Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 400224 |
| ensemblid | ENSG00000175985.10 |
| hgncid | 20148 |
| symbol | PLEKHD1 |
| name | pleckstrin homology and coiled-coil domain containing D1 |
| refseq_nuc | NM_001161498.2 |
| refseq_prot | NP_001154970.1 |
| ensembl_nuc | ENST00000322564.9 |
| ensembl_prot | ENSP00000317175.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 69484728 |
| end | 69531551 |
| strand | + |
| ver | v1.2 |
| region | chr14:69484728-69531551 |
| region5000 | chr14:69479728-69536551 |
| regionname0 | PLEKHD1_chr14_69484728_69531551 |
| regionname5000 | PLEKHD1_chr14_69479728_69536551 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 506 | 311 | 91 | 47 | 115 | 18 | 38 | 80 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0002 | 0/0 | 506 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0003 | 0/0 | 506 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0004 | 0/0 | 506 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0005 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0006 | 0/0 | 506 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0007 | 0/0 | 506 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| a0008 | 0/0 | 506 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | MFTSK others(501): Show |
chr14 | 69479728 | 69536551 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1518 | 217 | 65 | 34 | 81 | 12 | 24 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0002 | 0/0 | 1518 | 41 | 2 | 3 | 27 | 2 | 7 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0003 | 0/1 | 1518 | 40 | 14 | 10 | 7 | 4 | 4 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0004 | 0/0 | 1518 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0005 | 0/0 | 1518 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0006 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0007 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0009 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0010 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0017 | 0/0 | 1518 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0001c0018 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0002c0011 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0003c0013 | 0/0 | 1518 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0004c0014 | 0/0 | 1518 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0005c0016 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0006c0008 | 0/0 | 1518 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0007c0012 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 | ||
| a0008c0015 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | ATGTT others(1513): Show |
chr14 | 69479728 | 69536551 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4891 | 126 | 30 | 22 | 50 | 10 | 14 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0002 | 1/0 | 4891 | 32 | 15 | 3 | 4 | 0 | 9 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0003 | 0/0 | 4891 | 28 | 3 | 4 | 20 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0005 | 0/0 | 4891 | 4 | 0 | 0 | 3 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0006 | 0/0 | 4891 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0007 | 0/0 | 4891 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0008 | 0/0 | 4891 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0009 | 0/0 | 4887 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4882): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0010 | 0/0 | 4891 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0012 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0013 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0014 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0016 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0017 | 0/0 | 4887 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4882): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0018 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0019 | 0/0 | 4891 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0020 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0021 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0022 | 0/0 | 4864 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4859): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0023 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0025 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0001t0026 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0002t0001 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0002t0002 | 0/0 | 4891 | 29 | 1 | 3 | 17 | 2 | 6 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0002t0004 | 0/0 | 4891 | 9 | 0 | 0 | 9 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0002t0015 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0002t0024 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0003t0001 | 0/1 | 4891 | 25 | 1 | 8 | 7 | 4 | 4 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0003t0002 | 0/0 | 4891 | 8 | 7 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0003t0003 | 0/0 | 4891 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0003t0011 | 0/0 | 4891 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0004t0002 | 0/0 | 4891 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0005t0001 | 0/0 | 4891 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0006t0002 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0007t0002 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0009t0002 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0010t0002 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0017t0001 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0001c0018t0001 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0002c0011t0001 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0003c0013t0001 | 0/0 | 4891 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0004c0014t0005 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0005c0016t0001 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0006c0008t0001 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0007c0012t0003 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| a0008c0015t0001 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | GGAGT others(4886): Show |
chr14 | 69479728 | 69536551 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0008g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0016g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0017g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0018g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0019g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0020g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0021g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0022g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0023g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0025g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0001t0026g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0015g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0002t0024g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0003t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0004t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0004t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0004t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0004t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0004t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0006t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0007t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0009t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0010t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0017t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0001c0018t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0002c0011t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0003c0013t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0004c0014t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0005c0016t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0006c0008t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0007c0012t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| a0008c0015t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0077 | EUR | GBR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0244 | EUR | GBR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00140 | hp2 | a0001 | c0001 | t0023 | g0039 | EUR | GBR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0006 | EUR | FIN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0267 | EUR | FIN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00597 | hp1 | a0002 | c0011 | t0001 | g0021 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | CHS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00733 | hp1 | a0001 | c0003 | t0003 | g0194 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0255 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0241 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0107 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0238 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0098 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01257 | hp2 | a0001 | c0001 | t0019 | g0019 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01346 | hp1 | a0003 | c0013 | t0001 | g0224 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0210 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0208 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0109 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0220 | EUR | IBS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0221 | EUR | IBS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01884 | hp1 | a0001 | c0002 | t0024 | g0076 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01891 | hp1 | a0001 | c0018 | t0001 | g0195 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0239 | AMR | PEL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0249 | AMR | PEL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02055 | hp1 | a0001 | c0004 | t0002 | g0018 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0193 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | CDX | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | CDX | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | CDX | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02258 | hp1 | a0001 | c0003 | t0011 | g0041 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0302 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0203 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02602 | hp1 | a0004 | c0014 | t0005 | g0284 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02622 | hp1 | a0001 | c0001 | t0020 | g0254 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0181 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02717 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0166 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02723 | hp2 | a0005 | c0016 | t0001 | g0235 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0285 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0230 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0025 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02886 | hp2 | a0001 | c0010 | t0002 | g0170 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02896 | hp2 | a0001 | c0004 | t0002 | g0305 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02922 | hp1 | a0001 | c0009 | t0002 | g0204 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02922 | hp2 | a0001 | c0001 | t0025 | g0214 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0189 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02970 | hp2 | a0001 | c0004 | t0002 | g0303 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0306 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0231 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03130 | hp2 | a0001 | c0003 | t0011 | g0024 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03239 | hp2 | a0001 | c0017 | t0001 | g0084 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03453 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03486 | hp2 | a0001 | c0007 | t0002 | g0045 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0242 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03491 | hp2 | a0001 | c0005 | t0001 | g0030 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0215 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ESN | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03540 | hp2 | a0001 | c0006 | t0002 | g0299 | AFR | GWD | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0185 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0236 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0280 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0211 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03834 | hp2 | a0001 | c0005 | t0001 | g0016 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03927 | hp2 | a0001 | c0002 | t0015 | g0245 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0037 | SAS | BEB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04204 | hp2 | a0006 | c0008 | t0001 | g0243 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0217 | SAS | STU | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | YRI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | YRI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0043 | AFR | YRI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18949 | hp2 | a0007 | c0012 | t0003 | g0138 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0289 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18960 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18963 | hp2 | a0001 | c0001 | t0014 | g0117 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18979 | hp2 | a0008 | c0015 | t0001 | g0132 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19001 | hp2 | a0001 | c0001 | t0026 | g0119 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19002 | hp1 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19005 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0293 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0186 | AFR | LWK | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | LWK | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | LWK | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19064 | hp1 | a0001 | c0001 | t0016 | g0145 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0290 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19084 | hp1 | a0001 | c0001 | t0022 | g0073 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ASW | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0282 | SAS | GIH | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | GIH | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0044 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0258 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0180 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0071 | AFR | MSL | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | USA | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | USA | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | USA | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0212 | REF | REF | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0152 | REF | REF | PLEKHD1_chr14_69479728_69536551 | PLEKHD1 | chr14 | 69479728 | 69536551 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69502868 | G | C | 1 | a0002 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.544G>C | p.Glu182Gln | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/13 | 782/4891 | 544/1521 | 182/506 | chr14 | 69502868 | |||
| chr14:69524261 | G | T | 1 | a0006 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.683G>T | p.Gly228Val | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/13 | 921/4891 | 683/1521 | 228/506 | chr14 | 69524261 | |||
| chr14:69526037 | C | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.838C>T | p.Pro280Ser | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 9/13 | 1076/4891 | 838/1521 | 280/506 | chr14 | 69526037 | |||
| chr14:69526717 | G | A | 1 | a0007 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.944G>A | p.Arg315His | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 10/13 | 1182/4891 | 944/1521 | 315/506 | chr14 | 69526717 | |||
| chr14:69527282 | G | A | 1 | a0003 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1151G>A | p.Arg384Gln | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 11/13 | 1389/4891 | 1151/1521 | 384/506 | chr14 | 69527282 | |||
| chr14:69527909 | G | A | 1 | a0004 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1328G>A | p.Arg443Gln | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 12/13 | 1566/4891 | 1328/1521 | 443/506 | chr14 | 69527909 | |||
| chr14:69528342 | C | T | 1 | a0008 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1444C>T | p.Arg482Cys | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1682/4891 | 1444/1521 | 482/506 | chr14 | 69528342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69500133 | G | A | 6 | a0001c0003 a0001c0004 a0001c0006 others(3): Show |
48 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(45): Show |
synonymous_variant | LOW | c.168G>A | p.Glu56Glu | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/13 | 406/4891 | 168/1521 | 56/506 | chr14 | 69500133 | |||
| chr14:69500190 | C | T | 1 | a0001c0009 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.225C>T | p.Tyr75Tyr | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/13 | 463/4891 | 225/1521 | 75/506 | chr14 | 69500190 | |||
| chr14:69501798 | T | C | 1 | a0001c0010 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.475T>C | p.Leu159Leu | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/13 | 713/4891 | 475/1521 | 159/506 | chr14 | 69501798 | |||
| chr14:69522315 | C | T | 1 | a0001c0018 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.588C>T | p.Ala196Ala | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/13 | 826/4891 | 588/1521 | 196/506 | chr14 | 69522315 | |||
| chr14:69522330 | C | T | 1 | a0001c0017 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.603C>T | p.Phe201Phe | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/13 | 841/4891 | 603/1521 | 201/506 | chr14 | 69522330 | |||
| chr14:69526796 | G | A | 1 | a0001c0005 | 2 | HG03491.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.1023G>A | p.Thr341Thr | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 10/13 | 1261/4891 | 1023/1521 | 341/506 | chr14 | 69526796 | |||
| chr14:69527286 | T | C | 1 | a0001c0006 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1155T>C | p.Asn385Asn | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 11/13 | 1393/4891 | 1155/1521 | 385/506 | chr14 | 69527286 | |||
| chr14:69528290 | C | T | 1 | a0001c0009 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1392C>T | p.Ala464Ala | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1630/4891 | 1392/1521 | 464/506 | chr14 | 69528290 | |||
| chr14:69528305 | G | A | 2 | a0001c0004 a0001c0006 |
6 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.1407G>A | p.Glu469Glu | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1645/4891 | 1407/1521 | 469/506 | chr14 | 69528305 | |||
| chr14:69528395 | G | A | 2 | a0001c0002 a0001c0007 |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
synonymous_variant | LOW | c.1497G>A | p.Ser499Ser | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1735/4891 | 1497/1521 | 499/506 | chr14 | 69528395 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69484945 | G | T | 1 | a0001c0001t0026 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/13 | 21 | chr14 | 69484945 | ||||||
| chr14:69528424 | C | T | 1 | a0001c0001t0025 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 5 | chr14 | 69528424 | ||||||
| chr14:69528485 | G | A | 1 | a0001c0001t0012 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 66 | chr14 | 69528485 | ||||||
| chr14:69528590 | C | T | 2 | a0001c0001t0023 a0001c0002t0024 |
2 | HG00140.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*171C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 171 | chr14 | 69528590 | ||||||
| chr14:69528834 | C | G | 1 | a0001c0001t0022 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 415 | chr14 | 69528834 | ||||||
| chr14:69528837 | CCCTGCCC others(20): Show |
C | 1 | a0001c0001t0022 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*422_*448delGCCCGT others(21): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 422 | INFO_REALIGN_3_PRIME | chr14 | 69528837 | |||||
| chr14:69528844 | C | T | 7 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(4): Show |
15 | HG01175.hp2 HG02015.hp2 HG02602.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*425C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 425 | chr14 | 69528844 | ||||||
| chr14:69528898 | C | T | 2 | a0001c0001t0021 a0001c0001t0025 |
2 | HG02922.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*479C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 479 | chr14 | 69528898 | ||||||
| chr14:69528949 | A | G | 1 | a0001c0003t0011 | 2 | HG02258.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*530A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 530 | chr14 | 69528949 | ||||||
| chr14:69529051 | C | T | 1 | a0001c0001t0020 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*632C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 632 | chr14 | 69529051 | ||||||
| chr14:69529058 | C | G | 1 | a0001c0002t0004 | 9 | NA18956.hp2 NA18960.hp1 NA18965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*639C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 639 | chr14 | 69529058 | ||||||
| chr14:69529112 | T | G | 1 | a0001c0001t0007 | 3 | HG01175.hp2 HG02615.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*693T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 693 | chr14 | 69529112 | ||||||
| chr14:69529412 | T | C | 2 | a0001c0001t0021 a0001c0001t0025 |
2 | HG02922.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*993T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 993 | chr14 | 69529412 | ||||||
| chr14:69529504 | T | G | 1 | a0001c0001t0008 | 3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1085T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1085 | chr14 | 69529504 | ||||||
| chr14:69529624 | C | T | 2 | a0001c0001t0021 a0001c0001t0025 |
2 | HG02922.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1205C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1205 | chr14 | 69529624 | ||||||
| chr14:69529657 | T | C | 1 | a0001c0001t0009 | 2 | HG02145.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1238T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1238 | chr14 | 69529657 | ||||||
| chr14:69529678 | C | T | 1 | a0001c0002t0024 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1259C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1259 | chr14 | 69529678 | ||||||
| chr14:69529697 | C | T | 1 | a0001c0001t0019 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1278 | chr14 | 69529697 | ||||||
| chr14:69529852 | G | A | 2 | a0001c0001t0006 a0001c0001t0013 |
5 | HG02717.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1433G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1433 | chr14 | 69529852 | ||||||
| chr14:69530090 | G | A | 1 | a0001c0001t0014 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1671 | chr14 | 69530090 | ||||||
| chr14:69530187 | C | T | 3 | a0001c0001t0005 a0001c0001t0022 a0004c0014t0005 |
6 | HG02015.hp2 HG02602.hp1 HG04228.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1768C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1768 | chr14 | 69530187 | ||||||
| chr14:69530319 | C | T | 1 | a0001c0001t0010 | 2 | HG00738.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1900C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1900 | chr14 | 69530319 | ||||||
| chr14:69530342 | T | G | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(6): Show |
48 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1923T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 1923 | chr14 | 69530342 | ||||||
| chr14:69530531 | G | A | 1 | a0001c0002t0015 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2112G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 2112 | chr14 | 69530531 | ||||||
| chr14:69530594 | T | G | 1 | a0001c0001t0016 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2175T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 2175 | chr14 | 69530594 | ||||||
| chr14:69530868 | A | T | 17 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0018 others(14): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2449A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 2449 | chr14 | 69530868 | ||||||
| chr14:69530982 | C | T | 1 | a0001c0001t0013 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2563C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 2563 | chr14 | 69530982 | ||||||
| chr14:69530997 | C | T | 1 | a0001c0001t0008 | 3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2578C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 2578 | chr14 | 69530997 | ||||||
| chr14:69531211 | TTAAA | T | 2 | a0001c0001t0009 a0001c0001t0017 |
3 | HG02145.hp2 HG03579.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2794_*2797delAAAT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 2794 | INFO_REALIGN_3_PRIME | chr14 | 69531211 | |||||
| chr14:69531445 | G | A | 1 | a0001c0001t0018 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3026G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 13/13 | 3026 | chr14 | 69531445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69485382 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.149+268G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69485382 | |||||||
| chr14:69485573 | TA | T | 128 | a0001c0001t0001g0011 a0001c0001t0001g0190 a0001c0001t0001g0191 others(125): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.149+461delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69485573 | ||||||
| chr14:69485690 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0307 a0001c0003t0002g0302 others(3): Show |
6 | HG02451.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+576A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69485690 | |||||||
| chr14:69485701 | T | A | 3 | a0001c0001t0002g0187 a0001c0001t0009g0186 a0001c0001t0017g0185 |
3 | HG02280.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.149+587T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69485701 | |||||||
| chr14:69485702 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.149+588A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69485702 | |||||||
| chr14:69485801 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+687A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69485801 | |||||||
| chr14:69486108 | G | A | 1 | a0001c0003t0001g0188 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.149+994G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486108 | |||||||
| chr14:69486110 | G | A | 1 | a0001c0001t0007g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.149+996G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486110 | |||||||
| chr14:69486173 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+1059T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486173 | |||||||
| chr14:69486186 | G | A | 2 | a0001c0001t0001g0190 a0001c0003t0003g0189 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.149+1072G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486186 | |||||||
| chr14:69486285 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG00639.hp1 HG01256.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.149+1171A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486285 | |||||||
| chr14:69486450 | C | T | 1 | a0001c0002t0002g0300 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.149+1336C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486450 | |||||||
| chr14:69486582 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.149+1468C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486582 | |||||||
| chr14:69486616 | G | A | 4 | a0001c0001t0002g0187 a0001c0001t0002g0192 a0001c0001t0009g0186 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1502G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69486616 | |||||||
| chr14:69487017 | A | C | 30 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0307 others(27): Show |
32 | HG00735.hp1 HG02015.hp1 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.149+1903A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487017 | |||||||
| chr14:69487023 | A | T | 1 | a0001c0001t0012g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149+1909A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487023 | |||||||
| chr14:69487034 | C | G | 30 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0307 others(27): Show |
32 | HG00735.hp1 HG02015.hp1 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.149+1920C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487034 | |||||||
| chr14:69487182 | A | AAC | 65 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0074 others(62): Show |
68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.149+2109_149+2110d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | A | AACAC | 33 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(30): Show |
33 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.149+2107_149+2110d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | A | AACACAC | 23 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.149+2105_149+2110d others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | A | AACACACA others(1): Show |
8 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG00597.hp1 HG00673.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+2103_149+2110d others(10): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | A | AACACACA others(3): Show |
5 | a0001c0001t0001g0015 a0001c0001t0009g0193 a0001c0004t0002g0017 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2101_149+2110d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | A | AACACACA others(5): Show |
3 | a0001c0001t0001g0013 a0001c0001t0001g0307 a0001c0001t0007g0014 |
3 | HG02615.hp2 HG03209.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.149+2099_149+2110d others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | AAC | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0251 others(1): Show |
4 | HG01106.hp1 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2109_149+2110d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | AACAC | A | 11 | a0001c0001t0001g0177 a0001c0001t0002g0178 a0001c0001t0002g0253 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+2107_149+2110d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | AACACAC | A | 17 | a0001c0001t0001g0179 a0001c0001t0001g0264 a0001c0001t0003g0008 others(14): Show |
18 | HG00323.hp2 HG00544.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.149+2105_149+2110d others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | AACACACA others(1): Show |
A | 3 | a0001c0001t0002g0192 a0001c0001t0009g0186 a0001c0001t0018g0180 |
3 | HG02145.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.149+2103_149+2110d others(10): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | AACACACA others(3): Show |
A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0002g0187 others(2): Show |
6 | HG02280.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+2101_149+2110d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487182 | AACACACA others(5): Show |
A | 26 | a0001c0001t0001g0011 a0001c0001t0002g0297 a0001c0001t0002g0298 others(23): Show |
27 | HG00735.hp1 HG02015.hp1 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.149+2099_149+2110d others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487182 | ||||||
| chr14:69487244 | G | A | 64 | a0001c0001t0001g0011 a0001c0001t0001g0190 a0001c0001t0001g0191 others(61): Show |
66 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.149+2130G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487244 | |||||||
| chr14:69487276 | G | C | 1 | a0001c0001t0001g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+2162G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487276 | |||||||
| chr14:69487458 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.149+2344G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487458 | |||||||
| chr14:69487476 | G | A | 5 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(2): Show |
5 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+2362G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487476 | |||||||
| chr14:69487531 | T | C | 1 | a0001c0001t0009g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.149+2417T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487531 | |||||||
| chr14:69487560 | CT | C | 29 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0002g0297 others(26): Show |
31 | HG00735.hp1 HG02015.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.149+2450delT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69487560 | ||||||
| chr14:69487573 | G | C | 25 | a0001c0001t0001g0264 a0001c0001t0002g0250 a0001c0001t0002g0253 others(22): Show |
26 | HG00323.hp2 HG00544.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.149+2459G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487573 | |||||||
| chr14:69487659 | G | T | 25 | a0001c0001t0001g0264 a0001c0001t0002g0250 a0001c0001t0002g0253 others(22): Show |
26 | HG00323.hp2 HG00544.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.149+2545G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487659 | |||||||
| chr14:69487740 | T | C | 4 | a0001c0001t0002g0187 a0001c0001t0002g0192 a0001c0001t0009g0186 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2626T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69487740 | |||||||
| chr14:69488018 | C | T | 1 | a0001c0001t0009g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.149+2904C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488018 | |||||||
| chr14:69488220 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.149+3106G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488220 | |||||||
| chr14:69488234 | T | A | 1 | a0001c0001t0005g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.149+3120T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488234 | |||||||
| chr14:69488323 | A | C | 5 | a0001c0001t0001g0304 a0001c0003t0002g0302 a0001c0004t0002g0303 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+3209A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488323 | |||||||
| chr14:69488354 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.149+3240G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488354 | |||||||
| chr14:69488420 | C | A | 2 | a0001c0001t0001g0046 a0001c0007t0002g0045 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.149+3306C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488420 | |||||||
| chr14:69488534 | A | C | 71 | a0001c0001t0001g0116 a0001c0001t0001g0171 a0001c0001t0001g0172 others(68): Show |
74 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.149+3420A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488534 | |||||||
| chr14:69488602 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.149+3488G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488602 | |||||||
| chr14:69488868 | G | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG00544.hp1 HG02027.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+3754G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488868 | |||||||
| chr14:69488869 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG00544.hp1 HG02027.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+3755C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488869 | |||||||
| chr14:69488907 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.149+3793C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69488907 | |||||||
| chr14:69489002 | TG | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(52): Show |
56 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.149+3889delG | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489002 | |||||||
| chr14:69489018 | A | AGGCTTC | 90 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(87): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.149+3904_149+3905i others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489018 | |||||||
| chr14:69489201 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0169 others(18): Show |
22 | HG01081.hp1 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.149+4087A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489201 | |||||||
| chr14:69489251 | G | A | 30 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0002t0001g0274 others(27): Show |
31 | HG00733.hp1 HG00735.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.149+4137G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489251 | |||||||
| chr14:69489273 | G | A | 4 | a0001c0001t0002g0216 a0001c0001t0002g0232 a0001c0001t0021g0215 others(1): Show |
4 | HG02922.hp2 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+4159G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489273 | |||||||
| chr14:69489415 | C | A | 1 | a0001c0001t0026g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+4301C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489415 | |||||||
| chr14:69489558 | C | CA | 23 | a0001c0001t0001g0060 a0001c0001t0001g0092 a0001c0001t0001g0125 others(20): Show |
23 | HG01081.hp1 HG01261.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.149+4467dupA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | C | CAA | 54 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0033 others(51): Show |
56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.149+4466_149+4467d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | C | CAAA | 45 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(42): Show |
45 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.149+4465_149+4467d others(5): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | C | CAAAA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0169 others(21): Show |
26 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.149+4464_149+4467d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | C | CAAAAA | 22 | a0001c0001t0001g0276 a0001c0001t0003g0165 a0001c0001t0006g0009 others(19): Show |
24 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.149+4463_149+4467d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | C | CAAAAAA | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0275 others(3): Show |
6 | HG01346.hp2 HG02717.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+4462_149+4467d others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | CAAAAAA | C | 10 | a0001c0001t0003g0164 a0001c0001t0003g0252 a0001c0001t0003g0267 others(7): Show |
10 | HG00323.hp2 HG00544.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+4462_149+4467d others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0001g0249 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.149+4458_149+4467d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489558 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0171 a0001c0001t0002g0070 |
2 | HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.149+4457_149+4467d others(13): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489558 | ||||||
| chr14:69489592 | A | G | 9 | a0001c0001t0001g0213 a0001c0001t0001g0248 a0001c0001t0001g0251 others(6): Show |
10 | HG01106.hp1 HG02965.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+4478A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489592 | |||||||
| chr14:69489693 | C | T | 2 | a0001c0001t0002g0187 a0001c0002t0024g0076 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.149+4579C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489693 | |||||||
| chr14:69489723 | G | T | 6 | a0001c0001t0001g0304 a0001c0003t0002g0302 a0001c0004t0002g0303 others(3): Show |
6 | HG02451.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+4609G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489723 | |||||||
| chr14:69489857 | T | TTTTG | 6 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0161 others(3): Show |
6 | HG00323.hp1 HG00673.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+4768_149+4771d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489857 | ||||||
| chr14:69489857 | TTTTG | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(75): Show |
81 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.149+4768_149+4771d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69489857 | ||||||
| chr14:69489916 | G | C | 7 | a0001c0001t0002g0065 a0001c0001t0006g0066 a0001c0001t0007g0012 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+4802G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489916 | |||||||
| chr14:69489967 | A | C | 11 | a0001c0001t0001g0213 a0001c0001t0001g0248 a0001c0001t0001g0251 others(8): Show |
12 | HG01106.hp1 HG02965.hp1 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.149+4853A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69489967 | |||||||
| chr14:69490120 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.149+5006G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490120 | |||||||
| chr14:69490155 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0168 others(140): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.149+5041C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490155 | |||||||
| chr14:69490189 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0168 others(45): Show |
50 | HG00323.hp2 HG00544.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.149+5075G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490189 | |||||||
| chr14:69490243 | CA | C | 4 | a0001c0001t0002g0065 a0001c0001t0006g0066 a0001c0003t0011g0024 others(1): Show |
4 | HG02258.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+5130delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490243 | |||||||
| chr14:69490290 | T | C | 2 | a0001c0001t0001g0060 a0001c0003t0002g0026 |
2 | HG02976.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.149+5176T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490290 | |||||||
| chr14:69490309 | C | T | 10 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0248 others(7): Show |
11 | HG01106.hp1 HG01496.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+5195C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490309 | |||||||
| chr14:69490421 | G | A | 1 | a0001c0002t0002g0049 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.149+5307G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490421 | |||||||
| chr14:69490748 | G | A | 1 | a0001c0003t0002g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.149+5634G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490748 | |||||||
| chr14:69490825 | C | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.149+5711C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490825 | |||||||
| chr14:69490844 | C | T | 1 | a0001c0001t0003g0031 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.149+5730C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490844 | |||||||
| chr14:69490879 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.149+5765C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69490879 | |||||||
| chr14:69491055 | C | T | 4 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0248 others(1): Show |
4 | HG01106.hp1 HG01496.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+5941C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491055 | |||||||
| chr14:69491070 | A | C | 1 | a0001c0001t0022g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.149+5956A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491070 | |||||||
| chr14:69491126 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.149+6012C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491126 | |||||||
| chr14:69491481 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.149+6367C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491481 | |||||||
| chr14:69491522 | C | G | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.149+6408C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491522 | |||||||
| chr14:69491575 | C | G | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.149+6461C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491575 | |||||||
| chr14:69491590 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.149+6476C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491590 | |||||||
| chr14:69491677 | G | T | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.149+6563G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491677 | |||||||
| chr14:69491829 | G | T | 8 | a0001c0001t0002g0187 a0001c0001t0006g0175 a0001c0001t0007g0012 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+6715G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491829 | |||||||
| chr14:69491895 | T | C | 26 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0187 others(23): Show |
26 | HG01175.hp2 HG01433.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.149+6781T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491895 | |||||||
| chr14:69491910 | C | T | 1 | a0001c0002t0002g0300 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.149+6796C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491910 | |||||||
| chr14:69491944 | A | ATAAATT | 14 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0120 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.149+6834_149+6839d others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69491944 | ||||||
| chr14:69491966 | C | T | 1 | a0002c0011t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.149+6852C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69491966 | |||||||
| chr14:69492076 | A | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0159 others(3): Show |
6 | HG00323.hp1 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+6962A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492076 | |||||||
| chr14:69492079 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.149+6965G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492079 | |||||||
| chr14:69492096 | C | T | 2 | a0001c0001t0009g0186 a0001c0001t0009g0193 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.149+6982C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492096 | |||||||
| chr14:69492106 | C | A | 1 | a0001c0007t0002g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+6992C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492106 | |||||||
| chr14:69492243 | C | G | 8 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+7129C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492243 | |||||||
| chr14:69492286 | A | G | 7 | a0001c0001t0006g0175 a0001c0001t0007g0012 a0001c0001t0007g0014 others(4): Show |
7 | HG01175.hp2 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+7172A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492286 | |||||||
| chr14:69492376 | GGTCTTCA others(3): Show |
G | 1 | a0001c0001t0001g0115 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.149+7263_149+7272d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492376 | |||||||
| chr14:69492536 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.149+7422A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492536 | |||||||
| chr14:69492590 | C | T | 2 | a0001c0002t0002g0295 a0001c0002t0002g0296 |
2 | HG02165.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.149+7476C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492590 | |||||||
| chr14:69492600 | T | C | 36 | a0001c0001t0001g0095 a0001c0002t0001g0274 a0001c0002t0002g0002 others(33): Show |
38 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.149+7486T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492600 | |||||||
| chr14:69492732 | C | A | 15 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0120 others(12): Show |
16 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.150-7383C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69492732 | |||||||
| chr14:69492891 | TC | T | 7 | a0001c0003t0001g0210 a0001c0003t0001g0218 a0001c0003t0001g0219 others(4): Show |
7 | HG00741.hp1 HG01081.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-7221delC | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69492891 | ||||||
| chr14:69493046 | C | A | 2 | a0001c0001t0009g0186 a0001c0001t0009g0193 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.150-7069C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493046 | |||||||
| chr14:69493049 | G | A | 1 | a0001c0001t0018g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.150-7066G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493049 | |||||||
| chr14:69493061 | C | G | 2 | a0001c0003t0011g0024 a0001c0003t0011g0041 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.150-7054C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493061 | |||||||
| chr14:69493112 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.150-7003C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493112 | |||||||
| chr14:69493138 | G | A | 2 | a0001c0001t0002g0187 a0001c0002t0024g0076 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.150-6977G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493138 | |||||||
| chr14:69493254 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.150-6861A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493254 | |||||||
| chr14:69493266 | T | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0070 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.150-6849T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493266 | |||||||
| chr14:69493412 | C | A | 18 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0187 others(15): Show |
18 | HG01433.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.150-6703C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493412 | |||||||
| chr14:69493793 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.150-6322G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493793 | |||||||
| chr14:69493859 | G | A | 39 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(36): Show |
41 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.150-6256G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493859 | |||||||
| chr14:69493908 | G | A | 39 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(36): Show |
41 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.150-6207G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69493908 | |||||||
| chr14:69494058 | G | A | 2 | a0001c0001t0021g0215 a0001c0001t0025g0214 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.150-6057G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494058 | |||||||
| chr14:69494085 | T | C | 2 | a0001c0001t0002g0187 a0001c0002t0024g0076 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.150-6030T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494085 | |||||||
| chr14:69494212 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0116 others(132): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.150-5903T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494212 | |||||||
| chr14:69494257 | C | A | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.150-5858C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494257 | |||||||
| chr14:69494257 | C | T | 36 | a0001c0001t0001g0095 a0001c0002t0001g0274 a0001c0002t0002g0002 others(33): Show |
38 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.150-5858C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494257 | |||||||
| chr14:69494260 | T | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(29): Show |
34 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.150-5855T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494260 | |||||||
| chr14:69494332 | A | G | 1 | a0001c0004t0002g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-5783A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494332 | |||||||
| chr14:69494507 | CTA | C | 19 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0187 others(16): Show |
19 | HG01433.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.150-5607_150-5606d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494507 | |||||||
| chr14:69494598 | C | T | 8 | a0001c0003t0003g0189 a0001c0003t0003g0194 a0001c0003t0003g0203 others(5): Show |
8 | HG00733.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-5517C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494598 | |||||||
| chr14:69494658 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.150-5457G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494658 | |||||||
| chr14:69494678 | C | T | 10 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0141 others(7): Show |
11 | HG02683.hp2 HG03490.hp2 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-5437C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494678 | |||||||
| chr14:69494819 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.150-5296G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494819 | |||||||
| chr14:69494910 | C | A | 7 | a0001c0001t0001g0301 a0001c0001t0005g0217 a0001c0001t0006g0009 others(4): Show |
8 | HG02738.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-5205C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494910 | |||||||
| chr14:69494941 | T | C | 34 | a0001c0002t0002g0240 a0001c0003t0001g0006 a0001c0003t0001g0037 others(31): Show |
35 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.150-5174T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494941 | |||||||
| chr14:69494979 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0002g0057 a0001c0001t0002g0058 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-5136A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69494979 | |||||||
| chr14:69495116 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(42): Show |
47 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-4999T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495116 | |||||||
| chr14:69495244 | C | A | 10 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0141 others(7): Show |
11 | HG02683.hp2 HG03490.hp2 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-4871C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495244 | |||||||
| chr14:69495288 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.150-4827A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495288 | |||||||
| chr14:69495290 | C | T | 34 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0065 others(31): Show |
34 | HG01081.hp1 HG01175.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.150-4825C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495290 | |||||||
| chr14:69495346 | G | C | 1 | a0001c0002t0002g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.150-4769G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495346 | |||||||
| chr14:69495350 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0070 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.150-4765G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495350 | |||||||
| chr14:69495493 | A | C | 2 | a0001c0001t0002g0250 a0001c0001t0014g0117 |
2 | NA18963.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.150-4622A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495493 | |||||||
| chr14:69495576 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-4539G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495576 | |||||||
| chr14:69495593 | G | T | 2 | a0001c0001t0002g0187 a0001c0002t0024g0076 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.150-4522G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495593 | |||||||
| chr14:69495654 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.150-4461A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495654 | |||||||
| chr14:69495669 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.150-4446C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495669 | |||||||
| chr14:69495800 | C | A | 2 | a0001c0003t0002g0071 a0001c0003t0002g0166 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.150-4315C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495800 | |||||||
| chr14:69495910 | G | A | 19 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0187 others(16): Show |
19 | HG01433.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.150-4205G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495910 | |||||||
| chr14:69495917 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0248 a0001c0001t0001g0251 |
3 | HG01106.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.150-4198G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495917 | |||||||
| chr14:69495958 | G | A | 2 | a0001c0003t0001g0239 a0001c0003t0001g0249 |
2 | HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.150-4157G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69495958 | |||||||
| chr14:69496002 | G | C | 12 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0264 others(9): Show |
13 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-4113G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496002 | |||||||
| chr14:69496191 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.150-3924C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496191 | |||||||
| chr14:69496267 | T | A | 34 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0065 others(31): Show |
34 | HG01081.hp1 HG01175.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.150-3848T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496267 | |||||||
| chr14:69496283 | A | G | 34 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0065 others(31): Show |
34 | HG01081.hp1 HG01175.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.150-3832A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496283 | |||||||
| chr14:69496408 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.150-3707G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496408 | |||||||
| chr14:69496479 | A | G | 2 | a0001c0001t0021g0215 a0001c0001t0025g0214 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.150-3636A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496479 | |||||||
| chr14:69496525 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.150-3590G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496525 | |||||||
| chr14:69496608 | A | G | 11 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-3507A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496608 | |||||||
| chr14:69496702 | A | AT | 47 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0048 others(44): Show |
49 | HG00323.hp1 HG00544.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.150-3391dupT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69496702 | ||||||
| chr14:69496702 | A | ATT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0177 others(37): Show |
42 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.150-3392_150-3391d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69496702 | ||||||
| chr14:69496702 | A | ATTT | 9 | a0001c0001t0002g0121 a0001c0001t0002g0250 a0001c0001t0002g0256 others(6): Show |
9 | HG01192.hp1 HG01517.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-3393_150-3391d others(5): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69496702 | ||||||
| chr14:69496702 | A | ATTTTTTT | 11 | a0001c0001t0001g0099 a0001c0001t0001g0264 a0001c0001t0002g0007 others(8): Show |
12 | HG01175.hp2 HG02630.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.150-3397_150-3391d others(9): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69496702 | ||||||
| chr14:69496702 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0002g0065 a0001c0001t0002g0298 |
2 | HG02809.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.150-3400_150-3391d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69496702 | ||||||
| chr14:69496702 | AT | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0062 others(6): Show |
9 | HG00099.hp2 HG01257.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-3391delT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69496702 | ||||||
| chr14:69496725 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.150-3390A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496725 | |||||||
| chr14:69496896 | C | T | 3 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 |
3 | HG02145.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.150-3219C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496896 | |||||||
| chr14:69496900 | C | A | 1 | a0001c0002t0024g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.150-3215C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69496900 | |||||||
| chr14:69497116 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.150-2999G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497116 | |||||||
| chr14:69497338 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-2777C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497338 | |||||||
| chr14:69497403 | A | G | 131 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0099 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.150-2712A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497403 | |||||||
| chr14:69497484 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.150-2631C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497484 | |||||||
| chr14:69497596 | A | T | 73 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(70): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.150-2519A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497596 | |||||||
| chr14:69497606 | C | G | 1 | a0001c0001t0013g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.150-2509C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497606 | |||||||
| chr14:69497610 | A | T | 58 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0065 others(55): Show |
59 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.150-2505A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497610 | |||||||
| chr14:69497646 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.150-2469G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497646 | |||||||
| chr14:69497708 | A | C | 131 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0099 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.150-2407A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497708 | |||||||
| chr14:69497745 | G | A | 3 | a0001c0001t0007g0012 a0001c0001t0007g0014 a0001c0001t0007g0098 |
3 | HG01175.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.150-2370G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497745 | |||||||
| chr14:69497805 | C | A | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.150-2310C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497805 | |||||||
| chr14:69497805 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0173 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.150-2310C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497805 | |||||||
| chr14:69497853 | CTG | C | 3 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 |
3 | HG02145.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.150-2258_150-2257d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69497853 | ||||||
| chr14:69497909 | T | C | 12 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0264 others(9): Show |
13 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-2206T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69497909 | |||||||
| chr14:69498032 | G | GTTTTA | 10 | a0001c0003t0001g0160 a0001c0003t0001g0223 a0001c0003t0002g0043 others(7): Show |
10 | HG00673.hp2 HG01433.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-2059_150-2055d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498032 | ||||||
| chr14:69498032 | G | GTTTTATT others(3): Show |
1 | a0001c0003t0002g0026 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.150-2064_150-2055d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498032 | ||||||
| chr14:69498032 | G | GTTTTATT others(17): Show |
1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.150-2060_150-2059i others(26): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498032 | ||||||
| chr14:69498032 | G | GTTTTTTT others(157): Show |
1 | a0001c0002t0024g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.150-2079_150-2078i others(166): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498032 | ||||||
| chr14:69498033 | T | TTTTATTT others(2): Show |
3 | a0001c0001t0002g0253 a0001c0001t0010g0258 a0001c0001t0012g0181 |
3 | HG02109.hp2 HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-2078_150-2070d others(11): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498033 | ||||||
| chr14:69498038 | T | TTTTA | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(1): Show |
4 | HG01192.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-2073_150-2070d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498038 | ||||||
| chr14:69498042 | A | G | 8 | a0001c0002t0004g0010 a0001c0002t0004g0277 a0001c0002t0004g0288 others(5): Show |
9 | NA18956.hp2 NA18960.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-2073A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498042 | |||||||
| chr14:69498042 | AT | A | 4 | a0001c0001t0002g0256 a0001c0001t0010g0255 a0001c0001t0014g0117 others(1): Show |
4 | HG00738.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-2069delT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498042 | ||||||
| chr14:69498053 | TTTTA | T | 3 | a0001c0001t0002g0256 a0001c0001t0020g0254 a0001c0007t0002g0045 |
3 | HG02622.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.150-2054_150-2051d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498053 | ||||||
| chr14:69498056 | T | A | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.150-2059T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498056 | |||||||
| chr14:69498057 | A | AT | 11 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-2055dupT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTAT | 42 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0029 others(39): Show |
43 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.150-2013_150-2009d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTATTT others(3): Show |
23 | a0001c0001t0001g0159 a0001c0001t0001g0163 a0001c0001t0001g0183 others(20): Show |
23 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.150-2018_150-2009d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTATTT others(8): Show |
21 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0172 others(18): Show |
22 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.150-2023_150-2009d others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTATTT others(13): Show |
6 | a0001c0002t0002g0112 a0001c0002t0002g0280 a0001c0002t0002g0282 others(3): Show |
6 | HG02080.hp2 HG02155.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-2028_150-2009d others(22): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTATTT others(18): Show |
2 | a0001c0002t0001g0274 a0001c0002t0002g0281 |
2 | NA18956.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.150-2033_150-2009d others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTATTT others(23): Show |
1 | a0001c0002t0002g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.150-2038_150-2009d others(32): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTTATT others(3): Show |
7 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0003t0003g0194 others(4): Show |
7 | HG00733.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-2055_150-2054i others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTTATT others(8): Show |
16 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0218 others(13): Show |
16 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.150-2055_150-2054i others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTTATT others(13): Show |
1 | a0001c0003t0001g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.150-2055_150-2054i others(22): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTTATT others(18): Show |
1 | a0001c0003t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.150-2055_150-2054i others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTTATT others(18): Show |
8 | a0001c0002t0004g0010 a0001c0002t0004g0277 a0001c0002t0004g0288 others(5): Show |
8 | NA18956.hp2 NA18965.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-2055_150-2054i others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | ATTTTATT others(23): Show |
1 | a0001c0002t0004g0010 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.150-2055_150-2054i others(32): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | A | T | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.150-2058A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498057 | |||||||
| chr14:69498057 | ATTTAT | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01515.hp1 HG02257.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-2013_150-2009d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498057 | ATTTATTT others(3): Show |
A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0099 a0001c0001t0001g0169 others(10): Show |
13 | HG01175.hp2 HG02145.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-2018_150-2009d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498057 | ||||||
| chr14:69498061 | A | T | 21 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0002g0007 others(18): Show |
23 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.150-2054A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498061 | |||||||
| chr14:69498062 | T | A | 21 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0002g0007 others(18): Show |
23 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.150-2053T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498062 | |||||||
| chr14:69498105 | TA | T | 6 | a0001c0001t0002g0250 a0001c0001t0002g0256 a0001c0001t0002g0257 others(3): Show |
6 | HG00738.hp1 HG01192.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-2009delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498105 | |||||||
| chr14:69498106 | A | ATT | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.150-2009_150-2008i others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498106 | |||||||
| chr14:69498106 | A | ATTTT | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0253 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-2009_150-2008i others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498106 | |||||||
| chr14:69498389 | G | A | 6 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-1726G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498389 | |||||||
| chr14:69498452 | T | C | 65 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0099 others(62): Show |
68 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.150-1663T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498452 | |||||||
| chr14:69498588 | T | TTTCTC | 37 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0033 others(34): Show |
37 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.150-1457_150-1453d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(3): Show |
35 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0040 others(32): Show |
35 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.150-1462_150-1453d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(8): Show |
31 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0038 others(28): Show |
32 | HG01071.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.150-1467_150-1453d others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(13): Show |
23 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0052 others(20): Show |
24 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.150-1472_150-1453d others(22): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(18): Show |
12 | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0115 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.150-1477_150-1453d others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(23): Show |
7 | a0001c0003t0001g0210 a0001c0003t0001g0219 a0001c0003t0001g0220 others(4): Show |
7 | HG00140.hp1 HG01346.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-1499_150-1498i others(32): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(28): Show |
2 | a0001c0003t0001g0037 a0001c0003t0001g0218 |
2 | HG00741.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.150-1499_150-1498i others(37): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(33): Show |
2 | a0001c0003t0001g0241 a0001c0003t0001g0294 |
2 | HG00738.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.150-1499_150-1498i others(42): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(23): Show |
4 | a0001c0001t0001g0275 a0001c0001t0003g0093 a0001c0002t0002g0282 others(1): Show |
4 | HG02165.hp2 HG02717.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-1482_150-1453d others(32): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(28): Show |
2 | a0001c0001t0001g0105 a0001c0002t0002g0281 |
2 | HG01934.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.150-1487_150-1453d others(37): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(33): Show |
2 | a0001c0001t0001g0143 a0001c0002t0004g0288 |
2 | NA18965.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.150-1492_150-1453d others(42): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | T | TTTCTCTT others(48): Show |
1 | a0001c0002t0002g0280 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.150-1507_150-1453d others(57): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | TTTCTC | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0069 others(20): Show |
24 | HG00280.hp2 HG00544.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.150-1457_150-1453d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | TTTCTCTT others(3): Show |
T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02683.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-1462_150-1453d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | TTTCTCTT others(8): Show |
T | 10 | a0001c0001t0001g0157 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01515.hp2 HG01517.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-1467_150-1453d others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | TTTCTCTT others(13): Show |
T | 5 | a0001c0001t0002g0070 a0001c0001t0002g0199 a0001c0001t0002g0247 others(2): Show |
5 | HG02486.hp2 HG03098.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-1472_150-1453d others(22): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498588 | TTTCTCTT others(18): Show |
T | 13 | a0001c0001t0001g0264 a0001c0001t0002g0120 a0001c0001t0002g0121 others(10): Show |
13 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-1477_150-1453d others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498588 | ||||||
| chr14:69498592 | T | TCTTCTCT others(18): Show |
13 | a0001c0003t0001g0139 a0001c0003t0001g0160 a0001c0003t0001g0188 others(10): Show |
13 | HG00673.hp2 HG01081.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-1499_150-1498i others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498592 | ||||||
| chr14:69498597 | T | TCTTCTCT others(13): Show |
2 | a0001c0003t0001g0006 a0001c0003t0001g0239 |
3 | HG00280.hp1 HG00639.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.150-1499_150-1498i others(22): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498597 | ||||||
| chr14:69498602 | T | TCTTCTCT others(8): Show |
6 | a0001c0003t0001g0140 a0001c0003t0003g0194 a0001c0003t0003g0231 others(3): Show |
6 | HG00733.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1499_150-1498i others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498602 | ||||||
| chr14:69498638 | CTTCTCTT others(18): Show |
C | 1 | a0001c0001t0005g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.150-1475_150-1451d others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498638 | ||||||
| chr14:69498643 | CTTCTCTT others(13): Show |
C | 1 | a0001c0001t0022g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.150-1470_150-1451d others(22): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498643 | ||||||
| chr14:69498648 | CTTCTCTT others(8): Show |
C | 4 | a0001c0001t0003g0001 a0001c0001t0003g0270 a0001c0001t0021g0215 others(1): Show |
4 | HG01243.hp2 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-1465_150-1451d others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498648 | ||||||
| chr14:69498653 | CTTCTCTT others(3): Show |
C | 9 | a0001c0001t0001g0001 a0001c0001t0003g0097 a0001c0001t0003g0164 others(6): Show |
9 | HG02071.hp1 HG02083.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-1460_150-1451d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498653 | ||||||
| chr14:69498658 | CTTCTT | C | 13 | a0001c0001t0001g0177 a0001c0001t0001g0301 a0001c0001t0003g0001 others(10): Show |
15 | HG00323.hp2 HG00544.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-1455_150-1451d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69498658 | ||||||
| chr14:69498663 | T | C | 12 | a0001c0001t0001g0168 a0001c0001t0001g0276 a0001c0001t0002g0167 others(9): Show |
12 | HG00642.hp2 HG00735.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.150-1452T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498663 | |||||||
| chr14:69498846 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.150-1269C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498846 | |||||||
| chr14:69498894 | C | T | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.150-1221C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498894 | |||||||
| chr14:69498895 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0177 others(36): Show |
42 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.150-1220G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498895 | |||||||
| chr14:69498993 | G | A | 2 | a0001c0001t0021g0215 a0001c0001t0025g0214 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.150-1122G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69498993 | |||||||
| chr14:69499225 | G | GCA | 5 | a0001c0001t0001g0040 a0001c0001t0002g0070 a0001c0001t0007g0012 others(2): Show |
5 | HG01175.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-850_150-849dup others(2): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | G | GCACA | 3 | a0001c0001t0001g0174 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01515.hp2 HG01517.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.150-852_150-849dup others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCA | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.150-850_150-849del others(2): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACA | G | 28 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0046 others(25): Show |
28 | HG00673.hp1 HG01433.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-852_150-849del others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACACA | G | 14 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0088 others(11): Show |
15 | HG00280.hp1 HG00639.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-854_150-849del others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACACAC others(1): Show |
G | 59 | a0001c0001t0001g0028 a0001c0001t0001g0116 a0001c0001t0001g0134 others(56): Show |
61 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.150-856_150-849del others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACACAC others(3): Show |
G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0177 others(16): Show |
21 | HG00642.hp2 HG00735.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.150-858_150-849del others(10): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACACAC others(5): Show |
G | 47 | a0001c0001t0001g0095 a0001c0001t0002g0141 a0001c0001t0002g0197 others(44): Show |
49 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.150-860_150-849del others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACACAC others(7): Show |
G | 13 | a0001c0001t0001g0264 a0001c0001t0002g0120 a0001c0001t0002g0121 others(10): Show |
13 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-862_150-849del others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499225 | GCACACAC others(19): Show |
G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 |
3 | HG02145.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.150-874_150-849del others(26): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 69499225 | ||||||
| chr14:69499539 | G | T | 6 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-576G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499539 | |||||||
| chr14:69499627 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.150-488T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499627 | |||||||
| chr14:69499637 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.150-478G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499637 | |||||||
| chr14:69499707 | C | A | 52 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0134 others(49): Show |
55 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.150-408C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499707 | |||||||
| chr14:69499717 | T | G | 1 | a0001c0003t0001g0006 | 2 | HG00280.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.150-398T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499717 | |||||||
| chr14:69499799 | G | A | 24 | a0001c0003t0001g0006 a0001c0003t0001g0037 a0001c0003t0001g0139 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-316G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499799 | |||||||
| chr14:69499882 | G | T | 1 | a0001c0001t0002g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-233G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499882 | |||||||
| chr14:69499888 | C | T | 122 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0134 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.150-227C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499888 | |||||||
| chr14:69499908 | C | G | 1 | a0001c0003t0001g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-207C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69499908 | |||||||
| chr14:69500034 | C | A | 7 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(4): Show |
7 | HG01175.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-81C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 1/12 | chr14 | 69500034 | |||||||
| chr14:69500282 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.243+74G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/12 | chr14 | 69500282 | |||||||
| chr14:69500404 | C | G | 1 | a0001c0001t0003g0097 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.244-173C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/12 | chr14 | 69500404 | |||||||
| chr14:69500453 | G | C | 2 | a0001c0001t0021g0215 a0001c0001t0025g0214 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.244-124G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/12 | chr14 | 69500453 | |||||||
| chr14:69500461 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.244-116G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/12 | chr14 | 69500461 | |||||||
| chr14:69500543 | G | C | 2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.244-34G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/12 | chr14 | 69500543 | |||||||
| chr14:69500567 | T | C | 6 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-10T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 2/12 | chr14 | 69500567 | |||||||
| chr14:69500676 | G | A | 6 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+10G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 3/12 | chr14 | 69500676 | |||||||
| chr14:69500753 | C | T | 33 | a0001c0003t0001g0006 a0001c0003t0001g0037 a0001c0003t0001g0139 others(30): Show |
34 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.333+87C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 3/12 | chr14 | 69500753 | |||||||
| chr14:69500810 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.334-61G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 3/12 | chr14 | 69500810 | |||||||
| chr14:69501110 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0177 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.410+163T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 4/12 | chr14 | 69501110 | |||||||
| chr14:69501150 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.410+203G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 4/12 | chr14 | 69501150 | |||||||
| chr14:69501623 | G | A | 1 | a0001c0002t0024g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-111G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 4/12 | chr14 | 69501623 | |||||||
| chr14:69501641 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.411-93C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 4/12 | chr14 | 69501641 | |||||||
| chr14:69501727 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0019g0019 |
2 | HG00642.hp1 HG01257.hp2 |
splice_region_variant&intron_variant | LOW | c.411-7T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 4/12 | chr14 | 69501727 | |||||||
| chr14:69501830 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.502+5G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69501830 | |||||||
| chr14:69501831 | C | T | 12 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.502+6C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69501831 | |||||||
| chr14:69501961 | C | T | 1 | a0001c0003t0011g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.502+136C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69501961 | |||||||
| chr14:69501991 | C | A | 7 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(4): Show |
7 | HG01175.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+166C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69501991 | |||||||
| chr14:69502021 | G | A | 10 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0141 others(7): Show |
11 | HG02683.hp2 HG03490.hp2 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+196G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502021 | |||||||
| chr14:69502349 | G | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(5): Show |
8 | HG01175.hp2 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-478G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502349 | |||||||
| chr14:69502383 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.503-444G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502383 | |||||||
| chr14:69502464 | A | G | 7 | a0001c0003t0001g0210 a0001c0003t0001g0218 a0001c0003t0001g0219 others(4): Show |
7 | HG00741.hp1 HG01081.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-363A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502464 | |||||||
| chr14:69502641 | TG | T | 86 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0134 others(83): Show |
89 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.503-181delG | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 69502641 | ||||||
| chr14:69502650 | G | A | 4 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0122 others(1): Show |
4 | HG02280.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-177G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502650 | |||||||
| chr14:69502743 | C | T | 1 | a0001c0001t0009g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.503-84C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502743 | |||||||
| chr14:69502818 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.503-9T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 5/12 | chr14 | 69502818 | |||||||
| chr14:69502942 | G | T | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+63G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69502942 | |||||||
| chr14:69503004 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.555+125G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503004 | |||||||
| chr14:69503129 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0099 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.555+250G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503129 | |||||||
| chr14:69503285 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.555+406A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503285 | |||||||
| chr14:69503305 | G | A | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+426G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503305 | |||||||
| chr14:69503507 | A | G | 9 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0001g0190 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+628A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503507 | |||||||
| chr14:69503544 | A | G | 2 | a0001c0001t0009g0186 a0001c0001t0009g0193 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.555+665A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503544 | |||||||
| chr14:69503557 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.555+678A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503557 | |||||||
| chr14:69503560 | G | C | 5 | a0001c0003t0001g0160 a0001c0003t0001g0188 a0001c0003t0001g0222 others(2): Show |
5 | HG00673.hp2 HG02083.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.555+681G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503560 | |||||||
| chr14:69503607 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.555+728C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503607 | |||||||
| chr14:69503615 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.555+736C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503615 | |||||||
| chr14:69503622 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.555+743C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503622 | |||||||
| chr14:69503646 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555+767G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503646 | |||||||
| chr14:69503648 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(27): Show |
32 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.555+769G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503648 | |||||||
| chr14:69503669 | C | T | 1 | a0001c0006t0002g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.555+790C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503669 | |||||||
| chr14:69503690 | C | CA | 45 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0042 others(42): Show |
46 | HG00597.hp2 HG00741.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+835dupA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503690 | ||||||
| chr14:69503690 | C | CAA | 17 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0248 others(14): Show |
17 | HG00673.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.555+834_555+835dup others(2): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503690 | ||||||
| chr14:69503690 | C | CAAA | 6 | a0001c0001t0002g0178 a0001c0001t0002g0192 a0001c0001t0002g0250 others(3): Show |
6 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+833_555+835dup others(3): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503690 | ||||||
| chr14:69503690 | CA | C | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0184 others(9): Show |
12 | HG01175.hp2 HG01256.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.555+835delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503690 | ||||||
| chr14:69503690 | CAA | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0177 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.555+834_555+835del others(2): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503690 | ||||||
| chr14:69503690 | CAAA | C | 6 | a0001c0001t0003g0265 a0001c0001t0003g0273 a0001c0001t0006g0009 others(3): Show |
7 | HG02717.hp1 HG02965.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+833_555+835del others(3): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503690 | ||||||
| chr14:69503705 | A | T | 1 | a0001c0001t0001g0143 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.555+826A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503705 | |||||||
| chr14:69503714 | AT | A | 7 | a0001c0003t0002g0302 a0001c0004t0002g0017 a0001c0004t0002g0018 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+836delT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503714 | |||||||
| chr14:69503715 | T | A | 7 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(4): Show |
7 | HG01433.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+836T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503715 | |||||||
| chr14:69503833 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.555+954C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69503833 | |||||||
| chr14:69503863 | C | CA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.555+1010dupA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503863 | ||||||
| chr14:69503863 | C | CAA | 12 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(9): Show |
13 | HG00673.hp2 HG01175.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.555+1009_555+1010d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503863 | ||||||
| chr14:69503863 | CA | C | 61 | a0001c0001t0001g0038 a0001c0001t0001g0095 a0001c0001t0001g0161 others(58): Show |
62 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.555+1010delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503863 | ||||||
| chr14:69503863 | CAA | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0002g0120 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+1009_555+1010d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69503863 | ||||||
| chr14:69504035 | T | C | 70 | a0001c0001t0001g0095 a0001c0001t0002g0120 a0001c0001t0002g0121 others(67): Show |
72 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.555+1156T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504035 | |||||||
| chr14:69504228 | T | A | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+1349T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504228 | |||||||
| chr14:69504309 | T | G | 2 | a0001c0001t0002g0256 a0001c0001t0020g0254 |
2 | HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.555+1430T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504309 | |||||||
| chr14:69504363 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0002g0167 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.555+1484A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504363 | |||||||
| chr14:69504365 | C | T | 7 | a0001c0003t0002g0302 a0001c0004t0002g0017 a0001c0004t0002g0018 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+1486C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504365 | |||||||
| chr14:69504455 | T | C | 1 | a0001c0001t0003g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.555+1576T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504455 | |||||||
| chr14:69504513 | T | C | 1 | a0001c0001t0007g0098 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555+1634T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504513 | |||||||
| chr14:69504628 | TTTC | T | 3 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 |
3 | HG02145.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.555+1757_555+1759d others(5): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69504628 | ||||||
| chr14:69504793 | A | T | 11 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+1914A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504793 | |||||||
| chr14:69504881 | T | C | 44 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(41): Show |
46 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+2002T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504881 | |||||||
| chr14:69504967 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0159 others(3): Show |
6 | HG00323.hp1 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.555+2088G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504967 | |||||||
| chr14:69504981 | T | C | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+2102T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69504981 | |||||||
| chr14:69505270 | C | T | 1 | a0008c0015t0001g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.555+2391C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505270 | |||||||
| chr14:69505299 | C | A | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+2420C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505299 | |||||||
| chr14:69505445 | G | A | 2 | a0001c0001t0005g0217 a0001c0001t0022g0073 |
2 | HG04228.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.555+2566G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505445 | |||||||
| chr14:69505461 | A | T | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.555+2582A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505461 | |||||||
| chr14:69505752 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.555+2873C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505752 | |||||||
| chr14:69505762 | T | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.555+2883T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505762 | |||||||
| chr14:69505951 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.555+3072G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69505951 | |||||||
| chr14:69506411 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+3532C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506411 | |||||||
| chr14:69506474 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.555+3595C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506474 | |||||||
| chr14:69506718 | G | T | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+3839G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506718 | |||||||
| chr14:69506777 | C | T | 41 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(38): Show |
43 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.555+3898C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506777 | |||||||
| chr14:69506780 | C | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0095 others(129): Show |
138 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+3901C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506780 | |||||||
| chr14:69506807 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0001g0146 |
3 | HG02040.hp2 NA18965.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.555+3928T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506807 | |||||||
| chr14:69506830 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.555+3951A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506830 | |||||||
| chr14:69506891 | C | CT | 30 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0067 others(27): Show |
30 | HG00741.hp2 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.555+4040dupT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTT | 20 | a0001c0001t0001g0069 a0001c0001t0001g0148 a0001c0001t0001g0264 others(17): Show |
21 | HG00544.hp1 HG01258.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.555+4039_555+4040d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTT | 7 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0010g0255 others(4): Show |
7 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+4035_555+4040d others(8): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0009g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+4031_555+4040d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0009g0193 a0001c0001t0025g0214 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.555+4030_555+4040d others(13): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(5): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0002g0167 others(14): Show |
19 | HG00642.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.555+4029_555+4040d others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0001g0301 a0001c0001t0003g0051 a0001c0001t0003g0165 others(5): Show |
8 | HG00544.hp2 HG00735.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.555+4028_555+4040d others(15): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0003g0164 a0001c0001t0003g0267 a0001c0001t0003g0268 |
3 | HG00323.hp2 HG02083.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.555+4026_555+4040d others(17): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0003g0269 a0001c0001t0003g0272 |
2 | HG02071.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.555+4025_555+4040d others(18): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0007g0098 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555+4022_555+4040d others(21): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | CT | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0023 others(18): Show |
21 | HG00099.hp2 HG01069.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.555+4040delT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | CTTT | C | 11 | a0001c0001t0001g0225 a0001c0001t0002g0120 a0001c0001t0002g0121 others(8): Show |
11 | HG01261.hp2 HG01515.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+4038_555+4040d others(5): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506891 | CTTTT | C | 35 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(32): Show |
37 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.555+4037_555+4040d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69506891 | ||||||
| chr14:69506956 | G | A | 26 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(23): Show |
26 | HG00738.hp1 HG01192.hp1 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.555+4077G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69506956 | |||||||
| chr14:69507049 | C | T | 1 | a0001c0003t0002g0208 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.555+4170C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507049 | |||||||
| chr14:69507158 | G | A | 1 | a0001c0001t0002g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.555+4279G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507158 | |||||||
| chr14:69507369 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.555+4490C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507369 | |||||||
| chr14:69507637 | A | T | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+4758A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507637 | |||||||
| chr14:69507759 | C | A | 3 | a0001c0002t0001g0274 a0001c0002t0002g0281 a0001c0002t0002g0283 |
3 | NA18956.hp1 NA18993.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.555+4880C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507759 | |||||||
| chr14:69507863 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+4984C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507863 | |||||||
| chr14:69507883 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0095 others(99): Show |
108 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.555+5004A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69507883 | |||||||
| chr14:69508007 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0095 others(131): Show |
140 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.555+5128C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508007 | |||||||
| chr14:69508014 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.555+5135G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508014 | |||||||
| chr14:69508047 | G | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0099 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.555+5168G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508047 | |||||||
| chr14:69508129 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.555+5250C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508129 | |||||||
| chr14:69508146 | C | T | 1 | a0001c0003t0001g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.555+5267C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508146 | |||||||
| chr14:69508173 | C | T | 12 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.555+5294C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508173 | |||||||
| chr14:69508263 | G | A | 13 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.555+5384G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508263 | |||||||
| chr14:69508405 | CA | C | 12 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.555+5538delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69508405 | ||||||
| chr14:69508412 | A | C | 11 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+5533A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508412 | |||||||
| chr14:69508448 | G | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(41): Show |
47 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.555+5569G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508448 | |||||||
| chr14:69508576 | G | C | 26 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(23): Show |
26 | HG00738.hp1 HG01192.hp1 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.555+5697G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508576 | |||||||
| chr14:69508588 | A | G | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.555+5709A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508588 | |||||||
| chr14:69508621 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.555+5742G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508621 | |||||||
| chr14:69508965 | G | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+6086G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508965 | |||||||
| chr14:69508987 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.555+6108C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69508987 | |||||||
| chr14:69509198 | G | A | 1 | a0001c0002t0024g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.555+6319G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509198 | |||||||
| chr14:69509456 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.555+6577T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509456 | |||||||
| chr14:69509630 | T | C | 2 | a0001c0001t0009g0186 a0001c0001t0009g0193 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.555+6751T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509630 | |||||||
| chr14:69509665 | C | T | 2 | a0001c0001t0021g0215 a0001c0001t0025g0214 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.555+6786C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509665 | |||||||
| chr14:69509709 | G | A | 1 | a0001c0003t0001g0242 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.555+6830G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509709 | |||||||
| chr14:69509728 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0116 a0001c0001t0001g0134 |
3 | HG01243.hp1 HG01515.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.555+6849A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509728 | |||||||
| chr14:69509807 | G | A | 3 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 |
3 | HG02145.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.555+6928G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509807 | |||||||
| chr14:69509863 | A | G | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+6984A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509863 | |||||||
| chr14:69509877 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.555+6998G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509877 | |||||||
| chr14:69509949 | A | G | 41 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(38): Show |
43 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.555+7070A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69509949 | |||||||
| chr14:69510092 | T | C | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+7213T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510092 | |||||||
| chr14:69510251 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(44): Show |
50 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.555+7372T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510251 | |||||||
| chr14:69510425 | T | C | 1 | a0001c0004t0002g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.555+7546T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510425 | |||||||
| chr14:69510567 | A | G | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0003g0272 |
3 | HG02071.hp1 NA18982.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.555+7688A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510567 | |||||||
| chr14:69510755 | G | C | 13 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.555+7876G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510755 | |||||||
| chr14:69510790 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0072 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+7911T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510790 | |||||||
| chr14:69510963 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+8084C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69510963 | |||||||
| chr14:69511019 | T | C | 1 | a0001c0003t0001g0294 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.555+8140T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511019 | |||||||
| chr14:69511096 | A | G | 7 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(4): Show |
7 | HG01433.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+8217A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511096 | |||||||
| chr14:69511139 | T | TTTTG | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0003g0032 others(2): Show |
5 | HG00642.hp2 HG00735.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+8279_555+8282d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69511139 | ||||||
| chr14:69511139 | TTTTG | T | 20 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0057 others(17): Show |
21 | HG01256.hp2 HG01258.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.555+8279_555+8282d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69511139 | ||||||
| chr14:69511318 | C | A | 13 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.555+8439C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511318 | |||||||
| chr14:69511394 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.555+8515A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511394 | |||||||
| chr14:69511660 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | NA18964.hp1 NA18970.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.555+8781G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511660 | |||||||
| chr14:69511698 | C | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0232 a0001c0002t0002g0096 |
3 | HG02486.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.555+8819C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511698 | |||||||
| chr14:69511744 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.555+8865T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511744 | |||||||
| chr14:69511819 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0095 others(131): Show |
140 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.555+8940A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511819 | |||||||
| chr14:69511826 | T | C | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.555+8947T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69511826 | |||||||
| chr14:69512001 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(292): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.555+9122T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69512001 | |||||||
| chr14:69512065 | T | A | 1 | a0001c0002t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.555+9186T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69512065 | |||||||
| chr14:69512229 | CTG | C | 42 | a0001c0001t0001g0095 a0001c0001t0002g0216 a0001c0001t0002g0232 others(39): Show |
44 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.555+9352_555+9353d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69512229 | ||||||
| chr14:69512531 | C | T | 1 | a0001c0001t0010g0255 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.555+9652C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69512531 | |||||||
| chr14:69512531 | CATTT | C | 13 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.555+9653_555+9656d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69512531 | |||||||
| chr14:69512902 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.556-9381A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69512902 | |||||||
| chr14:69512987 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.556-9296G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69512987 | |||||||
| chr14:69513053 | A | G | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.556-9230A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513053 | |||||||
| chr14:69513219 | AAAAAT | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0144 |
3 | HG00673.hp1 HG02080.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.556-9041_556-9037d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69513219 | ||||||
| chr14:69513244 | T | TAAAATAA others(18): Show |
1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-9037_556-9036i others(27): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69513244 | ||||||
| chr14:69513244 | TAATAA | T | 18 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0264 others(15): Show |
19 | HG01081.hp1 HG01243.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.556-9011_556-9007d others(7): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69513244 | ||||||
| chr14:69513244 | TAATAAAA others(3): Show |
T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0066 a0001c0001t0006g0175 others(1): Show |
5 | HG02717.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-9016_556-9007d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69513244 | ||||||
| chr14:69513473 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0002g0056 |
2 | HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.556-8810C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513473 | |||||||
| chr14:69513488 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(41): Show |
47 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.556-8795G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513488 | |||||||
| chr14:69513615 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.556-8668A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513615 | |||||||
| chr14:69513794 | A | G | 13 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.556-8489A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513794 | |||||||
| chr14:69513823 | G | C | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.556-8460G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513823 | |||||||
| chr14:69513870 | C | G | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-8413C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513870 | |||||||
| chr14:69513948 | C | A | 12 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.556-8335C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69513948 | |||||||
| chr14:69514093 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.556-8190T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514093 | |||||||
| chr14:69514106 | C | CT | 7 | a0001c0002t0004g0010 a0001c0002t0004g0277 a0001c0002t0004g0288 others(4): Show |
8 | NA18956.hp2 NA18960.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.556-8176dupT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69514106 | ||||||
| chr14:69514224 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.556-8059C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514224 | |||||||
| chr14:69514252 | G | GT | 15 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0003t0002g0025 others(12): Show |
15 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.556-8019dupT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69514252 | ||||||
| chr14:69514378 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0095 others(131): Show |
140 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.556-7905A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514378 | |||||||
| chr14:69514389 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.556-7894T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514389 | |||||||
| chr14:69514514 | T | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-7769T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514514 | |||||||
| chr14:69514570 | C | G | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-7713C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514570 | |||||||
| chr14:69514866 | A | C | 1 | a0001c0002t0002g0300 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.556-7417A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514866 | |||||||
| chr14:69514876 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556-7407A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514876 | |||||||
| chr14:69514891 | C | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(125): Show |
134 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.556-7392C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514891 | |||||||
| chr14:69514928 | C | G | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-7355C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514928 | |||||||
| chr14:69514950 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556-7333C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514950 | |||||||
| chr14:69514971 | T | G | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-7312T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69514971 | |||||||
| chr14:69515019 | G | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0169 a0001c0001t0001g0173 others(3): Show |
6 | HG02258.hp2 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-7264G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515019 | |||||||
| chr14:69515042 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0001g0190 a0001c0001t0001g0209 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.556-7241A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515042 | |||||||
| chr14:69515069 | A | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0178 a0001c0001t0002g0192 |
3 | HG02145.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.556-7214A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515069 | |||||||
| chr14:69515105 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556-7178G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515105 | |||||||
| chr14:69515213 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-7070C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515213 | |||||||
| chr14:69515340 | G | C | 1 | a0001c0007t0002g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.556-6943G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515340 | |||||||
| chr14:69515526 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(138): Show |
147 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.556-6757A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515526 | |||||||
| chr14:69515552 | T | A | 15 | a0001c0001t0001g0264 a0001c0001t0002g0007 a0001c0001t0002g0056 others(12): Show |
16 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.556-6731T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515552 | |||||||
| chr14:69515704 | C | T | 1 | a0001c0003t0003g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556-6579C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515704 | |||||||
| chr14:69515855 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.556-6428G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515855 | |||||||
| chr14:69515864 | T | C | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-6419T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69515864 | |||||||
| chr14:69516088 | T | C | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-6195T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516088 | |||||||
| chr14:69516099 | C | T | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.556-6184C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516099 | |||||||
| chr14:69516199 | C | T | 4 | a0001c0001t0002g0122 a0001c0001t0002g0187 a0001c0001t0002g0216 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-6084C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516199 | |||||||
| chr14:69516281 | A | C | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-6002A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516281 | |||||||
| chr14:69516338 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.556-5945A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516338 | |||||||
| chr14:69516343 | AC | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.556-5939delC | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516343 | |||||||
| chr14:69516640 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.556-5643G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516640 | |||||||
| chr14:69516667 | T | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-5616T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516667 | |||||||
| chr14:69516686 | G | T | 1 | a0001c0002t0002g0049 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.556-5597G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516686 | |||||||
| chr14:69516754 | C | T | 1 | a0001c0001t0003g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.556-5529C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516754 | |||||||
| chr14:69516766 | C | G | 11 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-5517C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516766 | |||||||
| chr14:69516914 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556-5369G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516914 | |||||||
| chr14:69516984 | A | C | 40 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(37): Show |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.556-5299A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69516984 | |||||||
| chr14:69517192 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.556-5091G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517192 | |||||||
| chr14:69517273 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.556-5010G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517273 | |||||||
| chr14:69517298 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.556-4985G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517298 | |||||||
| chr14:69517338 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.556-4945T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517338 | |||||||
| chr14:69517415 | G | T | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-4868G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517415 | |||||||
| chr14:69517776 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556-4507T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517776 | |||||||
| chr14:69517842 | C | T | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-4441C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517842 | |||||||
| chr14:69517843 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.556-4440G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517843 | |||||||
| chr14:69517969 | C | G | 15 | a0001c0001t0001g0301 a0001c0001t0005g0217 a0001c0001t0006g0009 others(12): Show |
16 | HG01081.hp1 HG01175.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.556-4314C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69517969 | |||||||
| chr14:69517994 | T | TTTTA | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0253 others(2): Show |
5 | HG00738.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-4253_556-4250d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69517994 | ||||||
| chr14:69517994 | TTTTA | T | 27 | a0001c0001t0001g0061 a0001c0001t0001g0099 a0001c0001t0002g0122 others(24): Show |
28 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.556-4253_556-4250d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69517994 | ||||||
| chr14:69517994 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0001g0054 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.556-4261_556-4250d others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69517994 | ||||||
| chr14:69518022 | ATTTATTT others(5): Show |
A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.556-4257_556-4246d others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69518022 | ||||||
| chr14:69518026 | ATTTATTT others(1): Show |
A | 33 | a0001c0001t0001g0264 a0001c0001t0001g0301 a0001c0001t0002g0007 others(30): Show |
35 | HG00597.hp1 HG01175.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.556-4253_556-4246d others(10): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69518026 | ||||||
| chr14:69518026 | ATTTATTT others(5): Show |
A | 1 | a0001c0004t0002g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.556-4253_556-4242d others(14): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69518026 | ||||||
| chr14:69518030 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0158 |
2 | HG02735.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.556-4253A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518030 | |||||||
| chr14:69518030 | ATTTG | A | 36 | a0001c0001t0002g0065 a0001c0001t0002g0187 a0001c0001t0009g0186 others(33): Show |
38 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.556-4236_556-4233d others(6): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69518030 | ||||||
| chr14:69518034 | G | A | 29 | a0001c0001t0002g0070 a0001c0001t0002g0120 a0001c0001t0002g0121 others(26): Show |
29 | HG00738.hp1 HG01081.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.556-4249G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518034 | |||||||
| chr14:69518038 | G | A | 17 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0256 others(14): Show |
17 | HG01433.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.556-4245G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518038 | |||||||
| chr14:69518042 | GT | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(51): Show |
56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.556-4238delT | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69518042 | ||||||
| chr14:69518120 | C | T | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-4163C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518120 | |||||||
| chr14:69518152 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-4131C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518152 | |||||||
| chr14:69518173 | T | C | 1 | a0001c0003t0001g0294 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.556-4110T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518173 | |||||||
| chr14:69518189 | C | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.556-4094C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518189 | |||||||
| chr14:69518314 | T | C | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.556-3969T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518314 | |||||||
| chr14:69518316 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.556-3967C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518316 | |||||||
| chr14:69518447 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.556-3836A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518447 | |||||||
| chr14:69518641 | G | A | 1 | a0001c0003t0001g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.556-3642G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518641 | |||||||
| chr14:69518781 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.556-3502G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518781 | |||||||
| chr14:69518870 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.556-3413G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69518870 | |||||||
| chr14:69519109 | G | C | 28 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0120 others(25): Show |
28 | HG00738.hp1 HG01192.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.556-3174G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519109 | |||||||
| chr14:69519155 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(26): Show |
31 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.556-3128C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519155 | |||||||
| chr14:69519202 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.556-3081A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519202 | |||||||
| chr14:69519644 | T | G | 1 | a0001c0001t0017g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.556-2639T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519644 | |||||||
| chr14:69519743 | T | A | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.556-2540T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519743 | |||||||
| chr14:69519806 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.556-2477G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519806 | |||||||
| chr14:69519844 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.556-2439C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519844 | |||||||
| chr14:69519845 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.556-2438G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519845 | |||||||
| chr14:69519886 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.556-2397G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69519886 | |||||||
| chr14:69520044 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0179 a0001c0001t0002g0167 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-2239G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520044 | |||||||
| chr14:69520166 | C | CA | 45 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0035 others(42): Show |
45 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.556-2087dupA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69520166 | ||||||
| chr14:69520166 | C | CAA | 9 | a0001c0001t0001g0106 a0001c0001t0001g0191 a0001c0001t0001g0196 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-2088_556-2087d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69520166 | ||||||
| chr14:69520166 | C | CAAA | 8 | a0001c0001t0001g0116 a0001c0001t0002g0007 a0001c0001t0002g0056 others(5): Show |
9 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-2089_556-2087d others(5): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69520166 | ||||||
| chr14:69520166 | CA | C | 59 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0063 others(56): Show |
60 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.556-2087delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69520166 | ||||||
| chr14:69520166 | CAA | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0002g0167 others(29): Show |
34 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.556-2088_556-2087d others(4): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69520166 | ||||||
| chr14:69520166 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.556-2096_556-2087d others(12): Show |
PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 69520166 | ||||||
| chr14:69520190 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556-2093A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520190 | |||||||
| chr14:69520229 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.556-2054G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520229 | |||||||
| chr14:69520405 | T | C | 40 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(37): Show |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.556-1878T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520405 | |||||||
| chr14:69520433 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556-1850C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520433 | |||||||
| chr14:69520545 | C | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.556-1738C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520545 | |||||||
| chr14:69520771 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.556-1512T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520771 | |||||||
| chr14:69520875 | C | G | 14 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0120 others(11): Show |
14 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.556-1408C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69520875 | |||||||
| chr14:69521301 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.556-982A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521301 | |||||||
| chr14:69521323 | C | T | 12 | a0001c0001t0001g0301 a0001c0001t0005g0217 a0001c0001t0006g0009 others(9): Show |
13 | HG01175.hp2 HG02615.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-960C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521323 | |||||||
| chr14:69521456 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.556-827A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521456 | |||||||
| chr14:69521527 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.556-756G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521527 | |||||||
| chr14:69521598 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.556-685A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521598 | |||||||
| chr14:69521925 | G | T | 3 | a0001c0001t0008g0107 a0001c0001t0008g0108 a0001c0001t0008g0109 |
3 | HG01081.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.556-358G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521925 | |||||||
| chr14:69521984 | T | A | 18 | a0001c0001t0003g0008 a0001c0001t0003g0031 a0001c0001t0003g0164 others(15): Show |
19 | HG00323.hp2 HG00544.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.556-299T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521984 | |||||||
| chr14:69521985 | A | G | 13 | a0001c0001t0002g0007 a0001c0001t0002g0056 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.556-298A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69521985 | |||||||
| chr14:69522237 | T | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.556-46T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 6/12 | chr14 | 69522237 | |||||||
| chr14:69522458 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.650+81C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69522458 | |||||||
| chr14:69522694 | C | A | 2 | a0001c0005t0001g0016 a0001c0005t0001g0030 |
2 | HG03491.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.650+317C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69522694 | |||||||
| chr14:69522878 | A | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.650+501A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69522878 | |||||||
| chr14:69522963 | T | G | 1 | a0001c0001t0002g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.650+586T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69522963 | |||||||
| chr14:69523003 | G | A | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.650+626G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523003 | |||||||
| chr14:69523052 | C | A | 13 | a0001c0001t0002g0007 a0001c0001t0002g0056 a0001c0001t0002g0057 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.650+675C>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523052 | |||||||
| chr14:69523195 | G | T | 39 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(36): Show |
41 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.650+818G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523195 | |||||||
| chr14:69523229 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.650+852G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523229 | |||||||
| chr14:69523251 | T | A | 40 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(37): Show |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.650+874T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523251 | |||||||
| chr14:69523616 | A | C | 11 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0250 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.651-613A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523616 | |||||||
| chr14:69523618 | G | T | 1 | a0001c0007t0002g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.651-611G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523618 | |||||||
| chr14:69523676 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.651-553G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523676 | |||||||
| chr14:69523815 | T | G | 5 | a0001c0001t0001g0001 a0001c0001t0002g0167 a0001c0001t0003g0001 others(2): Show |
6 | HG01243.hp2 HG01884.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.651-414T>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523815 | |||||||
| chr14:69523825 | G | A | 1 | a0001c0002t0004g0289 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.651-404G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69523825 | |||||||
| chr14:69523885 | AC | A | 5 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0126 others(2): Show |
5 | HG00597.hp2 NA18964.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.651-342delC | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 69523885 | ||||||
| chr14:69524012 | C | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.651-217C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 7/12 | chr14 | 69524012 | |||||||
| chr14:69524344 | A | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.744+22A>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524344 | |||||||
| chr14:69524377 | A | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0070 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.744+55A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524377 | |||||||
| chr14:69524602 | C | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.744+280C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524602 | |||||||
| chr14:69524622 | G | A | 40 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(37): Show |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.744+300G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524622 | |||||||
| chr14:69524750 | A | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.744+428A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524750 | |||||||
| chr14:69524768 | G | A | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+446G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524768 | |||||||
| chr14:69524846 | T | A | 15 | a0001c0001t0001g0301 a0001c0001t0005g0217 a0001c0001t0006g0009 others(12): Show |
16 | HG01081.hp1 HG01175.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+524T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524846 | |||||||
| chr14:69524854 | G | A | 2 | a0001c0002t0002g0280 a0001c0002t0002g0282 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.744+532G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524854 | |||||||
| chr14:69524900 | CA | C | 14 | a0001c0003t0002g0025 a0001c0003t0002g0026 a0001c0003t0002g0043 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+580delA | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 69524900 | ||||||
| chr14:69524920 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.744+598G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69524920 | |||||||
| chr14:69525177 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.745-767A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525177 | |||||||
| chr14:69525227 | A | C | 1 | a0001c0010t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.745-717A>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525227 | |||||||
| chr14:69525498 | T | A | 1 | a0001c0001t0005g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.745-446T>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525498 | |||||||
| chr14:69525547 | A | G | 1 | a0001c0002t0015g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-397A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525547 | |||||||
| chr14:69525559 | T | C | 40 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(37): Show |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.745-385T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525559 | |||||||
| chr14:69525629 | G | A | 40 | a0001c0002t0001g0274 a0001c0002t0002g0002 a0001c0002t0002g0049 others(37): Show |
42 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.745-315G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525629 | |||||||
| chr14:69525682 | A | G | 1 | a0001c0002t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.745-262A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525682 | |||||||
| chr14:69525688 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.745-256C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525688 | |||||||
| chr14:69525695 | G | A | 15 | a0001c0001t0001g0301 a0001c0001t0005g0217 a0001c0001t0006g0009 others(12): Show |
16 | HG01081.hp1 HG01175.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.745-249G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525695 | |||||||
| chr14:69525863 | C | G | 4 | a0001c0002t0002g0079 a0001c0002t0002g0278 a0001c0002t0002g0295 others(1): Show |
4 | HG02135.hp2 HG02165.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-81C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 8/12 | chr14 | 69525863 | |||||||
| chr14:69526156 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.923+34A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 9/12 | chr14 | 69526156 | |||||||
| chr14:69526159 | T | C | 1 | a0001c0003t0001g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.923+37T>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 9/12 | chr14 | 69526159 | |||||||
| chr14:69526229 | G | A | 6 | a0001c0003t0001g0006 a0001c0003t0001g0037 a0001c0003t0001g0211 others(3): Show |
7 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+107G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 9/12 | chr14 | 69526229 | |||||||
| chr14:69526850 | G | T | 1 | a0001c0001t0009g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1056+21G>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 10/12 | chr14 | 69526850 | |||||||
| chr14:69527089 | C | T | 12 | a0001c0001t0002g0007 a0001c0001t0002g0057 a0001c0001t0002g0058 others(9): Show |
13 | HG01256.hp2 HG01258.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.1057-99C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 10/12 | chr14 | 69527089 | |||||||
| chr14:69527504 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0099 others(31): Show |
36 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1201+172C>T | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 11/12 | chr14 | 69527504 | |||||||
| chr14:69527544 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0038 |
2 | HG00673.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1201+212G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 11/12 | chr14 | 69527544 | |||||||
| chr14:69527675 | G | A | 3 | a0001c0001t0009g0186 a0001c0001t0009g0193 a0001c0001t0017g0185 |
3 | HG02145.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1202-108G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 11/12 | chr14 | 69527675 | |||||||
| chr14:69527756 | C | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(301): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1202-27C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 11/12 | chr14 | 69527756 | |||||||
| chr14:69527936 | A | G | 2 | a0001c0001t0021g0215 a0001c0001t0025g0214 |
2 | HG02922.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.1351+4A>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 12/12 | chr14 | 69527936 | |||||||
| chr14:69528070 | C | G | 2 | a0001c0001t0001g0040 a0001c0003t0001g0242 |
2 | HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1351+138C>G | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 12/12 | chr14 | 69528070 | |||||||
| chr14:69528071 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1351+139G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 12/12 | chr14 | 69528071 | |||||||
| chr14:69528172 | G | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0169 a0001c0001t0001g0173 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-78G>C | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 12/12 | chr14 | 69528172 | |||||||
| chr14:69528203 | G | A | 6 | a0001c0004t0002g0017 a0001c0004t0002g0018 a0001c0004t0002g0303 others(3): Show |
6 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-47G>A | PLEKHD1 | ENSG00000175985.10 | transcript | ENST00000322564.9 | protein_coding | 12/12 | chr14 | 69528203 |