025 | G | A | 3 | a0001c0001t0002g0192 a0001c0001t0007g0146 a0002c0002t0051g0078 |
3 | HG02895.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.345+1804G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948025 | |||||||
| chr8:38948085 | C | CA | 82 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0050 others(79): Show |
83 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.345+1883dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948085 | ||||||
| chr8:38948085 | C | CAAA | 72 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(69): Show |
73 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.345+1881_345+1883d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948085 | ||||||
| chr8:38948085 | CA | C | 11 | a0001c0001t0001g0226 a0001c0001t0001g0360 a0001c0001t0002g0305 others(8): Show |
11 | HG00733.hp1 HG02630.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.345+1883delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948085 | ||||||
| chr8:38948118 | CCTT | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0226 a0001c0001t0007g0159 others(2): Show |
5 | HG00733.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1901_345+1903d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948118 | ||||||
| chr8:38948315 | C | T | 76 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(73): Show |
77 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.345+2094C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948315 | |||||||
| chr8:38948341 | T | A | 49 | a0001c0001t0001g0024 a0001c0001t0001g0181 a0001c0001t0001g0183 others(46): Show |
49 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.345+2120T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948341 | |||||||
| chr8:38948380 | A | T | 2 | a0001c0001t0003g0204 a0001c0001t0013g0144 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.345+2159A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948380 | |||||||
| chr8:38948507 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.345+2286A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948507 | |||||||
| chr8:38948550 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(163): Show |
166 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.346-2300G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948550 | |||||||
| chr8:38948592 | G | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.346-2258G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948592 | |||||||
| chr8:38948638 | T | C | 2 | a0001c0001t0007g0161 a0001c0001t0053g0006 |
2 | HG01255.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.346-2212T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948638 | |||||||
| chr8:38948787 | G | A | 15 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0003g0081 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.346-2063G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948787 | |||||||
| chr8:38948868 | T | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0002g0087 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-1982T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948868 | |||||||
| chr8:38948901 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346-1949C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948901 | |||||||
| chr8:38948937 | C | T | 1 | a0001c0001t0011g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.346-1913C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948937 | |||||||
| chr8:38948946 | C | A | 54 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0096 others(51): Show |
55 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.346-1904C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948946 | |||||||
| chr8:38948985 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.346-1865C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948985 | |||||||
| chr8:38949006 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.346-1844G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949006 | |||||||
| chr8:38949051 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0226 a0001c0001t0007g0159 others(1): Show |
4 | HG00733.hp1 HG02148.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-1799A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949051 | |||||||
| chr8:38949114 | G | A | 237 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(234): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.346-1736G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949114 | |||||||
| chr8:38949189 | C | T | 1 | a0001c0001t0002g0340 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.346-1661C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949189 | |||||||
| chr8:38949235 | T | C | 1 | a0001c0001t0001g0321 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.346-1615T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949235 | |||||||
| chr8:38949350 | A | T | 11 | a0001c0001t0002g0011 a0001c0001t0007g0161 a0001c0001t0009g0080 others(8): Show |
11 | HG02257.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-1500A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949350 | |||||||
| chr8:38949416 | T | C | 15 | a0001c0001t0002g0013 a0001c0001t0002g0229 a0001c0001t0003g0204 others(12): Show |
16 | HG01192.hp1 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.346-1434T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949416 | |||||||
| chr8:38949636 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.346-1214A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949636 | |||||||
| chr8:38949696 | C | T | 40 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0051 others(37): Show |
40 | HG00323.hp2 HG00621.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.346-1154C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949696 | |||||||
| chr8:38949766 | A | G | 150 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0038 others(147): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.346-1084A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949766 | |||||||
| chr8:38949910 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.346-940C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949910 | |||||||
| chr8:38950019 | T | G | 3 | a0001c0001t0009g0093 a0001c0001t0020g0009 a0001c0001t0032g0094 |
3 | HG02055.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346-831T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950019 | |||||||
| chr8:38950055 | A | AT | 14 | a0001c0001t0001g0095 a0001c0001t0002g0011 a0001c0001t0003g0204 others(11): Show |
14 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.346-788dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38950055 | ||||||
| chr8:38950360 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0018g0130 |
2 | NA18982.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.346-490G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950360 | |||||||
| chr8:38950505 | G | GT | 118 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(115): Show |
118 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.346-336dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38950505 | ||||||
| chr8:38950529 | T | G | 1 | a0001c0001t0002g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-321T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950529 | |||||||
| chr8:38950530 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-320A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950530 | |||||||
| chr8:38950532 | C | A | 1 | a0001c0001t0002g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-318C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950532 | |||||||
| chr8:38950561 | C | T | 45 | a0001c0001t0001g0177 a0001c0001t0001g0230 a0001c0001t0001g0263 others(42): Show |
46 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.346-289C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950561 | |||||||
| chr8:38950699 | G | C | 53 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0046 others(50): Show |
53 | HG00408.hp2 HG00621.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.346-151G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950699 | |||||||
| chr8:38950730 | C | T | 10 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0067 others(7): Show |
10 | HG02132.hp1 HG02155.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.346-120C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950730 | |||||||
| chr8:38950735 | G | C | 1 | a0001c0001t0012g0224 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.346-115G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950735 | |||||||
| chr8:38950811 | G | T | 1 | a0001c0001t0002g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.346-39G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950811 | |||||||
| chr8:38951041 | A | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0095 a0001c0001t0002g0209 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+51A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951041 | |||||||
| chr8:38951072 | T | C | 41 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(38): Show |
41 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.486+82T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951072 | |||||||
| chr8:38951094 | A | G | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.486+104A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951094 | |||||||
| chr8:38951109 | G | C | 1 | a0001c0001t0003g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.486+119G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951109 | |||||||
| chr8:38951139 | T | G | 348 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(345): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.486+149T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951139 | |||||||
| chr8:38951229 | G | T | 1 | a0001c0001t0002g0019 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.486+239G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951229 | |||||||
| chr8:38951234 | G | A | 151 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(148): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.486+244G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951234 | |||||||
| chr8:38951239 | C | T | 39 | a0001c0001t0001g0220 a0001c0001t0001g0270 a0001c0001t0001g0275 others(36): Show |
39 | HG00621.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.486+249C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951239 | |||||||
| chr8:38951427 | G | A | 153 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(150): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.486+437G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951427 | |||||||
| chr8:38951469 | G | GT | 10 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0263 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.486+503dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | ||||||
| chr8:38951469 | GT | G | 26 | a0001c0001t0001g0048 a0001c0001t0001g0122 a0001c0001t0001g0214 others(23): Show |
26 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.486+503delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | ||||||
| chr8:38951469 | GTT | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0038 others(78): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.486+502_486+503del others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | ||||||
| chr8:38951469 | GTTT | G | 52 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(49): Show |
52 | HG00609.hp1 HG00733.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.486+501_486+503del others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | ||||||
| chr8:38951611 | A | C | 1 | a0001c0001t0011g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.487-555A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951611 | |||||||
| chr8:38951737 | C | T | 1 | a0001c0001t0015g0322 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.487-429C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951737 | |||||||
| chr8:38951863 | T | C | 1 | a0001c0001t0011g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487-303T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951863 | |||||||
| chr8:38951926 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.487-240T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951926 | |||||||
| chr8:38952003 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.487-163G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38952003 | |||||||
| chr8:38952138 | C | T | 1 | a0001c0001t0006g0267 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.487-28C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38952138 | |||||||
| chr8:38952145 | A | C | 339 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(336): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.487-21A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38952145 | |||||||
| chr8:38952342 | G | C | 2 | a0001c0001t0003g0114 a0001c0001t0013g0142 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.633+30G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952342 | |||||||
| chr8:38952344 | T | A | 1 | a0001c0001t0009g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633+32T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952344 | |||||||
| chr8:38952534 | G | A | 5 | a0001c0001t0012g0211 a0001c0001t0012g0213 a0001c0001t0027g0152 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.634-102G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952534 | |||||||
| chr8:38952603 | G | A | 2 | a0001c0001t0003g0058 a0001c0001t0011g0165 |
2 | NA18965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.634-33G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952603 | |||||||
| chr8:38952720 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.702+16G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38952720 | |||||||
| chr8:38952839 | A | G | 1 | a0001c0001t0027g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.702+135A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38952839 | |||||||
| chr8:38952876 | C | T | 4 | a0002c0002t0001g0194 a0002c0002t0004g0070 a0002c0002t0031g0034 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+172C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38952876 | |||||||
| chr8:38953189 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0043 others(62): Show |
67 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.703-108A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38953189 | |||||||
| chr8:38953588 | A | G | 1 | a0001c0001t0005g0353 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.773+221A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38953588 | |||||||
| chr8:38953840 | G | A | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.773+473G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38953840 | |||||||
| chr8:38953979 | C | T | 42 | a0001c0001t0001g0047 a0001c0001t0001g0214 a0001c0001t0001g0220 others(39): Show |
43 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.773+612C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38953979 | |||||||
| chr8:38954111 | G | A | 1 | a0002c0002t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.773+744G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954111 | |||||||
| chr8:38954186 | T | A | 1 | a0001c0001t0040g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.773+819T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954186 | |||||||
| chr8:38954214 | C | T | 1 | a0001c0001t0011g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.773+847C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954214 | |||||||
| chr8:38954383 | G | A | 7 | a0001c0001t0011g0162 a0001c0001t0012g0211 a0001c0001t0012g0213 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.773+1016G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954383 | |||||||
| chr8:38954447 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.773+1080C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954447 | |||||||
| chr8:38954730 | A | T | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.773+1363A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954730 | |||||||
| chr8:38954774 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.773+1407T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954774 | |||||||
| chr8:38954853 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.773+1486C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954853 | |||||||
| chr8:38954890 | C | T | 1 | a0001c0007t0016g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.773+1523C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954890 | |||||||
| chr8:38954958 | C | T | 39 | a0001c0001t0001g0047 a0001c0001t0001g0214 a0001c0001t0001g0220 others(36): Show |
40 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.773+1591C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954958 | |||||||
| chr8:38954966 | G | A | 1 | a0001c0001t0011g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.773+1599G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954966 | |||||||
| chr8:38954987 | T | C | 1 | a0001c0001t0032g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.773+1620T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954987 | |||||||
| chr8:38955313 | T | C | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.773+1946T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955313 | |||||||
| chr8:38955333 | G | A | 1 | a0001c0001t0019g0071 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.773+1966G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955333 | |||||||
| chr8:38955374 | A | T | 1 | a0001c0001t0001g0281 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.774-1949A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955374 | |||||||
| chr8:38955528 | C | T | 330 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.774-1795C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955528 | |||||||
| chr8:38955661 | C | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0095 a0001c0001t0003g0081 others(12): Show |
16 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.774-1662C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955661 | |||||||
| chr8:38955908 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.774-1415T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955908 | |||||||
| chr8:38955922 | C | T | 1 | a0001c0001t0004g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.774-1401C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955922 | |||||||
| chr8:38956014 | A | G | 5 | a0001c0001t0002g0022 a0001c0001t0002g0362 a0001c0001t0002g0363 others(2): Show |
5 | HG00735.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-1309A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956014 | |||||||
| chr8:38956041 | A | C | 2 | a0002c0002t0031g0034 a0002c0002t0051g0078 |
2 | HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.774-1282A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956041 | |||||||
| chr8:38956081 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(177): Show |
181 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.774-1242C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956081 | |||||||
| chr8:38956315 | G | A | 1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.774-1008G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956315 | |||||||
| chr8:38956327 | G | A | 129 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(126): Show |
130 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.774-996G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956327 | |||||||
| chr8:38956645 | T | C | 346 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(343): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.774-678T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956645 | |||||||
| chr8:38956667 | G | A | 1 | a0001c0001t0037g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.774-656G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956667 | |||||||
| chr8:38956696 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-627A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956696 | |||||||
| chr8:38956768 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0350 a0001c0001t0007g0299 |
3 | NA18995.hp1 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.774-555G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956768 | |||||||
| chr8:38956843 | G | A | 3 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0016g0148 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.774-480G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956843 | |||||||
| chr8:38956973 | A | G | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.774-350A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956973 | |||||||
| chr8:38957160 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774-163C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38957160 | |||||||
| chr8:38957176 | A | G | 1 | a0001c0001t0038g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.774-147A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38957176 | |||||||
| chr8:38957632 | G | T | 2 | a0001c0001t0001g0288 a0001c0001t0004g0257 |
2 | NA19007.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.837+246G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957632 | |||||||
| chr8:38957669 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.837+283G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957669 | |||||||
| chr8:38957675 | C | T | 105 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(102): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.837+289C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957675 | |||||||
| chr8:38957909 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG00642.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.837+523G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957909 | |||||||
| chr8:38957915 | C | T | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+529C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957915 | |||||||
| chr8:38957918 | A | G | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+532A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957918 | |||||||
| chr8:38957946 | G | A | 1 | a0001c0001t0019g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.837+560G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957946 | |||||||
| chr8:38958004 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.837+618C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958004 | |||||||
| chr8:38958176 | A | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(256): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.837+790A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958176 | |||||||
| chr8:38958246 | C | T | 1 | a0001c0001t0011g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.837+860C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958246 | |||||||
| chr8:38958322 | C | CA | 216 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.837+944dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38958322 | ||||||
| chr8:38958337 | C | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.837+951C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958337 | |||||||
| chr8:38958468 | C | T | 1 | a0001c0001t0017g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.837+1082C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958468 | |||||||
| chr8:38958536 | C | G | 140 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(137): Show |
140 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.837+1150C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958536 | |||||||
| chr8:38958547 | C | T | 2 | a0001c0001t0002g0199 a0001c0001t0002g0242 |
2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.837+1161C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958547 | |||||||
| chr8:38958785 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.837+1399G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958785 | |||||||
| chr8:38958830 | G | A | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+1444G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958830 | |||||||
| chr8:38958873 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.837+1487T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958873 | |||||||
| chr8:38958885 | C | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.837+1499C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958885 | |||||||
| chr8:38958981 | T | C | 291 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(288): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.837+1595T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958981 | |||||||
| chr8:38959356 | G | T | 1 | a0001c0001t0046g0197 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.837+1970G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959356 | |||||||
| chr8:38959505 | T | A | 70 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.837+2119T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959505 | |||||||
| chr8:38959645 | T | A | 11 | a0001c0001t0012g0086 a0001c0001t0012g0193 a0001c0001t0012g0211 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+2259T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959645 | |||||||
| chr8:38959768 | G | A | 1 | a0001c0001t0016g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.837+2382G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959768 | |||||||
| chr8:38959819 | G | A | 1 | a0001c0001t0049g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.837+2433G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959819 | |||||||
| chr8:38959894 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.837+2508A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959894 | |||||||
| chr8:38960304 | A | G | 1 | a0001c0001t0038g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.837+2918A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960304 | |||||||
| chr8:38960358 | C | T | 1 | a0001c0001t0003g0101 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.837+2972C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960358 | |||||||
| chr8:38960550 | AC | A | 3 | a0001c0001t0003g0121 a0001c0001t0003g0173 a0001c0001t0022g0185 |
3 | HG00280.hp2 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.837+3165delC | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960550 | |||||||
| chr8:38960552 | A | G | 1 | a0001c0001t0020g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.837+3166A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960552 | |||||||
| chr8:38960646 | A | G | 12 | a0001c0001t0009g0001 a0001c0001t0009g0080 a0001c0001t0009g0089 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+3260A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960646 | |||||||
| chr8:38960732 | G | C | 2 | a0001c0001t0019g0071 a0001c0001t0019g0090 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.837+3346G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960732 | |||||||
| chr8:38960855 | A | G | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+3469A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960855 | |||||||
| chr8:38960893 | A | G | 4 | a0001c0001t0020g0009 a0001c0001t0032g0094 a0002c0002t0031g0034 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+3507A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960893 | |||||||
| chr8:38960905 | G | C | 2 | a0001c0001t0022g0186 a0001c0001t0039g0273 |
2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.837+3519G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960905 | |||||||
| chr8:38961039 | T | G | 13 | a0001c0001t0012g0086 a0001c0001t0012g0193 a0001c0001t0012g0211 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+3653T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961039 | |||||||
| chr8:38961346 | G | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0227 a0001c0001t0007g0159 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+3960G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961346 | |||||||
| chr8:38961381 | AC | A | 3 | a0001c0001t0004g0109 a0001c0001t0004g0245 a0001c0001t0004g0285 |
3 | HG00408.hp2 HG02056.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.837+3996delC | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961381 | |||||||
| chr8:38961408 | G | A | 1 | a0001c0001t0034g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.837+4022G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961408 | |||||||
| chr8:38961485 | C | T | 1 | a0001c0001t0006g0267 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.837+4099C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961485 | |||||||
| chr8:38961534 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0002g0085 a0001c0001t0002g0087 others(3): Show |
6 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+4148C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961534 | |||||||
| chr8:38961822 | CGTTTAAC others(1): Show |
C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.837+4445_837+4452d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38961822 | ||||||
| chr8:38961910 | A | G | 1 | a0002c0002t0004g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837+4524A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961910 | |||||||
| chr8:38962007 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.837+4621A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962007 | |||||||
| chr8:38962287 | G | A | 12 | a0001c0001t0012g0086 a0001c0001t0012g0193 a0001c0001t0012g0211 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.837+4901G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962287 | |||||||
| chr8:38962393 | T | G | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+5007T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962393 | |||||||
| chr8:38962550 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.837+5164G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962550 | |||||||
| chr8:38962590 | A | G | 13 | a0001c0001t0012g0086 a0001c0001t0012g0193 a0001c0001t0012g0211 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+5204A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962590 | |||||||
| chr8:38962630 | A | C | 2 | a0001c0001t0032g0094 a0001c0001t0045g0301 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.837+5244A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962630 | |||||||
| chr8:38962845 | C | T | 177 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(174): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.837+5459C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962845 | |||||||
| chr8:38962919 | A | G | 161 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(158): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.837+5533A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962919 | |||||||
| chr8:38963050 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.838-5542A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963050 | |||||||
| chr8:38963280 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.838-5312A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963280 | |||||||
| chr8:38963403 | A | T | 44 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(41): Show |
45 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.838-5189A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963403 | |||||||
| chr8:38963405 | T | A | 2 | a0001c0001t0005g0203 a0001c0001t0005g0221 |
2 | NA18992.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.838-5187T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963405 | |||||||
| chr8:38963452 | G | A | 1 | a0001c0001t0005g0221 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.838-5140G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963452 | |||||||
| chr8:38963612 | G | A | 43 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(40): Show |
44 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.838-4980G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963612 | |||||||
| chr8:38963751 | T | C | 43 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(40): Show |
44 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.838-4841T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963751 | |||||||
| chr8:38963809 | A | G | 344 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.838-4783A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963809 | |||||||
| chr8:38963856 | G | A | 1 | a0001c0001t0009g0001 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.838-4736G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963856 | |||||||
| chr8:38964131 | G | A | 1 | a0001c0001t0034g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.838-4461G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964131 | |||||||
| chr8:38964147 | G | A | 178 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(175): Show |
180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.838-4445G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964147 | |||||||
| chr8:38964172 | A | T | 130 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(127): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.838-4420A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964172 | |||||||
| chr8:38964505 | C | T | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.838-4087C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964505 | |||||||
| chr8:38964516 | G | A | 43 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(40): Show |
44 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.838-4076G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964516 | |||||||
| chr8:38964708 | GA | G | 12 | a0001c0001t0009g0001 a0001c0001t0009g0080 a0001c0001t0009g0089 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-3874delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964708 | ||||||
| chr8:38964795 | T | C | 46 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(43): Show |
47 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.838-3797T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964795 | |||||||
| chr8:38964817 | A | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01928.hp1 HG01934.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-3775A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964817 | |||||||
| chr8:38964852 | C | CT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0045 others(89): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.838-3710dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38964852 | C | CTT | 26 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0100 others(23): Show |
26 | HG00673.hp1 HG01361.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.838-3711_838-3710d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38964852 | CT | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0038 others(34): Show |
37 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.838-3710delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38964852 | CTT | C | 67 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(64): Show |
67 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.838-3711_838-3710d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38964852 | CTTT | C | 11 | a0001c0001t0001g0368 a0001c0001t0003g0029 a0001c0001t0012g0086 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-3712_838-3710d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38964852 | CTTTTTTT others(1): Show |
C | 40 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(37): Show |
41 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.838-3717_838-3710d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38964852 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0016g0148 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-3722_838-3710d others(15): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | ||||||
| chr8:38965186 | G | T | 1 | a0001c0001t0002g0019 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.838-3406G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965186 | |||||||
| chr8:38965293 | G | A | 3 | a0001c0001t0016g0079 a0001c0001t0018g0243 a0001c0007t0016g0156 |
3 | HG02257.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838-3299G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965293 | |||||||
| chr8:38965763 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0350 a0001c0001t0007g0299 |
3 | NA18995.hp1 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.838-2829G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965763 | |||||||
| chr8:38965993 | C | G | 47 | a0001c0001t0001g0281 a0001c0001t0003g0003 a0001c0001t0003g0023 others(44): Show |
48 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.838-2599C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965993 | |||||||
| chr8:38966378 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.838-2214A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966378 | |||||||
| chr8:38966464 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.838-2128A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966464 | |||||||
| chr8:38966481 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.838-2111T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966481 | |||||||
| chr8:38966542 | T | C | 41 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0065 others(38): Show |
41 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.838-2050T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966542 | |||||||
| chr8:38966611 | C | T | 1 | a0001c0001t0004g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.838-1981C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966611 | |||||||
| chr8:38966733 | G | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(271): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.838-1859G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966733 | |||||||
| chr8:38966903 | G | A | 2 | a0001c0001t0020g0073 a0001c0001t0050g0166 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.838-1689G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966903 | |||||||
| chr8:38967134 | G | A | 2 | a0001c0001t0013g0145 a0001c0001t0013g0151 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.838-1458G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967134 | |||||||
| chr8:38967409 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0235 |
2 | NA19063.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.838-1183G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967409 | |||||||
| chr8:38967664 | C | CT | 17 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0368 others(14): Show |
17 | HG02165.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.838-913dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38967664 | ||||||
| chr8:38967696 | C | T | 1 | a0001c0001t0034g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.838-896C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967696 | |||||||
| chr8:38967720 | G | A | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.838-872G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967720 | |||||||
| chr8:38967723 | G | T | 1 | a0001c0001t0045g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.838-869G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967723 | |||||||
| chr8:38967733 | C | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0235 |
2 | NA19063.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.838-859C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967733 | |||||||
| chr8:38967952 | C | G | 2 | a0001c0001t0003g0114 a0001c0001t0013g0142 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.838-640C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967952 | |||||||
| chr8:38968035 | C | T | 12 | a0001c0001t0009g0001 a0001c0001t0009g0080 a0001c0001t0009g0089 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-557C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38968035 | |||||||
| chr8:38968183 | T | C | 12 | a0001c0001t0009g0001 a0001c0001t0009g0080 a0001c0001t0009g0089 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-409T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38968183 | |||||||
| chr8:38968691 | G | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0368 |
3 | NA18946.hp2 NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.915+22G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968691 | |||||||
| chr8:38968692 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0368 |
3 | NA18946.hp2 NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.915+23C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968692 | |||||||
| chr8:38968768 | C | T | 5 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0056 others(2): Show |
5 | HG01175.hp1 NA18948.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+99C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968768 | |||||||
| chr8:38968772 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(253): Show |
259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.915+103G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968772 | |||||||
| chr8:38968847 | T | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(270): Show |
276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.915+178T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968847 | |||||||
| chr8:38968898 | C | CT | 10 | a0001c0001t0001g0065 a0001c0001t0001g0096 a0001c0001t0001g0110 others(7): Show |
10 | HG01255.hp2 HG01981.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.915+247dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 38968898 | ||||||
| chr8:38968898 | CT | C | 12 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0250 others(9): Show |
12 | HG01106.hp2 HG01358.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.915+247delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 38968898 | ||||||
| chr8:38968938 | G | A | 1 | a0001c0001t0009g0089 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.915+269G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968938 | |||||||
| chr8:38968961 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.915+292C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968961 | |||||||
| chr8:38969065 | A | AT | 204 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(201): Show |
206 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.916-349dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 38969065 | ||||||
| chr8:38969154 | G | C | 2 | a0001c0001t0020g0073 a0001c0001t0050g0166 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.916-267G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969154 | |||||||
| chr8:38969250 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(203): Show |
207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.916-171G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969250 | |||||||
| chr8:38969274 | T | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(271): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.916-147T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969274 | |||||||
| chr8:38969367 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.916-54T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969367 |