Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 440107 |
|---|---|
| ensemblid | ENSG00000187510.11 |
| hgncid | 33829 |
| symbol | PLEKHG7 |
| name | pleckstrin homology and RhoGEF domain containing G7 |
| refseq_nuc | NM_001377329.1 |
| refseq_prot | NP_001364258.1 |
| ensembl_nuc | ENST00000344636.6 |
| ensembl_prot | ENSP00000344961.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 92702989 |
| end | 92772455 |
| strand | + |
| ver | v1.2 |
| region | chr12:92702989-92772455 |
| region5000 | chr12:92697989-92777455 |
| regionname0 | PLEKHG7_chr12_92702989_92772455 |
| regionname5000 | PLEKHG7_chr12_92697989_92777455 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 691 | 100 | 20 | 23 | 33 | 6 | 18 | 14 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002 | 1/1 | 691 | 96 | 38 | 18 | 17 | 9 | 12 | 10 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003 | 0/0 | 691 | 25 | 22 | 2 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0004 | 0/0 | 691 | 8 | 0 | 8 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0005 | 0/0 | 691 | 6 | 0 | 1 | 0 | 1 | 4 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0006 | 0/0 | 691 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0007 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0008 | 0/0 | 691 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0009 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0010 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0011 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0012 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0013 | 0/0 | 288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0014 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0015 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0016 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2076 | 89 | 18 | 20 | 32 | 5 | 14 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0002 | 0/1 | 2076 | 50 | 20 | 9 | 10 | 4 | 6 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0003 | 1/0 | 2076 | 34 | 7 | 9 | 6 | 5 | 6 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0004 | 0/0 | 2076 | 15 | 14 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0005 | 0/0 | 2076 | 8 | 2 | 3 | 0 | 0 | 3 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0006 | 0/0 | 2076 | 8 | 0 | 8 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0007 | 0/0 | 2076 | 7 | 5 | 1 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0008 | 0/0 | 2076 | 6 | 0 | 1 | 0 | 1 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0009 | 0/0 | 2076 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0010 | 0/0 | 2076 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0011 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0012 | 0/0 | 2076 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0013 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0014 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0015 | 0/0 | 2076 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0016 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0017 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0018 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0019 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0020 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0021 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0022 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0023 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0024 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0025 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0026 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0027 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0028 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| c0029 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2572 | 77 | 15 | 15 | 28 | 5 | 14 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0002 | 0/0 | 2574 | 23 | 2 | 6 | 4 | 2 | 9 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0003 | 0/1 | 2569 | 22 | 2 | 5 | 4 | 3 | 7 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0004 | 1/0 | 2566 | 21 | 7 | 3 | 6 | 3 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0005 | 0/0 | 2567 | 18 | 16 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0006 | 0/0 | 2570 | 16 | 11 | 5 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0007 | 0/0 | 2570 | 14 | 5 | 8 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0008 | 0/0 | 2572 | 13 | 1 | 4 | 1 | 2 | 5 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0009 | 0/0 | 2570 | 11 | 1 | 3 | 6 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0010 | 0/0 | 2566 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0011 | 0/0 | 2565 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0012 | 0/0 | 2570 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0013 | 0/0 | 2566 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0014 | 0/0 | 2576 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0015 | 0/0 | 2572 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0016 | 0/0 | 2570 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0017 | 0/0 | 2572 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0018 | 0/0 | 2582 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0019 | 0/0 | 2572 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0020 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0021 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0022 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0023 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0024 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0025 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0026 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| t0027 | 0/0 | 2567 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2076 | 89 | 18 | 20 | 32 | 5 | 14 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0005 | 0/0 | 2076 | 8 | 2 | 3 | 0 | 0 | 3 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0015 | 0/0 | 2076 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0018 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002 | 0/1 | 2076 | 50 | 20 | 9 | 10 | 4 | 6 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003 | 1/0 | 2076 | 34 | 7 | 9 | 6 | 5 | 6 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0009 | 0/0 | 2076 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0011 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0016 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0022 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0024 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0025 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004 | 0/0 | 2076 | 15 | 14 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0007 | 0/0 | 2076 | 7 | 5 | 1 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0013 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0021 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0004c0006 | 0/0 | 2076 | 8 | 0 | 8 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0005c0008 | 0/0 | 2076 | 6 | 0 | 1 | 0 | 1 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0006c0010 | 0/0 | 2076 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0007c0014 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0008c0012 | 0/0 | 2076 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0009c0028 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0010c0017 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0011c0027 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0012c0026 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0013c0023 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0014c0019 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0015c0020 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0016c0029 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4647 | 69 | 13 | 13 | 27 | 4 | 12 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0001t0002 | 0/0 | 4649 | 12 | 0 | 5 | 4 | 1 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0001t0006 | 0/0 | 4645 | 4 | 2 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0001t0007 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0001t0018 | 0/0 | 4657 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0001t0019 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0005t0001 | 0/0 | 4647 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0005t0002 | 0/0 | 4649 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0005t0006 | 0/0 | 4645 | 4 | 1 | 3 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0005t0020 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0015t0004 | 0/0 | 4641 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0001c0018t0001 | 0/0 | 4647 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0002 | 0/0 | 4649 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0003 | 0/1 | 4644 | 19 | 2 | 5 | 4 | 3 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0005 | 0/0 | 4642 | 14 | 13 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0006 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0007 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0009 | 0/0 | 4645 | 11 | 1 | 3 | 6 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0025 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0002t0027 | 0/0 | 4642 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003t0001 | 0/0 | 4647 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003t0002 | 0/0 | 4649 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003t0004 | 1/0 | 4641 | 15 | 4 | 3 | 5 | 2 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003t0008 | 0/0 | 4647 | 13 | 1 | 4 | 1 | 2 | 5 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003t0014 | 0/0 | 4651 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0003t0022 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0009t0010 | 0/0 | 4641 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0011t0005 | 0/0 | 4642 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0016t0004 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0022t0004 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0024t0014 | 0/0 | 4651 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0002c0025t0004 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0002 | 0/0 | 4649 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0005 | 0/0 | 4642 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0011 | 0/0 | 4640 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0013 | 0/0 | 4641 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0021 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0004t0023 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0007t0002 | 0/0 | 4649 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0007t0005 | 0/0 | 4642 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0007t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0007t0015 | 0/0 | 4647 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0007t0016 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0013t0004 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0013t0024 | 0/0 | 4640 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0003c0021t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0004c0006t0007 | 0/0 | 4645 | 8 | 0 | 8 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0005c0008t0002 | 0/0 | 4649 | 6 | 0 | 1 | 0 | 1 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0006c0010t0012 | 0/0 | 4645 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0007c0014t0006 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0008c0012t0003 | 0/0 | 4644 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0009c0028t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0010c0017t0001 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0011c0027t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0012c0026t0017 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0013c0023t0026 | 0/0 | 4640 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0014c0019t0003 | 0/0 | 4686 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0015c0020t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| a0016c0029t0001 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | copy fasta | chr12 | 92697989 | 92777455 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0018g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0019g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0020g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0015t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0015t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0018t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0007g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0025g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0027g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0022g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0011t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0011t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0016t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0022t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0024t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0025t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0013g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0013g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0013g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0021g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0023g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0015g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0013t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0013t0024g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0021t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0007c0014t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0007c0014t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0008c0012t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0009c0028t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0010c0017t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0011c0027t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0012c0026t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0013c0023t0026g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0014c0019t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0015c0020t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0016c0029t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0015 | t0004 | g0099 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0152 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00140 | hp1 | a0002 | c0002 | t0009 | g0008 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0169 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0170 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00639 | hp1 | a0004 | c0006 | t0007 | g0003 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00639 | hp2 | a0002 | c0002 | t0005 | g0176 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00642 | hp1 | a0004 | c0006 | t0007 | g0220 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0211 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00738 | hp1 | a0004 | c0006 | t0007 | g0221 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00738 | hp2 | a0002 | c0003 | t0004 | g0207 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0185 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01069 | hp1 | a0004 | c0006 | t0007 | g0003 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01081 | hp1 | a0004 | c0006 | t0007 | g0003 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01099 | hp2 | a0002 | c0003 | t0008 | g0194 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0168 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0116 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01167 | hp1 | a0003 | c0007 | t0005 | g0210 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01167 | hp2 | a0002 | c0002 | t0009 | g0008 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01168 | hp1 | a0001 | c0005 | t0006 | g0131 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01168 | hp2 | a0004 | c0006 | t0007 | g0219 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01169 | hp1 | a0002 | c0002 | t0009 | g0206 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01169 | hp2 | a0004 | c0006 | t0007 | g0218 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0159 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01192 | hp2 | a0002 | c0002 | t0009 | g0186 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01243 | hp1 | a0003 | c0004 | t0011 | g0180 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0107 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01255 | hp2 | a0002 | c0003 | t0008 | g0001 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0171 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01257 | hp2 | a0001 | c0005 | t0006 | g0047 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01261 | hp1 | a0002 | c0003 | t0004 | g0213 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01346 | hp1 | a0005 | c0008 | t0002 | g0026 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01346 | hp2 | a0002 | c0003 | t0008 | g0001 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01361 | hp1 | a0002 | c0003 | t0004 | g0208 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01516 | hp2 | a0002 | c0003 | t0008 | g0196 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0153 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01517 | hp2 | a0002 | c0003 | t0008 | g0001 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0147 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0166 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01891 | hp2 | a0003 | c0004 | t0021 | g0148 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01928 | hp1 | a0004 | c0006 | t0007 | g0222 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0151 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01975 | hp1 | a0001 | c0005 | t0006 | g0044 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0227 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0157 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02055 | hp1 | a0002 | c0003 | t0004 | g0013 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02055 | hp2 | a0003 | c0007 | t0016 | g0209 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02071 | hp1 | a0002 | c0002 | t0009 | g0204 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02071 | hp2 | a0001 | c0001 | t0018 | g0094 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02129 | hp2 | a0002 | c0002 | t0009 | g0201 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02135 | hp1 | a0002 | c0003 | t0008 | g0193 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02145 | hp1 | a0009 | c0028 | t0006 | g0048 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02165 | hp2 | a0002 | c0002 | t0009 | g0203 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02257 | hp1 | a0003 | c0021 | t0007 | g0019 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02257 | hp2 | a0003 | c0013 | t0004 | g0146 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02258 | hp1 | a0002 | c0003 | t0014 | g0143 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02280 | hp2 | a0002 | c0002 | t0009 | g0215 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02300 | hp1 | a0002 | c0003 | t0008 | g0195 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02572 | hp1 | a0002 | c0003 | t0022 | g0011 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02572 | hp2 | a0003 | c0007 | t0016 | g0177 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02602 | hp2 | a0005 | c0008 | t0002 | g0028 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02615 | hp2 | a0002 | c0003 | t0008 | g0199 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02622 | hp1 | a0006 | c0010 | t0012 | g0140 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02630 | hp1 | a0003 | c0004 | t0002 | g0145 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02630 | hp2 | a0002 | c0002 | t0005 | g0189 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02647 | hp1 | a0007 | c0014 | t0006 | g0049 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02647 | hp2 | a0015 | c0020 | t0006 | g0014 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02698 | hp2 | a0001 | c0005 | t0002 | g0051 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02717 | hp2 | a0003 | c0004 | t0011 | g0182 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02723 | hp1 | a0002 | c0016 | t0004 | g0017 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02723 | hp2 | a0002 | c0024 | t0014 | g0234 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0184 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02809 | hp1 | a0006 | c0010 | t0012 | g0139 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02809 | hp2 | a0002 | c0003 | t0004 | g0228 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02818 | hp1 | a0002 | c0002 | t0005 | g0230 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02818 | hp2 | a0002 | c0002 | t0005 | g0175 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02886 | hp1 | a0002 | c0002 | t0005 | g0174 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02886 | hp2 | a0007 | c0014 | t0006 | g0050 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02895 | hp1 | a0003 | c0004 | t0013 | g0226 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02896 | hp1 | a0003 | c0004 | t0013 | g0009 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02896 | hp2 | a0002 | c0002 | t0005 | g0232 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02897 | hp2 | a0003 | c0004 | t0013 | g0009 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02922 | hp1 | a0002 | c0011 | t0005 | g0018 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02922 | hp2 | a0002 | c0009 | t0010 | g0236 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02965 | hp1 | a0002 | c0025 | t0004 | g0136 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02965 | hp2 | a0002 | c0002 | t0005 | g0162 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02970 | hp1 | a0006 | c0010 | t0012 | g0141 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02970 | hp2 | a0010 | c0017 | t0001 | g0200 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02976 | hp1 | a0003 | c0004 | t0005 | g0225 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02976 | hp2 | a0002 | c0009 | t0010 | g0235 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03017 | hp1 | a0003 | c0007 | t0002 | g0154 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0163 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03041 | hp1 | a0003 | c0004 | t0023 | g0134 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03041 | hp2 | a0002 | c0002 | t0005 | g0231 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03098 | hp1 | a0002 | c0002 | t0006 | g0015 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03098 | hp2 | a0003 | c0004 | t0006 | g0149 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03139 | hp1 | a0002 | c0009 | t0010 | g0010 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03139 | hp2 | a0002 | c0002 | t0005 | g0191 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03195 | hp1 | a0002 | c0009 | t0010 | g0010 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03195 | hp2 | a0003 | c0007 | t0015 | g0205 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03209 | hp1 | a0003 | c0004 | t0007 | g0135 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03209 | hp2 | a0003 | c0004 | t0013 | g0223 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03225 | hp1 | a0016 | c0029 | t0001 | g0021 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03239 | hp1 | a0002 | c0002 | t0007 | g0183 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03453 | hp1 | a0002 | c0002 | t0006 | g0188 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0089 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03486 | hp1 | a0002 | c0003 | t0004 | g0012 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03486 | hp2 | a0001 | c0005 | t0020 | g0038 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03490 | hp1 | a0005 | c0008 | t0002 | g0031 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03490 | hp2 | a0014 | c0019 | t0003 | g0172 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03491 | hp2 | a0002 | c0003 | t0008 | g0002 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03492 | hp1 | a0005 | c0008 | t0002 | g0030 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03492 | hp2 | a0002 | c0003 | t0008 | g0002 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03516 | hp1 | a0003 | c0013 | t0024 | g0142 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03516 | hp2 | a0003 | c0004 | t0011 | g0178 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03540 | hp2 | a0006 | c0010 | t0012 | g0138 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03579 | hp1 | a0001 | c0005 | t0006 | g0052 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03579 | hp2 | a0002 | c0009 | t0010 | g0224 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0155 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03669 | hp1 | a0002 | c0002 | t0003 | g0160 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03688 | hp1 | a0001 | c0015 | t0004 | g0122 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03688 | hp2 | a0008 | c0012 | t0003 | g0007 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0167 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03710 | hp2 | a0005 | c0008 | t0002 | g0027 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03831 | hp1 | a0002 | c0003 | t0008 | g0197 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03834 | hp2 | a0001 | c0005 | t0001 | g0045 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03942 | hp1 | a0002 | c0002 | t0025 | g0156 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04115 | hp1 | a0002 | c0003 | t0008 | g0198 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04204 | hp1 | a0008 | c0012 | t0003 | g0007 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04204 | hp2 | a0002 | c0003 | t0008 | g0002 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0187 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18747 | hp1 | a0002 | c0002 | t0009 | g0202 | EAS | CHB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18906 | hp1 | a0002 | c0002 | t0005 | g0144 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18906 | hp2 | a0003 | c0007 | t0007 | g0190 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18939 | hp2 | a0002 | c0003 | t0004 | g0127 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18949 | hp2 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18964 | hp2 | a0002 | c0003 | t0004 | g0128 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0164 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18995 | hp2 | a0001 | c0018 | t0001 | g0121 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19004 | hp1 | a0002 | c0002 | t0009 | g0126 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0173 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19043 | hp2 | a0003 | c0007 | t0015 | g0217 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19054 | hp2 | a0002 | c0003 | t0004 | g0124 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19062 | hp2 | a0002 | c0022 | t0004 | g0129 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19084 | hp1 | a0002 | c0002 | t0009 | g0125 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19240 | hp1 | a0002 | c0003 | t0004 | g0239 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19240 | hp2 | a0001 | c0001 | t0019 | g0086 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20129 | hp1 | a0002 | c0009 | t0010 | g0237 | AFR | ASW | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20129 | hp2 | a0003 | c0004 | t0011 | g0179 | AFR | ASW | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20752 | hp1 | a0005 | c0008 | t0002 | g0025 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20752 | hp2 | a0002 | c0003 | t0004 | g0216 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20805 | hp1 | a0002 | c0003 | t0004 | g0212 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0046 | SAS | GIH | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02109 | hp1 | a0003 | c0004 | t0011 | g0181 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02109 | hp2 | a0011 | c0027 | t0006 | g0068 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02486 | hp2 | a0002 | c0002 | t0005 | g0229 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02559 | hp2 | a0002 | c0011 | t0005 | g0016 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03471 | hp1 | a0002 | c0002 | t0027 | g0192 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03471 | hp2 | a0006 | c0010 | t0012 | g0137 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG06807 | hp1 | a0012 | c0026 | t0017 | g0022 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0150 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20300 | hp1 | a0013 | c0023 | t0026 | g0233 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0161 | REF | REF | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0004 | g0214 | REF | REF | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92706690
|
C | G | 1 | a0016 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.59C>G | p.Pro20Arg | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 364/4641 | 59/2076 | 20/691 | chr12 | 92706690 | ||
| chr12:92706705
|
G | T | 1 | a0009 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.74G>T | p.Arg25Met | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 379/4641 | 74/2076 | 25/691 | chr12 | 92706705 | ||
| chr12:92706717
|
A | G | 1 | a0006 | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.86A>G | p.Lys29Arg | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 391/4641 | 86/2076 | 29/691 | chr12 | 92706717 | ||
| chr12:92707083
|
G | A | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.452G>A | p.Arg151Gln | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 757/4641 | 452/2076 | 151/691 | chr12 | 92707083 | ||
| chr12:92707119
|
T | A | 1 | a0005 | 6 | HG01346.hp1 HG02602.hp2 HG03490.hp1 others(3): Show |
missense_variant | MODERATE | c.488T>A | p.Leu163Gln | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 793/4641 | 488/2076 | 163/691 | chr12 | 92707119 | ||
| chr12:92737427
|
A | C | 7 | a0001a0004a0005others(4): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
missense_variant | MODERATE | c.845A>C | p.Asp282Ala | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/17 | 1150/4641 | 845/2076 | 282/691 | chr12 | 92737427 | ||
| chr12:92737447
|
C | T | 1 | a0013 | 1 | NA20300.hp1 | stop_gained | HIGH | c.865C>T | p.Gln289* | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/17 | 1170/4641 | 865/2076 | 289/691 | chr12 | 92737447 | ||
| chr12:92740901
|
G | A | 1 | a0012 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.988G>A | p.Asp330Asn | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/17 | 1293/4641 | 988/2076 | 330/691 | chr12 | 92740901 | ||
| chr12:92745554
|
G | C | 1 | a0015 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1214G>C | p.Ser405Thr | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/17 | 1519/4641 | 1214/2076 | 405/691 | chr12 | 92745554 | ||
| chr12:92745572
|
A | G | 1 | a0004 | 8 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(5): Show |
missense_variant | MODERATE | c.1232A>G | p.Asp411Gly | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/17 | 1537/4641 | 1232/2076 | 411/691 | chr12 | 92745572 | ||
| chr12:92754092
|
G | A | 1 | a0007 | 2 | HG02647.hp1 HG02886.hp2 |
stop_gained&splice_region_variant | HIGH | c.1254G>A | p.Trp418* | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/17 | 1559/4641 | 1254/2076 | 418/691 | chr12 | 92754092 | ||
| chr12:92756326
|
T | C | 8 | a0001a0003a0004others(5): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
missense_variant | MODERATE | c.1571T>C | p.Met524Thr | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/17 | 1876/4641 | 1571/2076 | 524/691 | chr12 | 92756326 | ||
| chr12:92764111
|
A | G | 1 | a0008 | 2 | HG03688.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.1787A>G | p.Glu596Gly | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/17 | 2092/4641 | 1787/2076 | 596/691 | chr12 | 92764111 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92706817
|
G | A | 2 | a0002c0011a0002c0016 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.186G>A | p.Arg62Arg | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 491/4641 | 186/2076 | 62/691 | chr12 | 92706817 | ||
| chr12:92729105
|
C | T | 1 | a0016c0029 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.643C>T | p.Leu215Leu | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/17 | 948/4641 | 643/2076 | 215/691 | chr12 | 92729105 | ||
| chr12:92737422
|
G | A | 1 | a0001c0018 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.840G>A | p.Pro280Pro | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/17 | 1145/4641 | 840/2076 | 280/691 | chr12 | 92737422 | ||
| chr12:92737438
|
C | T | 6 | a0002c0009a0002c0024a0002c0025others(3): Show | 26 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
synonymous_variant | LOW | c.856C>T | p.Leu286Leu | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/17 | 1161/4641 | 856/2076 | 286/691 | chr12 | 92737438 | ||
| chr12:92741511
|
C | T | 1 | a0002c0022 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.1056C>T | p.Asn352Asn | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/17 | 1361/4641 | 1056/2076 | 352/691 | chr12 | 92741511 | ||
| chr12:92754125
|
C | T | 3 | a0001c0005a0007c0014a0009c0028 | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
synonymous_variant | LOW | c.1287C>T | p.His429His | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/17 | 1592/4641 | 1287/2076 | 429/691 | chr12 | 92754125 | ||
| chr12:92754131
|
A | T | 15 | a0001c0001a0001c0005a0001c0015others(12): Show | 145 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
synonymous_variant | LOW | c.1293A>T | p.Pro431Pro | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/17 | 1598/4641 | 1293/2076 | 431/691 | chr12 | 92754131 | ||
| chr12:92761759
|
G | A | 21 | a0001c0001a0001c0005a0001c0018others(18): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
synonymous_variant | LOW | c.1644G>A | p.Thr548Thr | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/17 | 1949/4641 | 1644/2076 | 548/691 | chr12 | 92761759 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92706512
|
G | T | 1 | a0002c0002t0027 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 120 | chr12 | 92706512 | |||||
| chr12:92706551
|
G | A | 1 | a0012c0026t0017 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 81 | chr12 | 92706551 | |||||
| chr12:92706567
|
A | G | 1 | a0006c0010t0012 | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-65A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 65 | chr12 | 92706567 | |||||
| chr12:92706590
|
G | A | 1 | a0002c0003t0008 | 13 | HG01099.hp2 HG01255.hp2 HG01346.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/17 | 42 | chr12 | 92706590 | |||||
| chr12:92770230
|
T | C | 1 | a0002c0002t0009 | 11 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*35T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 35 | chr12 | 92770230 | |||||
| chr12:92770355
|
A | G | 10 | a0002c0002t0003a0002c0002t0005a0002c0002t0025others(7): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 160 | chr12 | 92770355 | |||||
| chr12:92770726
|
A | T | 1 | a0002c0009t0010 | 6 | HG02922.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 531 | chr12 | 92770726 | |||||
| chr12:92770782
|
C | T | 1 | a0003c0004t0013 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*587C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 587 | chr12 | 92770782 | |||||
| chr12:92770833
|
GA | G | 12 | a0002c0002t0003a0002c0002t0005a0002c0002t0025others(9): Show | 49 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*648delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 648 | INFO_REALIGN_3_PRIME | chr12 | 92770833 | ||||
| chr12:92770872
|
A | G | 2 | a0003c0004t0011a0003c0004t0023 | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*677A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 677 | chr12 | 92770872 | |||||
| chr12:92770996
|
G | GGT | 5 | a0002c0002t0005a0002c0002t0027a0002c0011t0005others(2): Show | 19 | HG00639.hp2 HG01167.hp1 HG01884.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*827dupGT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 828 | INFO_REALIGN_3_PRIME | chr12 | 92770996 | ||||
| chr12:92770996
|
G | GGTGT | 22 | a0001c0001t0006a0001c0001t0007a0001c0005t0006others(19): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*824_*827dupGTGT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 828 | INFO_REALIGN_3_PRIME | chr12 | 92770996 | ||||
| chr12:92770996
|
G | GGTGTGT | 11 | a0001c0001t0001a0001c0001t0019a0001c0005t0001others(8): Show | 95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*822_*827dupGTGTGT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 828 | INFO_REALIGN_3_PRIME | chr12 | 92770996 | ||||
| chr12:92770996
|
G | GGTGTGTG others(1): Show |
7 | a0001c0001t0002a0001c0005t0002a0002c0002t0002others(4): Show | 23 | HG00609.hp2 HG01070.hp1 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*820_*827dupGTGTGT others(2): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 828 | INFO_REALIGN_3_PRIME | chr12 | 92770996 | ||||
| chr12:92770996
|
G | GGTGTGTG others(3): Show |
2 | a0002c0003t0014a0002c0024t0014 | 2 | HG02258.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*818_*827dupGTGTGT others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 828 | INFO_REALIGN_3_PRIME | chr12 | 92770996 | ||||
| chr12:92770996
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0018 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*812_*827dupGTGTGT others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 828 | INFO_REALIGN_3_PRIME | chr12 | 92770996 | ||||
| chr12:92771116
|
G | T | 7 | a0001c0001t0007a0002c0002t0007a0002c0002t0009others(4): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*921G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 921 | chr12 | 92771116 | |||||
| chr12:92771160
|
G | A | 8 | a0001c0001t0007a0002c0002t0007a0002c0002t0009others(5): Show | 27 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*965G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 965 | chr12 | 92771160 | |||||
| chr12:92771772
|
T | C | 1 | a0001c0001t0019 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 1577 | chr12 | 92771772 | |||||
| chr12:92771843
|
C | T | 10 | a0001c0001t0007a0002c0002t0007a0002c0002t0009others(7): Show | 30 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 1648 | chr12 | 92771843 | |||||
| chr12:92771874
|
T | C | 2 | a0001c0005t0020a0002c0003t0022 | 2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1679T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 1679 | chr12 | 92771874 | |||||
| chr12:92772413
|
A | T | 1 | a0003c0004t0011 | 5 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2218A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 17/17 | 2218 | chr12 | 92772413 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92703183
|
C | T | 1 | a0002c0003t0004g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-162+51C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92703183 | ||||||
| chr12:92703591
|
G | A | 8 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-162+459G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92703591 | ||||||
| chr12:92703714
|
T | G | 2 | a0002c0002t0002g0020a0003c0021t0007g0019 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-162+582T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92703714 | ||||||
| chr12:92703729
|
T | C | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-162+597T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92703729 | ||||||
| chr12:92703740
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-162+608A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92703740 | ||||||
| chr12:92703759
|
T | C | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-162+627T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92703759 | ||||||
| chr12:92704021
|
G | T | 6 | a0002c0009t0010g0010a0002c0009t0010g0235a0002c0009t0010g0236others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-162+889G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704021 | ||||||
| chr12:92704067
|
C | T | 3 | a0002c0002t0005g0230a0002c0002t0005g0231a0002c0002t0005g0232 | 3 | HG02818.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-162+935C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704067 | ||||||
| chr12:92704267
|
G | GA | 10 | a0001c0001t0001g0023a0001c0001t0001g0238a0001c0001t0002g0024others(7): Show | 10 | HG01346.hp1 HG02155.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162+1146dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 92704267 | |||||
| chr12:92704337
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(113): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-162+1205G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704337 | ||||||
| chr12:92704440
|
G | A | 1 | a0003c0004t0023g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-162+1308G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704440 | ||||||
| chr12:92704552
|
C | T | 1 | a0002c0002t0005g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-162+1420C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704552 | ||||||
| chr12:92704588
|
C | T | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-162+1456C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704588 | ||||||
| chr12:92704669
|
G | A | 16 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-162+1537G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704669 | ||||||
| chr12:92704723
|
CCTGTTAG others(10): Show |
C | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-162+1593_-162+160 others(21): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 92704723 | |||||
| chr12:92704765
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-162+1633A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704765 | ||||||
| chr12:92704843
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-161-1628G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704843 | ||||||
| chr12:92704998
|
C | T | 1 | a0002c0002t0003g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-161-1473C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92704998 | ||||||
| chr12:92705014
|
T | A | 32 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.-161-1457T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705014 | ||||||
| chr12:92705037
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-161-1434C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705037 | ||||||
| chr12:92705090
|
G | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-161-1381G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705090 | ||||||
| chr12:92705330
|
TG | T | 8 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-1139delG | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 92705330 | |||||
| chr12:92705491
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-161-980T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705491 | ||||||
| chr12:92705642
|
G | A | 1 | a0003c0007t0016g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-161-829G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705642 | ||||||
| chr12:92705767
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-161-704G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705767 | ||||||
| chr12:92705807
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-161-664T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705807 | ||||||
| chr12:92705886
|
CA | C | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-584delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705886 | ||||||
| chr12:92705936
|
C | A | 24 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-161-535C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705936 | ||||||
| chr12:92705957
|
T | G | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-514T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705957 | ||||||
| chr12:92705980
|
G | A | 147 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(144): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-161-491G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92705980 | ||||||
| chr12:92706117
|
G | A | 1 | a0002c0002t0003g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-161-354G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92706117 | ||||||
| chr12:92706241
|
A | G | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-161-230A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92706241 | ||||||
| chr12:92706333
|
C | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-161-138C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 1/16 | chr12 | 92706333 | ||||||
| chr12:92707279
|
C | T | 1 | a0001c0005t0006g0131 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.507+141C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/16 | chr12 | 92707279 | ||||||
| chr12:92707441
|
C | G | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.508-209C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/16 | chr12 | 92707441 | ||||||
| chr12:92707555
|
G | A | 1 | a0002c0002t0007g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.508-95G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/16 | chr12 | 92707555 | ||||||
| chr12:92707635
|
T | C | 1 | a0003c0004t0013g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.508-15T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 2/16 | chr12 | 92707635 | ||||||
| chr12:92707754
|
C | T | 4 | a0002c0002t0005g0173a0002c0002t0005g0174a0002c0002t0005g0175others(1): Show | 4 | HG00639.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.530+82C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92707754 | ||||||
| chr12:92707999
|
A | T | 2 | a0002c0002t0003g0171a0014c0019t0003g0172 | 2 | HG01257.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.530+327A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92707999 | ||||||
| chr12:92708097
|
C | T | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+425C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708097 | ||||||
| chr12:92708166
|
G | A | 10 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.530+494G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708166 | ||||||
| chr12:92708243
|
T | C | 3 | a0002c0002t0007g0183a0002c0003t0001g0185a0002c0003t0002g0184 | 3 | HG00741.hp1 HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.530+571T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708243 | ||||||
| chr12:92708335
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.530+663C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708335 | ||||||
| chr12:92708519
|
G | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(131): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.530+847G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708519 | ||||||
| chr12:92708603
|
G | A | 1 | a0001c0005t0020g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.530+931G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708603 | ||||||
| chr12:92708609
|
G | A | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+937G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708609 | ||||||
| chr12:92708700
|
C | A | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+1028C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708700 | ||||||
| chr12:92708943
|
A | C | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+1271A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92708943 | ||||||
| chr12:92709016
|
A | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(113): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.530+1344A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92709016 | ||||||
| chr12:92709234
|
G | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1562G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92709234 | ||||||
| chr12:92709359
|
A | T | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.530+1687A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92709359 | ||||||
| chr12:92709769
|
A | C | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+2097A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92709769 | ||||||
| chr12:92710159
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530+2487C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710159 | ||||||
| chr12:92710188
|
C | T | 1 | a0002c0002t0005g0176 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.530+2516C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710188 | ||||||
| chr12:92710422
|
T | A | 1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.530+2750T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710422 | ||||||
| chr12:92710524
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+2852G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710524 | ||||||
| chr12:92710543
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(101): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.530+2871C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710543 | ||||||
| chr12:92710700
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.530+3028G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710700 | ||||||
| chr12:92710782
|
C | T | 1 | a0001c0015t0004g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.530+3110C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710782 | ||||||
| chr12:92710798
|
G | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+3126G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92710798 | ||||||
| chr12:92711136
|
T | A | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+3464T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711136 | ||||||
| chr12:92711140
|
C | G | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+3468C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711140 | ||||||
| chr12:92711204
|
A | G | 1 | a0002c0003t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.530+3532A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711204 | ||||||
| chr12:92711226
|
G | T | 1 | a0001c0018t0001g0121 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.530+3554G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711226 | ||||||
| chr12:92711262
|
T | C | 24 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.530+3590T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711262 | ||||||
| chr12:92711342
|
C | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+3670C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711342 | ||||||
| chr12:92711373
|
GAGACC | G | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.530+3703_530+3707d others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92711373 | |||||
| chr12:92711424
|
G | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+3752G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711424 | ||||||
| chr12:92711564
|
AC | A | 9 | a0002c0002t0005g0187a0002c0002t0005g0189a0002c0002t0005g0191others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+3895delC | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92711564 | |||||
| chr12:92711612
|
G | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.530+3940G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711612 | ||||||
| chr12:92711979
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.530+4307G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92711979 | ||||||
| chr12:92712472
|
C | G | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+4800C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92712472 | ||||||
| chr12:92712637
|
A | AT | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+4974dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92712637 | |||||
| chr12:92712705
|
C | T | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+5033C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92712705 | ||||||
| chr12:92712717
|
C | A | 1 | a0001c0001t0002g0053 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.530+5045C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92712717 | ||||||
| chr12:92712719
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.530+5047C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92712719 | ||||||
| chr12:92712921
|
T | C | 1 | a0002c0003t0008g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.530+5249T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92712921 | ||||||
| chr12:92713084
|
G | A | 15 | a0002c0003t0008g0001a0002c0003t0008g0002a0002c0003t0008g0193others(12): Show | 19 | HG01099.hp2 HG01243.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.530+5412G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713084 | ||||||
| chr12:92713107
|
C | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+5435C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713107 | ||||||
| chr12:92713108
|
G | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(118): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.530+5436G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713108 | ||||||
| chr12:92713123
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+5451C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713123 | ||||||
| chr12:92713158
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.530+5486T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713158 | ||||||
| chr12:92713210
|
G | T | 2 | a0005c0008t0002g0030a0005c0008t0002g0031 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.530+5538G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713210 | ||||||
| chr12:92713274
|
C | T | 24 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.530+5602C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713274 | ||||||
| chr12:92713425
|
T | C | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+5753T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713425 | ||||||
| chr12:92713512
|
T | G | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.530+5840T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713512 | ||||||
| chr12:92713548
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.530+5876A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713548 | ||||||
| chr12:92713670
|
A | G | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+5998A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713670 | ||||||
| chr12:92713947
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+6275G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92713947 | ||||||
| chr12:92714027
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.530+6355A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714027 | ||||||
| chr12:92714114
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.530+6442C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714114 | ||||||
| chr12:92714124
|
T | G | 15 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.530+6452T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714124 | ||||||
| chr12:92714255
|
G | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+6583G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714255 | ||||||
| chr12:92714309
|
G | C | 1 | a0001c0001t0007g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.530+6637G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714309 | ||||||
| chr12:92714337
|
A | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(143): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.530+6665A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714337 | ||||||
| chr12:92714386
|
C | T | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+6714C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714386 | ||||||
| chr12:92714443
|
T | C | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+6771T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714443 | ||||||
| chr12:92714463
|
G | A | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+6791G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714463 | ||||||
| chr12:92714500
|
A | G | 24 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.530+6828A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714500 | ||||||
| chr12:92714597
|
T | G | 1 | a0002c0003t0004g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.530+6925T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714597 | ||||||
| chr12:92714598
|
C | G | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+6926C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714598 | ||||||
| chr12:92714618
|
A | G | 1 | a0002c0002t0027g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530+6946A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714618 | ||||||
| chr12:92714800
|
A | G | 10 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.530+7128A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714800 | ||||||
| chr12:92714912
|
C | A | 1 | a0001c0001t0006g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.530+7240C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714912 | ||||||
| chr12:92714918
|
C | T | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.530+7246C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714918 | ||||||
| chr12:92714933
|
C | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+7261C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714933 | ||||||
| chr12:92714973
|
C | A | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+7301C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92714973 | ||||||
| chr12:92715017
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.530+7345G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715017 | ||||||
| chr12:92715018
|
G | GGATA | 18 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(15): Show | 18 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.530+7391_530+7394d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715018 | |||||
| chr12:92715018
|
GGATA | G | 76 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0064others(73): Show | 76 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.530+7391_530+7394d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715018 | |||||
| chr12:92715018
|
GGATAGAT others(1): Show |
G | 18 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0059others(15): Show | 19 | HG00609.hp2 HG01099.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.530+7387_530+7394d others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715018 | |||||
| chr12:92715018
|
GGATAGAT others(5): Show |
G | 6 | a0001c0001t0001g0057a0001c0001t0001g0133a0001c0001t0002g0056others(3): Show | 6 | HG02083.hp2 HG02129.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+7383_530+7394d others(14): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715018 | |||||
| chr12:92715108
|
A | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+7436A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715108 | ||||||
| chr12:92715131
|
G | A | 2 | a0002c0011t0005g0016a0002c0011t0005g0018 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.530+7459G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715131 | ||||||
| chr12:92715187
|
G | A | 23 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.530+7515G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715187 | ||||||
| chr12:92715241
|
A | G | 5 | a0002c0009t0010g0010a0002c0009t0010g0235a0002c0009t0010g0236others(2): Show | 6 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+7569A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715241 | ||||||
| chr12:92715346
|
G | T | 1 | a0002c0002t0006g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.530+7674G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715346 | ||||||
| chr12:92715384
|
A | G | 3 | a0002c0002t0005g0230a0002c0002t0005g0231a0002c0002t0005g0232 | 3 | HG02818.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.530+7712A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715384 | ||||||
| chr12:92715388
|
A | C | 1 | a0002c0025t0004g0136 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.530+7716A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715388 | ||||||
| chr12:92715396
|
T | C | 1 | a0008c0012t0003g0007 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.530+7724T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715396 | ||||||
| chr12:92715644
|
A | G | 24 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.530+7972A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715644 | ||||||
| chr12:92715716
|
C | CA | 50 | a0002c0002t0003g0150a0002c0002t0003g0152a0002c0002t0003g0153others(47): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.530+8066dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715716 | |||||
| chr12:92715716
|
C | CAA | 12 | a0002c0002t0003g0151a0002c0002t0005g0144a0002c0002t0005g0147others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.530+8065_530+8066d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715716 | |||||
| chr12:92715716
|
C | CAAA | 7 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(4): Show | 7 | HG02055.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.530+8064_530+8066d others(5): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715716 | |||||
| chr12:92715716
|
C | CAAAAA | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+8062_530+8066d others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715716 | |||||
| chr12:92715716
|
CA | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(106): Show | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.530+8066delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92715716 | |||||
| chr12:92715826
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.530+8154G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715826 | ||||||
| chr12:92715859
|
C | T | 24 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0006g0015others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.530+8187C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92715859 | ||||||
| chr12:92716081
|
T | TTTTTG | 3 | a0002c0002t0002g0020a0002c0002t0005g0187a0003c0021t0007g0019 | 3 | HG02257.hp1 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.530+8434_530+8438d others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92716081 | |||||
| chr12:92716081
|
TTTTTGTT others(3): Show |
T | 2 | a0001c0001t0001g0111a0001c0001t0006g0107 | 2 | HG01255.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.530+8429_530+8438d others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92716081 | |||||
| chr12:92716107
|
T | TTTTG | 13 | a0002c0002t0006g0015a0002c0003t0004g0013a0002c0003t0022g0011others(10): Show | 13 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+8438_530+8439i others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92716107 | |||||
| chr12:92716107
|
T | TTTTGTTT others(2): Show |
10 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0004g0012others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.530+8438_530+8439i others(11): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92716107 | |||||
| chr12:92716111
|
T | G | 3 | a0002c0002t0002g0020a0002c0002t0005g0187a0003c0021t0007g0019 | 3 | HG02257.hp1 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.530+8439T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92716111 | ||||||
| chr12:92716495
|
T | C | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+8823T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92716495 | ||||||
| chr12:92716550
|
C | T | 10 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.530+8878C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92716550 | ||||||
| chr12:92716708
|
G | A | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.530+9036G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92716708 | ||||||
| chr12:92716717
|
C | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(119): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.530+9045C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92716717 | ||||||
| chr12:92716777
|
A | C | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+9105A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92716777 | ||||||
| chr12:92717039
|
A | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(124): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.530+9367A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717039 | ||||||
| chr12:92717094
|
G | A | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+9422G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717094 | ||||||
| chr12:92717225
|
T | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(124): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.530+9553T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717225 | ||||||
| chr12:92717238
|
C | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+9566C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717238 | ||||||
| chr12:92717243
|
G | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(124): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.530+9571G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717243 | ||||||
| chr12:92717367
|
A | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0120 | 2 | HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.530+9695A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717367 | ||||||
| chr12:92717489
|
G | A | 3 | a0002c0003t0008g0001a0002c0003t0008g0195a0002c0003t0008g0196 | 5 | HG01255.hp2 HG01346.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+9817G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717489 | ||||||
| chr12:92717531
|
CA | C | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+9860delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717531 | ||||||
| chr12:92717550
|
T | C | 8 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.530+9878T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717550 | ||||||
| chr12:92717563
|
G | T | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+9891G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717563 | ||||||
| chr12:92717583
|
C | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(119): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.530+9911C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717583 | ||||||
| chr12:92717613
|
C | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(128): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.530+9941C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717613 | ||||||
| chr12:92717778
|
T | G | 6 | a0003c0007t0005g0210a0003c0007t0015g0205a0003c0007t0015g0217others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+10106T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717778 | ||||||
| chr12:92717834
|
G | A | 19 | a0002c0002t0003g0163a0002c0002t0005g0144a0002c0002t0005g0147others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+10162G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717834 | ||||||
| chr12:92717895
|
C | T | 3 | a0003c0007t0005g0210a0003c0007t0016g0177a0010c0017t0001g0200 | 3 | HG01167.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.530+10223C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717895 | ||||||
| chr12:92717923
|
C | T | 1 | a0002c0002t0005g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.530+10251C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92717923 | ||||||
| chr12:92718292
|
C | A | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.530+10620C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718292 | ||||||
| chr12:92718295
|
C | T | 2 | a0001c0001t0001g0106a0016c0029t0001g0021 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.530+10623C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718295 | ||||||
| chr12:92718327
|
G | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(130): Show | 138 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.530+10655G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718327 | ||||||
| chr12:92718352
|
G | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(124): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.531-10641G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718352 | ||||||
| chr12:92718377
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.531-10616G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718377 | ||||||
| chr12:92718433
|
T | C | 10 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-10560T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718433 | ||||||
| chr12:92718597
|
C | T | 1 | a0002c0002t0003g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.531-10396C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718597 | ||||||
| chr12:92718610
|
G | A | 8 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-10383G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718610 | ||||||
| chr12:92718624
|
C | T | 1 | a0002c0003t0004g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.531-10369C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718624 | ||||||
| chr12:92718647
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.531-10346C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718647 | ||||||
| chr12:92718648
|
A | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(113): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.531-10345A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718648 | ||||||
| chr12:92718733
|
T | G | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-10260T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718733 | ||||||
| chr12:92718796
|
G | A | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-10197G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718796 | ||||||
| chr12:92718809
|
G | A | 15 | a0002c0003t0008g0001a0002c0003t0008g0002a0002c0003t0008g0193others(12): Show | 19 | HG01099.hp2 HG01243.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.531-10184G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718809 | ||||||
| chr12:92718912
|
A | G | 1 | a0003c0007t0005g0210 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.531-10081A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92718912 | ||||||
| chr12:92719015
|
G | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531-9978G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719015 | ||||||
| chr12:92719043
|
T | C | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-9950T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719043 | ||||||
| chr12:92719118
|
C | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(117): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.531-9875C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719118 | ||||||
| chr12:92719133
|
G | A | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.531-9860G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719133 | ||||||
| chr12:92719465
|
C | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.531-9528C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719465 | ||||||
| chr12:92719467
|
G | C | 1 | a0002c0002t0005g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-9526G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719467 | ||||||
| chr12:92719469
|
C | G | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.531-9524C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719469 | ||||||
| chr12:92719544
|
C | T | 1 | a0003c0004t0007g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.531-9449C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719544 | ||||||
| chr12:92719612
|
T | C | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-9381T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719612 | ||||||
| chr12:92719713
|
G | T | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-9280G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719713 | ||||||
| chr12:92719846
|
A | G | 1 | a0002c0002t0009g0204 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.531-9147A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719846 | ||||||
| chr12:92719940
|
G | A | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.531-9053G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719940 | ||||||
| chr12:92719971
|
G | C | 1 | a0002c0002t0003g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.531-9022G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719971 | ||||||
| chr12:92719978
|
G | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(119): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.531-9015G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92719978 | ||||||
| chr12:92720024
|
T | C | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-8969T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720024 | ||||||
| chr12:92720047
|
G | A | 6 | a0002c0009t0010g0010a0002c0009t0010g0235a0002c0009t0010g0236others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-8946G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720047 | ||||||
| chr12:92720053
|
C | T | 1 | a0001c0005t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.531-8940C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720053 | ||||||
| chr12:92720074
|
C | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0037others(46): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.531-8919C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720074 | ||||||
| chr12:92720075
|
T | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0037others(47): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.531-8918T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720075 | ||||||
| chr12:92720273
|
G | A | 1 | a0002c0003t0004g0127 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.531-8720G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720273 | ||||||
| chr12:92720278
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.531-8715T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720278 | ||||||
| chr12:92720323
|
C | CT | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(113): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.531-8659dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92720323 | |||||
| chr12:92720323
|
CT | C | 10 | a0002c0002t0003g0151a0002c0002t0006g0015a0002c0003t0004g0012others(7): Show | 10 | HG01934.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-8659delT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92720323 | |||||
| chr12:92720365
|
A | G | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-8628A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720365 | ||||||
| chr12:92720387
|
G | A | 1 | a0002c0003t0004g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.531-8606G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720387 | ||||||
| chr12:92720486
|
G | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-8507G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720486 | ||||||
| chr12:92720556
|
C | T | 1 | a0009c0028t0006g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.531-8437C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720556 | ||||||
| chr12:92720586
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(140): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.531-8407G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720586 | ||||||
| chr12:92720686
|
G | A | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-8307G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720686 | ||||||
| chr12:92720707
|
A | G | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-8286A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720707 | ||||||
| chr12:92720887
|
A | G | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531-8106A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720887 | ||||||
| chr12:92720950
|
A | C | 1 | a0001c0005t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.531-8043A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92720950 | ||||||
| chr12:92721279
|
C | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.531-7714C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721279 | ||||||
| chr12:92721284
|
C | G | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(218): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.531-7709C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721284 | ||||||
| chr12:92721344
|
G | C | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-7649G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721344 | ||||||
| chr12:92721490
|
C | T | 6 | a0003c0007t0005g0210a0003c0007t0015g0205a0003c0007t0015g0217others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-7503C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721490 | ||||||
| chr12:92721491
|
G | A | 2 | a0002c0002t0005g0191a0002c0002t0006g0188 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.531-7502G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721491 | ||||||
| chr12:92721520
|
C | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531-7473C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721520 | ||||||
| chr12:92721534
|
G | C | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-7459G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721534 | ||||||
| chr12:92721702
|
C | A | 1 | a0003c0007t0005g0210 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.531-7291C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721702 | ||||||
| chr12:92721702
|
C | CA | 15 | a0002c0002t0003g0151a0002c0003t0004g0228a0002c0003t0008g0001others(12): Show | 19 | HG01099.hp2 HG01243.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.531-7265dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92721702 | |||||
| chr12:92721702
|
C | CAA | 5 | a0002c0002t0002g0020a0002c0003t0008g0197a0003c0004t0011g0178others(2): Show | 5 | HG02257.hp1 HG02717.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-7266_531-7265d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92721702 | |||||
| chr12:92721702
|
CAA | C | 18 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0001t0001g0132others(15): Show | 20 | HG01099.hp1 HG01934.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.531-7266_531-7265d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92721702 | |||||
| chr12:92721702
|
CAAA | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.531-7267_531-7265d others(5): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92721702 | |||||
| chr12:92721702
|
CAAAAAAA | C | 6 | a0002c0025t0004g0136a0003c0004t0007g0135a0006c0010t0012g0137others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-7271_531-7265d others(9): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92721702 | |||||
| chr12:92721702
|
CAAAAAAA others(1): Show |
C | 7 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-7272_531-7265d others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92721702 | |||||
| chr12:92721923
|
T | C | 1 | a0001c0001t0006g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.531-7070T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721923 | ||||||
| chr12:92722065
|
TA | T | 26 | a0002c0002t0005g0187a0002c0002t0005g0189a0002c0002t0005g0191others(23): Show | 30 | HG01099.hp2 HG01255.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.531-6915delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92722065 | |||||
| chr12:92722116
|
C | T | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-6877C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722116 | ||||||
| chr12:92722231
|
C | T | 8 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-6762C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722231 | ||||||
| chr12:92722371
|
C | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-6622C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722371 | ||||||
| chr12:92722589
|
C | T | 1 | a0003c0007t0016g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.531-6404C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722589 | ||||||
| chr12:92722605
|
C | T | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531-6388C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722605 | ||||||
| chr12:92722847
|
A | G | 1 | a0003c0007t0016g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.531-6146A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722847 | ||||||
| chr12:92722910
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.531-6083A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722910 | ||||||
| chr12:92722911
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.531-6082A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722911 | ||||||
| chr12:92722919
|
C | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-6074C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722919 | ||||||
| chr12:92722978
|
T | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(119): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.531-6015T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92722978 | ||||||
| chr12:92723008
|
TGGA | T | 9 | a0002c0003t0008g0001a0002c0003t0008g0002a0002c0003t0008g0193others(6): Show | 13 | HG01099.hp2 HG01255.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.531-5977_531-5975d others(5): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92723008 | |||||
| chr12:92723018
|
G | A | 9 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-5975G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723018 | ||||||
| chr12:92723078
|
G | T | 1 | a0002c0002t0003g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.531-5915G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723078 | ||||||
| chr12:92723119
|
A | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-5874A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723119 | ||||||
| chr12:92723172
|
A | G | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531-5821A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723172 | ||||||
| chr12:92723337
|
T | C | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-5656T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723337 | ||||||
| chr12:92723396
|
C | A | 3 | a0002c0002t0002g0020a0002c0003t0004g0228a0003c0021t0007g0019 | 3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.531-5597C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723396 | ||||||
| chr12:92723582
|
T | C | 3 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143 | 3 | HG01884.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.531-5411T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723582 | ||||||
| chr12:92723788
|
G | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(143): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.531-5205G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723788 | ||||||
| chr12:92723835
|
C | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-5158C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723835 | ||||||
| chr12:92723846
|
C | T | 8 | a0003c0004t0002g0145a0003c0004t0006g0149a0003c0013t0004g0146others(5): Show | 8 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-5147C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723846 | ||||||
| chr12:92723863
|
G | A | 1 | a0002c0002t0003g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.531-5130G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723863 | ||||||
| chr12:92723893
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.531-5100G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92723893 | ||||||
| chr12:92724024
|
G | A | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531-4969G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724024 | ||||||
| chr12:92724121
|
G | T | 9 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-4872G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724121 | ||||||
| chr12:92724156
|
T | C | 1 | a0001c0001t0006g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.531-4837T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724156 | ||||||
| chr12:92724209
|
C | T | 2 | a0002c0002t0005g0191a0002c0002t0006g0188 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.531-4784C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724209 | ||||||
| chr12:92724221
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.531-4772G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724221 | ||||||
| chr12:92724230
|
C | T | 9 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-4763C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724230 | ||||||
| chr12:92724248
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.531-4745T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724248 | ||||||
| chr12:92724336
|
A | G | 1 | a0002c0002t0009g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.531-4657A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724336 | ||||||
| chr12:92724394
|
T | A | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.531-4599T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724394 | ||||||
| chr12:92724498
|
A | T | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-4495A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724498 | ||||||
| chr12:92724518
|
C | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-4475C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724518 | ||||||
| chr12:92724555
|
T | C | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-4438T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724555 | ||||||
| chr12:92724589
|
A | G | 1 | a0001c0005t0006g0052 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531-4404A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724589 | ||||||
| chr12:92724753
|
T | G | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-4240T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724753 | ||||||
| chr12:92724759
|
T | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(143): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.531-4234T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724759 | ||||||
| chr12:92724977
|
G | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-4016G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92724977 | ||||||
| chr12:92725113
|
C | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-3880C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725113 | ||||||
| chr12:92725314
|
C | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.531-3679C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725314 | ||||||
| chr12:92725315
|
G | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-3678G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725315 | ||||||
| chr12:92725319
|
G | T | 8 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-3674G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725319 | ||||||
| chr12:92725548
|
G | A | 5 | a0002c0003t0004g0006a0002c0003t0004g0124a0002c0003t0004g0127others(2): Show | 6 | NA18939.hp2 NA18949.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-3445G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725548 | ||||||
| chr12:92725622
|
A | C | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-3371A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725622 | ||||||
| chr12:92725650
|
C | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(143): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.531-3343C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725650 | ||||||
| chr12:92725755
|
T | C | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-3238T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725755 | ||||||
| chr12:92725769
|
G | C | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.531-3224G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725769 | ||||||
| chr12:92725836
|
G | A | 1 | a0002c0016t0004g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.531-3157G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725836 | ||||||
| chr12:92725927
|
C | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-3066C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725927 | ||||||
| chr12:92725977
|
A | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-3016A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92725977 | ||||||
| chr12:92726113
|
C | A | 1 | a0002c0016t0004g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.531-2880C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726113 | ||||||
| chr12:92726154
|
A | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.531-2839A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726154 | ||||||
| chr12:92726159
|
C | G | 1 | a0002c0002t0009g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.531-2834C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726159 | ||||||
| chr12:92726163
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.531-2830T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726163 | ||||||
| chr12:92726504
|
A | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-2489A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726504 | ||||||
| chr12:92726713
|
T | C | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.531-2280T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726713 | ||||||
| chr12:92726953
|
G | A | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(133): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.531-2040G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92726953 | ||||||
| chr12:92727025
|
G | A | 3 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0022g0011 | 3 | HG02572.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.531-1968G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727025 | ||||||
| chr12:92727038
|
C | T | 1 | a0003c0004t0005g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.531-1955C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727038 | ||||||
| chr12:92727039
|
G | C | 29 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(26): Show | 31 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.531-1954G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727039 | ||||||
| chr12:92727095
|
A | G | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-1898A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727095 | ||||||
| chr12:92727108
|
A | G | 1 | a0002c0002t0003g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.531-1885A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727108 | ||||||
| chr12:92727118
|
A | T | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(148): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.531-1875A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727118 | ||||||
| chr12:92727312
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.531-1681G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727312 | ||||||
| chr12:92727344
|
T | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.531-1649T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727344 | ||||||
| chr12:92727497
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.531-1496G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727497 | ||||||
| chr12:92727739
|
C | G | 5 | a0002c0002t0003g0151a0002c0002t0003g0159a0002c0002t0003g0166others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-1254C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727739 | ||||||
| chr12:92727882
|
C | T | 3 | a0001c0001t0001g0111a0001c0001t0006g0107a0001c0005t0001g0046 | 3 | HG01255.hp1 HG01975.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.531-1111C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727882 | ||||||
| chr12:92727927
|
G | GGTGT | 6 | a0001c0001t0001g0084a0001c0001t0001g0091a0002c0009t0010g0010others(3): Show | 7 | HG01081.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-1033_531-1030d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727927
|
G | GGTGTGT | 7 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0005t0006g0131others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-1035_531-1030d others(8): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727927
|
G | GGTGTGTG others(1): Show |
11 | a0001c0001t0001g0072a0001c0001t0001g0079a0001c0001t0001g0088others(8): Show | 11 | HG00609.hp2 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-1037_531-1030d others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727927
|
G | GGTGTGTG others(3): Show |
5 | a0001c0001t0001g0064a0001c0001t0001g0090a0001c0001t0001g0132others(2): Show | 5 | HG01099.hp1 HG02145.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-1039_531-1030d others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727927
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.531-1041_531-1030d others(14): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727927
|
GGT | G | 36 | a0002c0002t0002g0020a0002c0002t0003g0150a0002c0002t0003g0151others(33): Show | 37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.531-1031_531-1030d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727927
|
GGTGT | G | 17 | a0002c0002t0003g0160a0002c0002t0005g0230a0002c0002t0005g0231others(14): Show | 18 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.531-1033_531-1030d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727927 | |||||
| chr12:92727960
|
G | GTA | 5 | a0001c0001t0001g0037a0002c0002t0003g0157a0002c0002t0003g0158others(2): Show | 5 | HG02015.hp2 HG02083.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-1032_531-1031i others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727960 | |||||
| chr12:92727962
|
G | A | 73 | a0001c0001t0001g0035a0001c0001t0001g0037a0002c0002t0003g0150others(70): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.531-1031G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727962 | ||||||
| chr12:92727962
|
G | GTA | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0002c0002t0005g0175others(1): Show | 4 | HG01106.hp1 HG02074.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-1018_531-1017d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTATA | 4 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG00323.hp1 HG00741.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-1020_531-1017d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTGTA | 10 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0097others(7): Show | 10 | HG01109.hp2 HG01516.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-1030_531-1029i others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTGTGTA | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(42): Show | 48 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.531-1030_531-1029i others(8): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTGTGTGT others(1): Show |
19 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0061others(16): Show | 19 | HG00673.hp1 HG01071.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.531-1030_531-1029i others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0002g0029 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.531-1030_531-1029i others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTGTGTGT others(3): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0105others(2): Show | 5 | HG00280.hp2 HG02040.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-1030_531-1029i others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
G | GTGTGTGT others(5): Show |
2 | a0005c0008t0002g0030a0005c0008t0002g0031 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.531-1030_531-1029i others(14): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727962
|
GTA | G | 11 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(8): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.531-1018_531-1017d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727962 | |||||
| chr12:92727964
|
A | G | 8 | a0002c0003t0004g0208a0002c0009t0010g0010a0002c0009t0010g0235others(5): Show | 9 | HG01361.hp1 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-1029A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727964 | ||||||
| chr12:92727966
|
A | G | 18 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(15): Show | 20 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.531-1027A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727966 | ||||||
| chr12:92727967
|
T | TATACACA others(36): Show |
2 | a0003c0004t0007g0135a0003c0013t0024g0142 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.531-1023_531-1022i others(45): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727967 | |||||
| chr12:92727979
|
C | CATATATA others(30): Show |
1 | a0002c0002t0003g0165 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.531-1006_531-970du others(38): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727979 | |||||
| chr12:92727987
|
C | CACACACC others(30): Show |
9 | a0002c0003t0004g0208a0002c0003t0004g0212a0002c0003t0004g0216others(6): Show | 10 | HG01361.hp1 HG02135.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-578_531-542dup others(37): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
C | CACACACC others(67): Show |
23 | a0002c0002t0002g0020a0002c0002t0003g0161a0002c0002t0003g0163others(20): Show | 23 | HG00280.hp1 HG00738.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.531-615_531-542dup others(74): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
C | CACACACC others(104): Show |
15 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(12): Show | 15 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.531-652_531-542dup others(111): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
C | CACACACC others(141): Show |
4 | a0002c0002t0003g0155a0002c0002t0003g0171a0002c0002t0025g0156others(1): Show | 4 | HG01257.hp1 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-689_531-542dup others(148): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
C | CACACACC others(215): Show |
1 | a0002c0002t0005g0232 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.531-763_531-542dup others(222): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
CACACACC others(30): Show |
C | 9 | a0002c0002t0009g0125a0002c0002t0009g0126a0002c0002t0009g0186others(6): Show | 9 | HG01192.hp2 HG02071.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-578_531-542del others(37): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
CACACACC others(67): Show |
C | 6 | a0002c0003t0004g0006a0002c0003t0004g0124a0002c0003t0004g0127others(3): Show | 7 | HG02922.hp1 NA18939.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-615_531-542del others(74): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
CACACACC others(104): Show |
C | 2 | a0002c0003t0004g0239a0003c0004t0021g0148 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.531-652_531-542del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
CACACACC others(141): Show |
C | 1 | a0002c0002t0003g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.531-689_531-542del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727987
|
CACACACC others(289): Show |
C | 1 | a0002c0003t0008g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.531-837_531-542del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92727987 | |||||
| chr12:92727989
|
C | T | 1 | a0002c0002t0027g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.531-1004C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92727989 | ||||||
| chr12:92728016
|
A | AATATATA others(79): Show |
3 | a0002c0009t0010g0224a0003c0004t0013g0009a0003c0004t0013g0223 | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-964_531-963ins others(86): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728016 | |||||
| chr12:92728016
|
A | AATATATA others(79): Show |
3 | a0002c0009t0010g0010a0002c0009t0010g0237a0002c0024t0014g0234 | 4 | HG02723.hp2 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-964_531-963ins others(86): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728016 | |||||
| chr12:92728016
|
A | AATATATA others(116): Show |
2 | a0002c0009t0010g0235a0002c0009t0010g0236 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.531-964_531-963ins others(123): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728016 | |||||
| chr12:92728016
|
A | AATATATA others(42): Show |
3 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143 | 3 | HG01884.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.531-964_531-963ins others(49): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728016 | |||||
| chr12:92728020
|
T | TATATACA others(42): Show |
2 | a0003c0004t0005g0225a0003c0004t0013g0226 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.531-964_531-963ins others(49): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728020 | |||||
| chr12:92728024
|
T | TACACATA others(5): Show |
5 | a0002c0025t0004g0136a0003c0004t0002g0145a0003c0004t0006g0149others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-964_531-963ins others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728024 | |||||
| chr12:92728034
|
A | T | 2 | a0001c0001t0001g0111a0001c0001t0006g0107 | 2 | HG01255.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.531-959A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728034 | ||||||
| chr12:92728039
|
A | ATGG | 6 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0061others(3): Show | 6 | HG01071.hp2 HG02040.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-951_531-949dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728039 | |||||
| chr12:92728042
|
GTGTATAT others(64): Show |
G | 9 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0073others(6): Show | 9 | HG00609.hp2 HG01071.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-948_531-878del others(71): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728042 | |||||
| chr12:92728042
|
GTGTATAT others(101): Show |
G | 1 | a0001c0001t0001g0072 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.531-948_531-841del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728042 | |||||
| chr12:92728053
|
A | C | 8 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-940A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728053 | ||||||
| chr12:92728076
|
A | ATGG | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(71): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.531-914_531-912dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728076 | |||||
| chr12:92728079
|
GTGTATAT others(64): Show |
G | 6 | a0001c0001t0001g0096a0001c0001t0001g0110a0001c0001t0001g0238others(3): Show | 6 | HG01928.hp1 HG02040.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-911_531-841del others(71): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728079 | |||||
| chr12:92728079
|
GTGTATAT others(101): Show |
G | 8 | a0001c0001t0001g0035a0001c0001t0001g0060a0001c0001t0001g0071others(5): Show | 8 | HG00609.hp1 HG02129.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-911_531-804del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728079 | |||||
| chr12:92728090
|
A | C | 8 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-903A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728090 | ||||||
| chr12:92728113
|
A | ATGG | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(71): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.531-877_531-875dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728113 | |||||
| chr12:92728116
|
GTGTATAT others(64): Show |
G | 6 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-874_531-804del others(71): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728116 | |||||
| chr12:92728127
|
A | C | 3 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143 | 3 | HG01884.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.531-866A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728127 | ||||||
| chr12:92728132
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.531-861A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728132 | ||||||
| chr12:92728150
|
A | ATGG | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(80): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.531-840_531-838dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728150 | |||||
| chr12:92728164
|
A | C | 1 | a0002c0002t0005g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.531-829A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728164 | ||||||
| chr12:92728187
|
A | ATGG | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(87): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.531-803_531-801dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728187 | |||||
| chr12:92728190
|
GTGTATAT others(64): Show |
G | 1 | a0007c0014t0006g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.531-800_531-730del others(71): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728190 | |||||
| chr12:92728194
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.531-799A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728194 | ||||||
| chr12:92728201
|
A | C | 1 | a0002c0002t0005g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.531-792A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728201 | ||||||
| chr12:92728224
|
A | ATGG | 38 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(35): Show | 38 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.531-766_531-764dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728224 | |||||
| chr12:92728224
|
A | ATGGTGGT others(36): Show |
4 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0112others(1): Show | 4 | HG00323.hp1 HG02155.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-764_531-763ins others(43): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728224 | |||||
| chr12:92728227
|
GTGTATAT others(27): Show |
G | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(60): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.531-763_531-730del others(34): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728227 | |||||
| chr12:92728227
|
GTGTATAT others(64): Show |
G | 7 | a0001c0005t0001g0045a0001c0005t0006g0044a0001c0005t0006g0047others(4): Show | 7 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-763_531-693del others(71): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728227 | |||||
| chr12:92728227
|
GTGTATAT others(101): Show |
G | 2 | a0001c0005t0002g0051a0012c0026t0017g0022 | 2 | HG02698.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.531-763_531-656del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728227 | |||||
| chr12:92728227
|
GTGTATAT others(138): Show |
G | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531-763_531-619del | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728227 | |||||
| chr12:92728261
|
A | ATGG | 42 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(39): Show | 42 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.531-729_531-727dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728261 | |||||
| chr12:92728264
|
GTGTATAT others(27): Show |
G | 1 | a0001c0005t0020g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.531-726_531-693del others(34): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728264 | |||||
| chr12:92728298
|
A | ATGG | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(103): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.531-692_531-690dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728298 | |||||
| chr12:92728335
|
A | ATGG | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.531-655_531-653dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728335 | |||||
| chr12:92728372
|
A | ATGG | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(114): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.531-618_531-616dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728372 | |||||
| chr12:92728409
|
A | ATGG | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(113): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.531-581_531-579dup others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728409
|
A | ATGGTGGT others(116): Show |
2 | a0001c0001t0007g0055a0002c0002t0006g0015 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.531-579_531-578ins others(123): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728409
|
A | ATGGTGGT others(236): Show |
1 | a0002c0003t0022g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.531-579_531-578ins others(243): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728409
|
A | ATGGTGTA others(33): Show |
2 | a0002c0003t0004g0213a0006c0010t0012g0137 | 2 | HG01261.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.531-523_531-484dup others(40): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728409
|
A | ATGGTGTA others(73): Show |
2 | a0002c0003t0004g0013a0015c0020t0006g0014 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.531-563_531-484dup others(80): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728409
|
A | ATGGTGTA others(153): Show |
1 | a0002c0003t0004g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.531-484_531-483ins others(160): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728409
|
A | ATGGTGTA others(218): Show |
2 | a0002c0002t0005g0230a0002c0002t0005g0231 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.531-542_531-541ins others(225): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728409 | |||||
| chr12:92728446
|
ATGG | A | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-541_531-539del others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728446 | |||||
| chr12:92728458
|
A | G | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.531-535A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728458 | ||||||
| chr12:92728473
|
C | T | 6 | a0003c0007t0005g0210a0003c0007t0015g0205a0003c0007t0015g0217others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-520C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728473 | ||||||
| chr12:92728486
|
ATGG | A | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-501_531-499del others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728486 | |||||
| chr12:92728510
|
G | A | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-483G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728510 | ||||||
| chr12:92728513
|
T | C | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-480T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728513 | ||||||
| chr12:92728515
|
T | C | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-478T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728515 | ||||||
| chr12:92728523
|
C | T | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-470C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728523 | ||||||
| chr12:92728550
|
T | C | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-443T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728550 | ||||||
| chr12:92728568
|
GT | G | 19 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(16): Show | 21 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.531-424delT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728568 | ||||||
| chr12:92728570
|
G | A | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.531-423G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728570 | ||||||
| chr12:92728572
|
G | A | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.531-421G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728572 | ||||||
| chr12:92728575
|
T | TAAATATA others(83): Show |
1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.531-418_531-417ins others(90): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728575 | ||||||
| chr12:92728576
|
G | A | 19 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(16): Show | 21 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.531-417G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728576 | ||||||
| chr12:92728576
|
G | T | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.531-417G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728576 | ||||||
| chr12:92728578
|
G | A | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-415G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728578 | ||||||
| chr12:92728581
|
C | A | 19 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(16): Show | 21 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.531-412C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728581 | ||||||
| chr12:92728581
|
C | T | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.531-412C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728581 | ||||||
| chr12:92728583
|
C | T | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-410C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728583 | ||||||
| chr12:92728585
|
T | C | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.531-408T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728585 | ||||||
| chr12:92728585
|
T | TATGTATA others(47): Show |
5 | a0002c0009t0010g0010a0002c0009t0010g0235a0002c0009t0010g0236others(2): Show | 6 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-407_531-406ins others(54): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728585 | |||||
| chr12:92728585
|
T | TATGTATA others(38): Show |
14 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(11): Show | 15 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-407_531-406ins others(45): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 92728585 | |||||
| chr12:92728619
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.531-374A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728619 | ||||||
| chr12:92728683
|
A | G | 1 | a0006c0010t0012g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.531-310A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728683 | ||||||
| chr12:92728960
|
C | T | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-33C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92728960 | ||||||
| chr12:92729317
|
G | A | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.658+197G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729317 | ||||||
| chr12:92729318
|
C | A | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.658+198C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729318 | ||||||
| chr12:92729402
|
G | A | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.658+282G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729402 | ||||||
| chr12:92729472
|
C | T | 5 | a0002c0002t0005g0162a0002c0002t0005g0173a0002c0002t0005g0174others(2): Show | 5 | HG00639.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.658+352C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729472 | ||||||
| chr12:92729571
|
G | A | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.658+451G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729571 | ||||||
| chr12:92729829
|
T | C | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.658+709T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729829 | ||||||
| chr12:92729904
|
A | C | 2 | a0001c0001t0007g0089a0011c0027t0006g0068 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.658+784A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92729904 | ||||||
| chr12:92729964
|
AAGG | A | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.658+847_658+849del others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 92729964 | |||||
| chr12:92730361
|
A | G | 20 | a0002c0003t0008g0001a0002c0003t0008g0002a0002c0003t0008g0193others(17): Show | 24 | HG01099.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.658+1241A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92730361 | ||||||
| chr12:92730479
|
G | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.658+1359G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92730479 | ||||||
| chr12:92730637
|
G | C | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.658+1517G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92730637 | ||||||
| chr12:92730769
|
T | C | 1 | a0002c0002t0003g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.659-1464T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92730769 | ||||||
| chr12:92730972
|
G | A | 7 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.659-1261G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92730972 | ||||||
| chr12:92731063
|
T | C | 1 | a0003c0004t0011g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.659-1170T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731063 | ||||||
| chr12:92731128
|
C | T | 5 | a0002c0009t0010g0010a0002c0009t0010g0235a0002c0009t0010g0236others(2): Show | 6 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-1105C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731128 | ||||||
| chr12:92731168
|
C | T | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.659-1065C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731168 | ||||||
| chr12:92731263
|
C | T | 20 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(17): Show | 22 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.659-970C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731263 | ||||||
| chr12:92731289
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(136): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.659-944A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731289 | ||||||
| chr12:92731435
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.659-798C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731435 | ||||||
| chr12:92731770
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.659-463G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731770 | ||||||
| chr12:92731853
|
A | G | 5 | a0002c0009t0010g0224a0003c0004t0005g0225a0003c0004t0013g0009others(2): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-380A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731853 | ||||||
| chr12:92731922
|
T | C | 6 | a0005c0008t0002g0025a0005c0008t0002g0026a0005c0008t0002g0027others(3): Show | 6 | HG01346.hp1 HG02602.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.659-311T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731922 | ||||||
| chr12:92731926
|
T | C | 3 | a0002c0025t0004g0136a0003c0004t0007g0135a0016c0029t0001g0021 | 3 | HG02965.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.659-307T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92731926 | ||||||
| chr12:92732195
|
A | G | 1 | a0002c0002t0003g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.659-38A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 4/16 | chr12 | 92732195 | ||||||
| chr12:92732390
|
G | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.699+117G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92732390 | ||||||
| chr12:92732418
|
G | A | 1 | a0002c0025t0004g0136 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.699+145G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92732418 | ||||||
| chr12:92732495
|
T | C | 21 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143others(18): Show | 23 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.699+222T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92732495 | ||||||
| chr12:92732981
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.699+708C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92732981 | ||||||
| chr12:92733049
|
T | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.699+776T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92733049 | ||||||
| chr12:92733389
|
T | C | 6 | a0003c0007t0005g0210a0003c0007t0015g0205a0003c0007t0015g0217others(3): Show | 6 | HG01167.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1116T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92733389 | ||||||
| chr12:92733465
|
G | A | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+1192G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92733465 | ||||||
| chr12:92733714
|
C | T | 29 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(26): Show | 31 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.699+1441C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92733714 | ||||||
| chr12:92733743
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.699+1470G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92733743 | ||||||
| chr12:92733816
|
C | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.699+1543C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92733816 | ||||||
| chr12:92734407
|
G | A | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.700-2075G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92734407 | ||||||
| chr12:92734460
|
C | A | 1 | a0002c0002t0005g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.700-2022C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92734460 | ||||||
| chr12:92734750
|
A | T | 1 | a0003c0004t0005g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700-1732A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92734750 | ||||||
| chr12:92734986
|
A | C | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-1496A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92734986 | ||||||
| chr12:92735016
|
C | T | 40 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(37): Show | 42 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.700-1466C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735016 | ||||||
| chr12:92735105
|
G | A | 5 | a0002c0002t0003g0151a0002c0002t0003g0159a0002c0002t0003g0166others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.700-1377G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735105 | ||||||
| chr12:92735491
|
T | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0105 | 3 | HG00280.hp2 HG01978.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.700-991T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735491 | ||||||
| chr12:92735496
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.700-986A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735496 | ||||||
| chr12:92735497
|
G | C | 5 | a0002c0003t0004g0006a0002c0003t0004g0124a0002c0003t0004g0127others(2): Show | 6 | NA18939.hp2 NA18949.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.700-985G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735497 | ||||||
| chr12:92735652
|
A | T | 1 | a0002c0002t0003g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.700-830A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735652 | ||||||
| chr12:92735816
|
T | C | 1 | a0002c0002t0005g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.700-666T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735816 | ||||||
| chr12:92735843
|
CTTTT | C | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-634_700-631del others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 92735843 | |||||
| chr12:92735909
|
T | A | 3 | a0002c0011t0005g0016a0002c0011t0005g0018a0002c0016t0004g0017 | 3 | HG02559.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700-573T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92735909 | ||||||
| chr12:92736117
|
T | A | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.700-365T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92736117 | ||||||
| chr12:92736119
|
T | C | 9 | a0002c0002t0005g0187a0002c0002t0005g0189a0002c0002t0005g0191others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-363T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92736119 | ||||||
| chr12:92736271
|
C | T | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.700-211C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92736271 | ||||||
| chr12:92736409
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.700-73T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92736409 | ||||||
| chr12:92736439
|
G | T | 4 | a0003c0007t0005g0210a0003c0007t0015g0205a0003c0007t0015g0217others(1): Show | 4 | HG01167.hp1 HG02055.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-43G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92736439 | ||||||
| chr12:92736446
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.700-36T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 5/16 | chr12 | 92736446 | ||||||
| chr12:92736644
|
G | A | 1 | a0001c0005t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.795+67G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92736644 | ||||||
| chr12:92736676
|
G | T | 1 | a0001c0018t0001g0121 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.795+99G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92736676 | ||||||
| chr12:92736889
|
C | T | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+312C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92736889 | ||||||
| chr12:92736990
|
C | T | 2 | a0002c0002t0003g0165a0012c0026t0017g0022 | 2 | HG06807.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.796-388C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92736990 | ||||||
| chr12:92737274
|
C | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.796-104C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92737274 | ||||||
| chr12:92737279
|
G | A | 1 | a0003c0004t0007g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.796-99G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92737279 | ||||||
| chr12:92737367
|
C | T | 3 | a0003c0004t0002g0145a0003c0004t0006g0149a0003c0013t0004g0146 | 3 | HG02257.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.796-11C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 6/16 | chr12 | 92737367 | ||||||
| chr12:92737573
|
T | C | 3 | a0002c0003t0004g0208a0002c0003t0004g0213a0002c0003t0004g0216 | 3 | HG01261.hp1 HG01361.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.939+52T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92737573 | ||||||
| chr12:92737695
|
A | AGAG | 24 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(21): Show | 26 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.939+174_939+175ins others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92737695 | ||||||
| chr12:92737739
|
G | GGGAGGGA others(21): Show |
98 | a0002c0002t0002g0020a0002c0002t0003g0150a0002c0002t0003g0151others(95): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.939+235_939+236ins others(28): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737739 | |||||
| chr12:92737745
|
G | GAGGAAGG others(29): Show |
1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.939+227_939+228ins others(36): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737745 | |||||
| chr12:92737745
|
GAGGGAGG others(1): Show |
G | 24 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(21): Show | 26 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.939+228_939+235del others(8): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737745 | |||||
| chr12:92737749
|
G | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.939+228G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92737749 | ||||||
| chr12:92737749
|
G | GAGGAAGG others(24): Show |
1 | a0001c0001t0001g0072 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.939+238_939+239ins others(31): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737749 | |||||
| chr12:92737749
|
G | GAGGAAGG others(22): Show |
17 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0077others(14): Show | 17 | HG01109.hp1 HG01109.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.939+239_939+240ins others(29): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737749 | |||||
| chr12:92737749
|
G | GAGGAAGG others(26): Show |
75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(72): Show | 76 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.939+239_939+240ins others(33): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737749 | |||||
| chr12:92737749
|
G | GAGGAAGG others(30): Show |
17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(14): Show | 19 | HG00639.hp1 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.939+239_939+240ins others(37): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737749 | |||||
| chr12:92737749
|
G | GAGGAAGG others(34): Show |
4 | a0001c0001t0001g0113a0001c0015t0004g0099a0004c0006t0007g0218others(1): Show | 4 | HG00099.hp1 HG00609.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+239_939+240ins others(41): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737749 | |||||
| chr12:92737753
|
A | AAGGGAGG others(17): Show |
1 | a0002c0002t0025g0156 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.939+235_939+236ins others(24): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737753 | |||||
| chr12:92737771
|
G | GGAAGGAA others(28): Show |
1 | a0001c0001t0002g0067 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.939+251_939+252ins others(35): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92737771 | |||||
| chr12:92737887
|
A | G | 23 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(20): Show | 25 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.939+366A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92737887 | ||||||
| chr12:92737890
|
T | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.939+369T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92737890 | ||||||
| chr12:92738123
|
G | C | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.939+602G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738123 | ||||||
| chr12:92738126
|
G | T | 17 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(14): Show | 19 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.939+605G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738126 | ||||||
| chr12:92738181
|
T | C | 1 | a0002c0003t0004g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.939+660T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738181 | ||||||
| chr12:92738199
|
C | A | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+678C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738199 | ||||||
| chr12:92738201
|
C | T | 1 | a0003c0004t0011g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.939+680C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738201 | ||||||
| chr12:92738217
|
T | G | 3 | a0002c0002t0005g0230a0002c0002t0005g0231a0002c0002t0005g0232 | 3 | HG02818.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.939+696T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738217 | ||||||
| chr12:92738260
|
A | AATAGAGC others(13): Show |
1 | a0001c0005t0006g0047 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.939+748_939+767dup others(20): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92738260 | |||||
| chr12:92738313
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0097 | 3 | HG01106.hp1 HG01109.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.939+792G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738313 | ||||||
| chr12:92738857
|
C | T | 9 | a0002c0003t0008g0001a0002c0003t0008g0002a0002c0003t0008g0193others(6): Show | 13 | HG01099.hp2 HG01255.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+1336C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738857 | ||||||
| chr12:92738941
|
G | A | 18 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(15): Show | 20 | HG01891.hp2 HG02257.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.939+1420G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738941 | ||||||
| chr12:92738990
|
C | T | 4 | a0003c0004t0005g0225a0003c0004t0013g0009a0003c0004t0013g0223others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+1469C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92738990 | ||||||
| chr12:92739112
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.939+1591C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739112 | ||||||
| chr12:92739454
|
G | A | 3 | a0002c0002t0002g0020a0002c0003t0004g0228a0003c0021t0007g0019 | 3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.940-1399G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739454 | ||||||
| chr12:92739478
|
T | A | 4 | a0003c0004t0002g0145a0003c0004t0006g0149a0003c0013t0004g0146others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1375T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739478 | ||||||
| chr12:92739482
|
A | C | 2 | a0003c0004t0013g0009a0003c0004t0013g0226 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.940-1371A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739482 | ||||||
| chr12:92739525
|
T | C | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.940-1328T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739525 | ||||||
| chr12:92739675
|
A | C | 3 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0022g0011 | 3 | HG02572.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.940-1178A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739675 | ||||||
| chr12:92739757
|
A | T | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-1096A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739757 | ||||||
| chr12:92739977
|
G | A | 1 | a0003c0007t0005g0210 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.940-876G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92739977 | ||||||
| chr12:92740018
|
A | G | 3 | a0003c0004t0002g0145a0003c0004t0006g0149a0003c0013t0004g0146 | 3 | HG02257.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.940-835A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740018 | ||||||
| chr12:92740050
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0132 | 2 | HG01099.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.940-803G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740050 | ||||||
| chr12:92740054
|
C | A | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.940-799C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740054 | ||||||
| chr12:92740067
|
A | C | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-786A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740067 | ||||||
| chr12:92740300
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(129): Show | 137 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.940-553A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740300 | ||||||
| chr12:92740318
|
A | G | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-535A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740318 | ||||||
| chr12:92740480
|
G | A | 5 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-373G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | chr12 | 92740480 | ||||||
| chr12:92740526
|
GTGT | G | 8 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.940-321_940-319del others(3): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 92740526 | |||||
| chr12:92741116
|
C | T | 1 | a0001c0005t0020g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1035+168C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/16 | chr12 | 92741116 | ||||||
| chr12:92741148
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1035+200G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/16 | chr12 | 92741148 | ||||||
| chr12:92741368
|
T | C | 1 | a0002c0002t0025g0156 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1036-123T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/16 | chr12 | 92741368 | ||||||
| chr12:92741372
|
T | G | 8 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036-119T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/16 | chr12 | 92741372 | ||||||
| chr12:92741401
|
C | T | 2 | a0012c0026t0017g0022a0015c0020t0006g0014 | 2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1036-90C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/16 | chr12 | 92741401 | ||||||
| chr12:92741479
|
C | T | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1036-12C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 8/16 | chr12 | 92741479 | ||||||
| chr12:92741585
|
T | TCACAAAG others(35): Show |
1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1131_1137+35dupCAC others(39): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 92741585 | |||||
| chr12:92741605
|
T | C | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137+13T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92741605 | ||||||
| chr12:92741893
|
T | C | 13 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(10): Show | 13 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1137+301T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92741893 | ||||||
| chr12:92742089
|
T | C | 12 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(9): Show | 12 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137+497T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742089 | ||||||
| chr12:92742481
|
A | G | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(217): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1137+889A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742481 | ||||||
| chr12:92742522
|
A | G | 12 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(9): Show | 12 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137+930A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742522 | ||||||
| chr12:92742591
|
G | GT | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(188): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1137+1014dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 92742591 | |||||
| chr12:92742591
|
G | GTT | 16 | a0001c0001t0001g0075a0001c0005t0001g0045a0001c0005t0001g0046others(13): Show | 16 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.1137+1013_1137+101 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 92742591 | |||||
| chr12:92742608
|
G | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137+1016G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742608 | ||||||
| chr12:92742649
|
G | A | 1 | a0003c0004t0007g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1137+1057G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742649 | ||||||
| chr12:92742704
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1137+1112G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742704 | ||||||
| chr12:92742786
|
A | G | 17 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(14): Show | 17 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1137+1194A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742786 | ||||||
| chr12:92742811
|
C | T | 1 | a0002c0003t0008g0199 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1137+1219C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742811 | ||||||
| chr12:92742975
|
A | G | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137+1383A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92742975 | ||||||
| chr12:92743284
|
A | T | 40 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(37): Show | 42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1137+1692A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743284 | ||||||
| chr12:92743288
|
C | T | 40 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(37): Show | 42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1137+1696C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743288 | ||||||
| chr12:92743549
|
A | AT | 18 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(15): Show | 18 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1138-1924dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 92743549 | |||||
| chr12:92743615
|
G | A | 4 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138-1863G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743615 | ||||||
| chr12:92743708
|
C | T | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1138-1770C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743708 | ||||||
| chr12:92743722
|
A | G | 147 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(144): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1138-1756A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743722 | ||||||
| chr12:92743762
|
A | G | 17 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(14): Show | 17 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1138-1716A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743762 | ||||||
| chr12:92743791
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1138-1687C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743791 | ||||||
| chr12:92743849
|
C | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1138-1629C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743849 | ||||||
| chr12:92743946
|
C | T | 1 | a0002c0002t0006g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1138-1532C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743946 | ||||||
| chr12:92744297
|
T | C | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1138-1181T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744297 | ||||||
| chr12:92744319
|
G | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(118): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1138-1159G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744319 | ||||||
| chr12:92744339
|
T | G | 1 | a0008c0012t0003g0007 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1138-1139T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744339 | ||||||
| chr12:92744349
|
G | A | 2 | a0002c0002t0003g0164a0002c0002t0003g0169 | 2 | HG00140.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1138-1129G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744349 | ||||||
| chr12:92744427
|
G | C | 3 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0003t0014g0143 | 3 | HG01884.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1138-1051G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744427 | ||||||
| chr12:92744572
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0112 | 2 | HG00323.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1138-906G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744572 | ||||||
| chr12:92744611
|
G | A | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138-867G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744611 | ||||||
| chr12:92744611
|
G | T | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1138-867G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744611 | ||||||
| chr12:92744626
|
C | T | 5 | a0002c0003t0004g0207a0002c0003t0004g0212a0002c0011t0005g0016others(2): Show | 5 | HG00738.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-852C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744626 | ||||||
| chr12:92744656
|
CT | C | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1138-808delT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 92744656 | |||||
| chr12:92744667
|
T | G | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1138-811T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744667 | ||||||
| chr12:92744671
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1138-807G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744671 | ||||||
| chr12:92744811
|
C | A | 16 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(13): Show | 16 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1138-667C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92744811 | ||||||
| chr12:92745229
|
T | C | 6 | a0004c0006t0007g0003a0004c0006t0007g0218a0004c0006t0007g0219others(3): Show | 8 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1138-249T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745229 | ||||||
| chr12:92745329
|
C | CCACTTTT others(97): Show |
5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-147_1138-146i others(106): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 92745329 | |||||
| chr12:92745332
|
T | G | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-146T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745332 | ||||||
| chr12:92745336
|
G | C | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-142G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745336 | ||||||
| chr12:92745337
|
T | C | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-141T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745337 | ||||||
| chr12:92745341
|
G | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-137G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745341 | ||||||
| chr12:92745343
|
C | T | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-135C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745343 | ||||||
| chr12:92745344
|
G | T | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-134G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745344 | ||||||
| chr12:92745347
|
T | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-131T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745347 | ||||||
| chr12:92745350
|
TTG | T | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-127_1138-126d others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745350 | ||||||
| chr12:92745354
|
T | C | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-124T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745354 | ||||||
| chr12:92745355
|
C | T | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-123C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745355 | ||||||
| chr12:92745356
|
A | C | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-122A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745356 | ||||||
| chr12:92745360
|
C | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-118C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745360 | ||||||
| chr12:92745365
|
C | G | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-113C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745365 | ||||||
| chr12:92745366
|
C | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-112C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745366 | ||||||
| chr12:92745367
|
T | G | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-111T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745367 | ||||||
| chr12:92745368
|
C | G | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-110C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745368 | ||||||
| chr12:92745370
|
A | AGAAGAAT others(2): Show |
5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-108_1138-107i others(11): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745370 | ||||||
| chr12:92745374
|
T | G | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-104T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745374 | ||||||
| chr12:92745375
|
T | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-103T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745375 | ||||||
| chr12:92745376
|
C | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-102C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745376 | ||||||
| chr12:92745458
|
C | T | 16 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0061others(13): Show | 16 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1138-20C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92745458 | ||||||
| chr12:92745616
|
T | C | 17 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(14): Show | 17 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1251+25T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92745616 | ||||||
| chr12:92745681
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1251+90G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92745681 | ||||||
| chr12:92745911
|
A | G | 1 | a0001c0001t0007g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1251+320A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92745911 | ||||||
| chr12:92745974
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1251+383G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92745974 | ||||||
| chr12:92745990
|
G | A | 4 | a0003c0004t0005g0225a0003c0004t0013g0009a0003c0004t0013g0223others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251+399G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92745990 | ||||||
| chr12:92746215
|
C | A | 1 | a0002c0002t0003g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1251+624C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746215 | ||||||
| chr12:92746347
|
G | T | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251+756G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746347 | ||||||
| chr12:92746382
|
A | G | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1251+791A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746382 | ||||||
| chr12:92746398
|
A | G | 17 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(14): Show | 17 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1251+807A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746398 | ||||||
| chr12:92746464
|
G | A | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251+873G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746464 | ||||||
| chr12:92746595
|
A | C | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1251+1004A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746595 | ||||||
| chr12:92746631
|
C | G | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251+1040C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746631 | ||||||
| chr12:92746825
|
C | T | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1251+1234C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92746825 | ||||||
| chr12:92747028
|
A | G | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1251+1437A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747028 | ||||||
| chr12:92747033
|
A | G | 28 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(25): Show | 30 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1251+1442A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747033 | ||||||
| chr12:92747126
|
A | T | 5 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251+1535A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747126 | ||||||
| chr12:92747259
|
G | GA | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(221): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1251+1680dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92747259 | |||||
| chr12:92747259
|
G | GAA | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251+1679_1251+168 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92747259 | |||||
| chr12:92747318
|
GAGATATC others(27): Show |
G | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(120): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1251+1755_1251+178 others(38): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92747318 | |||||
| chr12:92747472
|
T | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0037others(48): Show | 54 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1251+1881T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747472 | ||||||
| chr12:92747520
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1251+1929A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747520 | ||||||
| chr12:92747842
|
A | T | 11 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251+2251A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747842 | ||||||
| chr12:92747886
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(113): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1251+2295G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747886 | ||||||
| chr12:92747895
|
A | AG | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251+2308dupG | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92747895 | |||||
| chr12:92747930
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1251+2339G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747930 | ||||||
| chr12:92747948
|
A | G | 2 | a0002c0011t0005g0016a0002c0011t0005g0018 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1251+2357A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747948 | ||||||
| chr12:92748191
|
A | G | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251+2600A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748191 | ||||||
| chr12:92748250
|
C | CT | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(115): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1251+2673dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92748250 | |||||
| chr12:92748250
|
CT | C | 42 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(39): Show | 44 | HG01167.hp1 HG01168.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.1251+2673delT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92748250 | |||||
| chr12:92748302
|
G | A | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(213): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1251+2711G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748302 | ||||||
| chr12:92748332
|
C | T | 1 | a0005c0008t0002g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1251+2741C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748332 | ||||||
| chr12:92748348
|
G | A | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1251+2757G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748348 | ||||||
| chr12:92748396
|
G | T | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251+2805G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748396 | ||||||
| chr12:92748413
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1251+2822A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748413 | ||||||
| chr12:92748422
|
A | G | 1 | a0006c0010t0012g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1251+2831A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748422 | ||||||
| chr12:92748428
|
G | A | 1 | a0002c0002t0005g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251+2837G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748428 | ||||||
| chr12:92748553
|
G | C | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(120): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1251+2962G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748553 | ||||||
| chr12:92748602
|
C | T | 1 | a0001c0015t0004g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1251+3011C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748602 | ||||||
| chr12:92748725
|
C | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(131): Show | 137 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251+3134C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748725 | ||||||
| chr12:92748792
|
G | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1251+3201G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748792 | ||||||
| chr12:92748917
|
G | A | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1251+3326G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748917 | ||||||
| chr12:92748967
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3376G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748967 | ||||||
| chr12:92748968
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3377T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748968 | ||||||
| chr12:92748969
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3378T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748969 | ||||||
| chr12:92748973
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3382G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748973 | ||||||
| chr12:92748974
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3383T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748974 | ||||||
| chr12:92748975
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3384T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748975 | ||||||
| chr12:92748976
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3385T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748976 | ||||||
| chr12:92748977
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3386T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748977 | ||||||
| chr12:92748978
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3387T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748978 | ||||||
| chr12:92748980
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3389A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748980 | ||||||
| chr12:92748981
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3390G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748981 | ||||||
| chr12:92748982
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3391G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748982 | ||||||
| chr12:92748984
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3393G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748984 | ||||||
| chr12:92748985
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3394T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748985 | ||||||
| chr12:92748986
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3395T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748986 | ||||||
| chr12:92748987
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3396T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748987 | ||||||
| chr12:92748988
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3397A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748988 | ||||||
| chr12:92748989
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3398G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748989 | ||||||
| chr12:92748990
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3399A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748990 | ||||||
| chr12:92748994
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3403A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748994 | ||||||
| chr12:92748995
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3404T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748995 | ||||||
| chr12:92748996
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3405T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748996 | ||||||
| chr12:92748998
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3407G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748998 | ||||||
| chr12:92748999
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3408G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92748999 | ||||||
| chr12:92749013
|
G | C | 2 | a0007c0014t0006g0049a0007c0014t0006g0050 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1251+3422G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749013 | ||||||
| chr12:92749039
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1251+3448G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749039 | ||||||
| chr12:92749219
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3628A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749219 | ||||||
| chr12:92749219
|
A | G | 3 | a0002c0002t0005g0230a0002c0002t0005g0231a0002c0002t0005g0232 | 3 | HG02818.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1251+3628A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749219 | ||||||
| chr12:92749221
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3630T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749221 | ||||||
| chr12:92749223
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3632T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749223 | ||||||
| chr12:92749225
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3634T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749225 | ||||||
| chr12:92749230
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3639G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749230 | ||||||
| chr12:92749231
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3640T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749231 | ||||||
| chr12:92749232
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3641G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749232 | ||||||
| chr12:92749233
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3642T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749233 | ||||||
| chr12:92749234
|
A | ACCACCCA others(7): Show |
1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3644_1251+364 others(18): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749234 | |||||
| chr12:92749237
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3646T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749237 | ||||||
| chr12:92749273
|
T | A | 18 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(15): Show | 18 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1251+3682T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749273 | ||||||
| chr12:92749282
|
A | T | 32 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(29): Show | 35 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1251+3691A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749282 | ||||||
| chr12:92749314
|
CAG | C | 18 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(15): Show | 18 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1251+3726_1251+372 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749314 | |||||
| chr12:92749342
|
A | G | 1 | a0013c0023t0026g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1251+3751A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749342 | ||||||
| chr12:92749363
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3772C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749363 | ||||||
| chr12:92749364
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3773T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749364 | ||||||
| chr12:92749369
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3778G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749369 | ||||||
| chr12:92749387
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3796G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749387 | ||||||
| chr12:92749394
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3803T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749394 | ||||||
| chr12:92749427
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3836G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749427 | ||||||
| chr12:92749428
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3837A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749428 | ||||||
| chr12:92749434
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3843A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749434 | ||||||
| chr12:92749554
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3963C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749554 | ||||||
| chr12:92749555
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+3964A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749555 | ||||||
| chr12:92749559
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251+3968C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749559 | ||||||
| chr12:92749560
|
G | A | 18 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(15): Show | 18 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1251+3969G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749560 | ||||||
| chr12:92749587
|
G | A | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+3996G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749587 | ||||||
| chr12:92749633
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4042T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749633 | ||||||
| chr12:92749653
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4062T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749653 | ||||||
| chr12:92749669
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4078C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749669 | ||||||
| chr12:92749674
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4083T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749674 | ||||||
| chr12:92749675
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4084T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749675 | ||||||
| chr12:92749677
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4086T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749677 | ||||||
| chr12:92749687
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4096G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749687 | ||||||
| chr12:92749695
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4104T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749695 | ||||||
| chr12:92749697
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4106T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749697 | ||||||
| chr12:92749698
|
C | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4107C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749698 | ||||||
| chr12:92749724
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4133T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749724 | ||||||
| chr12:92749730
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4139A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749730 | ||||||
| chr12:92749731
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4140G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749731 | ||||||
| chr12:92749731
|
G | T | 5 | a0002c0003t0004g0207a0002c0003t0004g0212a0002c0011t0005g0016others(2): Show | 5 | HG00738.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251+4140G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749731 | ||||||
| chr12:92749732
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4141T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749732 | ||||||
| chr12:92749736
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4145T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749736 | ||||||
| chr12:92749739
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4148T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749739 | ||||||
| chr12:92749740
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4149G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749740 | ||||||
| chr12:92749746
|
A | G | 25 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(22): Show | 26 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1251+4155A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749746 | ||||||
| chr12:92749819
|
T | G | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+4228T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749819 | ||||||
| chr12:92749822
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4231T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749822 | ||||||
| chr12:92749823
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4232G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749823 | ||||||
| chr12:92749824
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4233C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749824 | ||||||
| chr12:92749825
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4234T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749825 | ||||||
| chr12:92749826
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4235G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749826 | ||||||
| chr12:92749829
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4238T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749829 | ||||||
| chr12:92749830
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4239C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749830 | ||||||
| chr12:92749831
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4240C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749831 | ||||||
| chr12:92749834
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4243C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749834 | ||||||
| chr12:92749835
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4244T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749835 | ||||||
| chr12:92749838
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1251+4247G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749838 | ||||||
| chr12:92749844
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4246T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749844 | ||||||
| chr12:92749845
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4245T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749845 | ||||||
| chr12:92749846
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4244T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749846 | ||||||
| chr12:92749848
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4242T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749848 | ||||||
| chr12:92749849
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4241T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749849 | ||||||
| chr12:92749851
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4239G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749851 | ||||||
| chr12:92749852
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4238G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749852 | ||||||
| chr12:92749854
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4236T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749854 | ||||||
| chr12:92749856
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4234T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749856 | ||||||
| chr12:92749859
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4231T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749859 | ||||||
| chr12:92749861
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4229T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749861 | ||||||
| chr12:92749862
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4228T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749862 | ||||||
| chr12:92749863
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4227T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749863 | ||||||
| chr12:92749864
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4226T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749864 | ||||||
| chr12:92749865
|
ATTTTATT others(10): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1252-4205_1252-418 others(21): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749865 | |||||
| chr12:92749866
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4224T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749866 | ||||||
| chr12:92749872
|
TTTA | T | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1252-4215_1252-421 others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749872 | |||||
| chr12:92749874
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4216T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749874 | ||||||
| chr12:92749876
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4214T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749876 | ||||||
| chr12:92749877
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4213T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749877 | ||||||
| chr12:92749878
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4212T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749878 | ||||||
| chr12:92749879
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4211T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749879 | ||||||
| chr12:92749880
|
ATT | A | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1252-4205_1252-420 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749880 | |||||
| chr12:92749881
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4209T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749881 | ||||||
| chr12:92749882
|
T | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4208T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749882 | ||||||
| chr12:92749883
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4207T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749883 | ||||||
| chr12:92749885
|
T | A | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1252-4205T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749885 | ||||||
| chr12:92749887
|
A | T | 1 | a0016c0029t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1252-4203A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749887 | ||||||
| chr12:92749901
|
T | C | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1252-4189T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749901 | ||||||
| chr12:92749906
|
C | A | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1252-4184C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749906 | ||||||
| chr12:92749906
|
C | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4184C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749906 | ||||||
| chr12:92749907
|
A | ATTTAT | 70 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1252-4165_1252-416 others(9): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749907 | |||||
| chr12:92749907
|
A | T | 2 | a0002c0009t0010g0010a0002c0009t0010g0237 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1252-4183A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749907 | ||||||
| chr12:92749922
|
TTTTA | T | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1252-4160_1252-415 others(8): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749922 | |||||
| chr12:92749923
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1252-4167T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749923 | ||||||
| chr12:92749926
|
A | ATTTTATT others(15): Show |
6 | a0002c0002t0005g0187a0002c0002t0005g0189a0002c0002t0005g0191others(3): Show | 6 | HG01192.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1252-4161_1252-416 others(26): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749926 | |||||
| chr12:92749930
|
A | T | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4160A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749930 | ||||||
| chr12:92749931
|
T | A | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4159T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749931 | ||||||
| chr12:92749937
|
TTTA | T | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1252-4151_1252-414 others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749937 | |||||
| chr12:92749942
|
A | T | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4148A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749942 | ||||||
| chr12:92749945
|
T | A | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4145T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749945 | ||||||
| chr12:92749945
|
TTATTTTA others(5): Show |
T | 2 | a0002c0003t0004g0207a0014c0019t0003g0172 | 2 | HG00738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1252-4119_1252-410 others(16): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749945 | |||||
| chr12:92749954
|
T | A | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1252-4136T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749954 | ||||||
| chr12:92749957
|
A | ATATTT | 88 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(85): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1252-4124_1252-412 others(9): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749957 | |||||
| chr12:92749957
|
A | ATATTTTA others(15): Show |
7 | a0001c0005t0006g0052a0003c0004t0011g0178a0003c0004t0011g0179others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-4120_1252-411 others(26): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749957 | |||||
| chr12:92749957
|
A | T | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1252-4133A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749957 | ||||||
| chr12:92749966
|
T | A | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4124T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749966 | ||||||
| chr12:92749969
|
A | AT | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-4120dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749969 | |||||
| chr12:92749969
|
A | T | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4121A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749969 | ||||||
| chr12:92749971
|
A | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(129): Show | 134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1252-4119A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749971 | ||||||
| chr12:92749973
|
T | TA | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(114): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1252-4117_1252-411 others(5): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749973 | ||||||
| chr12:92749973
|
T | TATATTTT others(28): Show |
10 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(7): Show | 10 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1252-4117_1252-411 others(39): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749973 | ||||||
| chr12:92749974
|
T | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-4116T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749974 | ||||||
| chr12:92749978
|
T | TTTA | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-4109_1252-410 others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749978 | |||||
| chr12:92749983
|
T | A | 1 | a0003c0007t0016g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-4107T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749983 | ||||||
| chr12:92749983
|
TTTA | T | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-4101_1252-409 others(7): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749983 | |||||
| chr12:92749989
|
A | T | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-4101A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749989 | ||||||
| chr12:92749991
|
T | A | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-4099T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749991 | ||||||
| chr12:92749997
|
T | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-4093T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749997 | ||||||
| chr12:92749999
|
A | ATT | 17 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(14): Show | 18 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1252-4090_1252-408 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749999 | |||||
| chr12:92749999
|
A | ATTATT | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(115): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1252-4065_1252-406 others(9): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749999 | |||||
| chr12:92749999
|
A | ATTATTTT others(3): Show |
1 | a0001c0001t0002g0029 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1252-4070_1252-406 others(14): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92749999 | |||||
| chr12:92749999
|
A | T | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-4091A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92749999 | ||||||
| chr12:92750007
|
ATT | A | 5 | a0002c0002t0006g0015a0002c0003t0004g0012a0002c0003t0004g0013others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-4080_1252-407 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92750007 | |||||
| chr12:92750080
|
A | T | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1252-4010A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92750080 | ||||||
| chr12:92750750
|
CTT | C | 4 | a0003c0004t0005g0225a0003c0004t0013g0009a0003c0004t0013g0223others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-3339_1252-333 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92750750 | ||||||
| chr12:92750754
|
T | A | 4 | a0003c0004t0005g0225a0003c0004t0013g0009a0003c0004t0013g0223others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-3336T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92750754 | ||||||
| chr12:92750816
|
T | A | 1 | a0006c0010t0012g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1252-3274T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92750816 | ||||||
| chr12:92750942
|
C | CAATA | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(126): Show | 131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1252-3129_1252-312 others(8): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92750942 | |||||
| chr12:92750955
|
A | C | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-3135A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92750955 | ||||||
| chr12:92751078
|
A | G | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1252-3012A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751078 | ||||||
| chr12:92751186
|
G | C | 5 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-2904G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751186 | ||||||
| chr12:92751514
|
C | T | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-2576C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751514 | ||||||
| chr12:92751515
|
G | A | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1252-2575G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751515 | ||||||
| chr12:92751532
|
A | AT | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(133): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1252-2545dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92751532 | |||||
| chr12:92751532
|
A | ATT | 12 | a0001c0001t0001g0057a0001c0005t0001g0045a0001c0005t0001g0046others(9): Show | 12 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1252-2546_1252-254 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92751532 | |||||
| chr12:92751656
|
G | A | 11 | a0002c0025t0004g0136a0003c0004t0002g0145a0003c0004t0005g0225others(8): Show | 12 | HG02257.hp2 HG02630.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1252-2434G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751656 | ||||||
| chr12:92751666
|
G | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1252-2424G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751666 | ||||||
| chr12:92751669
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1252-2421C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751669 | ||||||
| chr12:92751670
|
G | A | 1 | a0011c0027t0006g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1252-2420G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751670 | ||||||
| chr12:92751740
|
G | A | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1252-2350G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751740 | ||||||
| chr12:92751912
|
A | G | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-2178A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92751912 | ||||||
| chr12:92752027
|
TA | T | 5 | a0001c0001t0001g0088a0004c0006t0007g0003a0004c0006t0007g0220others(2): Show | 7 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1252-2051delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 92752027 | |||||
| chr12:92752028
|
A | T | 3 | a0002c0002t0002g0020a0002c0002t0006g0188a0003c0021t0007g0019 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1252-2062A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752028 | ||||||
| chr12:92752074
|
C | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1252-2016C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752074 | ||||||
| chr12:92752160
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1252-1930T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752160 | ||||||
| chr12:92752288
|
G | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1252-1802G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752288 | ||||||
| chr12:92752405
|
C | A | 12 | a0003c0007t0005g0210a0003c0007t0007g0190a0003c0007t0015g0205others(9): Show | 14 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1252-1685C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752405 | ||||||
| chr12:92752461
|
G | A | 35 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(32): Show | 38 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1252-1629G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752461 | ||||||
| chr12:92752509
|
C | A | 24 | a0002c0025t0004g0136a0003c0004t0002g0145a0003c0004t0005g0225others(21): Show | 27 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1252-1581C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752509 | ||||||
| chr12:92752548
|
G | A | 1 | a0002c0009t0010g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1252-1542G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752548 | ||||||
| chr12:92752603
|
C | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(96): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1252-1487C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752603 | ||||||
| chr12:92752767
|
A | G | 1 | a0001c0015t0004g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1252-1323A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752767 | ||||||
| chr12:92752779
|
C | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(185): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1252-1311C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752779 | ||||||
| chr12:92752970
|
C | T | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1252-1120C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752970 | ||||||
| chr12:92752973
|
A | G | 4 | a0003c0004t0005g0225a0003c0004t0013g0009a0003c0004t0013g0223others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-1117A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92752973 | ||||||
| chr12:92753053
|
T | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(90): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1252-1037T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753053 | ||||||
| chr12:92753092
|
G | A | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(135): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1252-998G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753092 | ||||||
| chr12:92753156
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1252-934C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753156 | ||||||
| chr12:92753277
|
G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(97): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1252-813G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753277 | ||||||
| chr12:92753575
|
T | C | 3 | a0002c0002t0005g0230a0002c0002t0005g0231a0002c0002t0005g0232 | 3 | HG02818.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1252-515T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753575 | ||||||
| chr12:92753660
|
C | T | 12 | a0003c0007t0005g0210a0003c0007t0007g0190a0003c0007t0015g0205others(9): Show | 14 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1252-430C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753660 | ||||||
| chr12:92753691
|
C | T | 3 | a0002c0002t0007g0183a0002c0003t0001g0185a0002c0003t0002g0184 | 3 | HG00741.hp1 HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1252-399C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753691 | ||||||
| chr12:92753742
|
C | T | 1 | a0002c0002t0003g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1252-348C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753742 | ||||||
| chr12:92753787
|
A | G | 42 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(39): Show | 45 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1252-303A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753787 | ||||||
| chr12:92753834
|
G | T | 1 | a0003c0004t0007g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1252-256G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92753834 | ||||||
| chr12:92754032
|
C | G | 42 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(39): Show | 45 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1252-58C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92754032 | ||||||
| chr12:92754562
|
G | A | 1 | a0015c0020t0006g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1426+298G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | chr12 | 92754562 | ||||||
| chr12:92754629
|
G | C | 6 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(3): Show | 7 | HG02723.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1426+365G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | chr12 | 92754629 | ||||||
| chr12:92754744
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(96): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1426+480G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | chr12 | 92754744 | ||||||
| chr12:92754775
|
G | A | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1426+511G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | chr12 | 92754775 | ||||||
| chr12:92754844
|
G | A | 2 | a0002c0003t0001g0211a0002c0003t0004g0124 | 2 | HG00642.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1426+580G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | chr12 | 92754844 | ||||||
| chr12:92755486
|
A | AT | 33 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(30): Show | 36 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1427-329dupT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 92755486 | |||||
| chr12:92755647
|
C | T | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1427-178C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 11/16 | chr12 | 92755647 | ||||||
| chr12:92756039
|
A | C | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542+99A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 12/16 | chr12 | 92756039 | ||||||
| chr12:92756099
|
G | A | 1 | a0003c0004t0013g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1542+159G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 12/16 | chr12 | 92756099 | ||||||
| chr12:92756219
|
T | C | 1 | a0002c0003t0004g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1543-79T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 12/16 | chr12 | 92756219 | ||||||
| chr12:92756284
|
G | A | 27 | a0001c0005t0001g0045a0001c0005t0001g0046a0001c0005t0002g0051others(24): Show | 28 | HG01168.hp1 HG01243.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1543-14G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 12/16 | chr12 | 92756284 | ||||||
| chr12:92756432
|
G | A | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636+41G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756432 | ||||||
| chr12:92756576
|
A | G | 7 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1636+185A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756576 | ||||||
| chr12:92756622
|
A | G | 6 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636+231A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756622 | ||||||
| chr12:92756661
|
C | T | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636+270C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756661 | ||||||
| chr12:92756713
|
A | G | 4 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0005g0173others(1): Show | 4 | HG01884.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1636+322A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756713 | ||||||
| chr12:92756748
|
C | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(96): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1636+357C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756748 | ||||||
| chr12:92756786
|
G | T | 7 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1636+395G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92756786 | ||||||
| chr12:92757161
|
C | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(127): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1636+770C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757161 | ||||||
| chr12:92757204
|
A | T | 84 | a0001c0001t0007g0055a0001c0001t0007g0089a0002c0002t0003g0150others(81): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.1636+813A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757204 | ||||||
| chr12:92757232
|
C | T | 2 | a0002c0002t0009g0186a0002c0002t0009g0215 | 2 | HG01192.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1636+841C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757232 | ||||||
| chr12:92757269
|
T | G | 84 | a0001c0001t0007g0055a0001c0001t0007g0089a0002c0002t0003g0150others(81): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.1636+878T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757269 | ||||||
| chr12:92757320
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0077others(4): Show | 8 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636+929A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757320 | ||||||
| chr12:92757460
|
T | C | 7 | a0002c0002t0005g0187a0002c0002t0005g0189a0002c0002t0005g0191others(4): Show | 7 | HG02486.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1636+1069T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757460 | ||||||
| chr12:92757584
|
G | A | 3 | a0003c0004t0013g0009a0003c0004t0013g0223a0003c0004t0013g0226 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1636+1193G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757584 | ||||||
| chr12:92757666
|
G | T | 43 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(40): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1636+1275G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757666 | ||||||
| chr12:92757832
|
T | C | 4 | a0002c0003t0008g0002a0002c0003t0008g0193a0002c0003t0008g0197others(1): Show | 6 | HG02135.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636+1441T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757832 | ||||||
| chr12:92757922
|
A | G | 8 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636+1531A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92757922 | ||||||
| chr12:92758044
|
C | G | 8 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636+1653C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758044 | ||||||
| chr12:92758227
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1636+1836T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758227 | ||||||
| chr12:92758247
|
T | C | 42 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1636+1856T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758247 | ||||||
| chr12:92758316
|
A | G | 1 | a0002c0002t0009g0204 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1636+1925A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758316 | ||||||
| chr12:92758339
|
G | A | 11 | a0002c0003t0001g0170a0002c0003t0001g0211a0002c0003t0002g0184others(8): Show | 13 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1636+1948G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758339 | ||||||
| chr12:92758377
|
T | C | 1 | a0010c0017t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1636+1986T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758377 | ||||||
| chr12:92758418
|
A | C | 5 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(2): Show | 6 | HG02922.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636+2027A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92758418 | ||||||
| chr12:92759125
|
T | G | 2 | a0002c0011t0005g0016a0002c0011t0005g0018 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1637-2627T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92759125 | ||||||
| chr12:92759274
|
T | C | 1 | a0003c0007t0002g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1637-2478T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92759274 | ||||||
| chr12:92759308
|
C | A | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1637-2444C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92759308 | ||||||
| chr12:92759576
|
G | T | 2 | a0002c0003t0008g0001a0002c0003t0008g0196 | 4 | HG01255.hp2 HG01346.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637-2176G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92759576 | ||||||
| chr12:92759703
|
C | T | 1 | a0002c0003t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1637-2049C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92759703 | ||||||
| chr12:92760021
|
C | T | 12 | a0002c0002t0002g0020a0002c0002t0006g0015a0002c0002t0006g0188others(9): Show | 12 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637-1731C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760021 | ||||||
| chr12:92760346
|
T | C | 1 | a0004c0006t0007g0003 | 3 | HG00639.hp1 HG01069.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1637-1406T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760346 | ||||||
| chr12:92760387
|
CT | C | 7 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637-1364delT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760387 | ||||||
| chr12:92760445
|
T | C | 5 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(2): Show | 6 | HG02922.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637-1307T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760445 | ||||||
| chr12:92760520
|
T | A | 10 | a0001c0015t0004g0122a0002c0003t0004g0006a0002c0003t0004g0124others(7): Show | 11 | HG00738.hp2 HG02723.hp1 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637-1232T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760520 | ||||||
| chr12:92760532
|
A | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1220A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760532 | ||||||
| chr12:92760533
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1219T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760533 | ||||||
| chr12:92760535
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1217T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760535 | ||||||
| chr12:92760539
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1213T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760539 | ||||||
| chr12:92760542
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1210A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760542 | ||||||
| chr12:92760543
|
A | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1209A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760543 | ||||||
| chr12:92760545
|
A | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1207A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760545 | ||||||
| chr12:92760547
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1205G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760547 | ||||||
| chr12:92760551
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1201A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760551 | ||||||
| chr12:92760552
|
A | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1200A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760552 | ||||||
| chr12:92760557
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1195A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760557 | ||||||
| chr12:92760558
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1194T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760558 | ||||||
| chr12:92760559
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1193T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760559 | ||||||
| chr12:92760563
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1189T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760563 | ||||||
| chr12:92760566
|
G | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1186G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760566 | ||||||
| chr12:92760571
|
C | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1181C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760571 | ||||||
| chr12:92760572
|
C | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1180C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760572 | ||||||
| chr12:92760579
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1173T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760579 | ||||||
| chr12:92760580
|
ACTCTAAG others(8): Show |
A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1171_1637-115 others(19): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760580 | ||||||
| chr12:92760597
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1155C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760597 | ||||||
| chr12:92760600
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1152C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760600 | ||||||
| chr12:92760607
|
T | C | 7 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637-1145T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760607 | ||||||
| chr12:92760618
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1134T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760618 | ||||||
| chr12:92760619
|
C | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1133C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760619 | ||||||
| chr12:92760620
|
C | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1132C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760620 | ||||||
| chr12:92760622
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1130C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760622 | ||||||
| chr12:92760625
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1127A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760625 | ||||||
| chr12:92760626
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1126A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760626 | ||||||
| chr12:92760627
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1125A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760627 | ||||||
| chr12:92760644
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1108C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760644 | ||||||
| chr12:92760647
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1105T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760647 | ||||||
| chr12:92760649
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1103T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760649 | ||||||
| chr12:92760650
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1102T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760650 | ||||||
| chr12:92760651
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1101C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760651 | ||||||
| chr12:92760654
|
A | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1098A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760654 | ||||||
| chr12:92760655
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1097T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760655 | ||||||
| chr12:92760656
|
T | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1096T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760656 | ||||||
| chr12:92760658
|
C | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1094C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760658 | ||||||
| chr12:92760659
|
T | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1093T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760659 | ||||||
| chr12:92760662
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1090G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760662 | ||||||
| chr12:92760664
|
G | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1088G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760664 | ||||||
| chr12:92760667
|
A | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1085A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760667 | ||||||
| chr12:92760673
|
A | C | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1079A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760673 | ||||||
| chr12:92760679
|
G | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1073G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760679 | ||||||
| chr12:92760681
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1071A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760681 | ||||||
| chr12:92760682
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1070A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760682 | ||||||
| chr12:92760683
|
G | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1069G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760683 | ||||||
| chr12:92760686
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1066G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760686 | ||||||
| chr12:92760690
|
C | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1062C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760690 | ||||||
| chr12:92760691
|
C | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1061C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760691 | ||||||
| chr12:92760699
|
G | A | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1053G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760699 | ||||||
| chr12:92760702
|
A | G | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1050A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760702 | ||||||
| chr12:92760703
|
C | T | 1 | a0014c0019t0003g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1637-1049C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760703 | ||||||
| chr12:92760752
|
AGCTATTT | A | 7 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637-997_1637-991d others(9): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92760752 | |||||
| chr12:92760836
|
A | G | 42 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1637-916A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92760836 | ||||||
| chr12:92761047
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0035others(32): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1637-705C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761047 | ||||||
| chr12:92761414
|
G | A | 1 | a0002c0003t0014g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1637-338G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761414 | ||||||
| chr12:92761540
|
AAAAG | A | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(142): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1637-210_1637-207d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761540 | |||||
| chr12:92761542
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1637-210A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761542 | ||||||
| chr12:92761546
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1637-206G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761546 | ||||||
| chr12:92761559
|
A | AGAAG | 3 | a0003c0004t0013g0009a0003c0004t0013g0223a0003c0004t0013g0226 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637-173_1637-170d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761559 | |||||
| chr12:92761559
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1637-193A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761559 | ||||||
| chr12:92761559
|
AGAAG | A | 48 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(45): Show | 50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.1637-173_1637-170d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761559 | |||||
| chr12:92761607
|
AAAAGAAA others(16): Show |
A | 1 | a0001c0001t0002g0024 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1637-126_1637-104d others(25): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761607 | |||||
| chr12:92761608
|
AAAGAAAG others(8): Show |
A | 3 | a0003c0004t0013g0009a0003c0004t0013g0226a0003c0007t0015g0217 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637-126_1637-112d others(17): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761608 | |||||
| chr12:92761621
|
AAGAAGAA others(6): Show |
A | 1 | a0002c0003t0014g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1637-129_1637-117d others(15): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761621 | |||||
| chr12:92761622
|
A | AGAAGAAA others(13): Show |
1 | a0002c0002t0005g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1637-129_1637-110d others(22): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761622 | |||||
| chr12:92761623
|
G | GAAGA | 6 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0007g0089others(3): Show | 6 | HG00673.hp2 HG02040.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637-69_1637-66dup others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
G | GAAGAAAG others(5): Show |
1 | a0002c0003t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1637-77_1637-66dup others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
GAAGA | G | 34 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0074others(31): Show | 35 | HG00738.hp2 HG01070.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1637-69_1637-66del others(4): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
GAAGAAAG others(1): Show |
G | 54 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0032others(51): Show | 55 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1637-73_1637-66del others(8): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
GAAGAAAG others(5): Show |
G | 33 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0059others(30): Show | 35 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1637-77_1637-66del others(12): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
GAAGAAAG others(9): Show |
G | 26 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0081others(23): Show | 28 | HG00609.hp2 HG00673.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1637-81_1637-66del others(16): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
GAAGAAAG others(13): Show |
G | 11 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0076others(8): Show | 11 | HG00323.hp1 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637-85_1637-66del others(20): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761623
|
GAAGAAAG others(17): Show |
G | 8 | a0001c0001t0001g0004a0001c0001t0001g0057a0001c0005t0006g0044others(5): Show | 9 | HG01243.hp1 HG01261.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637-89_1637-66del others(24): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761623 | |||||
| chr12:92761626
|
GAAAGAAA others(6): Show |
G | 1 | a0001c0015t0004g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1637-123_1637-111d others(15): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761626 | |||||
| chr12:92761626
|
GAAAGAAA others(10): Show |
G | 1 | a0001c0001t0001g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1637-123_1637-107d others(19): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761626 | |||||
| chr12:92761627
|
A | AAAGAAAG others(9): Show |
4 | a0002c0002t0003g0164a0002c0002t0003g0165a0002c0002t0025g0156others(1): Show | 4 | HG03471.hp1 HG03942.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637-110_1637-109i others(18): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761627 | |||||
| chr12:92761627
|
A | G | 1 | a0002c0002t0009g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1637-125A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761627 | ||||||
| chr12:92761631
|
A | AAAGAAAG others(5): Show |
8 | a0002c0002t0003g0150a0002c0002t0003g0153a0002c0002t0003g0157others(5): Show | 8 | HG00140.hp2 HG01517.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637-110_1637-109i others(14): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761631 | |||||
| chr12:92761632
|
A | G | 1 | a0003c0004t0013g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1637-120A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761632 | ||||||
| chr12:92761635
|
A | AAAGAAAG others(1): Show |
8 | a0002c0002t0003g0160a0002c0002t0003g0166a0002c0002t0003g0167others(5): Show | 8 | HG01106.hp2 HG01257.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637-110_1637-109i others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761635 | |||||
| chr12:92761639
|
A | AAAGG | 8 | a0002c0002t0003g0155a0002c0002t0003g0159a0002c0002t0003g0161others(5): Show | 9 | HG00639.hp2 HG01192.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637-110_1637-109i others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761639 | |||||
| chr12:92761642
|
GA | G | 2 | a0003c0004t0013g0009a0003c0004t0013g0226 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1637-107delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761642 | |||||
| chr12:92761643
|
A | G | 7 | a0002c0002t0005g0144a0002c0002t0005g0147a0002c0002t0005g0162others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1637-109A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761643 | ||||||
| chr12:92761647
|
A | G | 5 | a0002c0002t0003g0151a0002c0002t0003g0158a0002c0002t0005g0173others(2): Show | 5 | HG01167.hp1 HG01934.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1637-105A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761647 | ||||||
| chr12:92761658
|
GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1637-91_1637-79del others(13): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761658 | |||||
| chr12:92761666
|
GAAAGAAA others(6): Show |
G | 2 | a0002c0002t0009g0008a0002c0002t0009g0206 | 3 | HG00140.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1637-83_1637-71del others(13): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 92761666 | |||||
| chr12:92761686
|
G | GAAAGAAA others(11): Show |
1 | a0002c0002t0005g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1637-66_1637-65ins others(18): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761686 | ||||||
| chr12:92761687
|
G | A | 1 | a0002c0002t0005g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1637-65G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761687 | ||||||
| chr12:92761689
|
A | G | 1 | a0002c0002t0005g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1637-63A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761689 | ||||||
| chr12:92761719
|
G | A | 7 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637-33G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 13/16 | chr12 | 92761719 | ||||||
| chr12:92762002
|
G | GTAAA | 10 | a0002c0002t0003g0155a0002c0009t0010g0010a0002c0009t0010g0224others(7): Show | 12 | HG01891.hp2 HG02895.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1716+193_1716+196d others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 92762002 | |||||
| chr12:92762002
|
G | GTAAATAA others(1): Show |
6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1716+189_1716+196d others(10): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 92762002 | |||||
| chr12:92762033
|
C | CA | 7 | a0002c0002t0007g0183a0004c0006t0007g0003a0004c0006t0007g0218others(4): Show | 9 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+209dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 92762033 | |||||
| chr12:92762132
|
A | G | 1 | a0003c0007t0016g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1716+301A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92762132 | ||||||
| chr12:92762264
|
T | C | 1 | a0001c0001t0006g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1716+433T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92762264 | ||||||
| chr12:92762585
|
A | G | 15 | a0001c0001t0006g0114a0001c0001t0006g0116a0001c0001t0006g0117others(12): Show | 15 | HG01109.hp1 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1716+754A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92762585 | ||||||
| chr12:92762958
|
C | T | 1 | a0002c0009t0010g0224 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1717-1083C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92762958 | ||||||
| chr12:92763208
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1717-833T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92763208 | ||||||
| chr12:92763814
|
G | C | 1 | a0002c0002t0003g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1717-227G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92763814 | ||||||
| chr12:92764031
|
T | C | 1 | a0001c0001t0006g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1717-10T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 14/16 | chr12 | 92764031 | ||||||
| chr12:92764359
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1870+165C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92764359 | ||||||
| chr12:92764483
|
T | G | 5 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1870+289T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92764483 | ||||||
| chr12:92764530
|
T | C | 1 | a0002c0002t0003g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1870+336T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92764530 | ||||||
| chr12:92764584
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1870+390T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92764584 | ||||||
| chr12:92764669
|
C | T | 5 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(2): Show | 6 | HG02922.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1870+475C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92764669 | ||||||
| chr12:92764763
|
A | T | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1870+569A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92764763 | ||||||
| chr12:92765073
|
G | T | 1 | a0002c0003t0004g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1870+879G>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92765073 | ||||||
| chr12:92765325
|
T | TA | 6 | a0002c0003t0004g0012a0002c0003t0004g0013a0002c0003t0004g0228others(3): Show | 6 | HG02055.hp1 HG02135.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870+1151dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 92765325 | |||||
| chr12:92765325
|
TA | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(115): Show | 122 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1870+1151delA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 92765325 | |||||
| chr12:92765325
|
TAA | T | 81 | a0001c0001t0006g0114a0001c0001t0006g0116a0001c0001t0006g0117others(78): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.1870+1150_1870+115 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 92765325 | |||||
| chr12:92765498
|
G | A | 1 | a0002c0002t0002g0020 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1870+1304G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92765498 | ||||||
| chr12:92765510
|
C | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(142): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1870+1316C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92765510 | ||||||
| chr12:92765629
|
C | CA | 14 | a0001c0001t0001g0090a0001c0005t0006g0131a0002c0002t0003g0152others(11): Show | 15 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1870+1451dupA | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 92765629 | |||||
| chr12:92765849
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0120 | 2 | HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1870+1655T>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92765849 | ||||||
| chr12:92765930
|
A | G | 7 | a0006c0010t0012g0137a0006c0010t0012g0138a0006c0010t0012g0139others(4): Show | 7 | HG02109.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1870+1736A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92765930 | ||||||
| chr12:92765982
|
T | C | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1870+1788T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92765982 | ||||||
| chr12:92765995
|
TG | T | 5 | a0002c0009t0010g0010a0002c0009t0010g0224a0002c0009t0010g0235others(2): Show | 6 | HG02922.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1870+1804delG | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 92765995 | |||||
| chr12:92766147
|
G | C | 3 | a0003c0004t0013g0009a0003c0004t0013g0223a0003c0004t0013g0226 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870+1953G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766147 | ||||||
| chr12:92766177
|
T | C | 3 | a0003c0004t0013g0009a0003c0004t0013g0223a0003c0004t0013g0226 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870+1983T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766177 | ||||||
| chr12:92766319
|
C | A | 6 | a0003c0004t0011g0178a0003c0004t0011g0179a0003c0004t0011g0180others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1870+2125C>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766319 | ||||||
| chr12:92766444
|
A | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(104): Show | 108 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1870+2250A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766444 | ||||||
| chr12:92766613
|
C | T | 3 | a0003c0004t0013g0009a0003c0004t0013g0223a0003c0004t0013g0226 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1871-2370C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766613 | ||||||
| chr12:92766614
|
G | A | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1871-2369G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766614 | ||||||
| chr12:92766824
|
T | A | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1871-2159T>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766824 | ||||||
| chr12:92766927
|
C | T | 9 | a0002c0002t0006g0015a0002c0002t0006g0188a0006c0010t0012g0137others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1871-2056C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92766927 | ||||||
| chr12:92767088
|
A | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(216): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1871-1895A>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767088 | ||||||
| chr12:92767232
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1871-1751A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767232 | ||||||
| chr12:92767332
|
C | T | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1871-1651C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767332 | ||||||
| chr12:92767380
|
T | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(157): Show | 168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1871-1603T>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767380 | ||||||
| chr12:92767497
|
CTT | C | 52 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1871-1474_1871-147 others(6): Show |
PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 92767497 | |||||
| chr12:92767515
|
A | G | 3 | a0003c0004t0013g0009a0003c0004t0013g0223a0003c0004t0013g0226 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1871-1468A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767515 | ||||||
| chr12:92767663
|
G | A | 4 | a0002c0003t0004g0012a0002c0003t0004g0013a0002c0003t0022g0011others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1871-1320G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767663 | ||||||
| chr12:92767782
|
A | T | 3 | a0002c0002t0005g0230a0002c0002t0005g0231a0002c0002t0005g0232 | 3 | HG02818.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1871-1201A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767782 | ||||||
| chr12:92767933
|
C | T | 44 | a0001c0001t0006g0116a0001c0001t0006g0117a0002c0002t0003g0150others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1871-1050C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767933 | ||||||
| chr12:92767934
|
G | A | 1 | a0002c0003t0004g0127 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1871-1049G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92767934 | ||||||
| chr12:92768003
|
G | C | 1 | a0001c0001t0006g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1871-980G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768003 | ||||||
| chr12:92768034
|
C | T | 1 | a0002c0002t0002g0020 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1871-949C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768034 | ||||||
| chr12:92768069
|
G | A | 12 | a0002c0002t0002g0020a0002c0002t0006g0015a0002c0002t0006g0188others(9): Show | 12 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1871-914G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768069 | ||||||
| chr12:92768080
|
C | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(143): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1871-903C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768080 | ||||||
| chr12:92768103
|
G | A | 8 | a0001c0015t0004g0122a0002c0003t0004g0006a0002c0003t0004g0124others(5): Show | 9 | HG00738.hp2 HG03688.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.1871-880G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768103 | ||||||
| chr12:92768138
|
G | A | 38 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1871-845G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768138 | ||||||
| chr12:92768164
|
G | A | 1 | a0001c0005t0002g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1871-819G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768164 | ||||||
| chr12:92768202
|
G | A | 1 | a0003c0004t0021g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1871-781G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768202 | ||||||
| chr12:92768473
|
C | G | 1 | a0012c0026t0017g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1871-510C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768473 | ||||||
| chr12:92768671
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1871-312G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768671 | ||||||
| chr12:92768692
|
C | T | 2 | a0001c0001t0001g0103a0003c0004t0013g0223 | 2 | HG00673.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1871-291C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768692 | ||||||
| chr12:92768801
|
G | A | 1 | a0002c0003t0004g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1871-182G>A | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768801 | ||||||
| chr12:92768832
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1871-151A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 15/16 | chr12 | 92768832 | ||||||
| chr12:92769441
|
C | T | 1 | a0003c0013t0024g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1968+361C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769441 | ||||||
| chr12:92769446
|
A | G | 15 | a0001c0015t0004g0122a0002c0003t0004g0006a0002c0003t0004g0012others(12): Show | 16 | HG00738.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1968+366A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769446 | ||||||
| chr12:92769486
|
G | C | 7 | a0002c0002t0007g0183a0004c0006t0007g0003a0004c0006t0007g0218others(4): Show | 9 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+406G>C | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769486 | ||||||
| chr12:92769683
|
A | G | 42 | a0002c0002t0003g0150a0002c0002t0003g0151a0002c0002t0003g0152others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1969-405A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769683 | ||||||
| chr12:92769786
|
A | T | 1 | a0003c0007t0005g0210 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1969-302A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769786 | ||||||
| chr12:92769899
|
C | T | 1 | a0002c0002t0003g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1969-189C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769899 | ||||||
| chr12:92769999
|
AT | A | 22 | a0001c0001t0007g0055a0001c0001t0007g0089a0002c0002t0007g0183others(19): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1969-88delT | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 16/16 | chr12 | 92769999 |