Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0002 | 1/1 | 691 | 96 | 38 | 18 | 17 | 9 | 12 | 10 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0003 | 0/0 | 691 | 25 | 22 | 2 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0004 | 0/0 | 691 | 8 | 0 | 8 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0005 | 0/0 | 691 | 6 | 0 | 1 | 0 | 1 | 4 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0006 | 0/0 | 691 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0007 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(412): Show |
chr12 | 92697989 | 92777455 |
| a0008 | 0/0 | 691 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0009 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0010 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0011 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0012 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0013 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0014 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(700): Show |
chr12 | 92697989 | 92777455 |
| a0015 | 0/0 | 691 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(686): Show |
chr12 | 92697989 | 92777455 |
| a0016 | 0/0 | 288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | MEKTE others(283): Show |
chr12 | 92697989 | 92777455 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2073 | 89 | 18 | 20 | 32 | 5 | 14 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0001c0005 | 0/0 | 2073 | 8 | 2 | 3 | 0 | 0 | 3 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0001c0015 | 0/0 | 2073 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0001c0018 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0002 | 0/1 | 2073 | 50 | 20 | 9 | 10 | 4 | 6 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0003 | 1/0 | 2073 | 34 | 7 | 9 | 6 | 5 | 6 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0009 | 0/0 | 2073 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0011 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0016 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0022 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0024 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0002c0025 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0003c0004 | 0/0 | 2073 | 15 | 14 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0003c0007 | 0/0 | 2073 | 7 | 5 | 1 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0003c0013 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0003c0021 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0004c0006 | 0/0 | 2073 | 8 | 0 | 8 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0005c0008 | 0/0 | 2073 | 6 | 0 | 1 | 0 | 1 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0006c0010 | 0/0 | 2073 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0007c0014 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0008c0012 | 0/0 | 2073 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0009c0027 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0010c0028 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0011c0020 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0012c0017 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0013c0029 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0014c0019 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2110): Show |
chr12 | 92697989 | 92777455 | ||
| a0015c0026 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
chr12 | 92697989 | 92777455 | ||
| a0016c0023 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ATGGA others(2068): Show |
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 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0001c0001t0002 | 0/0 | 4649 | 12 | 0 | 5 | 4 | 1 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0001c0001t0006 | 0/0 | 4645 | 4 | 2 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0001c0001t0007 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0001c0001t0018 | 0/0 | 4657 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4652): Show |
chr12 | 92697989 | 92777455 |
| a0001c0001t0019 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0001c0005t0001 | 0/0 | 4647 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0001c0005t0002 | 0/0 | 4649 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0001c0005t0006 | 0/0 | 4645 | 4 | 1 | 3 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0001c0005t0020 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0001c0015t0004 | 0/0 | 4641 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0001c0018t0001 | 0/0 | 4647 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0002 | 0/0 | 4649 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0003 | 0/1 | 4644 | 19 | 2 | 5 | 4 | 3 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4639): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0005 | 0/0 | 4642 | 14 | 13 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4637): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0006 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0007 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0009 | 0/0 | 4645 | 11 | 1 | 3 | 6 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0025 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4641): Show |
chr12 | 92697989 | 92777455 |
| a0002c0002t0027 | 0/0 | 4642 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4637): Show |
chr12 | 92697989 | 92777455 |
| a0002c0003t0001 | 0/0 | 4647 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0002c0003t0002 | 0/0 | 4649 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0002c0003t0004 | 1/0 | 4641 | 15 | 4 | 3 | 5 | 2 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0002c0003t0008 | 0/0 | 4647 | 13 | 1 | 4 | 1 | 2 | 5 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0002c0003t0014 | 0/0 | 4651 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4646): Show |
chr12 | 92697989 | 92777455 |
| a0002c0003t0022 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0002c0009t0010 | 0/0 | 4641 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0002c0011t0005 | 0/0 | 4642 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4637): Show |
chr12 | 92697989 | 92777455 |
| a0002c0016t0004 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0002c0022t0004 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0002c0024t0014 | 0/0 | 4651 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4646): Show |
chr12 | 92697989 | 92777455 |
| a0002c0025t0004 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0002 | 0/0 | 4649 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0005 | 0/0 | 4642 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4637): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0011 | 0/0 | 4640 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4635): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0013 | 0/0 | 4641 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0021 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0003c0004t0023 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0003c0007t0002 | 0/0 | 4649 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0003c0007t0005 | 0/0 | 4642 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4637): Show |
chr12 | 92697989 | 92777455 |
| a0003c0007t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0003c0007t0015 | 0/0 | 4647 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0003c0007t0016 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0003c0013t0004 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4636): Show |
chr12 | 92697989 | 92777455 |
| a0003c0013t0024 | 0/0 | 4640 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4635): Show |
chr12 | 92697989 | 92777455 |
| a0003c0021t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0004c0006t0007 | 0/0 | 4645 | 8 | 0 | 8 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0005c0008t0002 | 0/0 | 4649 | 6 | 0 | 1 | 0 | 1 | 4 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4644): Show |
chr12 | 92697989 | 92777455 |
| a0006c0010t0012 | 0/0 | 4645 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0007c0014t0006 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0008c0012t0003 | 0/0 | 4644 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4639): Show |
chr12 | 92697989 | 92777455 |
| a0009c0027t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0010c0028t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0011c0020t0006 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4640): Show |
chr12 | 92697989 | 92777455 |
| a0012c0017t0001 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0013c0029t0001 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0014c0019t0003 | 0/0 | 4686 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4681): Show |
chr12 | 92697989 | 92777455 |
| a0015c0026t0017 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4642): Show |
chr12 | 92697989 | 92777455 |
| a0016c0023t0026 | 0/0 | 4640 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | ACTCA others(4635): Show |
chr12 | 92697989 | 92777455 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0086 | 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 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0001t0019g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0006g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0005t0020g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0015t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0015t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0001c0018t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0007g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0025g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0002t0027g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0014g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0003t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0009t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0011t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0011t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0016t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0022t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0024t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0002c0025t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0013g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0013g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0021g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0004t0023g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0015g0193 | 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 |
| a0003c0007t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0007t0016g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0013t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0013t0024g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0003c0021t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0004c0006t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0005c0008t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0006c0010t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0007c0014t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0007c0014t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0008c0012t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0009c0027t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0010c0028t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0011c0020t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0012c0017t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0013c0029t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0014c0019t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0015c0026t0017g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| a0016c0023t0026g0219 | 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 | g0100 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0144 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00140 | hp1 | a0002 | c0002 | t0009 | g0018 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0161 | EUR | GBR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0162 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00639 | hp1 | a0004 | c0006 | t0007 | g0004 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00639 | hp2 | a0002 | c0002 | t0005 | g0168 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00642 | hp1 | a0004 | c0006 | t0007 | g0208 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0199 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00738 | hp1 | a0004 | c0006 | t0007 | g0019 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00738 | hp2 | a0002 | c0003 | t0004 | g0195 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0175 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01069 | hp1 | a0004 | c0006 | t0007 | g0004 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01081 | hp1 | a0004 | c0006 | t0007 | g0004 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01099 | hp2 | a0002 | c0003 | t0008 | g0184 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0160 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0114 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01167 | hp1 | a0003 | c0007 | t0005 | g0198 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01167 | hp2 | a0002 | c0002 | t0009 | g0018 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01168 | hp1 | a0001 | c0005 | t0006 | g0125 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01168 | hp2 | a0004 | c0006 | t0007 | g0207 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01169 | hp1 | a0002 | c0002 | t0009 | g0194 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01169 | hp2 | a0004 | c0006 | t0007 | g0206 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0151 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01192 | hp2 | a0002 | c0002 | t0009 | g0176 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01243 | hp1 | a0003 | c0004 | t0011 | g0016 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0105 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01255 | hp2 | a0002 | c0003 | t0008 | g0002 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0163 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01257 | hp2 | a0001 | c0005 | t0006 | g0052 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01261 | hp1 | a0002 | c0003 | t0004 | g0201 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01346 | hp1 | a0005 | c0008 | t0002 | g0005 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01346 | hp2 | a0002 | c0003 | t0008 | g0002 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01361 | hp1 | a0002 | c0003 | t0004 | g0196 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01516 | hp2 | a0002 | c0003 | t0008 | g0186 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0145 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01517 | hp2 | a0002 | c0003 | t0008 | g0002 | EUR | IBS | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0139 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0158 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01891 | hp2 | a0003 | c0004 | t0021 | g0140 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01928 | hp1 | a0004 | c0006 | t0007 | g0019 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0143 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01975 | hp1 | a0001 | c0005 | t0006 | g0049 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0213 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0150 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02055 | hp1 | a0002 | c0003 | t0004 | g0024 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02055 | hp2 | a0003 | c0007 | t0016 | g0197 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02071 | hp1 | a0002 | c0002 | t0009 | g0192 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02071 | hp2 | a0001 | c0001 | t0018 | g0097 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0149 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02129 | hp2 | a0002 | c0002 | t0009 | g0017 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02135 | hp1 | a0002 | c0003 | t0008 | g0183 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02145 | hp1 | a0010 | c0028 | t0006 | g0053 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02165 | hp2 | a0002 | c0002 | t0009 | g0191 | EAS | CDX | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02257 | hp1 | a0003 | c0021 | t0007 | g0030 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02257 | hp2 | a0003 | c0013 | t0004 | g0138 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02258 | hp1 | a0002 | c0003 | t0014 | g0135 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02280 | hp2 | a0002 | c0002 | t0009 | g0203 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02300 | hp1 | a0002 | c0003 | t0008 | g0185 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02572 | hp1 | a0002 | c0003 | t0022 | g0022 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02572 | hp2 | a0003 | c0007 | t0016 | g0169 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02602 | hp2 | a0005 | c0008 | t0002 | g0037 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02615 | hp2 | a0002 | c0003 | t0008 | g0189 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02622 | hp1 | a0006 | c0010 | t0012 | g0014 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02630 | hp1 | a0003 | c0004 | t0002 | g0137 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02630 | hp2 | a0002 | c0002 | t0005 | g0179 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02647 | hp1 | a0007 | c0014 | t0006 | g0054 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02647 | hp2 | a0011 | c0020 | t0006 | g0025 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02698 | hp2 | a0001 | c0005 | t0002 | g0056 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02717 | hp2 | a0003 | c0004 | t0011 | g0172 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02723 | hp1 | a0002 | c0016 | t0004 | g0028 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02723 | hp2 | a0002 | c0024 | t0014 | g0220 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0174 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02809 | hp1 | a0006 | c0010 | t0012 | g0014 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02809 | hp2 | a0002 | c0003 | t0004 | g0214 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02818 | hp1 | a0002 | c0002 | t0005 | g0216 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02818 | hp2 | a0002 | c0002 | t0005 | g0167 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02886 | hp1 | a0002 | c0002 | t0005 | g0166 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02886 | hp2 | a0007 | c0014 | t0006 | g0055 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02895 | hp1 | a0003 | c0004 | t0013 | g0212 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02896 | hp1 | a0003 | c0004 | t0013 | g0020 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02896 | hp2 | a0002 | c0002 | t0005 | g0218 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02897 | hp2 | a0003 | c0004 | t0013 | g0020 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02922 | hp1 | a0002 | c0011 | t0005 | g0029 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02922 | hp2 | a0002 | c0009 | t0010 | g0222 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02965 | hp1 | a0002 | c0025 | t0004 | g0130 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02965 | hp2 | a0002 | c0002 | t0005 | g0154 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02970 | hp1 | a0006 | c0010 | t0012 | g0133 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02970 | hp2 | a0012 | c0017 | t0001 | g0190 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02976 | hp1 | a0003 | c0004 | t0005 | g0211 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02976 | hp2 | a0002 | c0009 | t0010 | g0221 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03017 | hp1 | a0003 | c0007 | t0002 | g0146 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0155 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03041 | hp1 | a0003 | c0004 | t0023 | g0128 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03041 | hp2 | a0002 | c0002 | t0005 | g0217 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03098 | hp1 | a0002 | c0002 | t0006 | g0026 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03098 | hp2 | a0003 | c0004 | t0006 | g0141 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03139 | hp1 | a0002 | c0009 | t0010 | g0021 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03139 | hp2 | a0002 | c0002 | t0005 | g0181 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03195 | hp1 | a0002 | c0009 | t0010 | g0021 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03195 | hp2 | a0003 | c0007 | t0015 | g0193 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03209 | hp1 | a0003 | c0004 | t0007 | g0129 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03209 | hp2 | a0003 | c0004 | t0013 | g0209 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03225 | hp1 | a0013 | c0029 | t0001 | g0032 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03239 | hp1 | a0002 | c0002 | t0007 | g0173 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03453 | hp1 | a0002 | c0002 | t0006 | g0178 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03486 | hp1 | a0002 | c0003 | t0004 | g0023 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03486 | hp2 | a0001 | c0005 | t0020 | g0045 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03490 | hp1 | a0005 | c0008 | t0002 | g0006 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03490 | hp2 | a0014 | c0019 | t0003 | g0164 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03491 | hp2 | a0002 | c0003 | t0008 | g0003 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03492 | hp1 | a0005 | c0008 | t0002 | g0006 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03492 | hp2 | a0002 | c0003 | t0008 | g0003 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03516 | hp1 | a0003 | c0013 | t0024 | g0134 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03516 | hp2 | a0003 | c0004 | t0011 | g0170 | AFR | ESN | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03540 | hp2 | a0006 | c0010 | t0012 | g0132 | AFR | GWD | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03579 | hp1 | a0001 | c0005 | t0006 | g0057 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03579 | hp2 | a0002 | c0009 | t0010 | g0210 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0147 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03669 | hp1 | a0002 | c0002 | t0003 | g0152 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03688 | hp1 | a0001 | c0015 | t0004 | g0120 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03688 | hp2 | a0008 | c0012 | t0003 | g0015 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0159 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03710 | hp2 | a0005 | c0008 | t0002 | g0005 | SAS | PJL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03831 | hp1 | a0002 | c0003 | t0008 | g0187 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03834 | hp2 | a0001 | c0005 | t0001 | g0050 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03942 | hp1 | a0002 | c0002 | t0025 | g0148 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04115 | hp1 | a0002 | c0003 | t0008 | g0188 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04204 | hp1 | a0008 | c0012 | t0003 | g0015 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG04204 | hp2 | a0002 | c0003 | t0008 | g0003 | SAS | STU | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0177 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18747 | hp1 | a0002 | c0002 | t0009 | g0017 | EAS | CHB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18906 | hp1 | a0002 | c0002 | t0005 | g0136 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18906 | hp2 | a0003 | c0007 | t0007 | g0180 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18939 | hp2 | a0002 | c0003 | t0004 | g0123 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18949 | hp2 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18964 | hp2 | a0002 | c0003 | t0004 | g0012 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0156 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA18995 | hp2 | a0001 | c0018 | t0001 | g0119 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19004 | hp1 | a0002 | c0002 | t0009 | g0011 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0165 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19043 | hp2 | a0003 | c0007 | t0015 | g0205 | AFR | LWK | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19054 | hp2 | a0002 | c0003 | t0004 | g0122 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0157 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19062 | hp2 | a0002 | c0022 | t0004 | g0012 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19084 | hp1 | a0002 | c0002 | t0009 | g0011 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19240 | hp1 | a0002 | c0003 | t0004 | g0225 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA19240 | hp2 | a0001 | c0001 | t0019 | g0091 | AFR | YRI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20129 | hp1 | a0002 | c0009 | t0010 | g0223 | AFR | ASW | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20129 | hp2 | a0003 | c0004 | t0011 | g0016 | AFR | ASW | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20752 | hp1 | a0005 | c0008 | t0002 | g0036 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20752 | hp2 | a0002 | c0003 | t0004 | g0204 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20805 | hp1 | a0002 | c0003 | t0004 | g0200 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0051 | SAS | GIH | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02109 | hp1 | a0003 | c0004 | t0011 | g0171 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02109 | hp2 | a0009 | c0027 | t0006 | g0073 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02486 | hp2 | a0002 | c0002 | t0005 | g0215 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG02559 | hp2 | a0002 | c0011 | t0005 | g0027 | AFR | ACB | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03471 | hp1 | a0002 | c0002 | t0027 | g0182 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG03471 | hp2 | a0006 | c0010 | t0012 | g0131 | AFR | MSL | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG06807 | hp1 | a0015 | c0026 | t0017 | g0033 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0142 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20300 | hp1 | a0016 | c0023 | t0026 | g0219 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0153 | REF | REF | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0004 | g0202 | REF | REF | PLEKHG7_chr12_92697989_92777455 | PLEKHG7 | chr12 | 92697989 | 92777455 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92706690 | C | G | 1 | a0013 | 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 | a0010 | 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 | a0012 | 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 | a0001 a0004 a0005 others(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 | a0016 | 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 | a0015 | 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 | a0011 | 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 | a0001 a0003 a0004 others(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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92706817 | G | A | 2 | a0002c0011 a0002c0016 |
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 | a0013c0029 | 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 | a0002c0009 a0002c0024 a0002c0025 others(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 | a0001c0005 a0007c0014 a0010c0028 |
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 | a0001c0001 a0001c0005 a0001c0015 others(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 | a0001c0001 a0001c0005 a0001c0018 others(18): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92706512 | 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 | a0015c0026t0017 | 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 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0025 others(7): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): 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 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0025 others(9): Show |
48 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(45): 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 | a0003c0004t0011 a0003c0004t0023 |
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 | a0002c0002t0005 a0002c0002t0027 a0002c0011t0005 others(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 | a0001c0001t0006 a0001c0001t0007 a0001c0005t0006 others(19): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): 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 | a0001c0001t0001 a0001c0001t0019 a0001c0005t0001 others(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 | a0001c0001t0002 a0001c0005t0002 a0002c0002t0002 others(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 | a0002c0003t0014 a0002c0024t0014 |
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 | a0001c0001t0007 a0002c0002t0007 a0002c0002t0009 others(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 | a0001c0001t0007 a0002c0002t0007 a0002c0002t0009 others(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 | a0001c0001t0007 a0002c0002t0007 a0002c0002t0009 others(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 | a0001c0005t0020 a0002c0003t0022 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92703183 | C | T | 1 | a0002c0003t0004g0225 | 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0002g0031 a0003c0021t0007g0030 |
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 | a0013c0029t0001g0032 | 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 | a0001c0001t0001g0224 | 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 | a0015c0026t0017g0033 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0221 a0002c0009t0010g0222 others(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 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 |
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 | 8 | a0001c0001t0001g0034 a0001c0001t0001g0224 a0001c0001t0002g0035 others(5): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): 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 | a0003c0004t0023g0128 | 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 | a0002c0002t0005g0215 | 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 | a0002c0003t0004g0214 | 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 | 15 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(12): 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0001g0127 | 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 | a0001c0001t0002g0041 | 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 | a0002c0002t0003g0213 | 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 | 31 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(29): 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 | a0001c0001t0001g0126 | 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 | a0015c0026t0017g0033 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0001g0042 | 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 | a0003c0007t0016g0169 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0044 | 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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 23 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(20): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): 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 | a0002c0002t0003g0142 | 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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | a0013c0029t0001g0032 | 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 | a0001c0005t0006g0125 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0002c0002t0007g0173 | 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 | a0003c0004t0013g0209 | 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 | a0002c0002t0005g0165 a0002c0002t0005g0166 a0002c0002t0005g0167 others(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 | a0002c0002t0003g0163 a0014c0019t0003g0164 |
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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0007g0173 a0002c0003t0001g0175 a0002c0003t0002g0174 |
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 | a0001c0001t0001g0034 | 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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): 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 | a0001c0005t0020g0045 | 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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | a0013c0029t0001g0032 | 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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0003t0004g0214 | 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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | a0001c0001t0001g0127 | 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 | a0002c0002t0005g0168 | 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 | a0001c0001t0002g0041 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): 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 | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): 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 | a0001c0001t0001g0121 | 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 | a0001c0015t0004g0120 | 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 | a0013c0029t0001g0032 | 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 | a0013c0029t0001g0032 | 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 | a0013c0029t0001g0032 | 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 | a0002c0003t0001g0162 | 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 | a0001c0018t0001g0119 | 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 | 23 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(20): 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 | a0013c0029t0001g0032 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0005g0177 a0002c0002t0005g0179 a0002c0002t0005g0181 others(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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | a0001c0001t0001g0121 | 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0001g0118 | 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 | a0002c0003t0008g0183 | 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 | 14 | a0002c0003t0008g0002 a0002c0003t0008g0003 a0002c0003t0008g0183 others(11): 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 | a0013c0029t0001g0032 | 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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): 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 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0059 | 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 | 1 | a0005c0008t0002g0006 | 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 | 23 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(20): 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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0001c0001t0002g0038 | 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 | a0013c0029t0001g0032 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0121 | 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 | 14 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(11): 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 | a0013c0029t0001g0032 | 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 | a0001c0001t0007g0060 | 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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): 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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 23 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(20): 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 | a0002c0003t0004g0225 | 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | a0002c0002t0027g0182 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0006g0112 | 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0013c0029t0001g0032 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 70 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0069 others(67): Show |
75 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(72): 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 | a0001c0001t0001g0008 a0001c0001t0001g0046 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0127 a0001c0001t0002g0061 others(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 | a0013c0029t0001g0032 | 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 | a0002c0011t0005g0027 a0002c0011t0005g0029 |
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 | 22 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(19): 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 | a0002c0009t0010g0021 a0002c0009t0010g0221 a0002c0009t0010g0222 others(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 | a0002c0002t0006g0026 | 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 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 |
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 | a0002c0025t0004g0130 | 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 | a0008c0012t0003g0015 | 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 | 23 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(20): 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 | 47 | a0002c0002t0003g0142 a0002c0002t0003g0144 a0002c0002t0003g0145 others(44): Show |
55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): 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 | a0002c0002t0003g0143 a0002c0002t0005g0136 a0002c0002t0005g0139 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | 23 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0006g0026 others(20): 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 | a0002c0002t0002g0031 a0002c0002t0005g0177 a0003c0021t0007g0030 |
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 | a0001c0001t0001g0109 a0001c0001t0006g0105 |
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 | 12 | a0002c0002t0006g0026 a0002c0003t0004g0024 a0002c0003t0022g0022 others(9): 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0004g0023 others(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 | a0002c0002t0002g0031 a0002c0002t0005g0177 a0003c0021t0007g0030 |
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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): 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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): 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 | a0013c0029t0001g0032 | 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): 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 | a0001c0001t0001g0085 a0001c0001t0001g0118 |
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 | a0002c0003t0008g0002 a0002c0003t0008g0185 a0002c0003t0008g0186 |
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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): 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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): 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 | a0003c0007t0005g0198 a0003c0007t0015g0193 a0003c0007t0015g0205 others(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 | a0002c0002t0003g0155 a0002c0002t0005g0136 a0002c0002t0005g0139 others(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 | a0003c0007t0005g0198 a0003c0007t0016g0169 a0012c0017t0001g0190 |
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 | a0002c0002t0005g0167 | 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0001c0001t0001g0104 a0013c0029t0001g0032 |
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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | |||||||
| chr12:92718610 | G | A | 8 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0003t0004g0204 | 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 | a0001c0001t0001g0084 | 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 14 | a0002c0003t0008g0002 a0002c0003t0008g0003 a0002c0003t0008g0183 others(11): 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 | a0003c0007t0005g0198 | 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 | a0015c0026t0017g0033 | 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): 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 | a0002c0003t0004g0214 | 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | a0002c0002t0005g0215 | 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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0003c0004t0007g0129 | 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | a0002c0002t0009g0192 | 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 | a0011c0020t0006g0025 | 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 | a0002c0002t0003g0213 | 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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): 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 | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | a0002c0009t0010g0021 a0002c0009t0010g0221 a0002c0009t0010g0222 others(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 | a0001c0005t0001g0051 | 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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(40): 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 | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): 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 | a0002c0003t0004g0123 | 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 | a0001c0001t0001g0096 | 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): 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 | a0002c0002t0003g0143 a0002c0002t0006g0026 a0002c0003t0004g0023 others(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 | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | a0002c0003t0004g0225 | 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 | a0003c0004t0021g0140 | 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 | a0010c0028t0006g0053 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | a0015c0026t0017g0033 | 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 | a0001c0005t0001g0050 | 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.531-7709C>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 3/16 | chr12 | 92721284 | |||||||
| chr12:92721344 | G | C | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | a0003c0007t0005g0198 a0003c0007t0015g0193 a0003c0007t0015g0205 others(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 | a0002c0002t0005g0181 a0002c0002t0006g0178 |
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 | a0013c0029t0001g0032 | 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | a0003c0007t0005g0198 | 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 | 14 | a0002c0002t0003g0143 a0002c0003t0004g0214 a0002c0003t0008g0002 others(11): 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 | a0002c0002t0002g0031 a0002c0003t0008g0187 a0003c0004t0011g0170 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0126 others(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 | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): 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 | 5 | a0002c0025t0004g0130 a0003c0004t0007g0129 a0006c0010t0012g0014 others(2): 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0006g0114 | 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 | a0002c0002t0005g0177 a0002c0002t0005g0179 a0002c0002t0005g0181 others(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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0003c0004t0021g0140 | 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 | a0003c0007t0016g0169 | 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 | a0015c0026t0017g0033 | 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 | a0003c0007t0016g0169 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0108 | 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 | a0003c0004t0021g0140 | 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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): 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 | a0002c0003t0008g0002 a0002c0003t0008g0003 a0002c0003t0008g0183 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0003g0152 | 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 | a0003c0004t0021g0140 | 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 | a0015c0026t0017g0033 | 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 | a0003c0004t0021g0140 | 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 | a0002c0002t0002g0031 a0002c0003t0004g0214 a0003c0021t0007g0030 |
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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 |
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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): 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 | a0003c0004t0021g0140 | 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 | 7 | a0003c0004t0002g0137 a0003c0004t0006g0141 a0003c0013t0004g0138 others(4): 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 | a0002c0002t0003g0156 | 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 | a0001c0001t0001g0043 | 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 | a0013c0029t0001g0032 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0006g0114 | 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 | a0002c0002t0005g0181 a0002c0002t0006g0178 |
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 | a0001c0001t0001g0088 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0001g0108 | 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 | a0002c0002t0009g0191 | 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 | a0001c0001t0002g0063 | 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | a0003c0004t0021g0140 | 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 | a0003c0004t0021g0140 | 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 | a0001c0005t0006g0057 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): 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 | a0003c0004t0021g0140 | 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 | a0003c0004t0021g0140 | 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 | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): 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 | a0003c0004t0021g0140 | 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0003t0004g0012 a0002c0003t0004g0013 a0002c0003t0004g0122 others(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 | a0003c0004t0021g0140 | 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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): 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 | a0003c0004t0021g0140 | 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 | a0002c0003t0004g0214 | 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 | a0002c0016t0004g0028 | 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 | a0003c0004t0021g0140 | 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 | a0003c0004t0021g0140 | 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 | a0002c0016t0004g0028 | 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): 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 | a0002c0002t0009g0203 | 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 | a0001c0001t0002g0035 | 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 | a0003c0004t0021g0140 | 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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0022g0022 |
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 | a0003c0004t0005g0211 | 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 | 28 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(25): Show |
30 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(27): 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0002c0002t0003g0161 | 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): 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 | a0001c0001t0001g0064 | 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): 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 | a0002c0002t0003g0143 a0002c0002t0003g0151 a0002c0002t0003g0158 others(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 | a0001c0001t0001g0109 a0001c0001t0006g0105 a0001c0005t0001g0051 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0002c0009t0010g0021 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0005t0006g0125 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0078 | 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 | 34 | a0002c0002t0002g0031 a0002c0002t0003g0142 a0002c0002t0003g0143 others(31): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(33): 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 | 15 | a0002c0002t0003g0152 a0002c0002t0005g0216 a0002c0002t0005g0217 others(12): 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 | a0001c0001t0001g0044 a0002c0002t0003g0149 a0002c0002t0003g0150 others(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 | 71 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0002c0002t0003g0142 others(68): 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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0002c0002t0005g0167 others(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 | 3 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0098 others(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 | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): 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 | a0001c0001t0001g0034 a0001c0001t0001g0043 a0001c0001t0001g0066 others(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 | a0001c0001t0002g0038 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0103 others(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 |
1 | a0005c0008t0002g0006 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0003t0004g0196 a0002c0009t0010g0021 a0002c0009t0010g0221 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0003c0004t0007g0129 a0003c0013t0024g0134 |
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 | a0002c0002t0003g0157 | 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 |
8 | a0002c0003t0004g0196 a0002c0003t0004g0200 a0002c0003t0004g0204 others(5): 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 |
21 | a0002c0002t0002g0031 a0002c0002t0003g0155 a0002c0002t0003g0156 others(18): Show |
22 | HG00280.hp1 HG00738.hp2 HG01106.hp2 others(19): 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 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(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 | a0002c0002t0003g0147 a0002c0002t0003g0163 a0002c0002t0025g0148 others(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 | a0002c0002t0005g0218 | 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 | 7 | a0002c0002t0009g0011 a0002c0002t0009g0017 a0002c0002t0009g0176 others(4): 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 | a0002c0003t0004g0012 a0002c0003t0004g0013 a0002c0003t0004g0122 others(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 | a0002c0003t0004g0225 a0003c0004t0021g0140 |
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 | a0002c0002t0003g0158 | 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 | a0002c0003t0008g0188 | 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 | a0002c0002t0027g0182 | 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 | a0002c0009t0010g0210 a0003c0004t0013g0020 a0003c0004t0013g0209 |
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 | a0002c0009t0010g0021 a0002c0009t0010g0223 a0002c0024t0014g0220 |
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 | a0002c0009t0010g0221 a0002c0009t0010g0222 |
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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 |
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 | a0003c0004t0005g0211 a0003c0004t0013g0212 |
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 | a0002c0025t0004g0130 a0003c0004t0002g0137 a0003c0004t0006g0141 others(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 | a0001c0001t0001g0109 a0001c0001t0006g0105 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0077 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): 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 | 5 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0224 others(2): 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 | a0001c0001t0001g0042 a0001c0001t0001g0065 a0001c0001t0001g0075 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): 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 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 |
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 | a0001c0001t0001g0096 | 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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): 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 | a0002c0002t0005g0139 | 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 | 82 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): 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 | a0007c0014t0006g0054 | 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 | a0001c0001t0001g0101 | 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 | a0002c0002t0005g0139 | 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 | 36 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0044 others(33): 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 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0110 others(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 | 59 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(56): 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 | a0001c0005t0001g0050 a0001c0005t0006g0049 a0001c0005t0006g0052 others(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 | a0001c0005t0002g0056 a0015c0026t0017g0033 |
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 | a0013c0029t0001g0032 | 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 | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0042 others(37): 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 | a0001c0005t0020g0045 | 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): 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 | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): 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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): 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 | a0001c0001t0007g0060 a0002c0002t0006g0026 |
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 | a0002c0003t0022g0022 | 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 | a0002c0003t0004g0201 a0006c0010t0012g0131 |
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 | a0002c0003t0004g0024 a0011c0020t0006g0025 |
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 | a0002c0003t0004g0023 | 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 | a0002c0002t0005g0216 a0002c0002t0005g0217 |
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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0003c0013t0024g0134 | 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 | a0003c0007t0005g0198 a0003c0007t0015g0193 a0003c0007t0015g0205 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0016c0023t0026g0219 | 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 | a0016c0023t0026g0219 | 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 | a0016c0023t0026g0219 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0016c0023t0026g0219 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0016c0023t0026g0219 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0016c0023t0026g0219 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0221 a0002c0009t0010g0222 others(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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0002g0076 | 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 | a0006c0010t0012g0131 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0005g0154 a0002c0002t0005g0165 a0002c0002t0005g0166 others(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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0001c0001t0007g0094 a0009c0027t0006g0073 |
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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 18 | a0002c0003t0008g0002 a0002c0003t0008g0003 a0002c0003t0008g0183 others(15): 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 | a0015c0026t0017g0033 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0002c0002t0003g0158 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0003c0004t0011g0172 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0221 a0002c0009t0010g0222 others(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 | a0015c0026t0017g0033 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(128): 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0126 | 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 | a0002c0009t0010g0210 a0003c0004t0005g0211 a0003c0004t0013g0020 others(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 | 4 | a0005c0008t0002g0005 a0005c0008t0002g0006 a0005c0008t0002g0036 others(1): 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 | a0002c0025t0004g0130 a0003c0004t0007g0129 a0013c0029t0001g0032 |
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 | a0002c0002t0003g0155 | 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 | a0015c0026t0017g0033 | 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 | a0002c0025t0004g0130 | 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 others(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 | a0001c0001t0001g0124 | 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 | a0003c0004t0021g0140 | 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 | a0003c0007t0005g0198 a0003c0007t0015g0193 a0003c0007t0015g0205 others(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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | 28 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(25): Show |
30 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(27): 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 | a0001c0001t0001g0224 | 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 | a0015c0026t0017g0033 | 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 | a0003c0013t0024g0134 | 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 | a0002c0002t0005g0167 | 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 | a0003c0004t0005g0211 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | 39 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(36): Show |
41 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(38): 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 | a0002c0002t0003g0143 a0002c0002t0003g0151 a0002c0002t0003g0158 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0103 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0002c0003t0004g0012 a0002c0003t0004g0013 a0002c0003t0004g0122 others(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 | a0002c0002t0003g0161 | 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 | a0002c0002t0005g0179 | 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0011t0005g0027 a0002c0011t0005g0029 a0002c0016t0004g0028 |
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 | a0002c0003t0004g0214 | 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 | a0002c0002t0005g0177 a0002c0002t0005g0179 a0002c0002t0005g0181 others(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 | a0016c0023t0026g0219 | 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 | a0001c0001t0002g0063 | 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 | a0003c0007t0005g0198 a0003c0007t0015g0193 a0003c0007t0015g0205 others(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 | a0001c0001t0001g0084 | 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 | a0001c0005t0001g0051 | 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 | a0001c0018t0001g0119 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0002c0002t0003g0157 a0015c0026t0017g0033 |
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 | a0003c0004t0021g0140 | 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 | a0003c0004t0007g0129 | 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 | a0003c0004t0002g0137 a0003c0004t0006g0141 a0003c0013t0004g0138 |
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 | a0002c0003t0004g0196 a0002c0003t0004g0201 a0002c0003t0004g0204 |
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 | 23 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(20): 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 |
94 | a0002c0002t0002g0031 a0002c0002t0003g0142 a0002c0002t0003g0143 others(91): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): 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 | a0015c0026t0017g0033 | 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 | 23 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(20): 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 | a0015c0026t0017g0033 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0071 others(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 |
68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): 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 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0111 a0001c0015t0004g0100 a0004c0006t0007g0206 others(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 | a0002c0002t0025g0148 | 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 | a0001c0001t0002g0072 | 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 | 22 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(19): 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 | a0003c0004t0021g0140 | 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 | a0016c0023t0026g0219 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0003t0004g0200 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0003c0004t0011g0172 | 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 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 |
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 | a0001c0005t0006g0052 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0098 |
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 | a0002c0003t0008g0002 a0002c0003t0008g0003 a0002c0003t0008g0183 others(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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0003c0004t0005g0211 a0003c0004t0013g0020 a0003c0004t0013g0209 others(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 | a0001c0001t0001g0075 | 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 | a0002c0002t0002g0031 a0002c0003t0004g0214 a0003c0021t0007g0030 |
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 | a0003c0004t0002g0137 a0003c0004t0006g0141 a0003c0013t0004g0138 others(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 | a0003c0004t0013g0020 a0003c0004t0013g0212 |
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 | a0003c0013t0024g0134 | 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0022g0022 |
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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0003c0007t0005g0198 | 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 | a0003c0004t0002g0137 a0003c0004t0006g0141 a0003c0013t0004g0138 |
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 | a0001c0001t0001g0095 a0001c0001t0001g0126 |
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 | a0015c0026t0017g0033 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 4 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(1): 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 | 7 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(4): 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 | a0001c0005t0020g0045 | 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 | a0001c0001t0001g0101 | 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 | a0002c0002t0025g0148 | 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 | 7 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(4): 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 | a0011c0020t0006g0025 a0015c0026t0017g0033 |
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 | a0016c0023t0026g0219 | 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 | a0014c0019t0003g0164 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | 209 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(206): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(178): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): 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 | 15 | a0001c0001t0001g0080 a0001c0005t0001g0050 a0001c0005t0001g0051 others(12): 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 | 7 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): 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 | a0003c0004t0007g0129 | 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 | a0001c0001t0001g0090 | 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 | 16 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(13): 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 | a0002c0003t0008g0189 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | 39 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(36): Show |
41 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1137+1692A>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743284 | |||||||
| chr12:92743288 | C | T | 39 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(36): Show |
41 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1137+1696C>T | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 9/16 | chr12 | 92743288 | |||||||
| chr12:92743549 | A | AT | 17 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(14): 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0011c0020t0006g0025 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): 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 | 16 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(13): 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 | a0001c0001t0001g0043 | 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 | a0014c0019t0003g0164 | 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 | a0002c0002t0006g0178 | 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 | a0011c0020t0006g0025 | 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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): 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 | a0008c0012t0003g0015 | 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 | a0002c0002t0003g0156 a0002c0002t0003g0161 |
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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0003t0014g0135 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0110 |
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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0003c0007t0016g0197 | 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 | a0002c0003t0004g0195 a0002c0003t0004g0200 a0002c0011t0005g0027 others(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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0011c0020t0006g0025 | 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 | a0001c0001t0001g0124 | 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 | 15 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(12): 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 | 5 | a0004c0006t0007g0004 a0004c0006t0007g0019 a0004c0006t0007g0206 others(2): 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0066 others(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 | 16 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(13): 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0007g0060 | 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 | a0001c0001t0001g0095 | 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 | a0003c0004t0005g0211 a0003c0004t0013g0020 a0003c0004t0013g0209 others(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 | a0002c0002t0003g0155 | 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0011c0020t0006g0025 | 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 | 16 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(13): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0011c0020t0006g0025 | 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 | a0003c0004t0021g0140 | 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 | 27 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(24): Show |
29 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1251+1442A>G | PLEKHG7 | ENSG00000187510.11 | transcript | ENST00000344636.6 | protein_coding | 10/16 | chr12 | 92747033 | |||||||
| chr12:92747126 | A | T | 4 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(1): 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(208): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): 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 | 45 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): 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 | a0001c0001t0001g0121 | 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0001c0001t0001g0111 | 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 | a0002c0011t0005g0027 a0002c0011t0005g0029 |
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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): 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 | 41 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(38): 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 | 205 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): 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 | a0005c0008t0002g0037 | 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 | a0013c0029t0001g0032 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0001c0001t0001g0092 | 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 | a0006c0010t0012g0131 | 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 | a0002c0002t0005g0167 | 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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): 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 | a0001c0015t0004g0120 | 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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): 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 | a0003c0004t0021g0140 | 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 | a0011c0020t0006g0025 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0007c0014t0006g0054 a0007c0014t0006g0055 |
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 | a0001c0001t0001g0080 | 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 | a0014c0019t0003g0164 | 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 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 |
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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | 17 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(14): 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 | 30 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(27): 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 | 17 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(14): 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 | a0016c0023t0026g0219 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0001c0001t0001g0075 | 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 | 17 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(14): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0002c0003t0004g0195 a0002c0003t0004g0200 a0002c0011t0005g0027 others(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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | 24 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(21): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0001c0001t0001g0099 | 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 | a0014c0019t0003g0164 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0013c0029t0001g0032 | 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 | a0013c0029t0001g0032 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0014c0019t0003g0164 | 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 | 67 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(64): Show |
75 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(72): 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 | a0002c0009t0010g0021 a0002c0009t0010g0223 |
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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | a0014c0019t0003g0164 | 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 | a0002c0002t0005g0177 a0002c0002t0005g0179 a0002c0002t0005g0181 others(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 | a0003c0007t0016g0197 | 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 | a0003c0007t0016g0197 | 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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | a0003c0007t0016g0197 | 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 | a0003c0007t0016g0197 | 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 | a0002c0003t0004g0195 a0014c0019t0003g0164 |
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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | 83 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(80): Show |
96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): 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 |
6 | a0001c0005t0006g0057 a0003c0004t0011g0016 a0003c0004t0011g0170 others(3): 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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | a0003c0007t0016g0197 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0003c0007t0016g0197 | 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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): 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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0003c0007t0016g0197 | 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): 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 | a0001c0001t0002g0038 | 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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0002c0002t0006g0026 a0002c0003t0004g0023 a0002c0003t0004g0024 others(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 | a0011c0020t0006g0025 | 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 | a0003c0004t0005g0211 a0003c0004t0013g0020 a0003c0004t0013g0209 others(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 | a0003c0004t0005g0211 a0003c0004t0013g0020 a0003c0004t0013g0209 others(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 | a0006c0010t0012g0132 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0003t0004g0214 | 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 | 4 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(1): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): 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 | a0001c0001t0001g0062 a0001c0005t0001g0050 a0001c0005t0001g0051 others(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 | a0002c0025t0004g0130 a0003c0004t0002g0137 a0003c0004t0005g0211 others(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 | a0003c0004t0021g0140 | 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 | a0001c0001t0001g0069 | 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 | a0009c0027t0006g0073 | 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 | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | 4 | a0001c0001t0001g0093 a0004c0006t0007g0004 a0004c0006t0007g0019 others(1): 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 | a0002c0002t0002g0031 a0002c0002t0006g0178 a0003c0021t0007g0030 |
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 | a0003c0004t0021g0140 | 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 | a0001c0001t0001g0081 | 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 | a0003c0004t0021g0140 | 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 | 11 | a0003c0007t0005g0198 a0003c0007t0007g0180 a0003c0007t0015g0193 others(8): 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 | 34 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(31): 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 | 23 | a0002c0025t0004g0130 a0003c0004t0002g0137 a0003c0004t0005g0211 others(20): 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 | a0002c0009t0010g0221 | 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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): 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 | a0001c0015t0004g0100 | 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 | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): 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 | a0003c0004t0021g0140 | 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 | a0003c0004t0005g0211 a0003c0004t0013g0020 a0003c0004t0013g0209 others(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 | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): 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 | a0001c0001t0001g0110 | 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 | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): 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 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 |
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 | 11 | a0003c0007t0005g0198 a0003c0007t0007g0180 a0003c0007t0015g0193 others(8): 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 | a0002c0002t0007g0173 a0002c0003t0001g0175 a0002c0003t0002g0174 |
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 | a0002c0002t0003g0151 | 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 | 40 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(37): 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 | a0003c0004t0007g0129 | 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 | 41 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 others(38): 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 | a0011c0020t0006g0025 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0002c0003t0001g0199 a0002c0003t0004g0122 |
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 | 32 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(29): 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 | a0003c0013t0024g0134 | 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0003c0004t0013g0020 | 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 | a0002c0003t0004g0200 | 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 | 26 | a0001c0005t0001g0050 a0001c0005t0001g0051 a0001c0005t0002g0056 others(23): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 6 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(3): 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 | 5 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(2): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0005g0165 others(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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): 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 | 6 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(3): 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 | 122 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): 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 | 79 | a0001c0001t0007g0060 a0001c0001t0007g0094 a0002c0002t0003g0142 others(76): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): 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 | a0002c0002t0009g0176 a0002c0002t0009g0203 |
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 | 79 | a0001c0001t0007g0060 a0001c0001t0007g0094 a0002c0002t0003g0142 others(76): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): 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 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0082 others(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 | a0002c0002t0005g0177 a0002c0002t0005g0179 a0002c0002t0005g0181 others(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 | a0003c0004t0013g0020 a0003c0004t0013g0209 a0003c0004t0013g0212 |
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 | 42 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(39): Show |
43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): 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 | a0002c0003t0008g0003 a0002c0003t0008g0183 a0002c0003t0008g0187 others(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 | 7 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(4): 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 | 7 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(4): 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 | a0001c0001t0002g0041 | 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 | 41 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(38): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): 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 | a0002c0002t0009g0192 | 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 | a0002c0003t0001g0162 a0002c0003t0001g0199 a0002c0003t0002g0174 others(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 | a0012c0017t0001g0190 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0002c0011t0005g0027 a0002c0011t0005g0029 |
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 | a0003c0007t0002g0146 | 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 | a0003c0013t0024g0134 | 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 | a0002c0003t0008g0002 a0002c0003t0008g0186 |
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 | a0002c0003t0001g0162 | 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 | 11 | a0002c0002t0002g0031 a0002c0002t0006g0026 a0002c0002t0006g0178 others(8): 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 | a0004c0006t0007g0004 | 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 | 6 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(3): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0001c0015t0004g0120 a0002c0003t0004g0012 a0002c0003t0004g0013 others(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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | 6 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(3): 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | a0014c0019t0003g0164 | 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 | 6 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(3): 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 | 41 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(38): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): 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 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0042 others(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 | a0002c0003t0014g0135 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0124 | 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 | a0003c0004t0013g0020 a0003c0004t0013g0209 a0003c0004t0013g0212 |
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 | a0001c0001t0001g0124 | 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 | 45 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(42): Show |
49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): 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 | a0001c0001t0002g0035 | 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 | a0003c0004t0013g0020 a0003c0004t0013g0212 a0003c0007t0015g0205 |
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 | a0002c0003t0014g0135 | 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 | a0002c0002t0005g0216 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0007g0094 others(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 | a0002c0003t0001g0162 | 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 | 32 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0077 others(29): 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 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0005t0006g0049 others(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 | a0001c0015t0004g0100 | 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 | a0001c0001t0001g0010 | 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 | a0002c0002t0003g0156 a0002c0002t0003g0157 a0002c0002t0025g0148 others(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 | a0002c0002t0009g0203 | 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 | a0002c0002t0003g0142 a0002c0002t0003g0145 a0002c0002t0003g0150 others(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 | a0003c0004t0013g0209 | 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 | a0002c0002t0003g0152 a0002c0002t0003g0158 a0002c0002t0003g0159 others(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 | 7 | a0002c0002t0003g0147 a0002c0002t0003g0151 a0002c0002t0005g0168 others(4): Show |
8 | HG00639.hp2 HG01192.hp1 HG02486.hp2 others(5): 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 | a0003c0004t0013g0020 a0003c0004t0013g0212 |
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 | a0002c0002t0005g0136 a0002c0002t0005g0139 a0002c0002t0005g0154 others(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 | a0002c0002t0003g0143 a0002c0002t0003g0149 a0002c0002t0005g0165 others(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 | a0001c0001t0001g0111 | 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 | a0002c0002t0009g0018 a0002c0002t0009g0194 |
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 | a0002c0002t0005g0167 | 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 | a0002c0002t0005g0167 | 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 | a0002c0002t0005g0167 | 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 | 6 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(3): 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 | a0002c0002t0003g0147 a0002c0009t0010g0021 a0002c0009t0010g0210 others(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 |
5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 6 | a0002c0002t0007g0173 a0004c0006t0007g0004 a0004c0006t0007g0019 others(3): 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 | a0003c0007t0016g0169 | 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 | a0001c0001t0006g0112 | 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 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(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 | a0002c0009t0010g0210 | 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 | a0001c0001t0001g0101 | 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 | a0002c0002t0003g0152 | 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 | a0001c0001t0006g0114 | 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 | a0001c0001t0001g0075 | 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 | 4 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(1): 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 | a0002c0002t0003g0142 | 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 | a0001c0001t0001g0111 | 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0001c0001t0001g0066 | 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 | a0002c0003t0004g0024 | 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 | a0002c0003t0004g0023 a0002c0003t0004g0024 a0002c0003t0004g0214 others(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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): 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 | 77 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(74): Show |
83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): 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 | a0002c0002t0002g0031 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): 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 | a0001c0001t0001g0095 a0001c0005t0006g0125 a0002c0002t0003g0144 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0118 |
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 | 6 | a0006c0010t0012g0014 a0006c0010t0012g0131 a0006c0010t0012g0132 others(3): 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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | a0002c0009t0010g0021 a0002c0009t0010g0210 a0002c0009t0010g0221 others(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 | a0003c0004t0013g0020 a0003c0004t0013g0209 a0003c0004t0013g0212 |
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 | a0003c0004t0013g0020 a0003c0004t0013g0209 a0003c0004t0013g0212 |
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 | 5 | a0003c0004t0011g0016 a0003c0004t0011g0170 a0003c0004t0011g0171 others(2): 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): 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 | a0003c0004t0013g0020 a0003c0004t0013g0209 a0003c0004t0013g0212 |
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 | a0003c0013t0024g0134 | 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 | a0001c0001t0002g0063 | 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 | 8 | a0002c0002t0006g0026 a0002c0002t0006g0178 a0006c0010t0012g0014 others(5): 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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): 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 | a0001c0001t0001g0126 | 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 | a0003c0013t0024g0134 | 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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): 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 | 50 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(47): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): 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 | a0003c0004t0013g0020 a0003c0004t0013g0209 a0003c0004t0013g0212 |
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 | a0002c0003t0004g0023 a0002c0003t0004g0024 a0002c0003t0022g0022 others(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 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 |
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 | 43 | a0001c0001t0006g0114 a0001c0001t0006g0115 a0002c0002t0003g0142 others(40): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): 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 | a0002c0003t0004g0123 | 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 | a0001c0001t0006g0115 | 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 | a0002c0002t0002g0031 | 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 | 11 | a0002c0002t0002g0031 a0002c0002t0006g0026 a0002c0002t0006g0178 others(8): 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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(132): 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 | a0001c0015t0004g0120 a0002c0003t0004g0012 a0002c0003t0004g0013 others(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 | 37 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(34): Show |
38 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(35): 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 | a0001c0005t0002g0056 | 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 | a0003c0004t0021g0140 | 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 | a0015c0026t0017g0033 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0101 a0003c0004t0013g0209 |
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 | a0002c0003t0004g0214 | 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 | a0001c0001t0001g0096 | 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 | a0003c0013t0024g0134 | 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 | a0001c0015t0004g0120 a0002c0003t0004g0012 a0002c0003t0004g0013 others(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 | 6 | a0002c0002t0007g0173 a0004c0006t0007g0004 a0004c0006t0007g0019 others(3): 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 | 41 | a0002c0002t0003g0142 a0002c0002t0003g0143 a0002c0002t0003g0144 others(38): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): 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 | a0003c0007t0005g0198 | 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 | a0002c0002t0003g0149 | 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 | 19 | a0001c0001t0007g0060 a0001c0001t0007g0094 a0002c0002t0007g0173 others(16): 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 |