| geneid | 130271 |
|---|---|
| ensemblid | ENSG00000152527.14 |
| hgncid | 30506 |
| symbol | PLEKHH2 |
| name | pleckstrin homology, MyTH4 and FERM domain containing H2 |
| refseq_nuc | NM_172069.4 |
| refseq_prot | NP_742066.2 |
| ensembl_nuc | ENST00000282406.9 |
| ensembl_prot | ENSP00000282406.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 43637260 |
| end | 43767987 |
| strand | + |
| ver | v1.2 |
| region | chr2:43637260-43767987 |
| region5000 | chr2:43632260-43772987 |
| regionname0 | PLEKHH2_chr2_43637260_43767987 |
| regionname5000 | PLEKHH2_chr2_43632260_43772987 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1493 | 146 | 29 | 37 | 40 | 8 | 30 | 25 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002 | 0/0 | 1493 | 38 | 23 | 3 | 7 | 1 | 4 | 6 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003 | 0/0 | 1493 | 31 | 21 | 8 | 0 | 1 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0004 | 0/0 | 1492 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0005 | 0/0 | 1493 | 6 | 0 | 2 | 2 | 0 | 2 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0006 | 0/0 | 1493 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0007 | 0/0 | 1493 | 4 | 2 | 0 | 2 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0008 | 0/0 | 1492 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0009 | 0/0 | 1492 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0010 | 0/0 | 1492 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0011 | 0/0 | 1493 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0012 | 0/0 | 1493 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0013 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0014 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0015 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0016 | 0/0 | 1493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0017 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0018 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0019 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0020 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0021 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0022 | 0/0 | 1493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0023 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4482 | 61 | 5 | 16 | 26 | 1 | 12 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0002 | 0/0 | 4482 | 31 | 3 | 6 | 14 | 3 | 5 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0003 | 0/1 | 4482 | 29 | 6 | 12 | 0 | 3 | 7 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0004 | 0/0 | 4482 | 17 | 8 | 7 | 0 | 1 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0005 | 0/0 | 4482 | 14 | 5 | 1 | 5 | 0 | 3 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0006 | 0/0 | 4482 | 9 | 7 | 0 | 0 | 1 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0007 | 0/0 | 4482 | 8 | 7 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0008 | 0/0 | 4482 | 6 | 0 | 2 | 2 | 0 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0009 | 0/0 | 4482 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0010 | 0/0 | 4479 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0011 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0012 | 0/0 | 4482 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0013 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0014 | 0/0 | 4482 | 3 | 2 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0015 | 0/0 | 4482 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0016 | 0/0 | 4482 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0017 | 0/0 | 4479 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0018 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0019 | 0/0 | 4479 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0020 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0021 | 0/0 | 4479 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0022 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0023 | 0/0 | 4482 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0024 | 0/0 | 4482 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0025 | 0/0 | 4482 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0026 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0027 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0028 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0029 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0030 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0031 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0032 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0033 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0034 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0035 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0036 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0037 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0038 | 0/0 | 4479 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0039 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0040 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0041 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0042 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0043 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0044 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0045 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0046 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0047 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0048 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0049 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0050 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0051 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0052 | 0/0 | 4479 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0053 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0054 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0055 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| c0056 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2513 | 99 | 17 | 29 | 28 | 5 | 18 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0002 | 0/0 | 2513 | 86 | 43 | 15 | 14 | 2 | 12 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0003 | 0/0 | 2513 | 21 | 9 | 3 | 0 | 1 | 8 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0004 | 0/0 | 2513 | 11 | 6 | 2 | 2 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0005 | 0/0 | 2513 | 7 | 5 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0006 | 0/0 | 2513 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0007 | 0/0 | 2513 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0008 | 0/0 | 2513 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0009 | 0/0 | 2513 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0010 | 0/0 | 2513 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0011 | 0/0 | 2513 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0012 | 0/0 | 2513 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0013 | 0/0 | 2513 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0014 | 0/0 | 2513 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0015 | 0/0 | 2513 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0016 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0017 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0018 | 0/0 | 2513 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| t0019 | 0/0 | 2513 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4482 | 61 | 5 | 16 | 26 | 1 | 12 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0002 | 0/0 | 4482 | 31 | 3 | 6 | 14 | 3 | 5 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0003 | 0/1 | 4482 | 29 | 6 | 12 | 0 | 3 | 7 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0007 | 0/0 | 4482 | 8 | 7 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0009 | 0/0 | 4482 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0018 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0024 | 0/0 | 4482 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0030 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0032 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0043 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0045 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0048 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0051 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0055 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0005 | 0/0 | 4482 | 14 | 5 | 1 | 5 | 0 | 3 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0006 | 0/0 | 4482 | 9 | 7 | 0 | 0 | 1 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0011 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0016 | 0/0 | 4482 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0020 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0023 | 0/0 | 4482 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0025 | 0/0 | 4482 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0040 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0047 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0004 | 0/0 | 4482 | 17 | 8 | 7 | 0 | 1 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0012 | 0/0 | 4482 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0013 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0022 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0037 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0039 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0044 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0050 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0004c0010 | 0/0 | 4479 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0004c0038 | 0/0 | 4479 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0005c0008 | 0/0 | 4482 | 6 | 0 | 2 | 2 | 0 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0006c0015 | 0/0 | 4482 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0006c0049 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0007c0014 | 0/0 | 4482 | 3 | 2 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0007c0035 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0008c0017 | 0/0 | 4479 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0009c0021 | 0/0 | 4479 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0010c0019 | 0/0 | 4479 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0011c0033 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0011c0034 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0012c0053 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0012c0054 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0013c0026 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0014c0027 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0015c0028 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0016c0029 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0017c0036 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0018c0041 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0019c0042 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0020c0046 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0021c0052 | 0/0 | 4479 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0022c0056 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0023c0031 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6994 | 45 | 4 | 11 | 23 | 0 | 6 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0001t0002 | 0/0 | 6994 | 10 | 0 | 2 | 1 | 1 | 6 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0001t0013 | 0/0 | 6994 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0001t0014 | 0/0 | 6994 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0001t0018 | 0/0 | 6994 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0001t0019 | 0/0 | 6994 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0002t0001 | 0/0 | 6994 | 6 | 0 | 0 | 2 | 2 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0002t0002 | 0/0 | 6994 | 20 | 3 | 6 | 7 | 1 | 3 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0002t0009 | 0/0 | 6994 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0002t0012 | 0/0 | 6994 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0003t0001 | 0/1 | 6994 | 25 | 2 | 12 | 0 | 3 | 7 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0003t0002 | 0/0 | 6994 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0007t0001 | 0/0 | 6994 | 8 | 7 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0009t0002 | 0/0 | 6994 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0018t0002 | 0/0 | 6994 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0024t0003 | 0/0 | 6994 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0030t0001 | 0/0 | 6994 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0032t0002 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0043t0004 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0045t0001 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0048t0001 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0051t0001 | 0/0 | 6994 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0001c0055t0001 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0005t0002 | 0/0 | 6994 | 5 | 0 | 0 | 5 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0005t0003 | 0/0 | 6994 | 8 | 4 | 1 | 0 | 0 | 3 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0005t0011 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0006t0002 | 0/0 | 6994 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0006t0003 | 0/0 | 6994 | 4 | 2 | 0 | 0 | 1 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0006t0004 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0006t0011 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0011t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0011t0008 | 0/0 | 6994 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0016t0002 | 0/0 | 6994 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0016t0003 | 0/0 | 6994 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0020t0002 | 0/0 | 6994 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0023t0004 | 0/0 | 6994 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0025t0004 | 0/0 | 6994 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0040t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0002c0047t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0004t0002 | 0/0 | 6994 | 13 | 7 | 5 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0004t0010 | 0/0 | 6994 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0004t0017 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0012t0004 | 0/0 | 6994 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0013t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0013t0007 | 0/0 | 6994 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0022t0002 | 0/0 | 6994 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0037t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0039t0004 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0044t0007 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0003c0050t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0004c0010t0005 | 0/0 | 6991 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0004c0010t0006 | 0/0 | 6991 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0004c0038t0006 | 0/0 | 6991 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0005c0008t0001 | 0/0 | 6994 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0005c0008t0002 | 0/0 | 6994 | 4 | 0 | 2 | 1 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0005c0008t0003 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0006c0015t0001 | 0/0 | 6994 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0006c0049t0001 | 0/0 | 6994 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0007c0014t0001 | 0/0 | 6994 | 3 | 2 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0007c0035t0001 | 0/0 | 6994 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0008c0017t0006 | 0/0 | 6991 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0009c0021t0005 | 0/0 | 6991 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0010c0019t0005 | 0/0 | 6991 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0011c0033t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0011c0034t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0012c0053t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0012c0054t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0013c0026t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0014c0027t0002 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0015c0028t0003 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0016c0029t0003 | 0/0 | 6994 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0017c0036t0001 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0018c0041t0003 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0019c0042t0015 | 0/0 | 6994 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0020c0046t0003 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0021c0052t0006 | 0/0 | 6991 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0022c0056t0003 | 0/0 | 6994 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| a0023c0031t0016 | 0/0 | 6994 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | copy fasta | chr2 | 43632260 | 43772987 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0013g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0013g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0018g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0001t0019g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0012g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0002t0012g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0009t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0009t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0009t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0009t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0009t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0009t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0018t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0018t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0024t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0024t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0030t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0032t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0043t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0045t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0048t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0051t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0001c0055t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0005t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0006t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0011t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0011t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0011t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0011t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0016t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0016t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0016t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0020t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0020t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0023t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0023t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0025t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0025t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0040t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0002c0047t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0010g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0010g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0004t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0012t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0012t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0012t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0012t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0013t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0013t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0013t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0013t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0022t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0022t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0037t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0039t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0044t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0003c0050t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0004c0010t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0004c0010t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0004c0010t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0004c0010t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0004c0010t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0004c0038t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0005c0008t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0005c0008t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0005c0008t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0005c0008t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0005c0008t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0005c0008t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0006c0015t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0006c0015t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0006c0015t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0006c0049t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0007c0014t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0007c0014t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0007c0014t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0007c0035t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0008c0017t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0008c0017t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0009c0021t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0009c0021t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0010c0019t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0010c0019t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0011c0033t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0011c0034t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0012c0053t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0012c0054t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0013c0026t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0014c0027t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0015c0028t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0016c0029t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0017c0036t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0018c0041t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0019c0042t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0020c0046t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0021c0052t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0022c0056t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| a0023c0031t0016g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0199 | EUR | GBR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0243 | EUR | GBR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0242 | EUR | FIN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00323 | hp2 | a0003 | c0004 | t0010 | g0136 | EUR | FIN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00597 | hp2 | a0001 | c0002 | t0009 | g0238 | EAS | CHS | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00639 | hp1 | a0002 | c0016 | t0003 | g0105 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00642 | hp1 | a0010 | c0019 | t0005 | g0071 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0189 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00735 | hp1 | a0001 | c0001 | t0013 | g0111 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00738 | hp1 | a0003 | c0012 | t0004 | g0176 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00738 | hp2 | a0003 | c0004 | t0002 | g0137 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00741 | hp1 | a0001 | c0051 | t0001 | g0082 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG00741 | hp2 | a0006 | c0015 | t0001 | g0156 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0197 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0155 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0157 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01074 | hp1 | a0003 | c0004 | t0002 | g0098 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01074 | hp2 | a0016 | c0029 | t0003 | g0161 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01099 | hp1 | a0003 | c0004 | t0002 | g0097 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01099 | hp2 | a0010 | c0019 | t0005 | g0073 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01106 | hp1 | a0003 | c0004 | t0002 | g0116 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01109 | hp1 | a0003 | c0004 | t0010 | g0139 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0064 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01168 | hp1 | a0001 | c0001 | t0013 | g0110 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01168 | hp2 | a0005 | c0008 | t0002 | g0255 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01175 | hp2 | a0006 | c0049 | t0001 | g0021 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01192 | hp2 | a0002 | c0005 | t0003 | g0002 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01243 | hp1 | a0001 | c0007 | t0001 | g0019 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01243 | hp2 | a0003 | c0004 | t0002 | g0107 | AMR | PUR | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01261 | hp1 | a0001 | c0030 | t0001 | g0215 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01261 | hp2 | a0002 | c0023 | t0004 | g0159 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0186 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0227 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01361 | hp1 | a0006 | c0015 | t0001 | g0007 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0171 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0178 | AMR | CLM | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0241 | EUR | IBS | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0158 | EUR | IBS | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01884 | hp1 | a0011 | c0033 | t0002 | g0103 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01884 | hp2 | a0004 | c0010 | t0006 | g0206 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01891 | hp1 | a0003 | c0004 | t0002 | g0248 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01975 | hp1 | a0005 | c0008 | t0002 | g0148 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01981 | hp1 | a0003 | c0004 | t0010 | g0102 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0196 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02027 | hp2 | a0001 | c0002 | t0009 | g0236 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02055 | hp1 | a0002 | c0011 | t0008 | g0145 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02055 | hp2 | a0001 | c0007 | t0001 | g0010 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02071 | hp1 | a0001 | c0002 | t0009 | g0235 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02074 | hp2 | a0007 | c0014 | t0001 | g0167 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02132 | hp1 | a0002 | c0005 | t0002 | g0045 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02132 | hp2 | a0019 | c0042 | t0015 | g0028 | EAS | KHV | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02145 | hp1 | a0001 | c0007 | t0001 | g0101 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0180 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | CDX | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02257 | hp1 | a0002 | c0025 | t0004 | g0015 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02257 | hp2 | a0001 | c0009 | t0002 | g0126 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0181 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02258 | hp2 | a0001 | c0007 | t0001 | g0003 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02280 | hp1 | a0006 | c0015 | t0001 | g0198 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02280 | hp2 | a0012 | c0053 | t0002 | g0121 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02451 | hp1 | a0001 | c0009 | t0002 | g0169 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02451 | hp2 | a0002 | c0006 | t0011 | g0239 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02572 | hp1 | a0003 | c0012 | t0004 | g0174 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0237 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02622 | hp1 | a0003 | c0004 | t0002 | g0100 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02622 | hp2 | a0002 | c0020 | t0002 | g0129 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02630 | hp1 | a0002 | c0006 | t0002 | g0182 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02630 | hp2 | a0002 | c0006 | t0002 | g0146 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02647 | hp1 | a0003 | c0004 | t0017 | g0117 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02647 | hp2 | a0003 | c0044 | t0007 | g0185 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02698 | hp2 | a0002 | c0005 | t0003 | g0033 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02717 | hp1 | a0002 | c0016 | t0002 | g0091 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02717 | hp2 | a0004 | c0010 | t0005 | g0092 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0087 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02738 | hp2 | a0005 | c0008 | t0002 | g0147 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02809 | hp1 | a0003 | c0022 | t0002 | g0140 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02818 | hp1 | a0003 | c0004 | t0002 | g0141 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02886 | hp2 | a0001 | c0009 | t0002 | g0106 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02895 | hp1 | a0001 | c0009 | t0002 | g0124 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0191 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02896 | hp1 | a0009 | c0021 | t0005 | g0253 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02896 | hp2 | a0002 | c0016 | t0002 | g0251 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02897 | hp1 | a0009 | c0021 | t0005 | g0254 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02897 | hp2 | a0001 | c0009 | t0002 | g0123 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02922 | hp1 | a0020 | c0046 | t0003 | g0165 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02922 | hp2 | a0002 | c0006 | t0004 | g0108 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02965 | hp1 | a0011 | c0034 | t0002 | g0151 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02965 | hp2 | a0003 | c0050 | t0002 | g0072 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02970 | hp1 | a0002 | c0006 | t0002 | g0096 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02970 | hp2 | a0008 | c0017 | t0006 | g0162 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02976 | hp1 | a0002 | c0040 | t0002 | g0081 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02976 | hp2 | a0021 | c0052 | t0006 | g0144 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03041 | hp1 | a0001 | c0009 | t0002 | g0128 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03041 | hp2 | a0003 | c0013 | t0002 | g0114 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03098 | hp1 | a0018 | c0041 | t0003 | g0204 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03098 | hp2 | a0007 | c0014 | t0001 | g0142 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03130 | hp1 | a0003 | c0013 | t0007 | g0134 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03130 | hp2 | a0002 | c0005 | t0003 | g0143 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03139 | hp1 | a0015 | c0028 | t0003 | g0212 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03139 | hp2 | a0002 | c0005 | t0011 | g0013 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03195 | hp1 | a0004 | c0038 | t0006 | g0093 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03195 | hp2 | a0002 | c0005 | t0003 | g0012 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0061 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03209 | hp2 | a0001 | c0018 | t0002 | g0150 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03225 | hp2 | a0002 | c0020 | t0002 | g0113 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03239 | hp2 | a0022 | c0056 | t0003 | g0245 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03453 | hp1 | a0003 | c0004 | t0002 | g0183 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03453 | hp2 | a0004 | c0010 | t0006 | g0135 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03486 | hp1 | a0003 | c0012 | t0004 | g0175 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03486 | hp2 | a0002 | c0006 | t0003 | g0163 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03490 | hp1 | a0001 | c0024 | t0003 | g0065 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0195 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03491 | hp1 | a0002 | c0005 | t0003 | g0032 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0202 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03516 | hp1 | a0007 | c0014 | t0001 | g0184 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0207 | AFR | ESN | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0122 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03540 | hp2 | a0004 | c0010 | t0005 | g0095 | AFR | GWD | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0063 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03579 | hp2 | a0012 | c0054 | t0002 | g0166 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0023 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0209 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03688 | hp2 | a0002 | c0005 | t0003 | g0190 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03704 | hp2 | a0001 | c0024 | t0003 | g0011 | SAS | PJL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04115 | hp1 | a0002 | c0006 | t0003 | g0193 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04184 | hp1 | a0005 | c0008 | t0003 | g0152 | SAS | BEB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04184 | hp2 | a0001 | c0055 | t0001 | g0256 | SAS | BEB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0179 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04199 | hp2 | a0001 | c0032 | t0002 | g0249 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04204 | hp2 | a0003 | c0004 | t0002 | g0080 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04228 | hp1 | a0001 | c0045 | t0001 | g0208 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | STU | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18522 | hp1 | a0003 | c0039 | t0004 | g0125 | AFR | YRI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18522 | hp2 | a0002 | c0011 | t0008 | g0120 | AFR | YRI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18747 | hp2 | a0001 | c0002 | t0012 | g0232 | EAS | CHB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18906 | hp1 | a0003 | c0012 | t0004 | g0177 | AFR | YRI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18906 | hp2 | a0001 | c0007 | t0001 | g0018 | AFR | YRI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18947 | hp1 | a0005 | c0008 | t0001 | g0153 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18962 | hp1 | a0002 | c0005 | t0002 | g0057 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18968 | hp2 | a0001 | c0001 | t0018 | g0055 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18970 | hp2 | a0007 | c0035 | t0001 | g0168 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18977 | hp1 | a0001 | c0001 | t0019 | g0053 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18977 | hp2 | a0002 | c0005 | t0002 | g0056 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18982 | hp2 | a0002 | c0005 | t0002 | g0020 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18986 | hp1 | a0002 | c0005 | t0002 | g0054 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18999 | hp2 | a0001 | c0002 | t0012 | g0226 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19012 | hp1 | a0002 | c0025 | t0004 | g0088 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19012 | hp2 | a0005 | c0008 | t0002 | g0230 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19030 | hp1 | a0003 | c0037 | t0002 | g0138 | AFR | LWK | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19030 | hp2 | a0003 | c0013 | t0007 | g0133 | AFR | LWK | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19043 | hp1 | a0003 | c0004 | t0002 | g0115 | AFR | LWK | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19043 | hp2 | a0023 | c0031 | t0016 | g0090 | AFR | LWK | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19060 | hp1 | a0002 | c0023 | t0004 | g0246 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19240 | hp1 | a0002 | c0005 | t0003 | g0083 | AFR | YRI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA19240 | hp2 | a0017 | c0036 | t0001 | g0099 | AFR | YRI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20129 | hp1 | a0001 | c0018 | t0002 | g0149 | AFR | ASW | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20129 | hp2 | a0002 | c0005 | t0003 | g0069 | AFR | ASW | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | TSI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20752 | hp2 | a0002 | c0006 | t0003 | g0194 | EUR | TSI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20805 | hp1 | a0001 | c0043 | t0004 | g0247 | EUR | TSI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0154 | EUR | TSI | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | GIH | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20905 | hp2 | a0001 | c0048 | t0001 | g0077 | SAS | GIH | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02109 | hp1 | a0002 | c0011 | t0008 | g0119 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02109 | hp2 | a0003 | c0022 | t0002 | g0164 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02486 | hp2 | a0013 | c0026 | t0002 | g0213 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02559 | hp1 | a0002 | c0006 | t0003 | g0132 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG02559 | hp2 | a0004 | c0010 | t0005 | g0094 | AFR | ACB | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03471 | hp1 | a0002 | c0011 | t0002 | g0127 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0062 | AFR | MSL | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0118 | AFR | USA | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| HG06807 | hp2 | a0003 | c0013 | t0007 | g0131 | AFR | USA | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20300 | hp1 | a0002 | c0047 | t0002 | g0014 | AFR | USA | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA20300 | hp2 | a0014 | c0027 | t0002 | g0214 | AFR | USA | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA21309 | hp1 | a0003 | c0004 | t0002 | g0160 | AFR | LWK | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| NA21309 | hp2 | a0008 | c0017 | t0006 | g0211 | AFR | LWK | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0188 | REF | REF | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0035 | REF | REF | PLEKHH2_chr2_43632260_43772987 | PLEKHH2 | chr2 | 43632260 | 43772987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43644758
|
G | A | 4 | a0008a0013a0014others(1): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.85G>A | p.Val29Ile | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/30 | 208/6994 | 85/4482 | 29/1493 | chr2 | 43644758 | ||
| chr2:43678896
|
G | A | 1 | a0023 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.157G>A | p.Glu53Lys | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/30 | 280/6994 | 157/4482 | 53/1493 | chr2 | 43678896 | ||
| chr2:43695168
|
G | A | 1 | a0016 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.446G>A | p.Arg149His | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/30 | 569/6994 | 446/4482 | 149/1493 | chr2 | 43695168 | ||
| chr2:43697278
|
C | T | 1 | a0022 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.610C>T | p.Pro204Ser | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/30 | 733/6994 | 610/4482 | 204/1493 | chr2 | 43697278 | ||
| chr2:43697350
|
A | G | 4 | a0008a0012a0015others(1): Show | 6 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
missense_variant | MODERATE | c.682A>G | p.Met228Val | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/30 | 805/6994 | 682/4482 | 228/1493 | chr2 | 43697350 | ||
| chr2:43700399
|
C | A | 5 | a0005a0007a0010others(2): Show | 15 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(12): Show |
missense_variant | MODERATE | c.1441C>A | p.Pro481Thr | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1564/6994 | 1441/4482 | 481/1493 | chr2 | 43700399 | ||
| chr2:43700400
|
C | T | 1 | a0017 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1442C>T | p.Pro481Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1565/6994 | 1442/4482 | 481/1493 | chr2 | 43700400 | ||
| chr2:43706328
|
C | T | 1 | a0020 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1733C>T | p.Ala578Val | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/30 | 1856/6994 | 1733/4482 | 578/1493 | chr2 | 43706328 | ||
| chr2:43707525
|
G | A | 1 | a0009 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1946G>A | p.Ser649Asn | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/30 | 2069/6994 | 1946/4482 | 649/1493 | chr2 | 43707525 | ||
| chr2:43710254
|
T | C | 1 | a0023 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2138T>C | p.Met713Thr | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 13/30 | 2261/6994 | 2138/4482 | 713/1493 | chr2 | 43710254 | ||
| chr2:43726298
|
G | C | 1 | a0018 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2568G>C | p.Trp856Cys | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/30 | 2691/6994 | 2568/4482 | 856/1493 | chr2 | 43726298 | ||
| chr2:43731569
|
A | C | 1 | a0015 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2910A>C | p.Glu970Asp | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/30 | 3033/6994 | 2910/4482 | 970/1493 | chr2 | 43731569 | ||
| chr2:43741028
|
G | A | 8 | a0002a0005a0015others(5): Show | 50 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(47): Show |
missense_variant | MODERATE | c.3206G>A | p.Arg1069Lys | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/30 | 3329/6994 | 3206/4482 | 1069/1493 | chr2 | 43741028 | ||
| chr2:43745960
|
A | G | 3 | a0003a0011a0014 | 34 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(31): Show |
missense_variant | MODERATE | c.3650A>G | p.Asn1217Ser | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/30 | 3773/6994 | 3650/4482 | 1217/1493 | chr2 | 43745960 | ||
| chr2:43762386
|
C | G | 1 | a0006 | 4 | HG00741.hp2 HG01175.hp2 HG01361.hp1 others(1): Show |
missense_variant | MODERATE | c.4154C>G | p.Ser1385Cys | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/30 | 4277/6994 | 4154/4482 | 1385/1493 | chr2 | 43762386 | ||
| chr2:43765494
|
C | T | 1 | a0019 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.4378C>T | p.Pro1460Ser | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 4501/6994 | 4378/4482 | 1460/1493 | chr2 | 43765494 | ||
| chr2:43765562
|
AAGC | A | 5 | a0004a0008a0009others(2): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
disruptive_inframe_deletion | MODERATE | c.4452_4454delCAG | p.Ser1484del | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 4575/6994 | 4452/4482 | 1484/1493 | INFO_REALIGN_3_PRIME | chr2 | 43765562 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43644784
|
T | C | 1 | a0016c0029 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.111T>C | p.Leu37Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/30 | 234/6994 | 111/4482 | 37/1493 | chr2 | 43644784 | ||
| chr2:43644785
|
T | C | 1 | a0001c0030 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.112T>C | p.Leu38Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/30 | 235/6994 | 112/4482 | 38/1493 | chr2 | 43644785 | ||
| chr2:43644787
|
A | G | 1 | a0001c0030 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.114A>G | p.Leu38Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/30 | 237/6994 | 114/4482 | 38/1493 | chr2 | 43644787 | ||
| chr2:43692660
|
G | A | 1 | a0001c0018 | 2 | HG03209.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.333G>A | p.Glu111Glu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/30 | 456/6994 | 333/4482 | 111/1493 | chr2 | 43692660 | ||
| chr2:43697286
|
A | T | 1 | a0001c0055 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.618A>T | p.Val206Val | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/30 | 741/6994 | 618/4482 | 206/1493 | chr2 | 43697286 | ||
| chr2:43699768
|
C | T | 1 | a0001c0051 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.810C>T | p.Ala270Ala | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 933/6994 | 810/4482 | 270/1493 | chr2 | 43699768 | ||
| chr2:43699804
|
T | A | 44 | a0001c0002a0001c0003a0001c0009others(41): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
synonymous_variant | LOW | c.846T>A | p.Pro282Pro | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 969/6994 | 846/4482 | 282/1493 | chr2 | 43699804 | ||
| chr2:43699834
|
C | T | 1 | a0003c0013 | 4 | HG03041.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.876C>T | p.Asp292Asp | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 999/6994 | 876/4482 | 292/1493 | chr2 | 43699834 | ||
| chr2:43700266
|
G | A | 1 | a0001c0032 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1308G>A | p.Leu436Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1431/6994 | 1308/4482 | 436/1493 | chr2 | 43700266 | ||
| chr2:43700320
|
C | G | 8 | a0001c0002a0001c0032a0001c0043others(5): Show | 40 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(37): Show |
synonymous_variant | LOW | c.1362C>G | p.Ala454Ala | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1485/6994 | 1362/4482 | 454/1493 | chr2 | 43700320 | ||
| chr2:43700429
|
C | T | 7 | a0005c0008a0007c0014a0007c0035others(4): Show | 15 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(12): Show |
synonymous_variant | LOW | c.1471C>T | p.Leu491Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1594/6994 | 1471/4482 | 491/1493 | chr2 | 43700429 | ||
| chr2:43700446
|
T | C | 7 | a0001c0009a0002c0011a0002c0020others(4): Show | 16 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
synonymous_variant | LOW | c.1488T>C | p.Ser496Ser | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1611/6994 | 1488/4482 | 496/1493 | chr2 | 43700446 | ||
| chr2:43700530
|
C | T | 2 | a0001c0007a0003c0050 | 9 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
synonymous_variant | LOW | c.1572C>T | p.Asp524Asp | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/30 | 1695/6994 | 1572/4482 | 524/1493 | chr2 | 43700530 | ||
| chr2:43704037
|
T | C | 30 | a0001c0002a0001c0003a0001c0030others(27): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
synonymous_variant | LOW | c.1707T>C | p.Asn569Asn | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/30 | 1830/6994 | 1707/4482 | 569/1493 | chr2 | 43704037 | ||
| chr2:43710051
|
C | T | 1 | a0002c0040 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.2028C>T | p.Ser676Ser | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 12/30 | 2151/6994 | 2028/4482 | 676/1493 | chr2 | 43710051 | ||
| chr2:43710060
|
G | A | 2 | a0003c0022a0011c0033 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
synonymous_variant | LOW | c.2037G>A | p.Thr679Thr | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 12/30 | 2160/6994 | 2037/4482 | 679/1493 | chr2 | 43710060 | ||
| chr2:43720704
|
A | G | 1 | a0007c0035 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.2496A>G | p.Thr832Thr | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/30 | 2619/6994 | 2496/4482 | 832/1493 | chr2 | 43720704 | ||
| chr2:43741008
|
C | A | 2 | a0001c0024a0023c0031 | 3 | HG03490.hp1 HG03704.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.3186C>A | p.Leu1062Leu | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/30 | 3309/6994 | 3186/4482 | 1062/1493 | chr2 | 43741008 | ||
| chr2:43742792
|
G | A | 1 | a0001c0048 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.3273G>A | p.Thr1091Thr | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/30 | 3396/6994 | 3273/4482 | 1091/1493 | chr2 | 43742792 | ||
| chr2:43757166
|
T | C | 1 | a0002c0047 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.3843T>C | p.His1281His | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/30 | 3966/6994 | 3843/4482 | 1281/1493 | chr2 | 43757166 | ||
| chr2:43765436
|
C | A | 6 | a0001c0043a0002c0023a0002c0025others(3): Show | 11 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(8): Show |
synonymous_variant | LOW | c.4320C>A | p.Ile1440Ile | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 4443/6994 | 4320/4482 | 1440/1493 | chr2 | 43765436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43765685
|
G | C | 1 | a0019c0042t0015 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 87 | chr2 | 43765685 | |||||
| chr2:43765903
|
C | T | 1 | a0001c0001t0014 | 2 | HG01109.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*305C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 305 | chr2 | 43765903 | |||||
| chr2:43765950
|
G | C | 7 | a0004c0010t0005a0004c0010t0006a0004c0038t0006others(4): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*352G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 352 | chr2 | 43765950 | |||||
| chr2:43766012
|
G | A | 1 | a0002c0011t0008 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*414G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 414 | chr2 | 43766012 | |||||
| chr2:43766089
|
T | A | 7 | a0004c0010t0005a0004c0010t0006a0004c0038t0006others(4): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*491T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 491 | chr2 | 43766089 | |||||
| chr2:43766105
|
G | A | 2 | a0003c0013t0007a0003c0044t0007 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 507 | chr2 | 43766105 | |||||
| chr2:43766119
|
C | T | 1 | a0002c0011t0008 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*521C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 521 | chr2 | 43766119 | |||||
| chr2:43766222
|
G | A | 1 | a0023c0031t0016 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 624 | chr2 | 43766222 | |||||
| chr2:43766224
|
C | A | 2 | a0002c0005t0011a0002c0006t0011 | 2 | HG02451.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*626C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 626 | chr2 | 43766224 | |||||
| chr2:43766236
|
T | C | 3 | a0004c0010t0005a0009c0021t0005a0010c0019t0005 | 7 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*638T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 638 | chr2 | 43766236 | |||||
| chr2:43766259
|
C | T | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 661 | chr2 | 43766259 | |||||
| chr2:43766309
|
G | C | 60 | a0001c0001t0002a0001c0001t0014a0001c0002t0002others(57): Show | 153 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*711G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 711 | chr2 | 43766309 | |||||
| chr2:43766370
|
A | T | 1 | a0001c0001t0013 | 2 | HG00735.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*772A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 772 | chr2 | 43766370 | |||||
| chr2:43766411
|
C | G | 1 | a0003c0004t0010 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*813C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 813 | chr2 | 43766411 | |||||
| chr2:43766582
|
C | T | 1 | a0003c0004t0017 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*984C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 984 | chr2 | 43766582 | |||||
| chr2:43766583
|
C | T | 10 | a0001c0024t0003a0002c0005t0003a0002c0006t0003others(7): Show | 21 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 985 | chr2 | 43766583 | |||||
| chr2:43766693
|
C | T | 1 | a0001c0002t0009 | 3 | HG00597.hp2 HG02027.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 1095 | chr2 | 43766693 | |||||
| chr2:43766756
|
C | G | 1 | a0001c0001t0018 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1158C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 1158 | chr2 | 43766756 | |||||
| chr2:43767241
|
C | G | 7 | a0004c0010t0005a0004c0010t0006a0004c0038t0006others(4): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1643C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 1643 | chr2 | 43767241 | |||||
| chr2:43767384
|
T | G | 9 | a0003c0013t0007a0003c0044t0007a0004c0010t0005others(6): Show | 17 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1786T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 1786 | chr2 | 43767384 | |||||
| chr2:43767558
|
T | A | 59 | a0001c0001t0002a0001c0001t0014a0001c0002t0002others(56): Show | 151 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*1960T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 1960 | chr2 | 43767558 | |||||
| chr2:43767731
|
T | G | 9 | a0003c0013t0007a0003c0044t0007a0004c0010t0005others(6): Show | 17 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2133T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 2133 | chr2 | 43767731 | |||||
| chr2:43767829
|
G | A | 1 | a0023c0031t0016 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2231G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 2231 | chr2 | 43767829 | |||||
| chr2:43767862
|
C | T | 7 | a0001c0043t0004a0002c0006t0004a0002c0023t0004others(4): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2264C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 30/30 | 2264 | chr2 | 43767862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43637387
|
A | G | 167 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
splice_region_variant&intron_variant | LOW | c.-4+8A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637387 | ||||||
| chr2:43637412
|
G | T | 1 | a0001c0055t0001g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-4+33G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637412 | ||||||
| chr2:43637416
|
T | C | 167 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-4+37T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637416 | ||||||
| chr2:43637427
|
T | G | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-4+48T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637427 | ||||||
| chr2:43637526
|
G | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+147G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637526 | ||||||
| chr2:43637811
|
C | T | 1 | a0005c0008t0002g0255 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-4+432C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637811 | ||||||
| chr2:43637845
|
G | A | 11 | a0001c0007t0001g0101a0002c0006t0002g0096a0002c0016t0002g0091others(8): Show | 11 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4+466G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637845 | ||||||
| chr2:43637901
|
G | T | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-4+522G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637901 | ||||||
| chr2:43637924
|
G | A | 1 | a0003c0004t0010g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-4+545G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43637924 | ||||||
| chr2:43638138
|
G | C | 1 | a0011c0033t0002g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-4+759G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638138 | ||||||
| chr2:43638202
|
G | C | 1 | a0011c0033t0002g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-4+823G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638202 | ||||||
| chr2:43638231
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-4+852G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638231 | ||||||
| chr2:43638243
|
C | A | 1 | a0002c0016t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4+864C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638243 | ||||||
| chr2:43638248
|
A | AAC | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0004c0010t0005g0094others(2): Show | 5 | HG01361.hp1 HG02040.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+908_-4+909dupAC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
A | AACAC | 8 | a0001c0001t0001g0006a0001c0002t0001g0005a0001c0003t0001g0004others(5): Show | 8 | HG01192.hp2 HG02074.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4+906_-4+909dupAC others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AAC | A | 23 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(20): Show | 23 | HG00642.hp1 HG00741.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4+908_-4+909delAC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACAC | A | 4 | a0001c0001t0002g0086a0001c0003t0001g0087a0001c0007t0001g0101others(1): Show | 4 | HG02145.hp1 HG02738.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+906_-4+909delAC others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACACAC | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0013g0110others(8): Show | 11 | HG00735.hp1 HG01106.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4+904_-4+909delAC others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACACACA others(1): Show |
A | 26 | a0001c0002t0002g0130a0001c0003t0002g0122a0001c0009t0002g0123others(23): Show | 26 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-4+902_-4+909delAC others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACACACA others(3): Show |
A | 25 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0003t0001g0157others(22): Show | 25 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-4+900_-4+909delAC others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACACACA others(5): Show |
A | 51 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(48): Show | 51 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4+898_-4+909delAC others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACACACA others(7): Show |
A | 39 | a0001c0001t0001g0222a0001c0002t0001g0104a0001c0002t0001g0225others(36): Show | 39 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.-4+896_-4+909delAC others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638248
|
AACACACA others(9): Show |
A | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-4+894_-4+909delAC others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638248 | |||||
| chr2:43638271
|
ACACACAC others(11): Show |
A | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-4+902_-4+919delAC others(16): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638271 | |||||
| chr2:43638292
|
C | T | 1 | a0003c0004t0002g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-4+913C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638292 | ||||||
| chr2:43638486
|
T | C | 9 | a0002c0005t0003g0143a0002c0011t0008g0119a0002c0011t0008g0120others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+1107T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638486 | ||||||
| chr2:43638639
|
T | G | 165 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.-4+1260T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638639 | ||||||
| chr2:43638742
|
C | G | 4 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0007t0001g0061others(1): Show | 4 | HG01109.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+1363C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638742 | ||||||
| chr2:43638743
|
G | A | 16 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(13): Show | 16 | HG01168.hp2 HG01884.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4+1364G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638743 | ||||||
| chr2:43638772
|
T | G | 1 | a0001c0007t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-4+1393T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638772 | ||||||
| chr2:43638785
|
G | A | 1 | a0001c0030t0001g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-4+1406G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638785 | ||||||
| chr2:43638815
|
T | TA | 136 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-4+1438dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43638815 | |||||
| chr2:43638989
|
A | G | 2 | a0001c0009t0002g0106a0003c0004t0002g0107 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-4+1610A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43638989 | ||||||
| chr2:43639203
|
T | C | 135 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-4+1824T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639203 | ||||||
| chr2:43639272
|
T | G | 15 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(12): Show | 15 | HG01168.hp2 HG01884.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+1893T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639272 | ||||||
| chr2:43639305
|
G | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-4+1926G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639305 | ||||||
| chr2:43639356
|
C | T | 10 | a0003c0004t0002g0115a0003c0004t0002g0116a0003c0004t0002g0137others(7): Show | 10 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4+1977C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639356 | ||||||
| chr2:43639460
|
C | CTT | 5 | a0008c0017t0006g0162a0008c0017t0006g0211a0013c0026t0002g0213others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+2082_-4+2083ins others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639460 | |||||
| chr2:43639486
|
C | T | 5 | a0008c0017t0006g0162a0008c0017t0006g0211a0013c0026t0002g0213others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+2107C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639486 | ||||||
| chr2:43639589
|
G | A | 1 | a0002c0006t0002g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-4+2210G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639589 | ||||||
| chr2:43639650
|
C | CT | 22 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0003t0002g0122others(19): Show | 22 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.-4+2295dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639650 | |||||
| chr2:43639650
|
CT | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0089others(23): Show | 26 | HG00639.hp1 HG00738.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-4+2295delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639650 | |||||
| chr2:43639650
|
CTT | C | 58 | a0001c0001t0001g0222a0001c0001t0002g0210a0001c0002t0001g0104others(55): Show | 58 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.-4+2294_-4+2295del others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639650 | |||||
| chr2:43639650
|
CTTT | C | 21 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0205others(18): Show | 21 | HG00735.hp1 HG01168.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.-4+2293_-4+2295del others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639650 | |||||
| chr2:43639650
|
CTTTT | C | 39 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(36): Show | 39 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-4+2292_-4+2295del others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639650 | |||||
| chr2:43639685
|
C | CT | 5 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+2307dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43639685 | |||||
| chr2:43639713
|
A | G | 151 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-4+2334A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639713 | ||||||
| chr2:43639771
|
C | G | 8 | a0002c0006t0003g0132a0002c0016t0003g0105a0003c0004t0002g0160others(5): Show | 8 | HG00639.hp1 HG02559.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4+2392C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639771 | ||||||
| chr2:43639845
|
C | T | 3 | a0001c0001t0001g0006a0003c0004t0002g0107a0004c0038t0006g0093 | 3 | HG01243.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4+2466C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639845 | ||||||
| chr2:43639989
|
G | A | 5 | a0008c0017t0006g0162a0008c0017t0006g0211a0013c0026t0002g0213others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+2610G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43639989 | ||||||
| chr2:43640068
|
T | C | 198 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0025others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-4+2689T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640068 | ||||||
| chr2:43640198
|
C | A | 1 | a0002c0005t0003g0012 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-4+2819C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640198 | ||||||
| chr2:43640211
|
CT | C | 167 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-4+2846delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43640211 | |||||
| chr2:43640249
|
C | T | 1 | a0002c0016t0002g0251 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-4+2870C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640249 | ||||||
| chr2:43640258
|
G | C | 16 | a0001c0007t0001g0101a0002c0006t0002g0096a0002c0016t0002g0091others(13): Show | 16 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4+2879G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640258 | ||||||
| chr2:43640281
|
C | T | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+2902C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640281 | ||||||
| chr2:43640297
|
C | T | 16 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(13): Show | 16 | HG01168.hp2 HG01884.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4+2918C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640297 | ||||||
| chr2:43640314
|
C | T | 16 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(13): Show | 16 | HG01168.hp2 HG01884.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4+2935C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640314 | ||||||
| chr2:43640337
|
G | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(11): Show | 14 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4+2958G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640337 | ||||||
| chr2:43640343
|
C | T | 2 | a0002c0006t0002g0096a0002c0011t0008g0145 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-4+2964C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640343 | ||||||
| chr2:43640346
|
C | T | 5 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+2967C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640346 | ||||||
| chr2:43640354
|
T | C | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-4+2975T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640354 | ||||||
| chr2:43640421
|
C | G | 167 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-4+3042C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640421 | ||||||
| chr2:43640442
|
C | A | 16 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(13): Show | 16 | HG01168.hp2 HG01884.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4+3063C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640442 | ||||||
| chr2:43640635
|
C | G | 1 | a0001c0002t0002g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-4+3256C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640635 | ||||||
| chr2:43640637
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-4+3258A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640637 | ||||||
| chr2:43640807
|
C | G | 167 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-4+3428C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640807 | ||||||
| chr2:43640808
|
G | A | 2 | a0001c0001t0001g0027a0019c0042t0015g0028 | 2 | HG01106.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-4+3429G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640808 | ||||||
| chr2:43640950
|
A | AT | 111 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0109others(108): Show | 111 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-4+3593dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43640950 | |||||
| chr2:43640950
|
A | ATT | 26 | a0001c0001t0002g0210a0001c0002t0001g0104a0001c0002t0001g0242others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-4+3592_-4+3593dup others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43640950 | |||||
| chr2:43640950
|
AT | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0074a0002c0016t0002g0091others(6): Show | 9 | HG01256.hp2 HG02486.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+3593delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43640950 | |||||
| chr2:43640950
|
ATT | A | 9 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+3592_-4+3593del others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43640950 | |||||
| chr2:43640979
|
G | C | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-4+3600G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640979 | ||||||
| chr2:43640995
|
C | A | 152 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-4+3616C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43640995 | ||||||
| chr2:43641048
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3-3623C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641048 | ||||||
| chr2:43641242
|
T | C | 1 | a0001c0002t0002g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-3-3429T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641242 | ||||||
| chr2:43641375
|
T | C | 1 | a0001c0045t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3-3296T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641375 | ||||||
| chr2:43641395
|
G | A | 134 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-3-3276G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641395 | ||||||
| chr2:43641501
|
A | AT | 163 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-3-3159dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43641501 | |||||
| chr2:43641588
|
G | A | 1 | a0005c0008t0002g0147 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-3-3083G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641588 | ||||||
| chr2:43641764
|
T | C | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3-2907T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641764 | ||||||
| chr2:43641902
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-3-2769G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43641902 | ||||||
| chr2:43642050
|
A | G | 17 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(14): Show | 17 | HG00639.hp1 HG02257.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3-2621A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43642050 | ||||||
| chr2:43642419
|
T | C | 2 | a0001c0003t0001g0178a0001c0003t0001g0179 | 2 | HG01496.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-3-2252T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43642419 | ||||||
| chr2:43642494
|
G | A | 165 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.-3-2177G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43642494 | ||||||
| chr2:43642839
|
G | A | 13 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(10): Show | 13 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-3-1832G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43642839 | ||||||
| chr2:43642843
|
A | G | 1 | a0004c0010t0006g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3-1828A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43642843 | ||||||
| chr2:43642933
|
T | G | 11 | a0001c0002t0002g0130a0003c0004t0002g0115a0003c0004t0002g0116others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3-1738T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43642933 | ||||||
| chr2:43643108
|
C | G | 2 | a0002c0006t0003g0163a0007c0014t0001g0142 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-3-1563C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643108 | ||||||
| chr2:43643206
|
A | G | 8 | a0002c0006t0003g0132a0002c0016t0003g0105a0003c0004t0002g0160others(5): Show | 8 | HG00639.hp1 HG02559.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-1465A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643206 | ||||||
| chr2:43643229
|
G | A | 167 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-3-1442G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643229 | ||||||
| chr2:43643351
|
A | C | 174 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-3-1320A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643351 | ||||||
| chr2:43643363
|
C | A | 2 | a0001c0009t0002g0106a0003c0004t0002g0107 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-3-1308C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643363 | ||||||
| chr2:43643493
|
T | C | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1178T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643493 | ||||||
| chr2:43643510
|
C | G | 1 | a0001c0002t0002g0233 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-3-1161C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643510 | ||||||
| chr2:43643559
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-3-1112G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643559 | ||||||
| chr2:43643566
|
A | G | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-3-1105A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643566 | ||||||
| chr2:43643632
|
G | A | 16 | a0001c0007t0001g0101a0002c0006t0002g0096a0002c0016t0002g0091others(13): Show | 16 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3-1039G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643632 | ||||||
| chr2:43643637
|
A | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-3-1034A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643637 | ||||||
| chr2:43643725
|
T | C | 1 | a0001c0003t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-3-946T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643725 | ||||||
| chr2:43643833
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0018g0055others(34): Show | 37 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3-838A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643833 | ||||||
| chr2:43643863
|
A | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0018g0055others(16): Show | 19 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3-808A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43643863 | ||||||
| chr2:43644136
|
T | A | 137 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-3-535T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43644136 | ||||||
| chr2:43644186
|
C | G | 1 | a0004c0010t0006g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-3-485C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43644186 | ||||||
| chr2:43644364
|
A | G | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-307A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43644364 | ||||||
| chr2:43644443
|
T | G | 30 | a0001c0003t0002g0122a0001c0007t0001g0101a0001c0018t0002g0149others(27): Show | 30 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-3-228T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43644443 | ||||||
| chr2:43644448
|
CTCCA | C | 166 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-3-218_-3-215delTC others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 43644448 | |||||
| chr2:43644550
|
C | T | 2 | a0012c0054t0002g0166a0020c0046t0003g0165 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-3-121C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43644550 | ||||||
| chr2:43644640
|
A | T | 19 | a0001c0001t0001g0085a0001c0001t0018g0055a0001c0002t0001g0005others(16): Show | 19 | HG01168.hp2 HG01975.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-3-31A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 1/29 | chr2 | 43644640 | ||||||
| chr2:43644844
|
T | C | 172 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.123+48T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43644844 | ||||||
| chr2:43644893
|
A | G | 33 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(30): Show | 33 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.123+97A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43644893 | ||||||
| chr2:43645044
|
A | T | 2 | a0012c0054t0002g0166a0020c0046t0003g0165 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.123+248A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645044 | ||||||
| chr2:43645135
|
T | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0018g0055others(17): Show | 20 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+339T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645135 | ||||||
| chr2:43645528
|
A | G | 3 | a0002c0006t0002g0146a0011c0033t0002g0103a0011c0034t0002g0151 | 3 | HG01884.hp1 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.123+732A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645528 | ||||||
| chr2:43645556
|
G | T | 1 | a0001c0003t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.123+760G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645556 | ||||||
| chr2:43645569
|
G | C | 2 | a0001c0002t0009g0235a0001c0002t0009g0236 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.123+773G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645569 | ||||||
| chr2:43645577
|
A | T | 2 | a0002c0006t0003g0163a0007c0014t0001g0142 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123+781A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645577 | ||||||
| chr2:43645584
|
G | T | 19 | a0001c0001t0001g0085a0001c0001t0018g0055a0001c0002t0001g0005others(16): Show | 19 | HG01168.hp2 HG01975.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+788G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645584 | ||||||
| chr2:43645607
|
G | T | 136 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.123+811G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645607 | ||||||
| chr2:43645658
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123+862A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43645658 | ||||||
| chr2:43645706
|
CACTTCTT others(3): Show |
C | 1 | a0001c0003t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123+915_123+924del others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43645706 | |||||
| chr2:43646005
|
A | C | 174 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.123+1209A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646005 | ||||||
| chr2:43646024
|
T | A | 1 | a0008c0017t0006g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.123+1228T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646024 | ||||||
| chr2:43646031
|
T | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0018g0055others(14): Show | 17 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.123+1235T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646031 | ||||||
| chr2:43646095
|
C | T | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123+1299C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646095 | ||||||
| chr2:43646137
|
T | G | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123+1341T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646137 | ||||||
| chr2:43646236
|
C | T | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+1440C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646236 | ||||||
| chr2:43646359
|
C | A | 5 | a0008c0017t0006g0162a0008c0017t0006g0211a0013c0026t0002g0213others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1563C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646359 | ||||||
| chr2:43646366
|
C | A | 42 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(39): Show | 42 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.123+1570C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646366 | ||||||
| chr2:43646398
|
G | A | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.123+1602G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646398 | ||||||
| chr2:43646408
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.123+1612A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646408 | ||||||
| chr2:43646635
|
A | G | 1 | a0016c0029t0003g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.123+1839A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646635 | ||||||
| chr2:43646674
|
T | C | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123+1878T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646674 | ||||||
| chr2:43646739
|
T | C | 149 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+1943T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646739 | ||||||
| chr2:43646979
|
T | C | 149 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+2183T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646979 | ||||||
| chr2:43646989
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0018g0055a0001c0002t0001g0005others(3): Show | 6 | HG02074.hp1 NA18962.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+2193C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43646989 | ||||||
| chr2:43647118
|
A | G | 3 | a0002c0006t0003g0163a0004c0010t0006g0135a0007c0014t0001g0142 | 3 | HG03098.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123+2322A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647118 | ||||||
| chr2:43647182
|
C | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+2386C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647182 | ||||||
| chr2:43647192
|
A | C | 1 | a0005c0008t0002g0147 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123+2396A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647192 | ||||||
| chr2:43647259
|
C | A | 41 | a0001c0001t0001g0222a0001c0001t0002g0210a0001c0002t0001g0104others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.123+2463C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647259 | ||||||
| chr2:43647389
|
C | T | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123+2593C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647389 | ||||||
| chr2:43647415
|
G | C | 4 | a0001c0001t0002g0031a0001c0001t0002g0075a0002c0005t0003g0032others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2619G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647415 | ||||||
| chr2:43647568
|
T | C | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123+2772T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647568 | ||||||
| chr2:43647650
|
G | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+2854G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647650 | ||||||
| chr2:43647672
|
C | T | 1 | a0001c0002t0012g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.123+2876C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647672 | ||||||
| chr2:43647769
|
G | T | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.123+2973G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647769 | ||||||
| chr2:43647848
|
C | T | 14 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(11): Show | 14 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+3052C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647848 | ||||||
| chr2:43647888
|
G | A | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123+3092G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647888 | ||||||
| chr2:43647994
|
A | G | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.123+3198A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43647994 | ||||||
| chr2:43648150
|
G | A | 135 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.123+3354G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648150 | ||||||
| chr2:43648180
|
TTTTGTTT others(5): Show |
T | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123+3396_123+3407d others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648180 | |||||
| chr2:43648184
|
G | T | 1 | a0003c0022t0002g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123+3388G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648184 | ||||||
| chr2:43648191
|
T | A | 1 | a0001c0001t0001g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.123+3395T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648191 | ||||||
| chr2:43648238
|
G | T | 2 | a0001c0003t0001g0216a0001c0003t0001g0217 | 2 | HG00735.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.123+3442G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648238 | ||||||
| chr2:43648295
|
T | A | 4 | a0001c0007t0001g0003a0001c0007t0001g0010a0001c0007t0001g0018others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3499T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648295 | ||||||
| chr2:43648319
|
G | A | 4 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3523G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648319 | ||||||
| chr2:43648337
|
T | C | 2 | a0001c0003t0001g0076a0001c0048t0001g0077 | 2 | HG01358.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.123+3541T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648337 | ||||||
| chr2:43648433
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123+3637C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648433 | ||||||
| chr2:43648434
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.123+3638G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648434 | ||||||
| chr2:43648435
|
C | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+3639C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648435 | ||||||
| chr2:43648496
|
G | T | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+3700G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648496 | ||||||
| chr2:43648525
|
G | A | 6 | a0002c0006t0003g0163a0008c0017t0006g0162a0008c0017t0006g0211others(3): Show | 6 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+3729G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648525 | ||||||
| chr2:43648560
|
C | CGT | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(91): Show | 94 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.123+3804_123+3805d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
C | CGTGT | 29 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0084others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.123+3802_123+3805d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
C | CGTGTGT | 17 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0109others(14): Show | 17 | HG00438.hp1 HG01192.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+3800_123+3805d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
C | CGTGTGTG others(5): Show |
1 | a0001c0003t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.123+3794_123+3805d others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
C | T | 1 | a0002c0005t0003g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.123+3764C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648560 | ||||||
| chr2:43648560
|
CGT | C | 32 | a0001c0001t0001g0192a0001c0001t0002g0031a0001c0003t0001g0178others(29): Show | 32 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.123+3804_123+3805d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
CGTGT | C | 18 | a0002c0016t0002g0091a0003c0004t0002g0137a0003c0004t0002g0141others(15): Show | 18 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+3802_123+3805d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
CGTGTGT | C | 5 | a0001c0002t0001g0104a0001c0032t0002g0249a0001c0045t0001g0208others(2): Show | 5 | HG01891.hp1 HG02896.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+3800_123+3805d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648560
|
CGTGTGTG others(1): Show |
C | 39 | a0001c0001t0001g0222a0001c0001t0002g0210a0001c0002t0001g0225others(36): Show | 39 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.123+3798_123+3805d others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43648560 | |||||
| chr2:43648645
|
A | G | 5 | a0008c0017t0006g0162a0008c0017t0006g0211a0013c0026t0002g0213others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3849A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648645 | ||||||
| chr2:43648745
|
T | C | 73 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(70): Show | 73 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.123+3949T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648745 | ||||||
| chr2:43648772
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.123+3976G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648772 | ||||||
| chr2:43648774
|
T | A | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.123+3978T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648774 | ||||||
| chr2:43648786
|
G | A | 1 | a0003c0039t0004g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.123+3990G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648786 | ||||||
| chr2:43648925
|
A | G | 1 | a0001c0009t0002g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123+4129A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648925 | ||||||
| chr2:43648957
|
T | C | 5 | a0002c0006t0003g0132a0003c0013t0002g0114a0003c0013t0007g0131others(2): Show | 5 | HG02559.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+4161T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43648957 | ||||||
| chr2:43649210
|
T | C | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123+4414T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43649210 | ||||||
| chr2:43649627
|
G | C | 1 | a0001c0002t0002g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123+4831G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43649627 | ||||||
| chr2:43649684
|
C | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+4888C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43649684 | ||||||
| chr2:43649685
|
G | A | 9 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+4889G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43649685 | ||||||
| chr2:43649784
|
G | C | 132 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.123+4988G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43649784 | ||||||
| chr2:43649935
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.123+5139G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43649935 | ||||||
| chr2:43650017
|
A | G | 62 | a0001c0001t0001g0222a0001c0001t0002g0210a0001c0002t0001g0005others(59): Show | 62 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.123+5221A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650017 | ||||||
| chr2:43650144
|
C | CT | 50 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0109others(47): Show | 50 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.123+5370dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43650144 | |||||
| chr2:43650144
|
CT | C | 67 | a0001c0001t0001g0025a0001c0001t0001g0222a0001c0002t0001g0005others(64): Show | 67 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.123+5370delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43650144 | |||||
| chr2:43650166
|
T | C | 2 | a0001c0007t0001g0061a0001c0007t0001g0062 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123+5370T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650166 | ||||||
| chr2:43650166
|
T | TTC | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG00741.hp2 HG01071.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+5370_123+5371i others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650166 | ||||||
| chr2:43650207
|
G | A | 1 | a0002c0023t0004g0246 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.123+5411G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650207 | ||||||
| chr2:43650411
|
A | G | 178 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.123+5615A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650411 | ||||||
| chr2:43650429
|
G | A | 1 | a0001c0045t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.123+5633G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650429 | ||||||
| chr2:43650502
|
T | C | 5 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0011g0013others(2): Show | 5 | HG01192.hp2 HG02257.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+5706T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650502 | ||||||
| chr2:43650650
|
C | CT | 21 | a0001c0001t0014g0064a0001c0009t0002g0123a0001c0009t0002g0124others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.123+5867dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43650650 | |||||
| chr2:43650726
|
A | T | 4 | a0001c0001t0001g0078a0001c0051t0001g0082a0002c0005t0003g0083others(1): Show | 4 | HG00741.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+5930A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650726 | ||||||
| chr2:43650789
|
T | G | 158 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.123+5993T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650789 | ||||||
| chr2:43650803
|
G | A | 137 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.123+6007G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650803 | ||||||
| chr2:43650831
|
G | A | 2 | a0002c0011t0008g0119a0002c0011t0008g0145 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.123+6035G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650831 | ||||||
| chr2:43650896
|
T | C | 170 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.123+6100T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650896 | ||||||
| chr2:43650934
|
C | A | 5 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+6138C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650934 | ||||||
| chr2:43650966
|
G | C | 158 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.123+6170G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650966 | ||||||
| chr2:43650971
|
A | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+6175A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43650971 | ||||||
| chr2:43651063
|
T | C | 136 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.123+6267T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651063 | ||||||
| chr2:43651071
|
T | C | 68 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(65): Show | 68 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.123+6275T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651071 | ||||||
| chr2:43651145
|
T | TTTCA | 20 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(17): Show | 20 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+6372_123+6375d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43651145 | |||||
| chr2:43651145
|
TTTCA | T | 46 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.123+6372_123+6375d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43651145 | |||||
| chr2:43651145
|
TTTCATTC others(1): Show |
T | 86 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(83): Show | 86 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.123+6368_123+6375d others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43651145 | |||||
| chr2:43651282
|
T | A | 1 | a0001c0003t0002g0237 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.123+6486T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651282 | ||||||
| chr2:43651356
|
C | T | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.123+6560C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651356 | ||||||
| chr2:43651362
|
C | T | 2 | a0011c0033t0002g0103a0011c0034t0002g0151 | 2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.123+6566C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651362 | ||||||
| chr2:43651430
|
G | A | 5 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+6634G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651430 | ||||||
| chr2:43651462
|
C | T | 5 | a0002c0005t0003g0143a0002c0011t0008g0119a0002c0011t0008g0145others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+6666C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651462 | ||||||
| chr2:43651569
|
C | CT | 20 | a0001c0001t0014g0064a0001c0009t0002g0123a0001c0009t0002g0124others(17): Show | 20 | HG00639.hp1 HG01109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+6782dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43651569 | |||||
| chr2:43651630
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0002g0051 | 3 | HG00639.hp2 HG01952.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.123+6834C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651630 | ||||||
| chr2:43651638
|
A | C | 1 | a0002c0005t0002g0020 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.123+6842A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651638 | ||||||
| chr2:43651856
|
A | C | 5 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0011g0013others(2): Show | 5 | HG01192.hp2 HG02257.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+7060A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651856 | ||||||
| chr2:43651863
|
G | A | 65 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(62): Show | 65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.123+7067G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651863 | ||||||
| chr2:43651903
|
T | A | 65 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(62): Show | 65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.123+7107T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43651903 | ||||||
| chr2:43652003
|
G | C | 5 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+7207G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652003 | ||||||
| chr2:43652063
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.123+7267T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652063 | ||||||
| chr2:43652099
|
G | C | 65 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(62): Show | 65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.123+7303G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652099 | ||||||
| chr2:43652106
|
A | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0002g0031others(2): Show | 5 | HG02486.hp1 HG03688.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+7310A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652106 | ||||||
| chr2:43652129
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.123+7333C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652129 | ||||||
| chr2:43652145
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0060 | 2 | NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.123+7349T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652145 | ||||||
| chr2:43652243
|
T | G | 65 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(62): Show | 65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.123+7447T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652243 | ||||||
| chr2:43652387
|
C | A | 1 | a0001c0003t0002g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.123+7591C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652387 | ||||||
| chr2:43652470
|
C | T | 46 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.123+7674C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652470 | ||||||
| chr2:43652550
|
T | C | 49 | a0001c0001t0002g0210a0001c0001t0014g0063a0001c0001t0014g0064others(46): Show | 49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.123+7754T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652550 | ||||||
| chr2:43652713
|
C | T | 46 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.123+7917C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652713 | ||||||
| chr2:43652714
|
C | T | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+7918C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652714 | ||||||
| chr2:43652837
|
T | C | 87 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.123+8041T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652837 | ||||||
| chr2:43652841
|
C | G | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.123+8045C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652841 | ||||||
| chr2:43652841
|
C | T | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+8045C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652841 | ||||||
| chr2:43652909
|
T | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+8113T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652909 | ||||||
| chr2:43652984
|
A | C | 6 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+8188A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43652984 | ||||||
| chr2:43653041
|
T | C | 51 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.123+8245T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653041 | ||||||
| chr2:43653182
|
T | C | 174 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.123+8386T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653182 | ||||||
| chr2:43653350
|
A | G | 51 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.123+8554A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653350 | ||||||
| chr2:43653447
|
G | T | 104 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.123+8651G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653447 | ||||||
| chr2:43653487
|
T | C | 10 | a0001c0001t0001g0009a0001c0018t0002g0149a0001c0018t0002g0150others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.123+8691T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653487 | ||||||
| chr2:43653509
|
C | T | 1 | a0020c0046t0003g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.123+8713C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653509 | ||||||
| chr2:43653546
|
G | T | 51 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.123+8750G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653546 | ||||||
| chr2:43653562
|
C | G | 4 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(1): Show | 4 | HG03041.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+8766C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653562 | ||||||
| chr2:43653571
|
C | A | 1 | a0008c0017t0006g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.123+8775C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653571 | ||||||
| chr2:43653651
|
C | G | 148 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.123+8855C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653651 | ||||||
| chr2:43653693
|
G | A | 1 | a0005c0008t0002g0148 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.123+8897G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653693 | ||||||
| chr2:43653712
|
G | T | 9 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(6): Show | 9 | HG00140.hp2 HG00323.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+8916G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653712 | ||||||
| chr2:43653828
|
G | GA | 19 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(16): Show | 19 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.123+9040dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43653828 | |||||
| chr2:43653999
|
A | C | 6 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+9203A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43653999 | ||||||
| chr2:43654022
|
G | A | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+9226G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654022 | ||||||
| chr2:43654064
|
C | T | 5 | a0002c0005t0003g0143a0002c0011t0008g0119a0002c0011t0008g0145others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+9268C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654064 | ||||||
| chr2:43654073
|
A | G | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+9277A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654073 | ||||||
| chr2:43654120
|
T | C | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.123+9324T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654120 | ||||||
| chr2:43654249
|
C | T | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+9453C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654249 | ||||||
| chr2:43654263
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0002g0030 | 2 | HG00438.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.123+9467C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654263 | ||||||
| chr2:43654279
|
C | G | 10 | a0001c0001t0001g0009a0001c0018t0002g0149a0001c0018t0002g0150others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.123+9483C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654279 | ||||||
| chr2:43654416
|
C | T | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+9620C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654416 | ||||||
| chr2:43654490
|
C | T | 1 | a0008c0017t0006g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.123+9694C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654490 | ||||||
| chr2:43654564
|
C | CT | 64 | a0001c0001t0001g0060a0001c0001t0002g0210a0001c0001t0014g0064others(61): Show | 64 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.123+9787dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654564 | |||||
| chr2:43654564
|
C | CTT | 7 | a0001c0002t0002g0221a0001c0032t0002g0249a0003c0004t0002g0100others(4): Show | 7 | HG01978.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+9786_123+9787d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654564 | |||||
| chr2:43654564
|
CT | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0038others(10): Show | 13 | HG01106.hp2 HG01168.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.123+9787delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654564 | |||||
| chr2:43654564
|
CTT | C | 78 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0187others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.123+9786_123+9787d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654564 | |||||
| chr2:43654564
|
CTTTT | C | 9 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+9784_123+9787d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654564 | |||||
| chr2:43654620
|
G | A | 51 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.123+9824G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654620 | ||||||
| chr2:43654679
|
A | G | 6 | a0003c0004t0002g0100a0004c0010t0005g0092a0004c0010t0005g0094others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+9883A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654679 | ||||||
| chr2:43654704
|
A | AC | 28 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0036others(25): Show | 28 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.123+9920dupC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654704 | |||||
| chr2:43654704
|
ACCCC | A | 96 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.123+9917_123+9920d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43654704 | |||||
| chr2:43654709
|
C | T | 2 | a0003c0004t0002g0097a0003c0004t0002g0098 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.123+9913C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654709 | ||||||
| chr2:43654711
|
C | CT | 50 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(47): Show | 50 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.123+9915_123+9916i others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654711 | ||||||
| chr2:43654711
|
C | T | 2 | a0008c0017t0006g0162a0015c0028t0003g0212 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.123+9915C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654711 | ||||||
| chr2:43654716
|
C | T | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.123+9920C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654716 | ||||||
| chr2:43654932
|
C | T | 1 | a0001c0003t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.123+10136C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654932 | ||||||
| chr2:43654933
|
G | A | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.123+10137G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654933 | ||||||
| chr2:43654937
|
G | T | 67 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(64): Show | 67 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.123+10141G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43654937 | ||||||
| chr2:43655065
|
G | C | 88 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(85): Show | 88 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.123+10269G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655065 | ||||||
| chr2:43655254
|
G | T | 134 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.123+10458G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655254 | ||||||
| chr2:43655280
|
A | G | 1 | a0008c0017t0006g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.123+10484A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655280 | ||||||
| chr2:43655292
|
CA | C | 4 | a0002c0006t0003g0163a0003c0004t0002g0100a0004c0038t0006g0093others(1): Show | 4 | HG02622.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+10503delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43655292 | |||||
| chr2:43655468
|
G | C | 136 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.123+10672G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655468 | ||||||
| chr2:43655488
|
G | A | 136 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.123+10692G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655488 | ||||||
| chr2:43655664
|
G | T | 3 | a0003c0004t0002g0100a0004c0038t0006g0093a0008c0017t0006g0211 | 3 | HG02622.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.123+10868G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655664 | ||||||
| chr2:43655749
|
T | G | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.123+10953T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655749 | ||||||
| chr2:43655783
|
C | A | 69 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(66): Show | 69 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.123+10987C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655783 | ||||||
| chr2:43655792
|
G | A | 142 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.123+10996G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655792 | ||||||
| chr2:43655863
|
A | C | 2 | a0001c0002t0002g0240a0002c0016t0002g0251 | 2 | HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.123+11067A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655863 | ||||||
| chr2:43655904
|
T | C | 6 | a0001c0007t0001g0191a0002c0006t0003g0163a0003c0004t0002g0100others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+11108T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43655904 | ||||||
| chr2:43655964
|
A | AT | 57 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.123+11180dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43655964 | |||||
| chr2:43655964
|
A | ATT | 71 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(68): Show | 71 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.123+11179_123+1118 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43655964 | |||||
| chr2:43656028
|
G | A | 142 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.123+11232G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656028 | ||||||
| chr2:43656104
|
G | C | 5 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+11308G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656104 | ||||||
| chr2:43656115
|
T | G | 142 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.123+11319T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656115 | ||||||
| chr2:43656200
|
G | A | 2 | a0001c0002t0002g0234a0001c0002t0002g0241 | 2 | HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.123+11404G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656200 | ||||||
| chr2:43656246
|
T | A | 4 | a0001c0001t0001g0048a0001c0001t0002g0031a0001c0001t0002g0047others(1): Show | 4 | HG03688.hp1 HG03831.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+11450T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656246 | ||||||
| chr2:43656451
|
AGAAGATA others(1): Show |
A | 158 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.123+11664_123+1167 others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43656451 | |||||
| chr2:43656472
|
A | G | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+11676A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656472 | ||||||
| chr2:43656481
|
A | G | 1 | a0002c0005t0003g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.123+11685A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656481 | ||||||
| chr2:43656572
|
A | G | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.123+11776A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656572 | ||||||
| chr2:43656626
|
A | C | 1 | a0001c0007t0001g0191 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.123+11830A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656626 | ||||||
| chr2:43656658
|
G | T | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123+11862G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656658 | ||||||
| chr2:43656717
|
A | C | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.123+11921A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656717 | ||||||
| chr2:43656807
|
T | C | 6 | a0001c0007t0001g0191a0002c0006t0003g0163a0003c0004t0002g0100others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+12011T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656807 | ||||||
| chr2:43656856
|
A | G | 1 | a0008c0017t0006g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.123+12060A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656856 | ||||||
| chr2:43656894
|
C | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(99): Show | 102 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.123+12098C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656894 | ||||||
| chr2:43656931
|
A | C | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+12135A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656931 | ||||||
| chr2:43656968
|
G | A | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+12172G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43656968 | ||||||
| chr2:43657013
|
C | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0109others(99): Show | 102 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.123+12217C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657013 | ||||||
| chr2:43657015
|
G | A | 1 | a0003c0012t0004g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123+12219G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657015 | ||||||
| chr2:43657035
|
CAAAACAA others(3): Show |
C | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+12249_123+1225 others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43657035 | |||||
| chr2:43657045
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0018g0055others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.123+12249T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657045 | ||||||
| chr2:43657061
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.123+12265T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657061 | ||||||
| chr2:43657202
|
C | T | 1 | a0003c0044t0007g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.123+12406C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657202 | ||||||
| chr2:43657272
|
C | T | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123+12476C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657272 | ||||||
| chr2:43657402
|
G | T | 1 | a0002c0016t0002g0251 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.123+12606G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657402 | ||||||
| chr2:43657417
|
C | T | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+12621C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657417 | ||||||
| chr2:43657443
|
C | G | 76 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.123+12647C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657443 | ||||||
| chr2:43657478
|
G | T | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+12682G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657478 | ||||||
| chr2:43657520
|
G | C | 9 | a0001c0007t0001g0101a0002c0006t0002g0096a0002c0011t0008g0119others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+12724G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657520 | ||||||
| chr2:43657621
|
A | G | 98 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.123+12825A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657621 | ||||||
| chr2:43657629
|
G | A | 1 | a0003c0004t0002g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+12833G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657629 | ||||||
| chr2:43657716
|
C | A | 4 | a0001c0003t0001g0195a0001c0003t0001g0196a0002c0006t0003g0193others(1): Show | 4 | HG01981.hp2 HG03490.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+12920C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657716 | ||||||
| chr2:43657758
|
G | A | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+12962G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657758 | ||||||
| chr2:43657799
|
G | A | 85 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+13003G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657799 | ||||||
| chr2:43657823
|
G | T | 1 | a0002c0005t0002g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+13027G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657823 | ||||||
| chr2:43657844
|
C | G | 111 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(108): Show | 111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.123+13048C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657844 | ||||||
| chr2:43657918
|
T | C | 171 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.123+13122T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657918 | ||||||
| chr2:43657986
|
G | C | 92 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(89): Show | 92 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.123+13190G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43657986 | ||||||
| chr2:43658052
|
T | C | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123+13256T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658052 | ||||||
| chr2:43658064
|
T | C | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+13268T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658064 | ||||||
| chr2:43658194
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.123+13398A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658194 | ||||||
| chr2:43658284
|
C | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(107): Show | 110 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.123+13488C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658284 | ||||||
| chr2:43658285
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+13489G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658285 | ||||||
| chr2:43658347
|
T | G | 2 | a0001c0003t0001g0188a0001c0003t0001g0189 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.123+13551T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658347 | ||||||
| chr2:43658389
|
T | C | 6 | a0001c0001t0001g0006a0001c0003t0001g0068a0001c0007t0001g0003others(3): Show | 6 | HG01192.hp1 HG01243.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+13593T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658389 | ||||||
| chr2:43658440
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+13644G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658440 | ||||||
| chr2:43658518
|
C | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+13722C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658518 | ||||||
| chr2:43658537
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+13741G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658537 | ||||||
| chr2:43658541
|
T | C | 3 | a0001c0009t0002g0106a0002c0006t0003g0163a0003c0004t0002g0107 | 3 | HG01243.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123+13745T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658541 | ||||||
| chr2:43658569
|
G | A | 1 | a0002c0006t0003g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.123+13773G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658569 | ||||||
| chr2:43658580
|
A | T | 1 | a0002c0006t0003g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.123+13784A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658580 | ||||||
| chr2:43658596
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+13800G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658596 | ||||||
| chr2:43658597
|
G | A | 1 | a0001c0002t0002g0223 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.123+13801G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658597 | ||||||
| chr2:43658751
|
G | A | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+13955G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658751 | ||||||
| chr2:43658877
|
A | G | 13 | a0001c0007t0001g0191a0001c0009t0002g0106a0002c0005t0003g0143others(10): Show | 13 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.123+14081A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658877 | ||||||
| chr2:43658911
|
T | C | 2 | a0002c0025t0004g0015a0002c0047t0002g0014 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.123+14115T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658911 | ||||||
| chr2:43658960
|
C | G | 4 | a0002c0005t0003g0143a0008c0017t0006g0162a0015c0028t0003g0212others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+14164C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658960 | ||||||
| chr2:43658961
|
T | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123+14165T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43658961 | ||||||
| chr2:43658973
|
C | CT | 95 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.123+14194dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43658973 | |||||
| chr2:43658973
|
C | CTT | 8 | a0001c0003t0001g0202a0002c0005t0003g0143a0003c0022t0002g0164others(5): Show | 8 | HG02109.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+14193_123+1419 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43658973 | |||||
| chr2:43658973
|
C | CTTT | 8 | a0001c0007t0001g0191a0001c0009t0002g0106a0002c0006t0003g0163others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+14192_123+1419 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43658973 | |||||
| chr2:43659104
|
A | C | 28 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(25): Show | 28 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.123+14308A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659104 | ||||||
| chr2:43659155
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.123+14359A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659155 | ||||||
| chr2:43659163
|
C | CTTTTTTT others(7): Show |
8 | a0001c0007t0001g0191a0001c0009t0002g0106a0003c0004t0002g0100others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+14375_123+1437 others(18): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43659163 | |||||
| chr2:43659163
|
C | CTTTTTTT others(8): Show |
4 | a0002c0005t0003g0143a0008c0017t0006g0162a0015c0028t0003g0212others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+14375_123+1437 others(19): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43659163 | |||||
| chr2:43659321
|
T | C | 25 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(22): Show | 25 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.123+14525T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659321 | ||||||
| chr2:43659349
|
C | G | 2 | a0010c0019t0005g0071a0010c0019t0005g0073 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.123+14553C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659349 | ||||||
| chr2:43659571
|
C | CT | 7 | a0002c0005t0003g0143a0002c0016t0002g0251a0007c0014t0001g0142others(4): Show | 7 | HG02896.hp2 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+14790dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43659571 | |||||
| chr2:43659619
|
C | G | 114 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(111): Show | 114 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.123+14823C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659619 | ||||||
| chr2:43659705
|
C | T | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+14909C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659705 | ||||||
| chr2:43659869
|
T | G | 1 | a0001c0003t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.123+15073T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659869 | ||||||
| chr2:43659873
|
T | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+15077T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659873 | ||||||
| chr2:43659879
|
T | A | 25 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(22): Show | 25 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.123+15083T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659879 | ||||||
| chr2:43659880
|
T | A | 7 | a0001c0007t0001g0191a0001c0009t0002g0106a0003c0004t0002g0100others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+15084T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659880 | ||||||
| chr2:43659882
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.123+15086T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659882 | ||||||
| chr2:43659916
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.123+15120G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659916 | ||||||
| chr2:43659959
|
A | G | 41 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.123+15163A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43659959 | ||||||
| chr2:43660029
|
C | T | 44 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.123+15233C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660029 | ||||||
| chr2:43660137
|
A | G | 8 | a0001c0007t0001g0191a0001c0009t0002g0106a0002c0006t0003g0163others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+15341A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660137 | ||||||
| chr2:43660183
|
GA | G | 8 | a0001c0007t0001g0191a0001c0009t0002g0106a0002c0006t0003g0163others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+15388delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660183 | ||||||
| chr2:43660332
|
G | A | 1 | a0001c0003t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.123+15536G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660332 | ||||||
| chr2:43660410
|
A | C | 1 | a0001c0001t0019g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.123+15614A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660410 | ||||||
| chr2:43660421
|
AAACATAT others(6072): Show |
A | 7 | a0001c0007t0001g0191a0001c0009t0002g0106a0003c0004t0002g0100others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+15642_124-1234 others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43660421 | |||||
| chr2:43660435
|
CT | C | 5 | a0001c0001t0013g0110a0001c0009t0002g0123a0002c0005t0002g0020others(2): Show | 5 | HG01168.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+15658delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43660435 | |||||
| chr2:43660471
|
A | AT | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.123+15688dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43660471 | |||||
| chr2:43660471
|
AT | A | 6 | a0001c0001t0002g0031a0002c0005t0003g0002a0002c0005t0003g0012others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+15688delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43660471 | |||||
| chr2:43660475
|
T | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0002t0009g0235others(7): Show | 10 | HG00597.hp2 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+15679T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660475 | ||||||
| chr2:43660511
|
C | T | 10 | a0001c0001t0001g0009a0001c0018t0002g0149a0001c0018t0002g0150others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.123+15715C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660511 | ||||||
| chr2:43660541
|
A | C | 19 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(16): Show | 19 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.123+15745A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660541 | ||||||
| chr2:43660634
|
C | A | 2 | a0001c0009t0002g0123a0001c0009t0002g0124 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+15838C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660634 | ||||||
| chr2:43660686
|
T | C | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+15890T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660686 | ||||||
| chr2:43660716
|
A | G | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.123+15920A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660716 | ||||||
| chr2:43660919
|
G | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+16123G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660919 | ||||||
| chr2:43660931
|
C | T | 1 | a0004c0010t0005g0095 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+16135C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660931 | ||||||
| chr2:43660932
|
G | A | 1 | a0001c0002t0002g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123+16136G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43660932 | ||||||
| chr2:43661002
|
G | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0018g0055others(16): Show | 19 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.123+16206G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661002 | ||||||
| chr2:43661091
|
A | G | 4 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0022t0002g0140others(1): Show | 4 | HG00738.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+16295A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661091 | ||||||
| chr2:43661296
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.123+16500C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661296 | ||||||
| chr2:43661346
|
G | C | 5 | a0001c0009t0002g0169a0003c0012t0004g0174a0003c0012t0004g0175others(2): Show | 5 | HG00738.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+16550G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661346 | ||||||
| chr2:43661432
|
G | C | 73 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(70): Show | 73 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.123+16636G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661432 | ||||||
| chr2:43661548
|
G | A | 78 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.123+16752G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661548 | ||||||
| chr2:43661610
|
C | T | 1 | a0001c0003t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123+16814C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661610 | ||||||
| chr2:43661752
|
C | G | 1 | a0001c0003t0001g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.123+16956C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661752 | ||||||
| chr2:43661946
|
C | T | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-16917C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661946 | ||||||
| chr2:43661947
|
G | A | 1 | a0001c0009t0002g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.124-16916G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43661947 | ||||||
| chr2:43662054
|
C | T | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124-16809C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662054 | ||||||
| chr2:43662218
|
A | C | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-16645A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662218 | ||||||
| chr2:43662250
|
A | G | 6 | a0002c0005t0003g0143a0002c0006t0003g0163a0007c0014t0001g0142others(3): Show | 6 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-16613A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662250 | ||||||
| chr2:43662292
|
G | C | 1 | a0016c0029t0003g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124-16571G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662292 | ||||||
| chr2:43662331
|
G | C | 55 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(52): Show | 55 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.124-16532G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662331 | ||||||
| chr2:43662397
|
A | T | 1 | a0001c0002t0002g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.124-16466A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662397 | ||||||
| chr2:43662398
|
A | G | 1 | a0001c0002t0002g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.124-16465A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662398 | ||||||
| chr2:43662416
|
G | A | 106 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(103): Show | 106 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.124-16447G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662416 | ||||||
| chr2:43662507
|
T | C | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-16356T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662507 | ||||||
| chr2:43662640
|
C | T | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-16223C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662640 | ||||||
| chr2:43662660
|
T | A | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.124-16203T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662660 | ||||||
| chr2:43662683
|
G | C | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-16180G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662683 | ||||||
| chr2:43662955
|
C | T | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-15908C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43662955 | ||||||
| chr2:43663223
|
T | G | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-15640T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663223 | ||||||
| chr2:43663341
|
T | C | 2 | a0001c0002t0009g0235a0001c0002t0009g0236 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.124-15522T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663341 | ||||||
| chr2:43663484
|
C | A | 17 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(14): Show | 17 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.124-15379C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663484 | ||||||
| chr2:43663540
|
T | G | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-15323T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663540 | ||||||
| chr2:43663544
|
AG | A | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-15318delG | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663544 | ||||||
| chr2:43663637
|
G | A | 8 | a0002c0006t0002g0146a0004c0010t0005g0092a0004c0010t0005g0094others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-15226G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663637 | ||||||
| chr2:43663666
|
T | A | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-15197T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663666 | ||||||
| chr2:43663684
|
G | A | 9 | a0001c0018t0002g0149a0001c0018t0002g0150a0005c0008t0001g0153others(6): Show | 9 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-15179G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663684 | ||||||
| chr2:43663893
|
C | G | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.124-14970C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663893 | ||||||
| chr2:43663896
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0041 | 2 | NA18978.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.124-14967T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43663896 | ||||||
| chr2:43663931
|
G | GA | 5 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0011g0013others(2): Show | 5 | HG01192.hp2 HG02257.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-14925dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43663931 | |||||
| chr2:43664011
|
C | A | 8 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0007t0001g0061others(5): Show | 8 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-14852C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664011 | ||||||
| chr2:43664045
|
A | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.124-14818A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664045 | ||||||
| chr2:43664079
|
A | G | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-14784A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664079 | ||||||
| chr2:43664169
|
C | A | 2 | a0002c0005t0003g0143a0021c0052t0006g0144 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.124-14694C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664169 | ||||||
| chr2:43664173
|
T | C | 1 | a0001c0002t0001g0242 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.124-14690T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664173 | ||||||
| chr2:43664251
|
C | A | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-14612C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664251 | ||||||
| chr2:43664287
|
G | C | 2 | a0010c0019t0005g0071a0010c0019t0005g0073 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.124-14576G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664287 | ||||||
| chr2:43664311
|
T | G | 9 | a0001c0007t0001g0061a0001c0007t0001g0062a0003c0004t0002g0137others(6): Show | 9 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-14552T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664311 | ||||||
| chr2:43664335
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.124-14528C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664335 | ||||||
| chr2:43664353
|
C | A | 88 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(85): Show | 88 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.124-14510C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664353 | ||||||
| chr2:43664367
|
C | T | 1 | a0001c0001t0019g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.124-14496C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664367 | ||||||
| chr2:43664406
|
A | T | 6 | a0002c0005t0003g0143a0002c0006t0003g0163a0007c0014t0001g0142others(3): Show | 6 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-14457A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664406 | ||||||
| chr2:43664441
|
T | C | 1 | a0001c0002t0002g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.124-14422T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664441 | ||||||
| chr2:43664457
|
A | C | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-14406A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664457 | ||||||
| chr2:43664539
|
T | A | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.124-14324T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664539 | ||||||
| chr2:43664603
|
G | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-14260G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664603 | ||||||
| chr2:43664610
|
A | G | 1 | a0001c0002t0002g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.124-14253A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664610 | ||||||
| chr2:43664684
|
C | G | 1 | a0022c0056t0003g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.124-14179C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664684 | ||||||
| chr2:43664727
|
T | G | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.124-14136T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664727 | ||||||
| chr2:43664822
|
A | C | 45 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.124-14041A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664822 | ||||||
| chr2:43664842
|
C | T | 4 | a0003c0012t0004g0174a0003c0012t0004g0175a0003c0012t0004g0176others(1): Show | 4 | HG00738.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-14021C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664842 | ||||||
| chr2:43664879
|
C | T | 1 | a0001c0030t0001g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.124-13984C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664879 | ||||||
| chr2:43664880
|
G | A | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-13983G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664880 | ||||||
| chr2:43664900
|
C | G | 7 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0010g0102others(4): Show | 7 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-13963C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664900 | ||||||
| chr2:43664905
|
C | T | 1 | a0002c0020t0002g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-13958C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43664905 | ||||||
| chr2:43665018
|
C | A | 1 | a0002c0005t0003g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.124-13845C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665018 | ||||||
| chr2:43665052
|
A | C | 1 | a0001c0003t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.124-13811A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665052 | ||||||
| chr2:43665092
|
G | C | 2 | a0001c0001t0001g0036a0003c0004t0002g0137 | 2 | HG00738.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.124-13771G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665092 | ||||||
| chr2:43665093
|
C | T | 1 | a0003c0004t0002g0137 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.124-13770C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665093 | ||||||
| chr2:43665094
|
A | G | 1 | a0003c0004t0002g0137 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.124-13769A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665094 | ||||||
| chr2:43665181
|
T | G | 1 | a0001c0002t0002g0224 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.124-13682T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665181 | ||||||
| chr2:43665207
|
G | A | 3 | a0003c0004t0002g0097a0003c0004t0002g0098a0020c0046t0003g0165 | 3 | HG01074.hp1 HG01099.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.124-13656G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665207 | ||||||
| chr2:43665262
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.124-13601G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665262 | ||||||
| chr2:43665274
|
C | G | 18 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-13589C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665274 | ||||||
| chr2:43665302
|
C | T | 6 | a0001c0003t0001g0195a0001c0003t0001g0196a0002c0006t0003g0193others(3): Show | 6 | HG01074.hp2 HG01981.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-13561C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665302 | ||||||
| chr2:43665343
|
C | G | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-13520C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665343 | ||||||
| chr2:43665428
|
C | T | 1 | a0002c0011t0008g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.124-13435C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665428 | ||||||
| chr2:43665429
|
G | A | 2 | a0002c0006t0003g0163a0007c0014t0001g0142 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.124-13434G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665429 | ||||||
| chr2:43665448
|
T | C | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-13415T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665448 | ||||||
| chr2:43665554
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0058 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.124-13309G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665554 | ||||||
| chr2:43665651
|
C | T | 12 | a0001c0001t0001g0044a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-13212C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665651 | ||||||
| chr2:43665652
|
G | T | 6 | a0002c0005t0003g0143a0002c0006t0003g0163a0007c0014t0001g0142others(3): Show | 6 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-13211G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665652 | ||||||
| chr2:43665754
|
C | T | 17 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(14): Show | 17 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.124-13109C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665754 | ||||||
| chr2:43665785
|
C | T | 4 | a0001c0001t0018g0055a0002c0005t0002g0054a0002c0005t0002g0056others(1): Show | 4 | NA18962.hp1 NA18968.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-13078C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665785 | ||||||
| chr2:43665786
|
C | G | 6 | a0001c0001t0018g0055a0001c0007t0001g0010a0001c0007t0001g0018others(3): Show | 6 | HG02055.hp2 NA18906.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-13077C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665786 | ||||||
| chr2:43665801
|
G | A | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-13062G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665801 | ||||||
| chr2:43665828
|
C | T | 4 | a0002c0006t0002g0146a0005c0008t0002g0147a0011c0033t0002g0103others(1): Show | 4 | HG01884.hp1 HG02630.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-13035C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665828 | ||||||
| chr2:43665853
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-13010T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665853 | ||||||
| chr2:43665944
|
C | T | 1 | a0001c0003t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.124-12919C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665944 | ||||||
| chr2:43665966
|
C | G | 153 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.124-12897C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665966 | ||||||
| chr2:43665967
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.124-12896G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43665967 | ||||||
| chr2:43666004
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0222 | 2 | NA18955.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.124-12859A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666004 | ||||||
| chr2:43666017
|
C | T | 6 | a0002c0005t0003g0143a0002c0006t0003g0163a0007c0014t0001g0142others(3): Show | 6 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-12846C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666017 | ||||||
| chr2:43666037
|
G | A | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-12826G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666037 | ||||||
| chr2:43666059
|
T | G | 6 | a0002c0005t0003g0143a0002c0006t0003g0163a0007c0014t0001g0142others(3): Show | 6 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-12804T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666059 | ||||||
| chr2:43666075
|
T | C | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-12788T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666075 | ||||||
| chr2:43666130
|
C | T | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-12733C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666130 | ||||||
| chr2:43666131
|
G | A | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.124-12732G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666131 | ||||||
| chr2:43666226
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.124-12637G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666226 | ||||||
| chr2:43666295
|
G | A | 20 | a0001c0001t0001g0192a0001c0003t0001g0024a0001c0003t0001g0068others(17): Show | 20 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-12568G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666295 | ||||||
| chr2:43666306
|
A | G | 18 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-12557A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666306 | ||||||
| chr2:43666438
|
G | A | 2 | a0001c0003t0001g0217a0001c0051t0001g0082 | 2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.124-12425G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666438 | ||||||
| chr2:43666446
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.124-12417C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666446 | ||||||
| chr2:43666463
|
C | T | 71 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(68): Show | 71 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.124-12400C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666463 | ||||||
| chr2:43666480
|
G | A | 1 | a0001c0003t0002g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124-12383G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666480 | ||||||
| chr2:43666546
|
C | G | 1 | a0002c0006t0011g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124-12317C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666546 | ||||||
| chr2:43666565
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-12298T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666565 | ||||||
| chr2:43666726
|
G | A | 2 | a0001c0003t0001g0076a0001c0048t0001g0077 | 2 | HG01358.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.124-12137G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666726 | ||||||
| chr2:43666739
|
T | C | 24 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(21): Show | 24 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.124-12124T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666739 | ||||||
| chr2:43666966
|
T | G | 2 | a0003c0004t0002g0137a0012c0054t0002g0166 | 2 | HG00738.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.124-11897T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43666966 | ||||||
| chr2:43667097
|
T | C | 5 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-11766T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667097 | ||||||
| chr2:43667132
|
T | C | 25 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(22): Show | 25 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-11731T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667132 | ||||||
| chr2:43667150
|
C | T | 10 | a0001c0001t0001g0009a0001c0018t0002g0149a0001c0018t0002g0150others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-11713C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667150 | ||||||
| chr2:43667172
|
G | GTCT | 24 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(21): Show | 24 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.124-11689_124-1168 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43667172 | |||||
| chr2:43667180
|
G | C | 24 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(21): Show | 24 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.124-11683G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667180 | ||||||
| chr2:43667288
|
A | G | 1 | a0004c0010t0006g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.124-11575A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667288 | ||||||
| chr2:43667290
|
A | G | 23 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(20): Show | 23 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-11573A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667290 | ||||||
| chr2:43667330
|
T | C | 1 | a0018c0041t0003g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124-11533T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667330 | ||||||
| chr2:43667457
|
A | G | 4 | a0001c0003t0001g0203a0003c0004t0002g0183a0004c0010t0006g0206others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-11406A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667457 | ||||||
| chr2:43667530
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.124-11333G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667530 | ||||||
| chr2:43667763
|
T | G | 13 | a0001c0007t0001g0191a0001c0009t0002g0106a0002c0005t0003g0143others(10): Show | 13 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.124-11100T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667763 | ||||||
| chr2:43667806
|
G | A | 2 | a0003c0004t0002g0097a0003c0004t0002g0098 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.124-11057G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667806 | ||||||
| chr2:43667811
|
T | C | 8 | a0001c0009t0002g0106a0002c0005t0003g0143a0002c0006t0003g0163others(5): Show | 8 | HG01243.hp2 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-11052T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667811 | ||||||
| chr2:43667890
|
T | C | 8 | a0001c0009t0002g0106a0002c0005t0003g0143a0002c0006t0003g0163others(5): Show | 8 | HG01243.hp2 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-10973T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667890 | ||||||
| chr2:43667893
|
T | TA | 7 | a0001c0001t0001g0044a0001c0001t0014g0064a0001c0002t0002g0221others(4): Show | 7 | HG00597.hp2 HG01109.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-10961dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43667893 | |||||
| chr2:43667902
|
A | AC | 7 | a0001c0001t0001g0009a0005c0008t0001g0153a0005c0008t0002g0147others(4): Show | 7 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-10960dupC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43667902 | |||||
| chr2:43667902
|
A | C | 4 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(1): Show | 4 | HG02922.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-10961A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667902 | ||||||
| chr2:43667910
|
T | C | 25 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0007t0001g0191others(22): Show | 25 | HG01168.hp2 HG01243.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-10953T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43667910 | ||||||
| chr2:43668124
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-10739C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668124 | ||||||
| chr2:43668275
|
A | G | 5 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-10588A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668275 | ||||||
| chr2:43668327
|
T | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(107): Show | 110 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.124-10536T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668327 | ||||||
| chr2:43668463
|
C | A | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-10400C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668463 | ||||||
| chr2:43668560
|
A | G | 105 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.124-10303A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668560 | ||||||
| chr2:43668616
|
C | A | 4 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145others(1): Show | 4 | HG02055.hp1 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-10247C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668616 | ||||||
| chr2:43668649
|
A | G | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-10214A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668649 | ||||||
| chr2:43668685
|
G | T | 1 | a0003c0004t0002g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-10178G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668685 | ||||||
| chr2:43668930
|
G | A | 1 | a0001c0003t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.124-9933G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43668930 | ||||||
| chr2:43669010
|
G | C | 5 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-9853G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669010 | ||||||
| chr2:43669234
|
A | G | 5 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-9629A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669234 | ||||||
| chr2:43669648
|
C | T | 1 | a0001c0003t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.124-9215C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669648 | ||||||
| chr2:43669702
|
G | C | 106 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(103): Show | 106 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.124-9161G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669702 | ||||||
| chr2:43669718
|
T | G | 1 | a0003c0004t0017g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.124-9145T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669718 | ||||||
| chr2:43669729
|
G | A | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-9134G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669729 | ||||||
| chr2:43669761
|
C | T | 2 | a0013c0026t0002g0213a0014c0027t0002g0214 | 2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.124-9102C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669761 | ||||||
| chr2:43669864
|
C | G | 105 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.124-8999C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669864 | ||||||
| chr2:43669905
|
G | A | 117 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(114): Show | 117 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(114): Show |
intron_variant | MODIFIER | c.124-8958G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43669905 | ||||||
| chr2:43670015
|
T | A | 83 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.124-8848T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670015 | ||||||
| chr2:43670016
|
T | C | 8 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0002g0160others(5): Show | 8 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-8847T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670016 | ||||||
| chr2:43670139
|
C | CA | 109 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.124-8719dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43670139 | |||||
| chr2:43670361
|
C | G | 109 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.124-8502C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670361 | ||||||
| chr2:43670441
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0031a0001c0001t0002g0058 | 3 | HG02486.hp1 HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.124-8422T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670441 | ||||||
| chr2:43670532
|
A | G | 46 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.124-8331A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670532 | ||||||
| chr2:43670565
|
C | G | 1 | a0001c0003t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.124-8298C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670565 | ||||||
| chr2:43670590
|
T | A | 4 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-8273T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670590 | ||||||
| chr2:43670623
|
AT | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0112others(45): Show | 48 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.124-8228delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43670623 | |||||
| chr2:43670623
|
ATT | A | 58 | a0001c0001t0001g0048a0001c0001t0001g0170a0001c0001t0001g0172others(55): Show | 58 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.124-8229_124-8228d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43670623 | |||||
| chr2:43670714
|
G | A | 1 | a0002c0023t0004g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.124-8149G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670714 | ||||||
| chr2:43670714
|
G | T | 6 | a0002c0005t0003g0143a0002c0006t0003g0163a0007c0014t0001g0142others(3): Show | 6 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-8149G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670714 | ||||||
| chr2:43670751
|
T | C | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-8112T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670751 | ||||||
| chr2:43670812
|
C | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.124-8051C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670812 | ||||||
| chr2:43670846
|
G | T | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-8017G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670846 | ||||||
| chr2:43670989
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.124-7874C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43670989 | ||||||
| chr2:43670989
|
CT | C | 8 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0010g0102others(5): Show | 8 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-7862delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43670989 | |||||
| chr2:43671045
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.124-7818G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671045 | ||||||
| chr2:43671143
|
C | T | 1 | a0005c0008t0003g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.124-7720C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671143 | ||||||
| chr2:43671177
|
G | A | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124-7686G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671177 | ||||||
| chr2:43671282
|
T | C | 109 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.124-7581T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671282 | ||||||
| chr2:43671490
|
A | T | 115 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(112): Show | 115 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.124-7373A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671490 | ||||||
| chr2:43671602
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.124-7261G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671602 | ||||||
| chr2:43671677
|
A | T | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-7186A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671677 | ||||||
| chr2:43671714
|
A | G | 4 | a0002c0005t0003g0143a0008c0017t0006g0162a0015c0028t0003g0212others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-7149A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671714 | ||||||
| chr2:43671723
|
T | C | 1 | a0001c0003t0002g0237 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.124-7140T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671723 | ||||||
| chr2:43671731
|
A | C | 1 | a0002c0006t0011g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124-7132A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671731 | ||||||
| chr2:43671788
|
C | G | 102 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(99): Show | 102 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.124-7075C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671788 | ||||||
| chr2:43671827
|
G | A | 101 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.124-7036G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671827 | ||||||
| chr2:43671883
|
G | A | 1 | a0002c0005t0002g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-6980G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43671883 | ||||||
| chr2:43672449
|
C | G | 100 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.124-6414C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672449 | ||||||
| chr2:43672541
|
T | C | 2 | a0001c0009t0002g0106a0003c0004t0002g0107 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.124-6322T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672541 | ||||||
| chr2:43672598
|
C | T | 2 | a0001c0009t0002g0106a0003c0004t0002g0107 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.124-6265C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672598 | ||||||
| chr2:43672608
|
T | C | 1 | a0008c0017t0006g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.124-6255T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672608 | ||||||
| chr2:43672753
|
T | A | 150 | a0001c0001t0001g0040a0001c0001t0001g0109a0001c0001t0001g0112others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-6110T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672753 | ||||||
| chr2:43672776
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.124-6087C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672776 | ||||||
| chr2:43672779
|
C | A | 103 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(100): Show | 103 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.124-6084C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672779 | ||||||
| chr2:43672835
|
A | G | 4 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-6028A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672835 | ||||||
| chr2:43672838
|
T | A | 148 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.124-6025T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672838 | ||||||
| chr2:43672904
|
A | C | 7 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0010g0102others(4): Show | 7 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-5959A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672904 | ||||||
| chr2:43672913
|
C | T | 3 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095 | 3 | HG02559.hp2 HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.124-5950C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672913 | ||||||
| chr2:43672941
|
C | T | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-5922C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672941 | ||||||
| chr2:43672977
|
A | C | 2 | a0001c0009t0002g0123a0001c0009t0002g0124 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.124-5886A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43672977 | ||||||
| chr2:43673159
|
C | T | 3 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093 | 3 | HG02622.hp1 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.124-5704C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673159 | ||||||
| chr2:43673222
|
A | T | 1 | a0002c0011t0008g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.124-5641A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673222 | ||||||
| chr2:43673251
|
C | A | 152 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-5612C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673251 | ||||||
| chr2:43673296
|
A | T | 174 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.124-5567A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673296 | ||||||
| chr2:43673490
|
C | T | 5 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(2): Show | 5 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-5373C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673490 | ||||||
| chr2:43673491
|
G | A | 4 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145others(1): Show | 4 | HG02055.hp1 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-5372G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673491 | ||||||
| chr2:43673859
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(156): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.124-5004T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673859 | ||||||
| chr2:43673891
|
C | G | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124-4972C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43673891 | ||||||
| chr2:43674040
|
G | C | 59 | a0001c0001t0001g0048a0001c0001t0001g0170a0001c0001t0001g0172others(56): Show | 59 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.124-4823G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674040 | ||||||
| chr2:43674073
|
T | A | 4 | a0001c0003t0001g0203a0003c0004t0002g0183a0004c0010t0006g0206others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-4790T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674073 | ||||||
| chr2:43674147
|
G | T | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.124-4716G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674147 | ||||||
| chr2:43674210
|
A | G | 1 | a0001c0002t0002g0233 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.124-4653A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674210 | ||||||
| chr2:43674347
|
T | C | 2 | a0001c0003t0001g0188a0001c0003t0001g0189 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.124-4516T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674347 | ||||||
| chr2:43674352
|
T | G | 3 | a0001c0007t0001g0191a0003c0004t0002g0100a0012c0053t0002g0121 | 3 | HG02280.hp2 HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.124-4511T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674352 | ||||||
| chr2:43674474
|
T | A | 154 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.124-4389T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674474 | ||||||
| chr2:43674648
|
C | A | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-4215C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674648 | ||||||
| chr2:43674651
|
C | T | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-4212C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674651 | ||||||
| chr2:43674712
|
T | C | 154 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.124-4151T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674712 | ||||||
| chr2:43674756
|
A | G | 158 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.124-4107A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674756 | ||||||
| chr2:43674757
|
T | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-4106T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674757 | ||||||
| chr2:43674776
|
G | A | 155 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-4087G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674776 | ||||||
| chr2:43674791
|
T | C | 158 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.124-4072T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674791 | ||||||
| chr2:43674933
|
C | T | 4 | a0001c0001t0001g0078a0001c0051t0001g0082a0002c0005t0003g0083others(1): Show | 4 | HG00741.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-3930C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674933 | ||||||
| chr2:43674984
|
C | CA | 12 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-3864dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43674984 | |||||
| chr2:43674991
|
A | C | 3 | a0001c0007t0001g0191a0003c0004t0002g0100a0004c0038t0006g0093 | 3 | HG02622.hp1 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.124-3872A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43674991 | ||||||
| chr2:43675289
|
G | A | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.124-3574G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675289 | ||||||
| chr2:43675372
|
G | C | 154 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.124-3491G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675372 | ||||||
| chr2:43675448
|
C | T | 1 | a0004c0010t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.124-3415C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675448 | ||||||
| chr2:43675618
|
C | G | 7 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0002g0160others(4): Show | 7 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-3245C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675618 | ||||||
| chr2:43675624
|
A | C | 2 | a0001c0003t0001g0004a0001c0003t0001g0087 | 2 | HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.124-3239A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675624 | ||||||
| chr2:43675709
|
C | A | 20 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(17): Show | 20 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-3154C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675709 | ||||||
| chr2:43675895
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0058 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.124-2968G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675895 | ||||||
| chr2:43675927
|
A | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-2936A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675927 | ||||||
| chr2:43675993
|
A | G | 5 | a0002c0005t0003g0143a0008c0017t0006g0162a0012c0054t0002g0166others(2): Show | 5 | HG02970.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-2870A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43675993 | ||||||
| chr2:43676025
|
G | C | 1 | a0001c0003t0001g0004 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.124-2838G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676025 | ||||||
| chr2:43676123
|
C | A | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-2740C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676123 | ||||||
| chr2:43676175
|
T | C | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.124-2688T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676175 | ||||||
| chr2:43676215
|
T | C | 142 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.124-2648T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676215 | ||||||
| chr2:43676344
|
T | C | 161 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0029others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.124-2519T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676344 | ||||||
| chr2:43676367
|
G | C | 2 | a0001c0007t0001g0191a0003c0004t0002g0100 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.124-2496G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676367 | ||||||
| chr2:43676381
|
G | A | 6 | a0001c0007t0001g0003a0001c0007t0001g0010a0001c0007t0001g0018others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-2482G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676381 | ||||||
| chr2:43676385
|
C | T | 2 | a0001c0007t0001g0191a0003c0004t0002g0100 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.124-2478C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676385 | ||||||
| chr2:43676433
|
T | A | 2 | a0001c0009t0002g0106a0003c0004t0002g0107 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.124-2430T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676433 | ||||||
| chr2:43676466
|
G | C | 1 | a0001c0001t0002g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.124-2397G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676466 | ||||||
| chr2:43676510
|
C | G | 2 | a0003c0004t0002g0097a0003c0004t0002g0098 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.124-2353C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676510 | ||||||
| chr2:43676648
|
T | A | 57 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(54): Show | 57 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.124-2215T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676648 | ||||||
| chr2:43676704
|
G | A | 3 | a0001c0009t0002g0106a0003c0004t0002g0107a0008c0017t0006g0211 | 3 | HG01243.hp2 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.124-2159G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676704 | ||||||
| chr2:43676872
|
C | T | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-1991C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676872 | ||||||
| chr2:43676933
|
A | G | 1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.124-1930A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676933 | ||||||
| chr2:43676999
|
A | G | 176 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.124-1864A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43676999 | ||||||
| chr2:43677048
|
C | T | 20 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(17): Show | 20 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-1815C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677048 | ||||||
| chr2:43677152
|
T | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-1711T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677152 | ||||||
| chr2:43677169
|
G | C | 156 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-1694G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677169 | ||||||
| chr2:43677203
|
G | GT | 49 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(46): Show | 49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.124-1647dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43677203 | |||||
| chr2:43677203
|
GT | G | 16 | a0001c0003t0002g0122a0001c0007t0001g0101a0001c0018t0002g0149others(13): Show | 16 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-1647delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43677203 | |||||
| chr2:43677320
|
G | A | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-1543G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677320 | ||||||
| chr2:43677334
|
A | G | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-1529A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677334 | ||||||
| chr2:43677463
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.124-1400C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677463 | ||||||
| chr2:43677489
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-1374A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677489 | ||||||
| chr2:43677603
|
C | T | 153 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.124-1260C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677603 | ||||||
| chr2:43677613
|
C | T | 51 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.124-1250C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677613 | ||||||
| chr2:43677624
|
C | T | 3 | a0002c0005t0002g0054a0002c0005t0002g0056a0002c0005t0002g0057 | 3 | NA18962.hp1 NA18977.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.124-1239C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677624 | ||||||
| chr2:43677625
|
G | A | 9 | a0001c0018t0002g0149a0001c0018t0002g0150a0005c0008t0001g0153others(6): Show | 9 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-1238G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677625 | ||||||
| chr2:43677665
|
C | T | 7 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-1198C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677665 | ||||||
| chr2:43677723
|
A | C | 107 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-1140A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677723 | ||||||
| chr2:43677729
|
G | A | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-1134G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677729 | ||||||
| chr2:43677776
|
T | C | 176 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.124-1087T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677776 | ||||||
| chr2:43677800
|
C | T | 107 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-1063C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677800 | ||||||
| chr2:43677809
|
C | T | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-1054C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677809 | ||||||
| chr2:43677810
|
A | G | 156 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-1053A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677810 | ||||||
| chr2:43677831
|
A | AC | 18 | a0001c0001t0001g0070a0001c0001t0001g0172a0001c0002t0002g0233others(15): Show | 18 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.124-1023dupC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43677831 | |||||
| chr2:43677834
|
C | T | 7 | a0001c0001t0001g0006a0001c0007t0001g0003a0001c0007t0001g0010others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-1029C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677834 | ||||||
| chr2:43677851
|
C | T | 13 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(10): Show | 13 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.124-1012C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677851 | ||||||
| chr2:43677855
|
C | T | 1 | a0002c0006t0003g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-1008C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677855 | ||||||
| chr2:43677856
|
G | A | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-1007G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677856 | ||||||
| chr2:43677869
|
G | C | 1 | a0003c0004t0002g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-994G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677869 | ||||||
| chr2:43677872
|
C | T | 6 | a0001c0002t0002g0218a0001c0002t0002g0223a0001c0002t0002g0224others(3): Show | 6 | HG02155.hp1 NA18952.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-991C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677872 | ||||||
| chr2:43677873
|
G | T | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-990G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677873 | ||||||
| chr2:43677885
|
T | C | 68 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(65): Show | 68 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.124-978T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677885 | ||||||
| chr2:43677885
|
T | G | 108 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.124-978T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677885 | ||||||
| chr2:43677901
|
GGACGGGG others(42): Show |
G | 107 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-948_124-900del others(49): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43677901 | |||||
| chr2:43677904
|
CGGGGCGG others(43): Show |
C | 1 | a0001c0003t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.124-955_124-906del others(50): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43677904 | |||||
| chr2:43677953
|
C | T | 1 | a0005c0008t0003g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.124-910C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677953 | ||||||
| chr2:43677958
|
C | T | 2 | a0001c0009t0002g0123a0001c0009t0002g0124 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.124-905C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677958 | ||||||
| chr2:43677970
|
G | A | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-893G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43677970 | ||||||
| chr2:43678038
|
C | T | 94 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(91): Show | 94 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.124-825C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678038 | ||||||
| chr2:43678043
|
TGGCAGAG others(33): Show |
T | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124-812_124-773del others(40): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43678043 | |||||
| chr2:43678111
|
C | G | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-752C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678111 | ||||||
| chr2:43678111
|
C | T | 20 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(17): Show | 20 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-752C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678111 | ||||||
| chr2:43678115
|
C | T | 2 | a0001c0007t0001g0191a0003c0004t0002g0100 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.124-748C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678115 | ||||||
| chr2:43678147
|
A | C | 176 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.124-716A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678147 | ||||||
| chr2:43678153
|
G | A | 1 | a0001c0003t0002g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124-710G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678153 | ||||||
| chr2:43678158
|
C | G | 108 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.124-705C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678158 | ||||||
| chr2:43678177
|
C | G | 3 | a0002c0005t0003g0002a0002c0005t0003g0069a0002c0005t0011g0013 | 3 | HG01192.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.124-686C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678177 | ||||||
| chr2:43678221
|
C | G | 48 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(45): Show | 48 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.124-642C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678221 | ||||||
| chr2:43678245
|
G | T | 51 | a0001c0001t0001g0048a0001c0001t0001g0170a0001c0001t0001g0172others(48): Show | 51 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.124-618G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678245 | ||||||
| chr2:43678285
|
G | A | 52 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(49): Show | 52 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.124-578G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678285 | ||||||
| chr2:43678297
|
C | G | 94 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(91): Show | 94 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.124-566C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678297 | ||||||
| chr2:43678299
|
A | G | 2 | a0002c0016t0002g0091a0017c0036t0001g0099 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-564A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678299 | ||||||
| chr2:43678302
|
C | G | 2 | a0001c0009t0002g0106a0003c0004t0002g0107 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.124-561C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678302 | ||||||
| chr2:43678385
|
C | T | 105 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.124-478C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678385 | ||||||
| chr2:43678386
|
C | G | 108 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.124-477C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678386 | ||||||
| chr2:43678412
|
T | C | 4 | a0001c0002t0002g0209a0001c0007t0001g0191a0003c0004t0002g0100others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-451T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678412 | ||||||
| chr2:43678524
|
A | G | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-339A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678524 | ||||||
| chr2:43678528
|
C | T | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-335C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678528 | ||||||
| chr2:43678580
|
C | T | 2 | a0001c0007t0001g0191a0003c0004t0002g0100 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.124-283C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678580 | ||||||
| chr2:43678581
|
G | A | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-282G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678581 | ||||||
| chr2:43678583
|
G | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0109others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-280G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678583 | ||||||
| chr2:43678602
|
C | G | 3 | a0003c0004t0002g0115a0003c0004t0002g0116a0003c0004t0017g0117 | 3 | HG01106.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124-261C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678602 | ||||||
| chr2:43678648
|
G | A | 1 | a0008c0017t0006g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.124-215G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678648 | ||||||
| chr2:43678679
|
C | T | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-184C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678679 | ||||||
| chr2:43678728
|
AGAGGTGG others(5): Show |
A | 3 | a0001c0009t0002g0106a0003c0004t0002g0107a0008c0017t0006g0211 | 3 | HG01243.hp2 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.124-126_124-115del others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43678728 | |||||
| chr2:43678737
|
A | AGTGGAGG others(5): Show |
12 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-99_124-88dupGG others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43678737 | |||||
| chr2:43678737
|
A | G | 44 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.124-126A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678737 | ||||||
| chr2:43678759
|
G | GAGGTGGA others(5): Show |
89 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0170others(86): Show | 89 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.124-93_124-92insCA others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43678759 | |||||
| chr2:43678759
|
G | GAGGTGGA others(11): Show |
4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-88_124-87insGC others(16): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 43678759 | |||||
| chr2:43678796
|
G | A | 2 | a0001c0007t0001g0191a0003c0004t0002g0100 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.124-67G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678796 | ||||||
| chr2:43678798
|
C | G | 5 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(2): Show | 5 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-65C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678798 | ||||||
| chr2:43678838
|
A | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-25A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 2/29 | chr2 | 43678838 | ||||||
| chr2:43679066
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.186+141T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679066 | ||||||
| chr2:43679217
|
T | G | 1 | a0003c0013t0002g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.186+292T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679217 | ||||||
| chr2:43679248
|
G | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186+323G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679248 | ||||||
| chr2:43679372
|
T | G | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.186+447T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679372 | ||||||
| chr2:43679396
|
A | C | 106 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(103): Show | 106 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.186+471A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679396 | ||||||
| chr2:43679407
|
TA | T | 176 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.186+491delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43679407 | |||||
| chr2:43679471
|
C | T | 1 | a0001c0003t0001g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.186+546C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679471 | ||||||
| chr2:43679494
|
CT | C | 13 | a0001c0001t0001g0222a0001c0003t0001g0155a0001c0003t0001g0157others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.186+588delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43679494 | |||||
| chr2:43679494
|
CTT | C | 91 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.186+587_186+588del others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43679494 | |||||
| chr2:43679494
|
CTTT | C | 50 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(47): Show | 50 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.186+586_186+588del others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43679494 | |||||
| chr2:43679494
|
CTTTT | C | 20 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(17): Show | 20 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(17): Show |
intron_variant | MODIFIER | c.186+585_186+588del others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43679494 | |||||
| chr2:43679567
|
C | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.186+642C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679567 | ||||||
| chr2:43679595
|
A | G | 1 | a0003c0044t0007g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186+670A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679595 | ||||||
| chr2:43679605
|
C | G | 93 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.186+680C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679605 | ||||||
| chr2:43679639
|
G | A | 1 | a0001c0030t0001g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.186+714G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679639 | ||||||
| chr2:43679650
|
C | A | 60 | a0001c0001t0001g0048a0001c0001t0001g0170a0001c0001t0001g0172others(57): Show | 60 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.186+725C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679650 | ||||||
| chr2:43679758
|
G | A | 11 | a0001c0003t0002g0122a0001c0018t0002g0149a0001c0018t0002g0150others(8): Show | 11 | HG01168.hp2 HG01975.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+833G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679758 | ||||||
| chr2:43679863
|
G | T | 3 | a0001c0007t0001g0191a0003c0004t0002g0100a0012c0053t0002g0121 | 3 | HG02280.hp2 HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.186+938G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679863 | ||||||
| chr2:43679877
|
G | A | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+952G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679877 | ||||||
| chr2:43679959
|
C | T | 1 | a0003c0004t0002g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.186+1034C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679959 | ||||||
| chr2:43679969
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.186+1044T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43679969 | ||||||
| chr2:43680022
|
T | TG | 176 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.186+1097_186+1098i others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680022 | ||||||
| chr2:43680152
|
T | A | 105 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.186+1227T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680152 | ||||||
| chr2:43680266
|
A | G | 4 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145others(1): Show | 4 | HG02055.hp1 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+1341A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680266 | ||||||
| chr2:43680320
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.186+1395G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680320 | ||||||
| chr2:43680368
|
TG | T | 82 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.186+1445delG | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43680368 | |||||
| chr2:43680448
|
A | G | 1 | a0003c0012t0004g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186+1523A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680448 | ||||||
| chr2:43680491
|
C | A | 31 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0187others(28): Show | 31 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.186+1566C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680491 | ||||||
| chr2:43680657
|
T | A | 107 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.186+1732T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680657 | ||||||
| chr2:43680707
|
G | A | 4 | a0001c0007t0001g0101a0002c0006t0002g0096a0003c0004t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+1782G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680707 | ||||||
| chr2:43680772
|
G | C | 175 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.186+1847G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680772 | ||||||
| chr2:43680794
|
C | A | 1 | a0003c0022t0002g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186+1869C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680794 | ||||||
| chr2:43680799
|
C | T | 106 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0001g0112others(103): Show | 106 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.186+1874C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680799 | ||||||
| chr2:43680816
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.186+1891T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680816 | ||||||
| chr2:43680993
|
A | G | 10 | a0001c0001t0001g0009a0001c0018t0002g0149a0001c0018t0002g0150others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+2068A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43680993 | ||||||
| chr2:43681012
|
C | G | 5 | a0002c0005t0003g0143a0008c0017t0006g0162a0012c0054t0002g0166others(2): Show | 5 | HG02970.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+2087C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681012 | ||||||
| chr2:43681136
|
C | T | 1 | a0003c0022t0002g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186+2211C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681136 | ||||||
| chr2:43681179
|
A | G | 7 | a0001c0001t0001g0006a0001c0007t0001g0003a0001c0007t0001g0010others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+2254A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681179 | ||||||
| chr2:43681338
|
T | C | 12 | a0001c0001t0001g0009a0001c0003t0002g0122a0001c0018t0002g0149others(9): Show | 12 | HG01168.hp2 HG01975.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.186+2413T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681338 | ||||||
| chr2:43681366
|
T | A | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186+2441T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681366 | ||||||
| chr2:43681405
|
T | C | 49 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(46): Show | 49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.186+2480T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681405 | ||||||
| chr2:43681499
|
C | T | 8 | a0002c0006t0002g0146a0004c0010t0005g0092a0004c0010t0005g0094others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+2574C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681499 | ||||||
| chr2:43681540
|
G | C | 1 | a0002c0005t0011g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.186+2615G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681540 | ||||||
| chr2:43681550
|
T | C | 105 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.186+2625T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681550 | ||||||
| chr2:43681623
|
A | G | 49 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(46): Show | 49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.186+2698A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681623 | ||||||
| chr2:43681646
|
A | G | 1 | a0001c0003t0001g0004 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.186+2721A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681646 | ||||||
| chr2:43681881
|
A | C | 43 | a0001c0001t0002g0210a0001c0002t0001g0005a0001c0002t0001g0104others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.186+2956A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681881 | ||||||
| chr2:43681912
|
T | A | 105 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0109others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.186+2987T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681912 | ||||||
| chr2:43681998
|
C | T | 46 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(43): Show | 46 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.186+3073C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43681998 | ||||||
| chr2:43682065
|
C | G | 4 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145others(1): Show | 4 | HG02055.hp1 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+3140C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682065 | ||||||
| chr2:43682129
|
C | T | 98 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0170others(95): Show | 98 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.186+3204C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682129 | ||||||
| chr2:43682184
|
A | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0170others(87): Show | 90 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.186+3259A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682184 | ||||||
| chr2:43682239
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(107): Show | 110 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.186+3314G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682239 | ||||||
| chr2:43682252
|
A | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.186+3327A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682252 | ||||||
| chr2:43682339
|
C | T | 1 | a0002c0006t0003g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186+3414C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682339 | ||||||
| chr2:43682465
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0002g0075 | 2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.186+3540C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682465 | ||||||
| chr2:43682473
|
AT | A | 4 | a0001c0002t0002g0130a0002c0006t0002g0146a0011c0033t0002g0103others(1): Show | 4 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+3554delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43682473 | |||||
| chr2:43682480
|
G | A | 5 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139others(2): Show | 5 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+3555G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682480 | ||||||
| chr2:43682521
|
G | A | 1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.186+3596G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682521 | ||||||
| chr2:43682527
|
G | A | 3 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0001g0179 | 3 | HG01109.hp2 HG03579.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.186+3602G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682527 | ||||||
| chr2:43682548
|
G | GC | 6 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+3629dupC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43682548 | |||||
| chr2:43682585
|
A | G | 1 | a0003c0022t0002g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186+3660A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682585 | ||||||
| chr2:43682589
|
G | A | 1 | a0002c0005t0002g0020 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.186+3664G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682589 | ||||||
| chr2:43682595
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.186+3670G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682595 | ||||||
| chr2:43682601
|
A | G | 1 | a0001c0002t0001g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.186+3676A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682601 | ||||||
| chr2:43682625
|
A | G | 9 | a0001c0003t0001g0195a0001c0003t0001g0196a0002c0005t0003g0190others(6): Show | 9 | HG01074.hp2 HG01361.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+3700A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682625 | ||||||
| chr2:43682639
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.186+3714G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682639 | ||||||
| chr2:43682675
|
C | T | 4 | a0001c0002t0002g0221a0001c0002t0002g0227a0001c0002t0002g0228others(1): Show | 4 | HG01358.hp2 HG01978.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+3750C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682675 | ||||||
| chr2:43682714
|
A | G | 5 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139others(2): Show | 5 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+3789A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682714 | ||||||
| chr2:43682739
|
C | A | 143 | a0001c0001t0001g0067a0001c0001t0001g0170a0001c0001t0001g0172others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.186+3814C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682739 | ||||||
| chr2:43682827
|
T | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0170others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.186+3902T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682827 | ||||||
| chr2:43682834
|
T | G | 13 | a0001c0018t0002g0149a0001c0018t0002g0150a0002c0006t0002g0146others(10): Show | 13 | HG01168.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.186+3909T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682834 | ||||||
| chr2:43682841
|
C | T | 45 | a0001c0001t0001g0001a0001c0002t0001g0005a0001c0002t0001g0104others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.186+3916C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682841 | ||||||
| chr2:43682902
|
C | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0170a0001c0001t0001g0172others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.186+3977C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682902 | ||||||
| chr2:43682939
|
T | TAC | 95 | a0001c0001t0001g0067a0001c0001t0001g0170a0001c0001t0001g0172others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.186+4036_186+4037d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43682939 | |||||
| chr2:43682939
|
T | TATACAC | 3 | a0002c0005t0003g0143a0012c0054t0002g0166a0021c0052t0006g0144 | 3 | HG02976.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.186+4015_186+4016i others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43682939 | |||||
| chr2:43682939
|
T | TATACACA others(1): Show |
11 | a0002c0006t0002g0146a0002c0006t0003g0163a0003c0013t0002g0114others(8): Show | 11 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+4015_186+4016i others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43682939 | |||||
| chr2:43682941
|
C | T | 100 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.186+4016C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682941 | ||||||
| chr2:43682967
|
G | C | 1 | a0004c0010t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.186+4042G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682967 | ||||||
| chr2:43682993
|
A | G | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.186+4068A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43682993 | ||||||
| chr2:43683023
|
G | A | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.186+4098G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683023 | ||||||
| chr2:43683024
|
A | G | 1 | a0003c0044t0007g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186+4099A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683024 | ||||||
| chr2:43683124
|
T | G | 7 | a0002c0005t0003g0143a0008c0017t0006g0162a0008c0017t0006g0211others(4): Show | 7 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+4199T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683124 | ||||||
| chr2:43683142
|
C | CT | 105 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0170others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.186+4237dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43683142 | |||||
| chr2:43683142
|
C | CTT | 44 | a0001c0001t0001g0001a0001c0001t0002g0210a0001c0002t0001g0005others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.186+4236_186+4237d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43683142 | |||||
| chr2:43683231
|
C | T | 1 | a0001c0045t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.186+4306C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683231 | ||||||
| chr2:43683240
|
C | T | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.186+4315C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683240 | ||||||
| chr2:43683311
|
G | C | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.186+4386G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683311 | ||||||
| chr2:43683348
|
G | A | 2 | a0007c0014t0001g0142a0017c0036t0001g0099 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.186+4423G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683348 | ||||||
| chr2:43683560
|
C | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+4635C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683560 | ||||||
| chr2:43683577
|
A | T | 15 | a0001c0001t0001g0009a0001c0018t0002g0149a0001c0018t0002g0150others(12): Show | 15 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+4652A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683577 | ||||||
| chr2:43683652
|
T | A | 168 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0187others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.186+4727T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683652 | ||||||
| chr2:43683695
|
A | T | 43 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.186+4770A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683695 | ||||||
| chr2:43683766
|
A | G | 16 | a0001c0002t0001g0104a0001c0002t0001g0242a0001c0002t0001g0243others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.186+4841A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683766 | ||||||
| chr2:43683784
|
C | CT | 46 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.186+4869dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43683784 | |||||
| chr2:43683871
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.186+4946G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43683871 | ||||||
| chr2:43684051
|
C | G | 14 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(11): Show | 14 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.186+5126C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684051 | ||||||
| chr2:43684177
|
T | C | 90 | a0001c0001t0001g0067a0001c0001t0001g0187a0001c0001t0001g0205others(87): Show | 90 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.186+5252T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684177 | ||||||
| chr2:43684214
|
T | A | 1 | a0001c0003t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.186+5289T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684214 | ||||||
| chr2:43684222
|
C | G | 15 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+5297C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684222 | ||||||
| chr2:43684282
|
C | A | 45 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.186+5357C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684282 | ||||||
| chr2:43684542
|
C | T | 41 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.186+5617C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684542 | ||||||
| chr2:43684616
|
C | T | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.186+5691C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684616 | ||||||
| chr2:43684628
|
A | T | 14 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(11): Show | 14 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.186+5703A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684628 | ||||||
| chr2:43684666
|
A | G | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.186+5741A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684666 | ||||||
| chr2:43684733
|
A | G | 15 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(12): Show | 15 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+5808A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684733 | ||||||
| chr2:43684784
|
A | G | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186+5859A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684784 | ||||||
| chr2:43684819
|
C | CA | 67 | a0001c0001t0001g0027a0001c0002t0002g0221a0001c0003t0001g0087others(64): Show | 67 | HG00738.hp1 HG00738.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.186+5911dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43684819 | |||||
| chr2:43684827
|
A | AG | 3 | a0001c0003t0001g0203a0003c0004t0002g0183a0004c0010t0006g0206 | 3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.186+5902_186+5903i others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684827 | ||||||
| chr2:43684835
|
A | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186+5910A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684835 | ||||||
| chr2:43684850
|
A | G | 5 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+5925A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684850 | ||||||
| chr2:43684870
|
G | T | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.186+5945G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684870 | ||||||
| chr2:43684877
|
C | G | 5 | a0003c0004t0002g0100a0003c0004t0002g0248a0007c0014t0001g0142others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+5952C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684877 | ||||||
| chr2:43684889
|
G | T | 78 | a0001c0001t0001g0067a0001c0001t0001g0187a0001c0001t0001g0205others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.186+5964G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684889 | ||||||
| chr2:43684925
|
C | G | 167 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0187others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.186+6000C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43684925 | ||||||
| chr2:43685074
|
T | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.186+6149T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685074 | ||||||
| chr2:43685094
|
G | A | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.186+6169G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685094 | ||||||
| chr2:43685213
|
A | T | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+6288A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685213 | ||||||
| chr2:43685350
|
A | G | 1 | a0001c0003t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.186+6425A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685350 | ||||||
| chr2:43685406
|
T | C | 154 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0187others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.186+6481T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685406 | ||||||
| chr2:43685422
|
C | G | 77 | a0001c0001t0001g0067a0001c0001t0001g0187a0001c0001t0001g0205others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.186+6497C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685422 | ||||||
| chr2:43685467
|
A | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+6542A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685467 | ||||||
| chr2:43685559
|
C | G | 14 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(11): Show | 14 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.186+6634C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685559 | ||||||
| chr2:43685596
|
G | T | 164 | a0001c0001t0001g0067a0001c0001t0001g0187a0001c0001t0001g0205others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.186+6671G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685596 | ||||||
| chr2:43685606
|
C | CT | 87 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0187others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.186+6697dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43685606 | |||||
| chr2:43685638
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.186+6713C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685638 | ||||||
| chr2:43685705
|
G | C | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186+6780G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685705 | ||||||
| chr2:43685918
|
A | G | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.187-6596A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685918 | ||||||
| chr2:43685926
|
T | C | 1 | a0013c0026t0002g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.187-6588T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43685926 | ||||||
| chr2:43686081
|
T | C | 54 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(51): Show | 54 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.187-6433T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686081 | ||||||
| chr2:43686146
|
TTCTTCCT others(6): Show |
T | 5 | a0001c0009t0002g0126a0001c0009t0002g0128a0002c0011t0002g0127others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-6347_187-6335d others(15): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43686146 | |||||
| chr2:43686168
|
C | G | 7 | a0002c0005t0003g0143a0008c0017t0006g0162a0008c0017t0006g0211others(4): Show | 7 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-6346C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686168 | ||||||
| chr2:43686275
|
C | G | 15 | a0001c0002t0001g0104a0001c0002t0001g0242a0001c0002t0001g0243others(12): Show | 15 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-6239C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686275 | ||||||
| chr2:43686285
|
C | T | 1 | a0001c0002t0002g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.187-6229C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686285 | ||||||
| chr2:43686408
|
G | A | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.187-6106G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686408 | ||||||
| chr2:43686611
|
T | A | 54 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(51): Show | 54 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.187-5903T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686611 | ||||||
| chr2:43686690
|
G | A | 1 | a0004c0010t0006g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.187-5824G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686690 | ||||||
| chr2:43686724
|
G | T | 1 | a0001c0002t0002g0221 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.187-5790G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686724 | ||||||
| chr2:43686787
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.187-5727T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686787 | ||||||
| chr2:43686857
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.187-5657T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686857 | ||||||
| chr2:43686896
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.187-5618G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686896 | ||||||
| chr2:43686908
|
G | A | 3 | a0001c0002t0002g0130a0002c0016t0002g0091a0020c0046t0003g0165 | 3 | HG02615.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.187-5606G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686908 | ||||||
| chr2:43686974
|
A | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0187a0001c0002t0002g0201others(36): Show | 39 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.187-5540A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686974 | ||||||
| chr2:43686976
|
A | C | 1 | a0004c0010t0006g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.187-5538A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43686976 | ||||||
| chr2:43686980
|
ATT | A | 166 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0187others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.187-5532_187-5531d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43686980 | |||||
| chr2:43687024
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.187-5490G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687024 | ||||||
| chr2:43687139
|
T | C | 167 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0187others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.187-5375T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687139 | ||||||
| chr2:43687170
|
A | T | 4 | a0001c0003t0001g0180a0002c0006t0002g0182a0003c0022t0002g0164others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-5344A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687170 | ||||||
| chr2:43687236
|
G | C | 53 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(50): Show | 53 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.187-5278G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687236 | ||||||
| chr2:43687241
|
T | A | 2 | a0002c0005t0002g0054a0002c0005t0002g0056 | 2 | NA18977.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.187-5273T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687241 | ||||||
| chr2:43687243
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.187-5271G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687243 | ||||||
| chr2:43687272
|
C | T | 1 | a0001c0003t0001g0195 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.187-5242C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687272 | ||||||
| chr2:43687304
|
G | A | 1 | a0002c0006t0002g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.187-5210G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687304 | ||||||
| chr2:43687325
|
T | G | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-5189T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687325 | ||||||
| chr2:43687373
|
A | G | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.187-5141A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687373 | ||||||
| chr2:43687435
|
G | A | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-5079G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687435 | ||||||
| chr2:43687630
|
C | G | 15 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(12): Show | 15 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-4884C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687630 | ||||||
| chr2:43687647
|
T | C | 44 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.187-4867T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687647 | ||||||
| chr2:43687710
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.187-4804T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687710 | ||||||
| chr2:43687820
|
A | C | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-4694A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687820 | ||||||
| chr2:43687908
|
C | T | 3 | a0001c0003t0002g0122a0002c0006t0004g0108a0023c0031t0016g0090 | 3 | HG02922.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187-4606C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687908 | ||||||
| chr2:43687986
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0041 | 2 | NA18978.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.187-4528A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687986 | ||||||
| chr2:43687988
|
A | G | 2 | a0003c0004t0002g0097a0003c0004t0002g0098 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.187-4526A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687988 | ||||||
| chr2:43687992
|
G | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.187-4522G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43687992 | ||||||
| chr2:43688049
|
C | G | 15 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(12): Show | 15 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-4465C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43688049 | ||||||
| chr2:43688246
|
A | C | 31 | a0001c0002t0002g0201a0001c0003t0001g0004a0001c0003t0001g0023others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.187-4268A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43688246 | ||||||
| chr2:43688593
|
G | A | 9 | a0001c0003t0001g0076a0001c0003t0001g0154a0001c0003t0001g0155others(6): Show | 9 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.187-3921G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43688593 | ||||||
| chr2:43688755
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.187-3759G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43688755 | ||||||
| chr2:43688807
|
G | A | 15 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(12): Show | 15 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-3707G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43688807 | ||||||
| chr2:43688902
|
G | C | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.187-3612G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43688902 | ||||||
| chr2:43688995
|
GC | G | 44 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.187-3515delC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43688995 | |||||
| chr2:43689153
|
G | A | 1 | a0001c0007t0001g0062 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.187-3361G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689153 | ||||||
| chr2:43689196
|
G | A | 2 | a0001c0003t0001g0188a0001c0003t0001g0189 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.187-3318G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689196 | ||||||
| chr2:43689210
|
C | T | 15 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(12): Show | 15 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-3304C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689210 | ||||||
| chr2:43689224
|
G | C | 2 | a0001c0003t0002g0122a0002c0006t0004g0108 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.187-3290G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689224 | ||||||
| chr2:43689226
|
A | C | 1 | a0002c0005t0003g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.187-3288A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689226 | ||||||
| chr2:43689349
|
A | T | 1 | a0005c0008t0002g0255 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.187-3165A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689349 | ||||||
| chr2:43689364
|
C | A | 45 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.187-3150C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689364 | ||||||
| chr2:43689500
|
T | G | 3 | a0001c0001t0002g0031a0001c0001t0002g0058a0001c0001t0002g0210 | 3 | HG03688.hp1 HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.187-3014T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689500 | ||||||
| chr2:43689599
|
A | G | 167 | a0001c0001t0001g0009a0001c0002t0001g0005a0001c0002t0001g0104others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.187-2915A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689599 | ||||||
| chr2:43689625
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.187-2889T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689625 | ||||||
| chr2:43689816
|
C | T | 43 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.187-2698C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43689816 | ||||||
| chr2:43690170
|
G | A | 14 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(11): Show | 14 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.187-2344G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43690170 | ||||||
| chr2:43690346
|
C | CT | 7 | a0002c0005t0003g0143a0008c0017t0006g0162a0008c0017t0006g0211others(4): Show | 7 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-2157dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43690346 | |||||
| chr2:43690562
|
T | G | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.187-1952T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43690562 | ||||||
| chr2:43690564
|
C | A | 51 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.187-1950C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43690564 | ||||||
| chr2:43690648
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.187-1866T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43690648 | ||||||
| chr2:43690795
|
T | C | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.187-1719T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43690795 | ||||||
| chr2:43690918
|
T | C | 1 | a0002c0006t0003g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.187-1596T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43690918 | ||||||
| chr2:43691227
|
A | C | 3 | a0001c0009t0002g0126a0001c0009t0002g0128a0003c0039t0004g0125 | 3 | HG02257.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.187-1287A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691227 | ||||||
| chr2:43691227
|
A | G | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-1287A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691227 | ||||||
| chr2:43691231
|
A | T | 6 | a0001c0003t0002g0122a0002c0006t0004g0108a0004c0010t0005g0092others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-1283A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691231 | ||||||
| chr2:43691282
|
G | A | 1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.187-1232G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691282 | ||||||
| chr2:43691501
|
G | A | 1 | a0003c0013t0002g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.187-1013G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691501 | ||||||
| chr2:43691508
|
C | T | 1 | a0011c0034t0002g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187-1006C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691508 | ||||||
| chr2:43691549
|
G | T | 1 | a0002c0006t0002g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.187-965G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691549 | ||||||
| chr2:43691600
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.187-914A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691600 | ||||||
| chr2:43691686
|
T | A | 1 | a0003c0013t0002g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.187-828T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43691686 | ||||||
| chr2:43691686
|
TA | T | 7 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0003g0069others(4): Show | 7 | HG01192.hp2 HG02257.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-821delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 43691686 | |||||
| chr2:43692043
|
T | C | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.187-471T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43692043 | ||||||
| chr2:43692213
|
C | T | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-301C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43692213 | ||||||
| chr2:43692255
|
T | C | 46 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.187-259T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 3/29 | chr2 | 43692255 | ||||||
| chr2:43692777
|
C | T | 2 | a0010c0019t0005g0071a0010c0019t0005g0073 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.336+114C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43692777 | ||||||
| chr2:43692795
|
G | C | 42 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.336+132G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43692795 | ||||||
| chr2:43692815
|
AG | A | 41 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.336+154delG | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43692815 | |||||
| chr2:43692882
|
A | T | 53 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(50): Show | 53 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.336+219A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43692882 | ||||||
| chr2:43692896
|
G | A | 1 | a0003c0004t0002g0137 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.336+233G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43692896 | ||||||
| chr2:43692943
|
T | G | 2 | a0001c0003t0001g0155a0001c0003t0001g0157 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.336+280T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43692943 | ||||||
| chr2:43692979
|
T | G | 6 | a0001c0003t0002g0122a0002c0006t0004g0108a0004c0010t0005g0092others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.336+316T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43692979 | ||||||
| chr2:43693102
|
AT | A | 150 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.336+450delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693102 | |||||
| chr2:43693102
|
ATT | A | 13 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(10): Show | 13 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.336+449_336+450del others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693102 | |||||
| chr2:43693116
|
G | A | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.336+453G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693116 | ||||||
| chr2:43693123
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.336+460A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693123 | ||||||
| chr2:43693199
|
A | G | 46 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.336+536A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693199 | ||||||
| chr2:43693204
|
C | T | 1 | a0001c0002t0002g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.336+541C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693204 | ||||||
| chr2:43693218
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0067others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.336+555C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693218 | ||||||
| chr2:43693289
|
A | C | 13 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(10): Show | 13 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.336+626A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693289 | ||||||
| chr2:43693528
|
A | G | 12 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.336+865A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693528 | ||||||
| chr2:43693552
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.337-879G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693552 | ||||||
| chr2:43693592
|
C | T | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.337-839C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693592 | ||||||
| chr2:43693658
|
A | G | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.337-773A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693658 | ||||||
| chr2:43693705
|
C | G | 33 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(30): Show | 33 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.337-726C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693705 | ||||||
| chr2:43693706
|
T | C | 51 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(48): Show | 51 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.337-725T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693706 | ||||||
| chr2:43693708
|
A | G | 146 | a0001c0001t0001g0009a0001c0002t0001g0005a0001c0002t0001g0104others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.337-723A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693708 | ||||||
| chr2:43693723
|
C | CAAAAAAA others(3): Show |
6 | a0001c0018t0002g0149a0001c0018t0002g0150a0002c0006t0004g0108others(3): Show | 6 | HG01099.hp2 HG02074.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-700_337-691dup others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693723
|
C | CAAAAAAA others(4): Show |
73 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0242others(70): Show | 73 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.337-701_337-691dup others(11): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693723
|
C | CAAAAAAA others(5): Show |
44 | a0001c0002t0001g0225a0001c0002t0002g0130a0001c0002t0002g0224others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.337-702_337-691dup others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693723
|
C | CAAAAAAA others(6): Show |
24 | a0001c0002t0002g0201a0001c0003t0001g0023a0001c0003t0001g0076others(21): Show | 24 | HG00140.hp1 HG00642.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.337-703_337-691dup others(13): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693723
|
C | CAAAAAAA others(7): Show |
5 | a0002c0006t0002g0146a0002c0006t0003g0163a0002c0011t0002g0127others(2): Show | 5 | HG02630.hp2 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-704_337-691dup others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693723
|
C | CAAAAAAA others(8): Show |
4 | a0001c0009t0002g0106a0003c0004t0002g0248a0003c0013t0007g0133others(1): Show | 4 | HG01891.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-705_337-691dup others(15): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693723
|
C | CAAAAAAA others(10): Show |
1 | a0003c0004t0002g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.337-707_337-691dup others(17): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 43693723 | |||||
| chr2:43693915
|
C | G | 1 | a0001c0002t0002g0228 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.337-516C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693915 | ||||||
| chr2:43693935
|
C | A | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.337-496C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693935 | ||||||
| chr2:43693999
|
A | G | 1 | a0005c0008t0002g0148 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.337-432A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43693999 | ||||||
| chr2:43694062
|
A | G | 1 | a0001c0002t0002g0228 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.337-369A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43694062 | ||||||
| chr2:43694152
|
T | A | 13 | a0002c0005t0003g0143a0002c0006t0002g0146a0002c0006t0003g0163others(10): Show | 13 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.337-279T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43694152 | ||||||
| chr2:43694271
|
C | T | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.337-160C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43694271 | ||||||
| chr2:43694350
|
A | T | 165 | a0001c0001t0001g0009a0001c0002t0001g0005a0001c0002t0001g0104others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.337-81A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 4/29 | chr2 | 43694350 | ||||||
| chr2:43694600
|
A | G | 15 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.420+86A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43694600 | ||||||
| chr2:43694619
|
G | A | 1 | a0020c0046t0003g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.420+105G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43694619 | ||||||
| chr2:43694630
|
C | T | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.420+116C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43694630 | ||||||
| chr2:43694668
|
T | C | 1 | a0001c0001t0019g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.420+154T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43694668 | ||||||
| chr2:43694816
|
A | T | 45 | a0001c0002t0002g0201a0001c0003t0001g0004a0001c0003t0001g0023others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.420+302A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43694816 | ||||||
| chr2:43694891
|
T | C | 1 | a0001c0045t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.421-252T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43694891 | ||||||
| chr2:43695042
|
T | C | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.421-101T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43695042 | ||||||
| chr2:43695074
|
A | G | 15 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-69A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 5/29 | chr2 | 43695074 | ||||||
| chr2:43695271
|
A | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.502+47A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695271 | ||||||
| chr2:43695348
|
G | A | 1 | a0003c0012t0004g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502+124G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695348 | ||||||
| chr2:43695490
|
G | T | 1 | a0001c0003t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.502+266G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695490 | ||||||
| chr2:43695536
|
C | T | 5 | a0001c0002t0002g0218a0001c0002t0002g0223a0001c0002t0002g0224others(2): Show | 5 | HG02155.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+312C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695536 | ||||||
| chr2:43695537
|
C | G | 81 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.502+313C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695537 | ||||||
| chr2:43695603
|
G | A | 1 | a0003c0004t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502+379G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695603 | ||||||
| chr2:43695627
|
C | T | 4 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(1): Show | 4 | HG03041.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+403C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695627 | ||||||
| chr2:43695789
|
C | A | 80 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(77): Show | 80 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.502+565C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695789 | ||||||
| chr2:43695821
|
G | A | 1 | a0001c0003t0001g0195 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.502+597G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695821 | ||||||
| chr2:43695886
|
C | T | 15 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.502+662C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43695886 | ||||||
| chr2:43696041
|
T | A | 1 | a0003c0004t0002g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.502+817T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696041 | ||||||
| chr2:43696194
|
C | T | 6 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0003g0069others(3): Show | 6 | HG01192.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+970C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696194 | ||||||
| chr2:43696197
|
G | T | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.502+973G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696197 | ||||||
| chr2:43696302
|
A | T | 164 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.503-869A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696302 | ||||||
| chr2:43696412
|
C | T | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.503-759C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696412 | ||||||
| chr2:43696487
|
C | CA | 103 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0066others(100): Show | 103 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.503-668dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr2 | 43696487 | |||||
| chr2:43696608
|
G | A | 1 | a0001c0003t0001g0024 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.503-563G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696608 | ||||||
| chr2:43696636
|
A | G | 3 | a0001c0003t0002g0122a0002c0006t0004g0108a0023c0031t0016g0090 | 3 | HG02922.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.503-535A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696636 | ||||||
| chr2:43696894
|
C | T | 12 | a0001c0018t0002g0149a0001c0018t0002g0150a0005c0008t0001g0153others(9): Show | 12 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-277C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696894 | ||||||
| chr2:43696928
|
G | C | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.503-243G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696928 | ||||||
| chr2:43696989
|
A | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.503-182A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696989 | ||||||
| chr2:43696990
|
A | T | 2 | a0007c0014t0001g0184a0020c0046t0003g0165 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.503-181A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43696990 | ||||||
| chr2:43697032
|
T | A | 161 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.503-139T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43697032 | ||||||
| chr2:43697045
|
A | G | 1 | a0005c0008t0002g0230 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.503-126A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43697045 | ||||||
| chr2:43697090
|
A | C | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.503-81A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 6/29 | chr2 | 43697090 | ||||||
| chr2:43697394
|
T | A | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.688+38T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43697394 | ||||||
| chr2:43697432
|
T | C | 15 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+76T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43697432 | ||||||
| chr2:43697927
|
CTCT | C | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.688+579_688+581del others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr2 | 43697927 | |||||
| chr2:43698037
|
G | A | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.688+681G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698037 | ||||||
| chr2:43698251
|
C | CT | 147 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.688+909dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr2 | 43698251 | |||||
| chr2:43698251
|
C | CTT | 10 | a0001c0002t0002g0200a0001c0003t0001g0154a0001c0003t0001g0155others(7): Show | 10 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.688+908_688+909dup others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr2 | 43698251 | |||||
| chr2:43698401
|
C | A | 127 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.688+1045C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698401 | ||||||
| chr2:43698510
|
A | T | 1 | a0003c0004t0002g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.689-1137A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698510 | ||||||
| chr2:43698537
|
C | G | 1 | a0001c0007t0001g0003 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.689-1110C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698537 | ||||||
| chr2:43698544
|
C | T | 38 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.689-1103C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698544 | ||||||
| chr2:43698596
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.689-1051C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698596 | ||||||
| chr2:43698622
|
T | C | 1 | a0001c0007t0001g0003 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.689-1025T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698622 | ||||||
| chr2:43698704
|
G | C | 2 | a0007c0014t0001g0142a0020c0046t0003g0165 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.689-943G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698704 | ||||||
| chr2:43698719
|
A | C | 1 | a0020c0046t0003g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.689-928A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698719 | ||||||
| chr2:43698833
|
T | A | 1 | a0001c0003t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.689-814T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698833 | ||||||
| chr2:43698932
|
G | A | 160 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.689-715G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43698932 | ||||||
| chr2:43699059
|
C | T | 160 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.689-588C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43699059 | ||||||
| chr2:43699207
|
GT | G | 160 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.689-430delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr2 | 43699207 | |||||
| chr2:43699326
|
G | T | 144 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.689-321G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43699326 | ||||||
| chr2:43699629
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.689-18T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 7/29 | chr2 | 43699629 | ||||||
| chr2:43700638
|
G | A | 1 | a0020c0046t0003g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1650+30G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43700638 | ||||||
| chr2:43700692
|
G | A | 15 | a0005c0008t0001g0153a0005c0008t0002g0147a0005c0008t0002g0148others(12): Show | 15 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1650+84G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43700692 | ||||||
| chr2:43700713
|
C | A | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1650+105C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43700713 | ||||||
| chr2:43700897
|
G | A | 12 | a0005c0008t0001g0153a0005c0008t0002g0147a0005c0008t0002g0148others(9): Show | 12 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650+289G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43700897 | ||||||
| chr2:43700953
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1650+345C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43700953 | ||||||
| chr2:43701077
|
T | G | 10 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650+469T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701077 | ||||||
| chr2:43701264
|
A | G | 1 | a0002c0006t0011g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1650+656A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701264 | ||||||
| chr2:43701314
|
T | C | 163 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1650+706T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701314 | ||||||
| chr2:43701445
|
T | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1650+837T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701445 | ||||||
| chr2:43701517
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1650+909G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701517 | ||||||
| chr2:43701543
|
A | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1650+935A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701543 | ||||||
| chr2:43701589
|
A | AT | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1650+985dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43701589 | |||||
| chr2:43701612
|
C | A | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1650+1004C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701612 | ||||||
| chr2:43701629
|
A | G | 86 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(83): Show | 86 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1650+1021A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701629 | ||||||
| chr2:43701638
|
C | T | 3 | a0003c0004t0002g0100a0003c0004t0002g0248a0018c0041t0003g0204 | 3 | HG01891.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1650+1030C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701638 | ||||||
| chr2:43701706
|
T | TA | 10 | a0003c0004t0010g0136a0005c0008t0001g0153a0005c0008t0002g0147others(7): Show | 10 | HG00323.hp2 HG01168.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650+1113dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43701706 | |||||
| chr2:43701767
|
A | AT | 140 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1650+1176dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43701767 | |||||
| chr2:43701811
|
G | A | 163 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1650+1203G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701811 | ||||||
| chr2:43701851
|
T | C | 163 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1650+1243T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701851 | ||||||
| chr2:43701857
|
A | T | 163 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1650+1249A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701857 | ||||||
| chr2:43701903
|
A | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1650+1295A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43701903 | ||||||
| chr2:43702003
|
A | G | 2 | a0001c0003t0001g0180a0003c0022t0002g0164 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1650+1395A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702003 | ||||||
| chr2:43702053
|
C | G | 2 | a0002c0025t0004g0015a0002c0047t0002g0014 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1650+1445C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702053 | ||||||
| chr2:43702055
|
C | T | 11 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1650+1447C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702055 | ||||||
| chr2:43702271
|
T | A | 37 | a0001c0003t0001g0087a0001c0003t0001g0180a0001c0003t0001g0186others(34): Show | 37 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1650+1663T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702271 | ||||||
| chr2:43702305
|
G | A | 1 | a0001c0003t0002g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1651-1676G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702305 | ||||||
| chr2:43702314
|
T | A | 3 | a0001c0003t0002g0122a0002c0006t0004g0108a0023c0031t0016g0090 | 3 | HG02922.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1651-1667T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702314 | ||||||
| chr2:43702366
|
A | C | 1 | a0002c0006t0002g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1651-1615A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702366 | ||||||
| chr2:43702527
|
C | CT | 27 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0066others(24): Show | 27 | HG00735.hp1 HG01071.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1651-1432dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTT | 10 | a0001c0007t0001g0101a0002c0005t0003g0002a0002c0005t0003g0012others(7): Show | 10 | HG01192.hp2 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1651-1433_1651-143 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTT | 30 | a0001c0003t0001g0068a0001c0003t0001g0171a0001c0003t0002g0237others(27): Show | 30 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1651-1434_1651-143 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTT | 43 | a0001c0003t0001g0004a0001c0003t0001g0023a0001c0003t0001g0024others(40): Show | 43 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1651-1435_1651-143 others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTTT | 6 | a0001c0003t0001g0216a0001c0009t0002g0123a0001c0009t0002g0124others(3): Show | 6 | HG01978.hp2 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-1436_1651-143 others(9): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTTTTT | 33 | a0001c0002t0001g0243a0001c0003t0001g0087a0001c0003t0001g0180others(30): Show | 33 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1651-1438_1651-143 others(11): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTTTTT others(1): Show |
31 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1651-1439_1651-143 others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTTTTT others(2): Show |
12 | a0001c0002t0002g0200a0001c0002t0002g0209a0001c0002t0002g0223others(9): Show | 12 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1651-1440_1651-143 others(13): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTTTTT others(3): Show |
2 | a0001c0003t0002g0122a0013c0026t0002g0213 | 2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-1441_1651-143 others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702527
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0002g0221 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1651-1442_1651-143 others(15): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43702527 | |||||
| chr2:43702661
|
A | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1651-1320A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702661 | ||||||
| chr2:43702844
|
G | A | 162 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1651-1137G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702844 | ||||||
| chr2:43702920
|
C | G | 12 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(9): Show | 12 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-1061C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702920 | ||||||
| chr2:43702932
|
C | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1651-1049C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702932 | ||||||
| chr2:43702936
|
C | T | 40 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1651-1045C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702936 | ||||||
| chr2:43702993
|
C | T | 8 | a0001c0003t0001g0186a0001c0003t0002g0181a0003c0004t0002g0107others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-988C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43702993 | ||||||
| chr2:43703102
|
G | A | 1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1651-879G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703102 | ||||||
| chr2:43703109
|
G | A | 2 | a0001c0001t0001g0008a0001c0002t0002g0252 | 2 | HG01993.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1651-872G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703109 | ||||||
| chr2:43703114
|
A | T | 161 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1651-867A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703114 | ||||||
| chr2:43703177
|
G | A | 162 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1651-804G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703177 | ||||||
| chr2:43703179
|
G | T | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1651-802G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703179 | ||||||
| chr2:43703310
|
C | G | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1651-671C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703310 | ||||||
| chr2:43703389
|
A | G | 3 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134 | 3 | HG03130.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1651-592A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703389 | ||||||
| chr2:43703441
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1651-540C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703441 | ||||||
| chr2:43703477
|
G | C | 162 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1651-504G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703477 | ||||||
| chr2:43703570
|
A | G | 50 | a0001c0003t0001g0004a0001c0003t0001g0023a0001c0003t0001g0024others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1651-411A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703570 | ||||||
| chr2:43703594
|
A | C | 12 | a0005c0008t0001g0153a0005c0008t0002g0147a0005c0008t0002g0148others(9): Show | 12 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-387A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703594 | ||||||
| chr2:43703690
|
T | C | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1651-291T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703690 | ||||||
| chr2:43703703
|
TCTTA | T | 12 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(9): Show | 12 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-274_1651-271d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43703703 | |||||
| chr2:43703707
|
A | G | 1 | a0018c0041t0003g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1651-274A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703707 | ||||||
| chr2:43703738
|
C | G | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1651-243C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703738 | ||||||
| chr2:43703773
|
A | T | 145 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1651-208A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | chr2 | 43703773 | ||||||
| chr2:43703916
|
C | CT | 8 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0109others(5): Show | 8 | HG01257.hp1 HG02145.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-40dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43703916 | |||||
| chr2:43703916
|
C | CTT | 10 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1651-41_1651-40dup others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43703916 | |||||
| chr2:43703916
|
CT | C | 11 | a0005c0008t0001g0153a0005c0008t0002g0148a0005c0008t0002g0230others(8): Show | 11 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1651-40delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43703916 | |||||
| chr2:43703916
|
CTTTT | C | 5 | a0001c0002t0002g0231a0001c0003t0001g0004a0001c0003t0002g0237others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-43_1651-40del others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43703916 | |||||
| chr2:43703916
|
CTTTTT | C | 125 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1651-44_1651-40del others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 43703916 | |||||
| chr2:43704120
|
A | T | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1726+64A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704120 | ||||||
| chr2:43704182
|
G | A | 140 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1726+126G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704182 | ||||||
| chr2:43704220
|
G | T | 1 | a0004c0010t0006g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1726+164G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704220 | ||||||
| chr2:43704250
|
G | T | 5 | a0008c0017t0006g0162a0008c0017t0006g0211a0012c0053t0002g0121others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726+194G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704250 | ||||||
| chr2:43704338
|
A | G | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1726+282A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704338 | ||||||
| chr2:43704338
|
A | T | 1 | a0020c0046t0003g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1726+282A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704338 | ||||||
| chr2:43704389
|
C | T | 3 | a0001c0003t0002g0122a0002c0006t0004g0108a0023c0031t0016g0090 | 3 | HG02922.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1726+333C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704389 | ||||||
| chr2:43704446
|
A | G | 135 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1726+390A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704446 | ||||||
| chr2:43704507
|
A | G | 1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1726+451A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704507 | ||||||
| chr2:43704614
|
G | C | 11 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1726+558G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704614 | ||||||
| chr2:43704662
|
T | TA | 77 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0192others(74): Show | 77 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1726+630dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAA | 12 | a0001c0002t0002g0200a0001c0002t0002g0224a0001c0002t0009g0236others(9): Show | 12 | HG00597.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726+629_1726+630d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAA | 6 | a0008c0017t0006g0162a0008c0017t0006g0211a0012c0053t0002g0121others(3): Show | 6 | HG02280.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1726+628_1726+630d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAA | 9 | a0002c0006t0002g0146a0002c0006t0003g0163a0002c0011t0008g0119others(6): Show | 9 | HG02109.hp1 HG02630.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1726+627_1726+630d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAA | 22 | a0001c0003t0001g0004a0001c0003t0001g0023a0001c0003t0001g0024others(19): Show | 22 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1726+625_1726+630d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA | 9 | a0001c0003t0001g0068a0001c0003t0001g0076a0001c0003t0001g0171others(6): Show | 9 | HG01109.hp1 HG01192.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1726+624_1726+630d others(9): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA others(4): Show |
1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1726+620_1726+630d others(13): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA others(7): Show |
2 | a0011c0033t0002g0103a0011c0034t0002g0151 | 2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1726+617_1726+630d others(16): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA others(8): Show |
2 | a0010c0019t0005g0071a0010c0019t0005g0073 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1726+616_1726+630d others(17): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA others(9): Show |
3 | a0005c0008t0002g0148a0007c0014t0001g0167a0007c0035t0001g0168 | 3 | HG01975.hp1 HG02074.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1726+615_1726+630d others(18): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA others(10): Show |
4 | a0005c0008t0001g0153a0005c0008t0002g0147a0005c0008t0002g0230others(1): Show | 4 | HG02738.hp2 HG04184.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+614_1726+630d others(19): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
T | TAAAAAAA others(12): Show |
1 | a0005c0008t0002g0255 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1726+612_1726+630d others(21): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704662
|
TAAAAAA | T | 12 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(9): Show | 12 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1726+625_1726+630d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43704662 | |||||
| chr2:43704745
|
A | C | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1726+689A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704745 | ||||||
| chr2:43704800
|
T | C | 12 | a0001c0009t0002g0106a0001c0009t0002g0123a0001c0009t0002g0124others(9): Show | 12 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1726+744T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704800 | ||||||
| chr2:43704892
|
C | T | 1 | a0002c0005t0003g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1726+836C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704892 | ||||||
| chr2:43704984
|
A | T | 79 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0225others(76): Show | 79 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1726+928A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704984 | ||||||
| chr2:43704985
|
T | C | 1 | a0002c0005t0003g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1726+929T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43704985 | ||||||
| chr2:43705055
|
C | A | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1726+999C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705055 | ||||||
| chr2:43705120
|
C | G | 1 | a0003c0004t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1726+1064C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705120 | ||||||
| chr2:43705126
|
A | C | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1726+1070A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705126 | ||||||
| chr2:43705251
|
C | CT | 6 | a0001c0001t0001g0044a0001c0001t0002g0030a0001c0007t0001g0101others(3): Show | 6 | HG00438.hp1 HG00741.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1727-1049dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43705251 | |||||
| chr2:43705251
|
C | CTTT | 9 | a0002c0006t0004g0108a0003c0004t0002g0248a0004c0010t0005g0092others(6): Show | 9 | HG00642.hp1 HG01099.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1727-1051_1727-104 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43705251 | |||||
| chr2:43705251
|
C | CTTTT | 37 | a0001c0003t0001g0068a0001c0003t0001g0171a0001c0003t0001g0180others(34): Show | 37 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1727-1052_1727-104 others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43705251 | |||||
| chr2:43705251
|
C | CTTTTT | 62 | a0001c0002t0001g0005a0001c0002t0001g0225a0001c0002t0001g0242others(59): Show | 62 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1727-1053_1727-104 others(9): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43705251 | |||||
| chr2:43705251
|
C | CTTTTTT | 21 | a0001c0002t0001g0104a0001c0002t0002g0201a0001c0002t0002g0220others(18): Show | 21 | HG00642.hp2 HG01106.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1727-1054_1727-104 others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43705251 | |||||
| chr2:43705251
|
CTTT | C | 20 | a0001c0009t0002g0123a0001c0009t0002g0124a0001c0009t0002g0126others(17): Show | 20 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1727-1051_1727-104 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr2 | 43705251 | |||||
| chr2:43705406
|
C | A | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1727-916C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705406 | ||||||
| chr2:43705444
|
A | T | 1 | a0001c0009t0002g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1727-878A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705444 | ||||||
| chr2:43705472
|
G | A | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1727-850G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705472 | ||||||
| chr2:43705761
|
A | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0170a0001c0001t0001g0172others(2): Show | 5 | HG01071.hp2 HG01257.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1727-561A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705761 | ||||||
| chr2:43705903
|
C | G | 8 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0170others(5): Show | 8 | HG01071.hp2 HG01257.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1727-419C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705903 | ||||||
| chr2:43705911
|
A | G | 2 | a0002c0016t0002g0251a0014c0027t0002g0214 | 2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1727-411A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43705911 | ||||||
| chr2:43706007
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1727-315T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43706007 | ||||||
| chr2:43706215
|
C | G | 35 | a0001c0002t0001g0005a0001c0002t0001g0225a0001c0002t0001g0242others(32): Show | 35 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1727-107C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43706215 | ||||||
| chr2:43706244
|
C | A | 3 | a0001c0002t0002g0200a0004c0038t0006g0093a0020c0046t0003g0165 | 3 | HG02886.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1727-78C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 9/29 | chr2 | 43706244 | ||||||
| chr2:43706522
|
C | T | 2 | a0001c0002t0002g0200a0004c0038t0006g0093 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1821+106C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43706522 | ||||||
| chr2:43706669
|
C | T | 2 | a0001c0002t0002g0200a0004c0038t0006g0093 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1821+253C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43706669 | ||||||
| chr2:43706924
|
A | G | 1 | a0017c0036t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1822-477A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43706924 | ||||||
| chr2:43706969
|
G | A | 2 | a0001c0001t0001g0009a0020c0046t0003g0165 | 2 | HG02040.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1822-432G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43706969 | ||||||
| chr2:43706997
|
A | C | 1 | a0002c0016t0002g0251 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1822-404A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43706997 | ||||||
| chr2:43707003
|
C | T | 3 | a0001c0002t0002g0200a0004c0038t0006g0093a0017c0036t0001g0099 | 3 | HG02886.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1822-398C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43707003 | ||||||
| chr2:43707037
|
A | T | 3 | a0001c0002t0002g0200a0004c0038t0006g0093a0017c0036t0001g0099 | 3 | HG02886.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1822-364A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43707037 | ||||||
| chr2:43707180
|
G | T | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1822-221G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43707180 | ||||||
| chr2:43707196
|
C | CA | 12 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0002g0017others(9): Show | 12 | HG01168.hp2 HG01175.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1822-185dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAA | 17 | a0001c0002t0001g0225a0001c0002t0002g0218a0001c0002t0002g0223others(14): Show | 17 | HG00438.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1822-186_1822-185d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAAA | 9 | a0001c0002t0001g0005a0001c0002t0002g0219a0001c0002t0002g0229others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1822-187_1822-185d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAAAA | 76 | a0001c0002t0001g0242a0001c0002t0001g0244a0001c0002t0002g0130others(73): Show | 76 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1822-188_1822-185d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAAAAA | 40 | a0001c0002t0001g0243a0001c0002t0002g0240a0001c0002t0009g0236others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1822-189_1822-185d others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAAAAAA | 6 | a0001c0003t0001g0189a0001c0030t0001g0215a0005c0008t0002g0147others(3): Show | 6 | HG00642.hp2 HG01261.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-190_1822-185d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAAAAAAA | 5 | a0002c0005t0011g0013a0003c0004t0002g0248a0010c0019t0005g0071others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1822-191_1822-185d others(9): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707196
|
C | CAAAAAAA others(4): Show |
1 | a0002c0016t0002g0251 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1822-195_1822-185d others(13): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 43707196 | |||||
| chr2:43707349
|
T | C | 2 | a0005c0008t0002g0255a0008c0017t0006g0211 | 2 | HG01168.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1822-52T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43707349 | ||||||
| chr2:43707388
|
C | G | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1822-13C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 10/29 | chr2 | 43707388 | ||||||
| chr2:43707638
|
C | T | 5 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+93C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43707638 | ||||||
| chr2:43707744
|
A | G | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1966+199A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43707744 | ||||||
| chr2:43707745
|
G | GT | 98 | a0001c0002t0001g0225a0001c0002t0001g0242a0001c0002t0001g0243others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1966+211dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr2 | 43707745 | |||||
| chr2:43707745
|
GT | G | 59 | a0001c0002t0002g0231a0001c0002t0002g0240a0001c0003t0001g0087others(56): Show | 59 | HG00738.hp1 HG01074.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.1966+211delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr2 | 43707745 | |||||
| chr2:43707783
|
G | C | 1 | a0001c0002t0002g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1966+238G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43707783 | ||||||
| chr2:43707794
|
T | G | 1 | a0001c0003t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1966+249T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43707794 | ||||||
| chr2:43707879
|
C | A | 1 | a0001c0003t0001g0195 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1966+334C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43707879 | ||||||
| chr2:43707953
|
T | C | 17 | a0001c0001t0001g0006a0001c0002t0002g0200a0001c0009t0002g0106others(14): Show | 17 | HG00738.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1966+408T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43707953 | ||||||
| chr2:43708135
|
C | T | 4 | a0001c0003t0001g0180a0003c0004t0002g0097a0003c0004t0002g0098others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1966+590C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708135 | ||||||
| chr2:43708307
|
G | A | 26 | a0001c0003t0001g0068a0001c0003t0001g0171a0001c0003t0001g0186others(23): Show | 26 | HG00323.hp2 HG00738.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1966+762G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708307 | ||||||
| chr2:43708333
|
C | G | 108 | a0001c0001t0001g0006a0001c0001t0014g0063a0001c0001t0014g0064others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1966+788C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708333 | ||||||
| chr2:43708335
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1966+790G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708335 | ||||||
| chr2:43708452
|
G | A | 6 | a0002c0005t0011g0013a0002c0006t0011g0239a0002c0016t0002g0251others(3): Show | 6 | HG02451.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1966+907G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708452 | ||||||
| chr2:43708497
|
A | G | 35 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0041others(32): Show | 35 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1966+952A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708497 | ||||||
| chr2:43708579
|
T | C | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1966+1034T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708579 | ||||||
| chr2:43708586
|
T | C | 160 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0041others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1966+1041T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708586 | ||||||
| chr2:43708597
|
T | C | 57 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0243others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1966+1052T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708597 | ||||||
| chr2:43708734
|
T | C | 25 | a0001c0002t0001g0243a0001c0003t0001g0024a0001c0003t0001g0076others(22): Show | 25 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1966+1189T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708734 | ||||||
| chr2:43708783
|
A | T | 1 | a0011c0034t0002g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1967-1207A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43708783 | ||||||
| chr2:43709031
|
A | G | 1 | a0001c0002t0002g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1967-959A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709031 | ||||||
| chr2:43709073
|
T | C | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1967-917T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709073 | ||||||
| chr2:43709091
|
G | A | 32 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(29): Show | 32 | HG00738.hp2 HG01168.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1967-899G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709091 | ||||||
| chr2:43709219
|
T | G | 173 | a0001c0001t0001g0006a0001c0001t0002g0031a0001c0001t0002g0051others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1967-771T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709219 | ||||||
| chr2:43709223
|
T | G | 37 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1967-767T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709223 | ||||||
| chr2:43709379
|
C | T | 31 | a0001c0002t0002g0130a0001c0002t0002g0200a0001c0002t0002g0240others(28): Show | 31 | HG00738.hp2 HG01168.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1967-611C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709379 | ||||||
| chr2:43709396
|
G | A | 33 | a0001c0002t0002g0130a0001c0002t0002g0200a0001c0002t0002g0240others(30): Show | 33 | HG00738.hp2 HG01168.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1967-594G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709396 | ||||||
| chr2:43709612
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0001t0018g0055others(1): Show | 4 | HG02071.hp2 NA18968.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-378C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709612 | ||||||
| chr2:43709619
|
C | T | 7 | a0001c0003t0001g0186a0002c0005t0011g0013a0002c0006t0011g0239others(4): Show | 7 | HG01346.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967-371C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709619 | ||||||
| chr2:43709633
|
C | G | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1967-357C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709633 | ||||||
| chr2:43709696
|
C | T | 7 | a0001c0003t0001g0186a0002c0005t0011g0013a0002c0006t0011g0239others(4): Show | 7 | HG01346.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967-294C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709696 | ||||||
| chr2:43709705
|
G | A | 1 | a0005c0008t0002g0255 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1967-285G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709705 | ||||||
| chr2:43709801
|
A | C | 3 | a0001c0002t0009g0235a0001c0002t0009g0236a0001c0002t0009g0238 | 3 | HG00597.hp2 HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1967-189A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709801 | ||||||
| chr2:43709813
|
T | C | 174 | a0001c0001t0001g0006a0001c0001t0001g0192a0001c0001t0002g0031others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1967-177T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709813 | ||||||
| chr2:43709835
|
A | G | 173 | a0001c0001t0001g0006a0001c0001t0001g0192a0001c0001t0002g0031others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1967-155A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709835 | ||||||
| chr2:43709947
|
C | T | 7 | a0001c0003t0001g0186a0002c0005t0011g0013a0002c0006t0011g0239others(4): Show | 7 | HG01346.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967-43C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 11/29 | chr2 | 43709947 | ||||||
| chr2:43710361
|
T | C | 37 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.2214+31T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 13/29 | chr2 | 43710361 | ||||||
| chr2:43710385
|
C | T | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2214+55C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 13/29 | chr2 | 43710385 | ||||||
| chr2:43710584
|
C | CT | 68 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0222others(65): Show | 68 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.2301+33dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43710584 | |||||
| chr2:43710584
|
CTT | C | 11 | a0001c0002t0002g0200a0002c0006t0004g0108a0003c0013t0002g0114others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2301+32_2301+33del others(2): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43710584 | |||||
| chr2:43710584
|
CTTT | C | 20 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(17): Show | 20 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2301+31_2301+33del others(3): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43710584 | |||||
| chr2:43710584
|
CTTTTTTT others(2): Show |
C | 6 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0002g0160others(3): Show | 6 | HG00738.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2301+25_2301+33del others(9): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43710584 | |||||
| chr2:43710729
|
C | A | 29 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(26): Show | 29 | HG00738.hp2 HG01884.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.2301+154C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43710729 | ||||||
| chr2:43710806
|
A | G | 5 | a0003c0013t0002g0114a0004c0010t0006g0135a0004c0010t0006g0206others(2): Show | 5 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2301+231A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43710806 | ||||||
| chr2:43710829
|
A | G | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2301+254A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43710829 | ||||||
| chr2:43710926
|
C | T | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2301+351C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43710926 | ||||||
| chr2:43710928
|
G | A | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2301+353G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43710928 | ||||||
| chr2:43710956
|
T | C | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2301+381T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43710956 | ||||||
| chr2:43711135
|
C | T | 1 | a0001c0048t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2301+560C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711135 | ||||||
| chr2:43711419
|
C | A | 165 | a0001c0001t0001g0006a0001c0001t0002g0031a0001c0001t0002g0051others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2302-806C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711419 | ||||||
| chr2:43711464
|
T | C | 3 | a0001c0002t0002g0130a0002c0016t0002g0091a0018c0041t0003g0204 | 3 | HG02615.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2302-761T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711464 | ||||||
| chr2:43711619
|
C | T | 28 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.2302-606C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711619 | ||||||
| chr2:43711666
|
C | T | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2302-559C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711666 | ||||||
| chr2:43711687
|
C | T | 1 | a0002c0005t0002g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2302-538C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711687 | ||||||
| chr2:43711749
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0029others(17): Show | 20 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.2302-476C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711749 | ||||||
| chr2:43711786
|
C | T | 8 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139others(5): Show | 8 | HG00323.hp2 HG01109.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2302-439C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711786 | ||||||
| chr2:43711787
|
G | A | 31 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(28): Show | 31 | HG00738.hp2 HG01168.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.2302-438G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711787 | ||||||
| chr2:43711825
|
C | A | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2302-400C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711825 | ||||||
| chr2:43711862
|
C | T | 7 | a0001c0003t0001g0186a0002c0005t0011g0013a0002c0006t0011g0239others(4): Show | 7 | HG01346.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2302-363C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711862 | ||||||
| chr2:43711893
|
C | CA | 109 | a0001c0001t0001g0006a0001c0001t0002g0031a0001c0001t0002g0051others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2302-316dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43711893 | |||||
| chr2:43711893
|
C | CAA | 11 | a0001c0002t0002g0224a0001c0002t0002g0227a0002c0005t0002g0045others(8): Show | 11 | HG01243.hp2 HG01358.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.2302-317_2302-316d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43711893 | |||||
| chr2:43711893
|
CA | C | 32 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(29): Show | 32 | HG00738.hp2 HG01168.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.2302-316delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr2 | 43711893 | |||||
| chr2:43711940
|
A | G | 202 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0066others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.2302-285A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43711940 | ||||||
| chr2:43712040
|
G | A | 1 | a0005c0008t0001g0153 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2302-185G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 14/29 | chr2 | 43712040 | ||||||
| chr2:43712386
|
A | G | 32 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.2460+3A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43712386 | ||||||
| chr2:43712567
|
G | T | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2460+184G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43712567 | ||||||
| chr2:43712689
|
T | C | 35 | a0001c0001t0001g0192a0001c0001t0002g0031a0001c0001t0002g0047others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.2460+306T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43712689 | ||||||
| chr2:43712719
|
C | T | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2460+336C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43712719 | ||||||
| chr2:43712735
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2460+352A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43712735 | ||||||
| chr2:43712905
|
A | G | 1 | a0022c0056t0003g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2460+522A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43712905 | ||||||
| chr2:43713099
|
A | AACACAAA others(9): Show |
3 | a0001c0002t0002g0130a0002c0016t0002g0091a0018c0041t0003g0204 | 3 | HG02615.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2460+721_2460+722i others(18): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(3): Show |
32 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.2460+725_2460+734d others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(5): Show |
2 | a0005c0008t0001g0153a0005c0008t0002g0148 | 2 | HG01975.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2460+723_2460+734d others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(17): Show |
3 | a0003c0022t0002g0140a0003c0022t0002g0164a0011c0033t0002g0103 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2460+729_2460+730i others(26): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(7): Show |
5 | a0003c0013t0002g0114a0004c0010t0006g0135a0004c0010t0006g0206others(2): Show | 5 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2460+721_2460+734d others(16): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(9): Show |
4 | a0003c0004t0002g0137a0003c0004t0002g0160a0003c0050t0002g0072others(1): Show | 4 | HG00738.hp2 HG02965.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460+719_2460+734d others(18): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(11): Show |
20 | a0001c0002t0002g0240a0001c0003t0002g0122a0001c0009t0002g0123others(17): Show | 20 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2460+717_2460+734d others(20): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713099
|
A | AACACACA others(15): Show |
2 | a0001c0003t0001g0180a0001c0009t0002g0128 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2460+734_2460+735i others(24): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713099 | |||||
| chr2:43713122
|
A | G | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2460+739A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713122 | ||||||
| chr2:43713127
|
T | C | 32 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.2460+744T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713127 | ||||||
| chr2:43713140
|
A | G | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2460+757A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713140 | ||||||
| chr2:43713290
|
G | T | 28 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0180others(25): Show | 28 | HG00738.hp2 HG01884.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2460+907G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713290 | ||||||
| chr2:43713393
|
G | T | 27 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(24): Show | 27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460+1010G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713393 | ||||||
| chr2:43713629
|
T | A | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2460+1246T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713629 | ||||||
| chr2:43713660
|
G | GT | 14 | a0001c0002t0002g0130a0001c0003t0001g0024a0001c0003t0001g0202others(11): Show | 14 | HG00738.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2460+1291dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713660 | |||||
| chr2:43713660
|
G | GTT | 32 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.2460+1290_2460+129 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43713660 | |||||
| chr2:43713760
|
A | C | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2460+1377A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713760 | ||||||
| chr2:43713883
|
T | C | 1 | a0002c0006t0003g0194 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2460+1500T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713883 | ||||||
| chr2:43713989
|
T | C | 2 | a0001c0002t0002g0130a0002c0016t0002g0091 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2460+1606T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43713989 | ||||||
| chr2:43714154
|
G | C | 1 | a0003c0004t0002g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2460+1771G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714154 | ||||||
| chr2:43714277
|
C | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0192a0001c0001t0002g0031others(87): Show | 90 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.2460+1894C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714277 | ||||||
| chr2:43714319
|
A | T | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2460+1936A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714319 | ||||||
| chr2:43714344
|
C | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2460+1961C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714344 | ||||||
| chr2:43714362
|
T | C | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2460+1979T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714362 | ||||||
| chr2:43714392
|
G | T | 29 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2460+2009G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714392 | ||||||
| chr2:43714394
|
C | T | 8 | a0001c0003t0001g0186a0002c0005t0011g0013a0002c0006t0004g0108others(5): Show | 8 | HG01346.hp2 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2460+2011C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714394 | ||||||
| chr2:43714437
|
A | G | 30 | a0001c0002t0002g0130a0001c0002t0002g0200a0001c0002t0002g0240others(27): Show | 30 | HG00738.hp2 HG01168.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2460+2054A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714437 | ||||||
| chr2:43714534
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2460+2151T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714534 | ||||||
| chr2:43714601
|
G | A | 1 | a0002c0006t0002g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2460+2218G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714601 | ||||||
| chr2:43714627
|
A | G | 7 | a0001c0003t0001g0195a0002c0005t0003g0190a0002c0006t0003g0193others(4): Show | 7 | HG01074.hp2 HG02280.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2460+2244A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714627 | ||||||
| chr2:43714632
|
G | T | 9 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2460+2249G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714632 | ||||||
| chr2:43714635
|
A | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2460+2252A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714635 | ||||||
| chr2:43714805
|
A | G | 179 | a0001c0001t0001g0006a0001c0001t0001g0192a0001c0001t0002g0030others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.2460+2422A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714805 | ||||||
| chr2:43714897
|
G | A | 1 | a0001c0009t0002g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2460+2514G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714897 | ||||||
| chr2:43714986
|
A | C | 3 | a0003c0022t0002g0140a0003c0022t0002g0164a0011c0033t0002g0103 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2460+2603A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43714986 | ||||||
| chr2:43715042
|
C | G | 1 | a0001c0003t0002g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2460+2659C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715042 | ||||||
| chr2:43715099
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2460+2716G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715099 | ||||||
| chr2:43715126
|
A | G | 14 | a0001c0002t0002g0240a0001c0003t0001g0180a0001c0003t0002g0122others(11): Show | 14 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2460+2743A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715126 | ||||||
| chr2:43715145
|
G | A | 9 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2460+2762G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715145 | ||||||
| chr2:43715149
|
A | G | 5 | a0003c0004t0002g0137a0003c0004t0002g0141a0003c0004t0002g0160others(2): Show | 5 | HG00738.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2460+2766A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715149 | ||||||
| chr2:43715156
|
A | G | 9 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2460+2773A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715156 | ||||||
| chr2:43715191
|
G | A | 2 | a0002c0025t0004g0015a0002c0047t0002g0014 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2460+2808G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715191 | ||||||
| chr2:43715259
|
A | C | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2460+2876A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715259 | ||||||
| chr2:43715291
|
GA | G | 6 | a0002c0006t0002g0146a0002c0006t0003g0163a0002c0011t0008g0119others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2460+2918delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43715291 | |||||
| chr2:43715327
|
G | C | 2 | a0001c0003t0001g0186a0007c0014t0001g0142 | 2 | HG01346.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2460+2944G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715327 | ||||||
| chr2:43715334
|
G | A | 63 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.2460+2951G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715334 | ||||||
| chr2:43715367
|
A | T | 9 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2460+2984A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715367 | ||||||
| chr2:43715396
|
G | T | 7 | a0001c0003t0001g0186a0002c0005t0011g0013a0002c0006t0011g0239others(4): Show | 7 | HG01346.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2460+3013G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715396 | ||||||
| chr2:43715406
|
C | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2460+3023C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715406 | ||||||
| chr2:43715422
|
A | G | 1 | a0005c0008t0002g0255 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2460+3039A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715422 | ||||||
| chr2:43715446
|
A | G | 1 | a0006c0015t0001g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2460+3063A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715446 | ||||||
| chr2:43715506
|
A | T | 1 | a0002c0006t0002g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2460+3123A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715506 | ||||||
| chr2:43715613
|
A | G | 9 | a0003c0013t0002g0114a0003c0013t0007g0131a0003c0013t0007g0133others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2460+3230A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715613 | ||||||
| chr2:43715723
|
G | A | 2 | a0002c0006t0002g0146a0002c0006t0003g0163 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2460+3340G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715723 | ||||||
| chr2:43715773
|
G | T | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2460+3390G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715773 | ||||||
| chr2:43715830
|
A | G | 65 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2460+3447A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715830 | ||||||
| chr2:43715863
|
T | C | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2460+3480T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715863 | ||||||
| chr2:43715866
|
G | A | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2460+3483G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715866 | ||||||
| chr2:43715916
|
G | C | 1 | a0001c0003t0001g0216 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2460+3533G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715916 | ||||||
| chr2:43715919
|
A | G | 63 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.2460+3536A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715919 | ||||||
| chr2:43715977
|
G | T | 62 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.2460+3594G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715977 | ||||||
| chr2:43715984
|
A | T | 2 | a0004c0038t0006g0093a0008c0017t0006g0211 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2460+3601A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43715984 | ||||||
| chr2:43716018
|
G | C | 1 | a0001c0001t0018g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2460+3635G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716018 | ||||||
| chr2:43716386
|
A | G | 127 | a0001c0001t0001g0006a0001c0001t0001g0192a0001c0001t0002g0017others(124): Show | 127 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.2460+4003A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716386 | ||||||
| chr2:43716551
|
C | T | 20 | a0001c0002t0002g0130a0001c0003t0001g0023a0002c0005t0003g0002others(17): Show | 20 | HG01192.hp2 HG01261.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2461-4118C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716551 | ||||||
| chr2:43716599
|
T | C | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2461-4070T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716599 | ||||||
| chr2:43716668
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2461-4001A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716668 | ||||||
| chr2:43716739
|
C | T | 7 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(4): Show | 7 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2461-3930C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716739 | ||||||
| chr2:43716770
|
G | A | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2461-3899G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716770 | ||||||
| chr2:43716840
|
C | T | 2 | a0002c0005t0011g0013a0002c0006t0011g0239 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2461-3829C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716840 | ||||||
| chr2:43716882
|
C | G | 39 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2461-3787C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716882 | ||||||
| chr2:43716883
|
T | C | 1 | a0001c0002t0002g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2461-3786T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43716883 | ||||||
| chr2:43717186
|
G | A | 4 | a0002c0005t0011g0013a0002c0006t0011g0239a0002c0047t0002g0014others(1): Show | 4 | HG02451.hp2 HG03139.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461-3483G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717186 | ||||||
| chr2:43717334
|
C | G | 1 | a0001c0003t0002g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2461-3335C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717334 | ||||||
| chr2:43717391
|
C | G | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2461-3278C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717391 | ||||||
| chr2:43717411
|
C | G | 4 | a0001c0003t0002g0237a0001c0009t0002g0106a0002c0006t0004g0108others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461-3258C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717411 | ||||||
| chr2:43717416
|
T | TCAAA | 3 | a0001c0001t0019g0053a0001c0007t0001g0003a0001c0007t0001g0101 | 3 | HG02145.hp1 HG02258.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2461-3223_2461-322 others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43717416 | |||||
| chr2:43717416
|
TCAAA | T | 58 | a0001c0002t0002g0240a0001c0003t0001g0068a0001c0003t0001g0171others(55): Show | 58 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2461-3223_2461-322 others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43717416 | |||||
| chr2:43717416
|
TCAAACAA others(1): Show |
T | 117 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2461-3227_2461-322 others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43717416 | |||||
| chr2:43717416
|
TCAAACAA others(5): Show |
T | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2461-3231_2461-322 others(16): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43717416 | |||||
| chr2:43717467
|
G | T | 1 | a0002c0005t0003g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2461-3202G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717467 | ||||||
| chr2:43717478
|
G | A | 4 | a0001c0003t0002g0237a0001c0009t0002g0106a0002c0006t0004g0108others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461-3191G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717478 | ||||||
| chr2:43717638
|
G | C | 20 | a0001c0003t0002g0181a0003c0004t0002g0080a0003c0004t0002g0097others(17): Show | 20 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2461-3031G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717638 | ||||||
| chr2:43717646
|
T | A | 172 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.2461-3023T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717646 | ||||||
| chr2:43717728
|
C | A | 49 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2461-2941C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717728 | ||||||
| chr2:43717757
|
C | T | 18 | a0001c0001t0001g0192a0001c0001t0002g0031a0001c0001t0002g0047others(15): Show | 18 | HG00597.hp2 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2461-2912C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717757 | ||||||
| chr2:43717917
|
A | T | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2461-2752A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43717917 | ||||||
| chr2:43718117
|
C | T | 176 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2461-2552C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718117 | ||||||
| chr2:43718153
|
A | T | 176 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2461-2516A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718153 | ||||||
| chr2:43718252
|
A | G | 59 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0068others(56): Show | 59 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.2461-2417A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718252 | ||||||
| chr2:43718306
|
G | A | 1 | a0016c0029t0003g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2461-2363G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718306 | ||||||
| chr2:43718353
|
C | T | 45 | a0001c0002t0002g0130a0001c0003t0002g0181a0002c0005t0003g0002others(42): Show | 45 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2461-2316C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718353 | ||||||
| chr2:43718376
|
A | T | 1 | a0001c0045t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2461-2293A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718376 | ||||||
| chr2:43718532
|
C | T | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2461-2137C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718532 | ||||||
| chr2:43718537
|
CA | C | 14 | a0001c0002t0002g0130a0001c0002t0009g0235a0001c0002t0009g0236others(11): Show | 14 | HG00597.hp2 HG02027.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2461-2117delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43718537 | |||||
| chr2:43718698
|
A | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2461-1971A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718698 | ||||||
| chr2:43718864
|
A | T | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2461-1805A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718864 | ||||||
| chr2:43718899
|
A | G | 1 | a0001c0002t0002g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2461-1770A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718899 | ||||||
| chr2:43718906
|
C | T | 45 | a0001c0002t0002g0130a0001c0003t0002g0181a0002c0005t0003g0002others(42): Show | 45 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2461-1763C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718906 | ||||||
| chr2:43718907
|
G | T | 43 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2461-1762G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718907 | ||||||
| chr2:43718929
|
T | C | 1 | a0001c0003t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2461-1740T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718929 | ||||||
| chr2:43718955
|
C | T | 1 | a0001c0002t0002g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2461-1714C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718955 | ||||||
| chr2:43718968
|
G | T | 1 | a0002c0016t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2461-1701G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43718968 | ||||||
| chr2:43719456
|
T | G | 1 | a0013c0026t0002g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2461-1213T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43719456 | ||||||
| chr2:43719596
|
C | A | 43 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2461-1073C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43719596 | ||||||
| chr2:43719624
|
G | C | 1 | a0022c0056t0003g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2461-1045G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43719624 | ||||||
| chr2:43720168
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2461-501T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720168 | ||||||
| chr2:43720175
|
C | A | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2461-494C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720175 | ||||||
| chr2:43720179
|
A | G | 39 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.2461-490A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720179 | ||||||
| chr2:43720204
|
T | C | 9 | a0001c0003t0002g0237a0001c0009t0002g0106a0001c0024t0003g0011others(6): Show | 9 | HG02615.hp2 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2461-465T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720204 | ||||||
| chr2:43720252
|
G | A | 5 | a0004c0010t0006g0135a0004c0010t0006g0206a0008c0017t0006g0162others(2): Show | 5 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2461-417G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720252 | ||||||
| chr2:43720252
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2461-417G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720252 | ||||||
| chr2:43720280
|
CT | C | 122 | a0001c0001t0001g0006a0001c0001t0014g0063a0001c0001t0014g0064others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2461-374delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43720280 | |||||
| chr2:43720280
|
CTT | C | 50 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2461-375_2461-374d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 43720280 | |||||
| chr2:43720295
|
T | A | 56 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.2461-374T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720295 | ||||||
| chr2:43720319
|
G | A | 2 | a0010c0019t0005g0071a0010c0019t0005g0073 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2461-350G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720319 | ||||||
| chr2:43720360
|
G | A | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2461-309G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720360 | ||||||
| chr2:43720402
|
A | G | 1 | a0005c0008t0002g0230 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2461-267A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720402 | ||||||
| chr2:43720487
|
A | T | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2461-182A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720487 | ||||||
| chr2:43720531
|
A | G | 5 | a0004c0010t0006g0135a0004c0010t0006g0206a0008c0017t0006g0162others(2): Show | 5 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2461-138A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720531 | ||||||
| chr2:43720621
|
T | C | 36 | a0001c0001t0001g0192a0001c0001t0002g0017a0001c0001t0002g0030others(33): Show | 36 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.2461-48T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 15/29 | chr2 | 43720621 | ||||||
| chr2:43720805
|
A | G | 122 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2541+56A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43720805 | ||||||
| chr2:43720990
|
A | G | 1 | a0002c0005t0003g0002 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2541+241A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43720990 | ||||||
| chr2:43721011
|
C | T | 2 | a0003c0004t0002g0141a0003c0004t0002g0160 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2541+262C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721011 | ||||||
| chr2:43721014
|
A | G | 68 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0068others(65): Show | 68 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.2541+265A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721014 | ||||||
| chr2:43721163
|
C | G | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2541+414C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721163 | ||||||
| chr2:43721272
|
A | G | 2 | a0002c0005t0011g0013a0002c0006t0011g0239 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2541+523A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721272 | ||||||
| chr2:43721312
|
G | T | 1 | a0001c0003t0002g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2541+563G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721312 | ||||||
| chr2:43721459
|
A | G | 177 | a0001c0001t0001g0022a0001c0001t0002g0017a0001c0001t0002g0030others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2541+710A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721459 | ||||||
| chr2:43721465
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2541+716C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721465 | ||||||
| chr2:43721599
|
T | A | 6 | a0001c0018t0002g0149a0001c0018t0002g0150a0003c0013t0007g0131others(3): Show | 6 | HG02647.hp2 HG03130.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2541+850T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721599 | ||||||
| chr2:43721632
|
C | G | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2541+883C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721632 | ||||||
| chr2:43721665
|
C | G | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2541+916C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721665 | ||||||
| chr2:43721718
|
T | C | 1 | a0012c0053t0002g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2541+969T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43721718 | ||||||
| chr2:43722150
|
G | A | 1 | a0001c0003t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2541+1401G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722150 | ||||||
| chr2:43722255
|
C | CA | 20 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(17): Show | 20 | HG01175.hp2 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2541+1523dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr2 | 43722255 | |||||
| chr2:43722255
|
CA | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0074a0001c0001t0001g0084others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2541+1523delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr2 | 43722255 | |||||
| chr2:43722255
|
CAA | C | 48 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.2541+1522_2541+152 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr2 | 43722255 | |||||
| chr2:43722378
|
A | G | 1 | a0002c0011t0008g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2541+1629A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722378 | ||||||
| chr2:43722587
|
G | A | 1 | a0002c0025t0004g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2541+1838G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722587 | ||||||
| chr2:43722622
|
C | T | 3 | a0002c0006t0003g0194a0002c0016t0003g0105a0006c0015t0001g0198 | 3 | HG00639.hp1 HG02280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2541+1873C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722622 | ||||||
| chr2:43722639
|
C | T | 3 | a0001c0001t0014g0063a0001c0001t0014g0064a0023c0031t0016g0090 | 3 | HG01109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2541+1890C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722639 | ||||||
| chr2:43722651
|
T | C | 1 | a0001c0009t0002g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2541+1902T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722651 | ||||||
| chr2:43722781
|
G | A | 4 | a0001c0003t0002g0237a0001c0009t0002g0106a0002c0006t0004g0108others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2541+2032G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722781 | ||||||
| chr2:43722808
|
A | T | 169 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.2541+2059A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722808 | ||||||
| chr2:43722919
|
A | G | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2541+2170A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722919 | ||||||
| chr2:43722998
|
T | G | 25 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(22): Show | 25 | HG00438.hp1 HG00438.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.2541+2249T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43722998 | ||||||
| chr2:43723118
|
C | G | 169 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.2541+2369C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723118 | ||||||
| chr2:43723162
|
A | G | 43 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2541+2413A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723162 | ||||||
| chr2:43723200
|
A | T | 175 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2541+2451A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723200 | ||||||
| chr2:43723341
|
C | G | 39 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.2541+2592C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723341 | ||||||
| chr2:43723495
|
G | C | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2541+2746G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723495 | ||||||
| chr2:43723674
|
C | T | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2542-2598C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723674 | ||||||
| chr2:43723785
|
G | A | 1 | a0002c0006t0002g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2542-2487G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723785 | ||||||
| chr2:43723790
|
G | A | 57 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0068others(54): Show | 57 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.2542-2482G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723790 | ||||||
| chr2:43723837
|
A | G | 5 | a0002c0005t0003g0190a0002c0006t0003g0194a0002c0016t0003g0105others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2542-2435A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723837 | ||||||
| chr2:43723838
|
C | T | 3 | a0001c0003t0001g0186a0007c0014t0001g0142a0017c0036t0001g0099 | 3 | HG01346.hp2 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2542-2434C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723838 | ||||||
| chr2:43723872
|
T | A | 57 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2542-2400T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723872 | ||||||
| chr2:43723879
|
G | C | 2 | a0003c0004t0002g0097a0003c0004t0002g0098 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2542-2393G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723879 | ||||||
| chr2:43723894
|
C | G | 3 | a0002c0005t0011g0013a0002c0006t0011g0239a0003c0037t0002g0138 | 3 | HG02451.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2542-2378C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723894 | ||||||
| chr2:43723984
|
T | G | 185 | a0001c0001t0001g0006a0001c0001t0002g0017a0001c0001t0002g0030others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.2542-2288T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43723984 | ||||||
| chr2:43724002
|
T | G | 2 | a0001c0002t0002g0220a0001c0043t0004g0247 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2542-2270T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724002 | ||||||
| chr2:43724112
|
AGAGCAGG others(31): Show |
A | 56 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.2542-2159_2542-212 others(42): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724112 | ||||||
| chr2:43724130
|
G | T | 112 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(109): Show | 112 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.2542-2142G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724130 | ||||||
| chr2:43724253
|
G | A | 1 | a0002c0047t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2542-2019G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724253 | ||||||
| chr2:43724311
|
C | T | 1 | a0001c0003t0001g0216 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2542-1961C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724311 | ||||||
| chr2:43724382
|
A | G | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2542-1890A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724382 | ||||||
| chr2:43724408
|
A | G | 1 | a0001c0043t0004g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2542-1864A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724408 | ||||||
| chr2:43724468
|
A | C | 5 | a0001c0024t0003g0011a0001c0024t0003g0065a0002c0006t0002g0096others(2): Show | 5 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2542-1804A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724468 | ||||||
| chr2:43724635
|
A | G | 1 | a0001c0003t0001g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2542-1637A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724635 | ||||||
| chr2:43724732
|
A | G | 178 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.2542-1540A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724732 | ||||||
| chr2:43724783
|
T | A | 168 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2542-1489T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724783 | ||||||
| chr2:43724934
|
C | T | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2542-1338C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43724934 | ||||||
| chr2:43725269
|
G | C | 175 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2542-1003G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725269 | ||||||
| chr2:43725278
|
T | G | 7 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150others(4): Show | 7 | HG02647.hp2 HG02886.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2542-994T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725278 | ||||||
| chr2:43725293
|
C | G | 2 | a0001c0024t0003g0011a0001c0024t0003g0065 | 2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2542-979C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725293 | ||||||
| chr2:43725331
|
G | A | 1 | a0001c0055t0001g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2542-941G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725331 | ||||||
| chr2:43725400
|
A | G | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2542-872A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725400 | ||||||
| chr2:43725461
|
G | T | 1 | a0015c0028t0003g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2542-811G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725461 | ||||||
| chr2:43725541
|
C | G | 1 | a0003c0013t0002g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2542-731C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725541 | ||||||
| chr2:43725556
|
G | T | 115 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2542-716G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725556 | ||||||
| chr2:43725831
|
A | G | 175 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2542-441A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725831 | ||||||
| chr2:43725883
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0172 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2542-389G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725883 | ||||||
| chr2:43725926
|
T | C | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2542-346T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43725926 | ||||||
| chr2:43725945
|
C | CA | 8 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150others(5): Show | 8 | HG02647.hp2 HG02886.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2542-318dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr2 | 43725945 | |||||
| chr2:43725957
|
A | AT | 58 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0068others(55): Show | 58 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2542-306dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr2 | 43725957 | |||||
| chr2:43726099
|
G | C | 1 | a0022c0056t0003g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2542-173G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43726099 | ||||||
| chr2:43726124
|
CAA | C | 168 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2542-133_2542-132d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr2 | 43726124 | |||||
| chr2:43726240
|
G | C | 1 | a0002c0005t0003g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2542-32G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 16/29 | chr2 | 43726240 | ||||||
| chr2:43726511
|
G | A | 1 | a0001c0001t0019g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2721+60G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726511 | ||||||
| chr2:43726525
|
A | G | 163 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2721+74A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726525 | ||||||
| chr2:43726613
|
C | T | 168 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2721+162C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726613 | ||||||
| chr2:43726614
|
G | C | 37 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.2721+163G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726614 | ||||||
| chr2:43726654
|
T | C | 1 | a0002c0047t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2721+203T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726654 | ||||||
| chr2:43726675
|
G | A | 7 | a0001c0024t0003g0011a0001c0024t0003g0065a0002c0005t0003g0032others(4): Show | 7 | HG02698.hp2 HG03239.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.2721+224G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726675 | ||||||
| chr2:43726774
|
A | G | 6 | a0001c0007t0001g0003a0001c0007t0001g0019a0001c0007t0001g0061others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+323A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726774 | ||||||
| chr2:43726941
|
A | G | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2721+490A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726941 | ||||||
| chr2:43726957
|
T | TTTTTCAT others(35): Show |
6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+543_2721+584d others(44): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43726957 | |||||
| chr2:43726969
|
T | A | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2721+518T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43726969 | ||||||
| chr2:43727184
|
C | T | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+733C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727184 | ||||||
| chr2:43727185
|
G | A | 7 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(4): Show | 7 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2721+734G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727185 | ||||||
| chr2:43727189
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2721+738G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727189 | ||||||
| chr2:43727249
|
C | T | 207 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0067others(204): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2721+798C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727249 | ||||||
| chr2:43727251
|
A | T | 2 | a0002c0006t0003g0132a0018c0041t0003g0204 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2721+800A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727251 | ||||||
| chr2:43727327
|
G | A | 22 | a0001c0003t0001g0068a0001c0003t0001g0171a0001c0003t0002g0181others(19): Show | 22 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2721+876G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727327 | ||||||
| chr2:43727406
|
G | A | 64 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0068others(61): Show | 64 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.2721+955G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727406 | ||||||
| chr2:43727410
|
C | CAAAAAAA others(3): Show |
56 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2721+961_2721+970d others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43727410 | |||||
| chr2:43727410
|
C | CAAAAAAA others(4): Show |
108 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0001g0242others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2721+960_2721+970d others(13): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43727410 | |||||
| chr2:43727410
|
C | CAAAAAAA others(5): Show |
5 | a0001c0003t0002g0237a0001c0009t0002g0106a0002c0006t0004g0108others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721+970_2721+971i others(14): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43727410 | |||||
| chr2:43727422
|
G | A | 1 | a0013c0026t0002g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2721+971G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727422 | ||||||
| chr2:43727588
|
T | C | 1 | a0001c0001t0018g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2721+1137T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727588 | ||||||
| chr2:43727620
|
A | G | 1 | a0013c0026t0002g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2721+1169A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727620 | ||||||
| chr2:43727653
|
C | T | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2721+1202C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727653 | ||||||
| chr2:43727816
|
T | C | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+1365T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727816 | ||||||
| chr2:43727870
|
C | G | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+1419C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727870 | ||||||
| chr2:43727871
|
T | C | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+1420T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43727871 | ||||||
| chr2:43728050
|
A | C | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-1587A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728050 | ||||||
| chr2:43728066
|
G | A | 1 | a0001c0001t0018g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2722-1571G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728066 | ||||||
| chr2:43728273
|
G | A | 1 | a0001c0032t0002g0249 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2722-1364G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728273 | ||||||
| chr2:43728340
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2722-1297G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728340 | ||||||
| chr2:43728417
|
G | A | 41 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2722-1220G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728417 | ||||||
| chr2:43728426
|
C | T | 3 | a0001c0003t0002g0237a0001c0009t0002g0106a0020c0046t0003g0165 | 3 | HG02615.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2722-1211C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728426 | ||||||
| chr2:43728451
|
C | G | 1 | a0001c0003t0002g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2722-1186C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728451 | ||||||
| chr2:43728477
|
C | CA | 17 | a0001c0001t0013g0111a0001c0002t0002g0200a0001c0002t0002g0231others(14): Show | 17 | HG00735.hp1 HG00741.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2722-1142dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43728477 | |||||
| chr2:43728477
|
C | CAA | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-1143_2722-114 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43728477 | |||||
| chr2:43728537
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2722-1100T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728537 | ||||||
| chr2:43728541
|
T | C | 1 | a0003c0004t0010g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2722-1096T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728541 | ||||||
| chr2:43728541
|
T | G | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2722-1096T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728541 | ||||||
| chr2:43728562
|
C | CT | 6 | a0001c0001t0001g0079a0001c0001t0001g0187a0001c0002t0001g0104others(3): Show | 6 | HG01361.hp1 HG02738.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-1058dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43728562 | |||||
| chr2:43728562
|
CT | C | 112 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(109): Show | 112 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.2722-1058delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 43728562 | |||||
| chr2:43728575
|
T | A | 2 | a0001c0003t0001g0202a0005c0008t0002g0147 | 2 | HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2722-1062T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728575 | ||||||
| chr2:43728576
|
T | A | 35 | a0001c0001t0002g0042a0001c0001t0002g0058a0001c0002t0001g0242others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.2722-1061T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728576 | ||||||
| chr2:43728577
|
T | A | 96 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2722-1060T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728577 | ||||||
| chr2:43728578
|
T | A | 157 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.2722-1059T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728578 | ||||||
| chr2:43728579
|
T | A | 168 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2722-1058T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728579 | ||||||
| chr2:43728605
|
A | C | 85 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0002t0002g0130others(82): Show | 85 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.2722-1032A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728605 | ||||||
| chr2:43728622
|
C | A | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2722-1015C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728622 | ||||||
| chr2:43728631
|
G | T | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-1006G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728631 | ||||||
| chr2:43728644
|
C | G | 6 | a0004c0010t0006g0135a0004c0010t0006g0206a0004c0038t0006g0093others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-993C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728644 | ||||||
| chr2:43728753
|
C | T | 1 | a0001c0001t0013g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2722-884C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728753 | ||||||
| chr2:43728793
|
C | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2722-844C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728793 | ||||||
| chr2:43728800
|
G | T | 33 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.2722-837G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728800 | ||||||
| chr2:43728994
|
T | A | 7 | a0003c0004t0002g0118a0003c0004t0002g0137a0003c0004t0002g0141others(4): Show | 7 | HG00738.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2722-643T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43728994 | ||||||
| chr2:43729291
|
A | T | 1 | a0002c0023t0004g0246 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2722-346A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43729291 | ||||||
| chr2:43729426
|
A | G | 1 | a0001c0002t0002g0233 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2722-211A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43729426 | ||||||
| chr2:43729528
|
G | A | 33 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.2722-109G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 17/29 | chr2 | 43729528 | ||||||
| chr2:43729802
|
G | A | 1 | a0018c0041t0003g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2830+57G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43729802 | ||||||
| chr2:43729865
|
A | G | 4 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2830+120A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43729865 | ||||||
| chr2:43730005
|
T | C | 1 | a0001c0003t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2830+260T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730005 | ||||||
| chr2:43730022
|
C | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2830+277C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730022 | ||||||
| chr2:43730061
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0038 | 2 | NA18950.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2830+316C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730061 | ||||||
| chr2:43730290
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2830+545C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730290 | ||||||
| chr2:43730570
|
T | G | 3 | a0001c0003t0002g0237a0001c0009t0002g0106a0020c0046t0003g0165 | 3 | HG02615.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2830+825T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730570 | ||||||
| chr2:43730629
|
G | A | 1 | a0001c0003t0002g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2831-861G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730629 | ||||||
| chr2:43730675
|
A | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0043 | 2 | HG01106.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2831-815A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730675 | ||||||
| chr2:43730764
|
G | A | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2831-726G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730764 | ||||||
| chr2:43730771
|
G | C | 6 | a0003c0004t0002g0107a0003c0012t0004g0174a0003c0012t0004g0175others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2831-719G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43730771 | ||||||
| chr2:43731091
|
A | G | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2831-399A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731091 | ||||||
| chr2:43731166
|
G | A | 8 | a0001c0018t0002g0149a0001c0018t0002g0150a0002c0005t0011g0013others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2831-324G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731166 | ||||||
| chr2:43731299
|
A | T | 1 | a0002c0005t0002g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2831-191A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731299 | ||||||
| chr2:43731370
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2831-120C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731370 | ||||||
| chr2:43731378
|
C | T | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2831-112C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731378 | ||||||
| chr2:43731396
|
G | T | 3 | a0001c0003t0002g0237a0001c0009t0002g0106a0020c0046t0003g0165 | 3 | HG02615.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2831-94G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731396 | ||||||
| chr2:43731419
|
G | T | 3 | a0001c0003t0002g0237a0001c0009t0002g0106a0020c0046t0003g0165 | 3 | HG02615.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2831-71G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 18/29 | chr2 | 43731419 | ||||||
| chr2:43731722
|
A | G | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2943+120A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43731722 | ||||||
| chr2:43731949
|
A | G | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2943+347A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43731949 | ||||||
| chr2:43732112
|
C | G | 1 | a0002c0006t0004g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2943+510C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732112 | ||||||
| chr2:43732294
|
T | C | 1 | a0001c0003t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2943+692T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732294 | ||||||
| chr2:43732319
|
C | T | 1 | a0001c0003t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2943+717C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732319 | ||||||
| chr2:43732376
|
T | G | 19 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(16): Show | 19 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2943+774T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732376 | ||||||
| chr2:43732379
|
T | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2943+777T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732379 | ||||||
| chr2:43732408
|
C | T | 137 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(134): Show | 137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.2943+806C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732408 | ||||||
| chr2:43732557
|
T | C | 1 | a0002c0047t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2943+955T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732557 | ||||||
| chr2:43732661
|
C | A | 19 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(16): Show | 19 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2943+1059C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732661 | ||||||
| chr2:43732665
|
T | A | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2943+1063T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732665 | ||||||
| chr2:43732666
|
C | A | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2943+1064C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732666 | ||||||
| chr2:43732706
|
A | T | 6 | a0002c0005t0011g0013a0002c0006t0011g0239a0002c0011t0008g0119others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2943+1104A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732706 | ||||||
| chr2:43732716
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0041others(3): Show | 6 | HG00639.hp2 HG01993.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.2943+1114C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732716 | ||||||
| chr2:43732904
|
A | C | 44 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2943+1302A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732904 | ||||||
| chr2:43732959
|
T | G | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2943+1357T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732959 | ||||||
| chr2:43732967
|
C | A | 19 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(16): Show | 19 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2943+1365C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732967 | ||||||
| chr2:43732969
|
T | TC | 44 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2943+1372dupC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr2 | 43732969 | |||||
| chr2:43732971
|
C | T | 55 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(52): Show | 55 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.2943+1369C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732971 | ||||||
| chr2:43732997
|
C | T | 3 | a0001c0018t0002g0149a0001c0018t0002g0150a0001c0051t0001g0082 | 3 | HG00741.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2943+1395C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43732997 | ||||||
| chr2:43733362
|
CA | C | 19 | a0001c0001t0001g0187a0001c0001t0014g0063a0001c0001t0014g0064others(16): Show | 19 | HG00323.hp1 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2943+1781delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr2 | 43733362 | |||||
| chr2:43733362
|
CAA | C | 113 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(110): Show | 113 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.2943+1780_2943+178 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr2 | 43733362 | |||||
| chr2:43733362
|
CAAA | C | 22 | a0001c0009t0002g0124a0002c0006t0002g0096a0002c0006t0002g0182others(19): Show | 22 | HG00323.hp2 HG00738.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2943+1779_2943+178 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr2 | 43733362 | |||||
| chr2:43733519
|
T | A | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2943+1917T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733519 | ||||||
| chr2:43733571
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0043 | 2 | HG01106.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2943+1969A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733571 | ||||||
| chr2:43733600
|
G | A | 55 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(52): Show | 55 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.2943+1998G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733600 | ||||||
| chr2:43733681
|
G | A | 138 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(135): Show | 138 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.2943+2079G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733681 | ||||||
| chr2:43733691
|
C | T | 6 | a0002c0005t0011g0013a0002c0006t0011g0239a0002c0011t0008g0119others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2943+2089C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733691 | ||||||
| chr2:43733756
|
A | G | 1 | a0001c0018t0002g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2943+2154A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733756 | ||||||
| chr2:43733777
|
T | C | 1 | a0001c0002t0002g0252 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2943+2175T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733777 | ||||||
| chr2:43733786
|
G | A | 137 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(134): Show | 137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.2943+2184G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733786 | ||||||
| chr2:43733817
|
A | G | 22 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251others(19): Show | 22 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2943+2215A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43733817 | ||||||
| chr2:43734138
|
A | C | 17 | a0001c0002t0002g0200a0001c0003t0001g0180a0001c0003t0002g0237others(14): Show | 17 | HG00738.hp2 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2943+2536A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734138 | ||||||
| chr2:43734310
|
A | G | 138 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(135): Show | 138 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.2943+2708A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734310 | ||||||
| chr2:43734353
|
C | T | 1 | a0002c0023t0004g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2943+2751C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734353 | ||||||
| chr2:43734576
|
C | T | 1 | a0002c0020t0002g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2943+2974C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734576 | ||||||
| chr2:43734613
|
A | G | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2943+3011A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734613 | ||||||
| chr2:43734617
|
T | A | 1 | a0003c0012t0004g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2943+3015T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734617 | ||||||
| chr2:43734691
|
G | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2943+3089G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734691 | ||||||
| chr2:43734890
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0089 | 2 | HG02155.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2943+3288A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734890 | ||||||
| chr2:43734978
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0060 | 2 | NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2944-3363A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43734978 | ||||||
| chr2:43735138
|
C | T | 40 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(37): Show | 40 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2944-3203C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735138 | ||||||
| chr2:43735335
|
A | G | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2944-3006A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735335 | ||||||
| chr2:43735423
|
G | T | 131 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0047others(128): Show | 131 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2944-2918G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735423 | ||||||
| chr2:43735434
|
G | A | 4 | a0001c0024t0003g0011a0001c0024t0003g0065a0002c0006t0003g0193others(1): Show | 4 | HG03239.hp2 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2944-2907G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735434 | ||||||
| chr2:43735452
|
G | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2944-2889G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735452 | ||||||
| chr2:43735555
|
C | G | 1 | a0001c0002t0002g0218 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2944-2786C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735555 | ||||||
| chr2:43735618
|
T | C | 4 | a0001c0002t0002g0220a0001c0002t0002g0234a0001c0002t0002g0241others(1): Show | 4 | HG01175.hp1 HG01256.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2944-2723T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735618 | ||||||
| chr2:43735639
|
T | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2944-2702T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735639 | ||||||
| chr2:43735851
|
C | T | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2944-2490C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43735851 | ||||||
| chr2:43736048
|
A | G | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2944-2293A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736048 | ||||||
| chr2:43736057
|
GTTA | G | 2 | a0001c0003t0001g0196a0001c0045t0001g0208 | 2 | HG01981.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2944-2269_2944-226 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr2 | 43736057 | |||||
| chr2:43736145
|
T | G | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2944-2196T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736145 | ||||||
| chr2:43736416
|
C | T | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2944-1925C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736416 | ||||||
| chr2:43736449
|
C | T | 13 | a0001c0003t0001g0180a0002c0006t0004g0108a0003c0004t0002g0118others(10): Show | 13 | HG00738.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2944-1892C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736449 | ||||||
| chr2:43736453
|
G | T | 1 | a0002c0011t0002g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2944-1888G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736453 | ||||||
| chr2:43736455
|
A | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2944-1886A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736455 | ||||||
| chr2:43736563
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2944-1778G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736563 | ||||||
| chr2:43736575
|
T | C | 2 | a0001c0003t0001g0188a0001c0003t0001g0189 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2944-1766T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736575 | ||||||
| chr2:43736790
|
C | T | 1 | a0001c0002t0002g0218 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2944-1551C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736790 | ||||||
| chr2:43736827
|
A | C | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2944-1514A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736827 | ||||||
| chr2:43736831
|
A | C | 34 | a0001c0002t0002g0200a0001c0003t0001g0068a0001c0003t0001g0171others(31): Show | 34 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2944-1510A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736831 | ||||||
| chr2:43736857
|
G | A | 1 | a0001c0003t0001g0216 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2944-1484G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736857 | ||||||
| chr2:43736861
|
G | C | 1 | a0007c0014t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2944-1480G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736861 | ||||||
| chr2:43736939
|
C | T | 91 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0001g0180others(88): Show | 91 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.2944-1402C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43736939 | ||||||
| chr2:43737008
|
C | T | 32 | a0001c0003t0001g0180a0002c0006t0004g0108a0003c0004t0002g0080others(29): Show | 32 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.2944-1333C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737008 | ||||||
| chr2:43737357
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2944-984T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737357 | ||||||
| chr2:43737604
|
C | T | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2944-737C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737604 | ||||||
| chr2:43737613
|
G | T | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2944-728G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737613 | ||||||
| chr2:43737630
|
A | C | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2944-711A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737630 | ||||||
| chr2:43737698
|
A | G | 88 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(85): Show | 88 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2944-643A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737698 | ||||||
| chr2:43737868
|
C | T | 42 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2944-473C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737868 | ||||||
| chr2:43737887
|
T | C | 70 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(67): Show | 70 | HG00639.hp1 HG01074.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.2944-454T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737887 | ||||||
| chr2:43737942
|
G | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2944-399G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43737942 | ||||||
| chr2:43738025
|
G | C | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2944-316G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43738025 | ||||||
| chr2:43738119
|
T | C | 2 | a0001c0003t0001g0203a0001c0007t0001g0018 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2944-222T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43738119 | ||||||
| chr2:43738159
|
G | A | 16 | a0002c0005t0002g0020a0002c0005t0002g0045a0002c0005t0002g0054others(13): Show | 16 | HG01168.hp2 HG01975.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.2944-182G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43738159 | ||||||
| chr2:43738306
|
C | T | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2944-35C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 19/29 | chr2 | 43738306 | ||||||
| chr2:43738561
|
G | GT | 65 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(62): Show | 65 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(62): Show |
intron_variant | MODIFIER | c.3123+50dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 43738561 | |||||
| chr2:43738566
|
T | C | 57 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(54): Show | 57 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3123+46T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43738566 | ||||||
| chr2:43738639
|
A | T | 5 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3123+119A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43738639 | ||||||
| chr2:43738640
|
G | A | 30 | a0002c0006t0004g0108a0003c0004t0002g0080a0003c0004t0002g0097others(27): Show | 30 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.3123+120G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43738640 | ||||||
| chr2:43738786
|
G | A | 1 | a0002c0047t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3123+266G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43738786 | ||||||
| chr2:43738948
|
A | T | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3123+428A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43738948 | ||||||
| chr2:43738962
|
G | A | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3123+442G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43738962 | ||||||
| chr2:43739052
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3123+532C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739052 | ||||||
| chr2:43739073
|
C | T | 123 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(120): Show | 123 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.3123+553C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739073 | ||||||
| chr2:43739106
|
G | T | 3 | a0001c0003t0001g0186a0007c0014t0001g0142a0017c0036t0001g0099 | 3 | HG01346.hp2 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3123+586G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739106 | ||||||
| chr2:43739133
|
C | T | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3123+613C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739133 | ||||||
| chr2:43739138
|
G | A | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3123+618G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739138 | ||||||
| chr2:43739198
|
A | G | 4 | a0001c0003t0001g0203a0001c0007t0001g0018a0003c0004t0002g0118others(1): Show | 4 | HG02818.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3123+678A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739198 | ||||||
| chr2:43739310
|
C | G | 7 | a0001c0001t0002g0051a0001c0002t0002g0221a0001c0002t0002g0227others(4): Show | 7 | HG01358.hp2 HG01952.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.3123+790C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739310 | ||||||
| chr2:43739328
|
C | T | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3123+808C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739328 | ||||||
| chr2:43739469
|
C | A | 2 | a0001c0018t0002g0149a0001c0018t0002g0150 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3123+949C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739469 | ||||||
| chr2:43739483
|
G | A | 1 | a0003c0012t0004g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3123+963G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739483 | ||||||
| chr2:43739501
|
T | C | 2 | a0002c0005t0011g0013a0002c0006t0011g0239 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3123+981T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739501 | ||||||
| chr2:43739509
|
C | T | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3123+989C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739509 | ||||||
| chr2:43739571
|
C | T | 1 | a0013c0026t0002g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3123+1051C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739571 | ||||||
| chr2:43739702
|
G | T | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3123+1182G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739702 | ||||||
| chr2:43739733
|
A | G | 1 | a0001c0003t0001g0179 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3123+1213A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739733 | ||||||
| chr2:43739748
|
T | G | 158 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0002g0017others(155): Show | 158 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.3124-1198T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739748 | ||||||
| chr2:43739853
|
T | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3124-1093T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43739853 | ||||||
| chr2:43740049
|
C | G | 1 | a0001c0002t0002g0218 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3124-897C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740049 | ||||||
| chr2:43740067
|
A | G | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3124-879A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740067 | ||||||
| chr2:43740094
|
A | G | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3124-852A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740094 | ||||||
| chr2:43740095
|
C | T | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3124-851C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740095 | ||||||
| chr2:43740283
|
G | T | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3124-663G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740283 | ||||||
| chr2:43740289
|
A | T | 1 | a0001c0003t0002g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3124-657A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740289 | ||||||
| chr2:43740294
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3124-652A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740294 | ||||||
| chr2:43740295
|
A | T | 2 | a0002c0011t0008g0119a0002c0011t0008g0145 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3124-651A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740295 | ||||||
| chr2:43740296
|
T | A | 10 | a0002c0005t0002g0020a0002c0005t0002g0045a0002c0005t0002g0054others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.3124-650T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740296 | ||||||
| chr2:43740350
|
A | G | 33 | a0001c0002t0002g0200a0001c0002t0002g0218a0001c0003t0001g0068others(30): Show | 33 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.3124-596A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740350 | ||||||
| chr2:43740383
|
A | G | 156 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(153): Show | 156 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.3124-563A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740383 | ||||||
| chr2:43740389
|
T | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3124-557T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740389 | ||||||
| chr2:43740434
|
G | A | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3124-512G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740434 | ||||||
| chr2:43740533
|
G | C | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3124-413G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740533 | ||||||
| chr2:43740655
|
C | A | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3124-291C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740655 | ||||||
| chr2:43740667
|
T | C | 2 | a0001c0003t0001g0196a0001c0045t0001g0208 | 2 | HG01981.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3124-279T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740667 | ||||||
| chr2:43740776
|
G | C | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3124-170G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740776 | ||||||
| chr2:43740885
|
C | T | 13 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3124-61C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740885 | ||||||
| chr2:43740910
|
C | T | 1 | a0001c0032t0002g0249 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3124-36C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 20/29 | chr2 | 43740910 | ||||||
| chr2:43741080
|
G | A | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3221+37G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741080 | ||||||
| chr2:43741101
|
A | G | 4 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3221+58A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741101 | ||||||
| chr2:43741177
|
G | A | 13 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3221+134G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741177 | ||||||
| chr2:43741192
|
G | A | 19 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0003g0032others(16): Show | 19 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.3221+149G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741192 | ||||||
| chr2:43741255
|
G | C | 29 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(26): Show | 29 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.3221+212G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741255 | ||||||
| chr2:43741361
|
C | T | 14 | a0003c0004t0002g0107a0003c0004t0002g0137a0003c0004t0002g0141others(11): Show | 14 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.3221+318C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741361 | ||||||
| chr2:43741373
|
C | G | 31 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(28): Show | 31 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.3221+330C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741373 | ||||||
| chr2:43741511
|
C | T | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3221+468C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741511 | ||||||
| chr2:43741576
|
C | T | 3 | a0002c0005t0011g0013a0002c0006t0004g0108a0002c0006t0011g0239 | 3 | HG02451.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3221+533C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741576 | ||||||
| chr2:43741713
|
T | C | 5 | a0001c0002t0002g0200a0001c0003t0002g0237a0001c0009t0002g0106others(2): Show | 5 | HG02615.hp2 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3221+670T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741713 | ||||||
| chr2:43741717
|
C | T | 13 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3221+674C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741717 | ||||||
| chr2:43741796
|
G | T | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3221+753G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741796 | ||||||
| chr2:43741861
|
T | C | 2 | a0009c0021t0005g0253a0009c0021t0005g0254 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3221+818T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741861 | ||||||
| chr2:43741940
|
G | T | 55 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.3222-801G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43741940 | ||||||
| chr2:43742101
|
A | G | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3222-640A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742101 | ||||||
| chr2:43742146
|
G | A | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3222-595G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742146 | ||||||
| chr2:43742158
|
C | A | 53 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3222-583C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742158 | ||||||
| chr2:43742161
|
C | T | 1 | a0001c0007t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3222-580C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742161 | ||||||
| chr2:43742277
|
C | T | 1 | a0001c0018t0002g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3222-464C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742277 | ||||||
| chr2:43742309
|
A | AT | 31 | a0001c0003t0001g0068a0001c0003t0001g0171a0003c0004t0002g0080others(28): Show | 31 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.3222-419dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr2 | 43742309 | |||||
| chr2:43742310
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3222-431T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742310 | ||||||
| chr2:43742343
|
G | A | 53 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3222-398G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742343 | ||||||
| chr2:43742449
|
A | T | 15 | a0001c0003t0001g0068a0001c0003t0001g0171a0003c0004t0002g0080others(12): Show | 15 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3222-292A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 21/29 | chr2 | 43742449 | ||||||
| chr2:43742986
|
G | C | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3399+68G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43742986 | ||||||
| chr2:43743113
|
A | T | 53 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3399+195A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743113 | ||||||
| chr2:43743114
|
C | T | 103 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(100): Show | 103 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3399+196C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743114 | ||||||
| chr2:43743148
|
A | G | 42 | a0001c0024t0003g0011a0001c0024t0003g0065a0002c0005t0002g0020others(39): Show | 42 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.3399+230A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743148 | ||||||
| chr2:43743156
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3399+238G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743156 | ||||||
| chr2:43743182
|
C | T | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3399+264C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743182 | ||||||
| chr2:43743183
|
G | A | 7 | a0001c0001t0002g0031a0001c0001t0002g0047a0001c0001t0002g0058others(4): Show | 7 | HG02698.hp1 HG03688.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.3399+265G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743183 | ||||||
| chr2:43743200
|
A | G | 6 | a0001c0001t0002g0031a0001c0001t0002g0047a0001c0001t0002g0058others(3): Show | 6 | HG02698.hp1 HG03688.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399+282A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743200 | ||||||
| chr2:43743210
|
C | T | 1 | a0002c0047t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3399+292C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743210 | ||||||
| chr2:43743620
|
G | A | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3400-214G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 22/29 | chr2 | 43743620 | ||||||
| chr2:43744124
|
GA | G | 6 | a0001c0003t0001g0180a0003c0004t0002g0137a0003c0004t0002g0141others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3555+145delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr2 | 43744124 | |||||
| chr2:43744153
|
C | T | 50 | a0002c0005t0002g0020a0002c0005t0002g0045a0002c0005t0002g0054others(47): Show | 50 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.3555+164C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744153 | ||||||
| chr2:43744421
|
C | T | 1 | a0003c0004t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3555+432C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744421 | ||||||
| chr2:43744550
|
G | T | 24 | a0002c0005t0003g0002a0002c0005t0003g0012a0002c0005t0003g0032others(21): Show | 24 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.3555+561G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744550 | ||||||
| chr2:43744606
|
G | A | 51 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(48): Show | 51 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.3555+617G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744606 | ||||||
| chr2:43744678
|
G | A | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3555+689G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744678 | ||||||
| chr2:43744683
|
C | T | 1 | a0002c0005t0003g0012 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3555+694C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744683 | ||||||
| chr2:43744741
|
A | G | 56 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3555+752A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744741 | ||||||
| chr2:43744828
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3555+839A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744828 | ||||||
| chr2:43744867
|
C | CA | 11 | a0001c0001t0001g0079a0001c0007t0001g0101a0002c0005t0003g0002others(8): Show | 11 | HG01175.hp2 HG01192.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3555+898dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr2 | 43744867 | |||||
| chr2:43744867
|
CA | C | 27 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0014g0063others(24): Show | 27 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3555+898delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr2 | 43744867 | |||||
| chr2:43744882
|
A | G | 64 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(61): Show | 64 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.3555+893A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744882 | ||||||
| chr2:43744884
|
A | G | 32 | a0001c0003t0001g0068a0001c0003t0001g0171a0003c0004t0002g0080others(29): Show | 32 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3555+895A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744884 | ||||||
| chr2:43744947
|
A | G | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3556-919A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43744947 | ||||||
| chr2:43745036
|
G | A | 1 | a0003c0004t0002g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3556-830G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745036 | ||||||
| chr2:43745041
|
T | A | 1 | a0001c0001t0002g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3556-825T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745041 | ||||||
| chr2:43745056
|
G | A | 1 | a0007c0014t0001g0167 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3556-810G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745056 | ||||||
| chr2:43745093
|
C | A | 1 | a0005c0008t0002g0147 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3556-773C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745093 | ||||||
| chr2:43745139
|
C | T | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3556-727C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745139 | ||||||
| chr2:43745293
|
G | A | 50 | a0002c0005t0002g0020a0002c0005t0002g0045a0002c0005t0002g0054others(47): Show | 50 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.3556-573G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745293 | ||||||
| chr2:43745346
|
A | G | 6 | a0001c0003t0002g0181a0002c0006t0003g0193a0004c0010t0006g0135others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3556-520A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745346 | ||||||
| chr2:43745361
|
A | G | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3556-505A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745361 | ||||||
| chr2:43745393
|
T | C | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3556-473T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745393 | ||||||
| chr2:43745451
|
G | A | 4 | a0002c0005t0011g0013a0002c0006t0004g0108a0002c0006t0011g0239others(1): Show | 4 | HG02451.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3556-415G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745451 | ||||||
| chr2:43745478
|
T | C | 1 | a0013c0026t0002g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3556-388T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745478 | ||||||
| chr2:43745527
|
G | A | 43 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.3556-339G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745527 | ||||||
| chr2:43745569
|
A | G | 55 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.3556-297A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745569 | ||||||
| chr2:43745672
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3556-194A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745672 | ||||||
| chr2:43745738
|
A | T | 1 | a0002c0005t0002g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3556-128A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 23/29 | chr2 | 43745738 | ||||||
| chr2:43746027
|
C | A | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3653+64C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746027 | ||||||
| chr2:43746048
|
G | A | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3653+85G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746048 | ||||||
| chr2:43746072
|
G | C | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3653+109G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746072 | ||||||
| chr2:43746339
|
G | C | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3653+376G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746339 | ||||||
| chr2:43746385
|
C | T | 4 | a0006c0015t0001g0007a0006c0015t0001g0156a0006c0015t0001g0198others(1): Show | 4 | HG00741.hp2 HG01175.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.3653+422C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746385 | ||||||
| chr2:43746533
|
TAC | T | 149 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(146): Show | 149 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.3653+587_3653+588d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43746533 | |||||
| chr2:43746551
|
C | T | 1 | a0001c0003t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3653+588C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746551 | ||||||
| chr2:43746607
|
A | G | 1 | a0001c0003t0001g0171 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3653+644A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746607 | ||||||
| chr2:43746690
|
C | T | 12 | a0001c0001t0002g0030a0001c0001t0002g0051a0001c0002t0001g0225others(9): Show | 12 | HG00438.hp1 HG00438.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.3653+727C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746690 | ||||||
| chr2:43746699
|
T | C | 1 | a0005c0008t0002g0230 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3653+736T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746699 | ||||||
| chr2:43746750
|
C | T | 52 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3653+787C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746750 | ||||||
| chr2:43746752
|
C | T | 2 | a0001c0003t0001g0186a0007c0014t0001g0142 | 2 | HG01346.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3653+789C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746752 | ||||||
| chr2:43746804
|
A | G | 10 | a0001c0002t0002g0130a0001c0002t0002g0240a0001c0003t0002g0122others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3653+841A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746804 | ||||||
| chr2:43746812
|
T | C | 25 | a0001c0043t0004g0247a0002c0005t0003g0002a0002c0005t0003g0012others(22): Show | 25 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.3653+849T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746812 | ||||||
| chr2:43746830
|
C | T | 1 | a0002c0011t0008g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3653+867C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746830 | ||||||
| chr2:43746901
|
C | T | 52 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3653+938C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746901 | ||||||
| chr2:43746909
|
G | A | 3 | a0003c0022t0002g0140a0003c0022t0002g0164a0011c0033t0002g0103 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3653+946G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746909 | ||||||
| chr2:43746964
|
T | C | 104 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(101): Show | 104 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.3653+1001T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43746964 | ||||||
| chr2:43747065
|
T | G | 2 | a0002c0005t0003g0032a0002c0005t0003g0033 | 2 | HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.3653+1102T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747065 | ||||||
| chr2:43747082
|
C | G | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3653+1119C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747082 | ||||||
| chr2:43747092
|
G | GTC | 30 | a0002c0005t0002g0020a0002c0005t0002g0045a0002c0005t0002g0054others(27): Show | 30 | HG01168.hp2 HG01975.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.3653+1144_3653+114 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747092 | |||||
| chr2:43747092
|
G | GTCTCTCT others(17): Show |
19 | a0001c0043t0004g0247a0002c0005t0003g0002a0002c0005t0003g0012others(16): Show | 19 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.3653+1145_3653+114 others(28): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747092 | |||||
| chr2:43747107
|
T | TCTCCCTC others(19): Show |
1 | a0005c0008t0003g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3653+1145_3653+114 others(30): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747107 | |||||
| chr2:43747109
|
C | CCT | 19 | a0001c0001t0001g0067a0001c0001t0001g0078a0001c0001t0001g0170others(16): Show | 19 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.3653+1170_3653+117 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747109 | |||||
| chr2:43747109
|
C | T | 1 | a0005c0008t0003g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3653+1146C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747109 | ||||||
| chr2:43747109
|
CCT | C | 54 | a0001c0001t0002g0017a0001c0001t0002g0031a0001c0001t0002g0042others(51): Show | 54 | HG00597.hp2 HG00642.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3653+1170_3653+117 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747109 | |||||
| chr2:43747109
|
CCTCT | C | 4 | a0001c0002t0002g0200a0001c0002t0002g0209a0001c0018t0002g0149others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.3653+1168_3653+117 others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747109 | |||||
| chr2:43747109
|
CCTCTCT | C | 12 | a0001c0001t0002g0030a0001c0001t0002g0051a0001c0002t0001g0225others(9): Show | 12 | HG00438.hp1 HG00438.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.3653+1166_3653+117 others(10): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43747109 | |||||
| chr2:43747219
|
T | C | 66 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(63): Show | 66 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.3653+1256T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747219 | ||||||
| chr2:43747260
|
T | A | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3653+1297T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747260 | ||||||
| chr2:43747298
|
A | G | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3653+1335A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747298 | ||||||
| chr2:43747329
|
C | T | 1 | a0002c0025t0004g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3653+1366C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747329 | ||||||
| chr2:43747376
|
G | A | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3653+1413G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747376 | ||||||
| chr2:43747482
|
G | C | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3653+1519G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747482 | ||||||
| chr2:43747530
|
A | G | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3653+1567A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747530 | ||||||
| chr2:43747553
|
G | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3653+1590G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747553 | ||||||
| chr2:43747666
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0172 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3653+1703C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747666 | ||||||
| chr2:43747796
|
G | A | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3653+1833G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747796 | ||||||
| chr2:43747827
|
A | G | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3653+1864A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747827 | ||||||
| chr2:43747845
|
A | G | 1 | a0001c0002t0002g0220 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3653+1882A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747845 | ||||||
| chr2:43747897
|
G | A | 1 | a0001c0003t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3653+1934G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747897 | ||||||
| chr2:43747924
|
T | C | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3653+1961T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43747924 | ||||||
| chr2:43748042
|
C | A | 142 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(139): Show | 142 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.3653+2079C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748042 | ||||||
| chr2:43748085
|
G | A | 7 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150others(4): Show | 7 | HG02647.hp2 HG02886.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.3653+2122G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748085 | ||||||
| chr2:43748173
|
T | C | 13 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3653+2210T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748173 | ||||||
| chr2:43748307
|
A | T | 152 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(149): Show | 152 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.3653+2344A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748307 | ||||||
| chr2:43748311
|
T | G | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3653+2348T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748311 | ||||||
| chr2:43748464
|
C | A | 17 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(14): Show | 17 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.3653+2501C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748464 | ||||||
| chr2:43748508
|
C | T | 4 | a0006c0015t0001g0007a0006c0015t0001g0156a0006c0015t0001g0198others(1): Show | 4 | HG00741.hp2 HG01175.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.3653+2545C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748508 | ||||||
| chr2:43748552
|
C | T | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3653+2589C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748552 | ||||||
| chr2:43748571
|
C | T | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3653+2608C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748571 | ||||||
| chr2:43748624
|
A | T | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3653+2661A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748624 | ||||||
| chr2:43748655
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3653+2692C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748655 | ||||||
| chr2:43748691
|
C | T | 50 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3653+2728C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748691 | ||||||
| chr2:43748760
|
C | CT | 65 | a0001c0001t0002g0075a0001c0001t0014g0063a0001c0001t0014g0064others(62): Show | 65 | HG00639.hp1 HG01074.hp2 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.3653+2810dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43748760 | |||||
| chr2:43748760
|
C | CTT | 48 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3653+2809_3653+281 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43748760 | |||||
| chr2:43748760
|
CT | C | 17 | a0003c0004t0002g0107a0003c0004t0002g0137a0003c0004t0002g0141others(14): Show | 17 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.3653+2810delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43748760 | |||||
| chr2:43748818
|
A | G | 153 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(150): Show | 153 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.3653+2855A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748818 | ||||||
| chr2:43748830
|
T | C | 92 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(89): Show | 92 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.3653+2867T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748830 | ||||||
| chr2:43748855
|
C | G | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3653+2892C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748855 | ||||||
| chr2:43748876
|
C | T | 2 | a0001c0003t0002g0237a0001c0009t0002g0106 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3653+2913C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748876 | ||||||
| chr2:43748946
|
T | G | 111 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(108): Show | 111 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.3653+2983T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748946 | ||||||
| chr2:43748949
|
T | G | 111 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(108): Show | 111 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.3653+2986T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43748949 | ||||||
| chr2:43749003
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3653+3040C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749003 | ||||||
| chr2:43749045
|
C | A | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3653+3082C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749045 | ||||||
| chr2:43749058
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3653+3095A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749058 | ||||||
| chr2:43749124
|
T | C | 10 | a0001c0002t0001g0243a0001c0003t0001g0076a0001c0003t0001g0154others(7): Show | 10 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.3653+3161T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749124 | ||||||
| chr2:43749249
|
A | T | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3653+3286A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749249 | ||||||
| chr2:43749402
|
G | C | 153 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(150): Show | 153 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.3653+3439G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749402 | ||||||
| chr2:43749431
|
G | A | 9 | a0001c0001t0014g0063a0001c0001t0014g0064a0001c0003t0002g0181others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3653+3468G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749431 | ||||||
| chr2:43749433
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3653+3470C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749433 | ||||||
| chr2:43749528
|
T | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3653+3565T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749528 | ||||||
| chr2:43749757
|
T | A | 1 | a0002c0005t0003g0143 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3653+3794T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749757 | ||||||
| chr2:43749783
|
G | T | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3653+3820G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749783 | ||||||
| chr2:43749837
|
G | C | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3654-3782G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43749837 | ||||||
| chr2:43750128
|
A | G | 1 | a0005c0008t0002g0255 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3654-3491A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750128 | ||||||
| chr2:43750176
|
A | G | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3654-3443A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750176 | ||||||
| chr2:43750370
|
G | C | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3654-3249G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750370 | ||||||
| chr2:43750467
|
C | T | 41 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(38): Show | 41 | HG00438.hp1 HG00597.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.3654-3152C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750467 | ||||||
| chr2:43750480
|
C | CA | 55 | a0001c0001t0001g0109a0001c0001t0002g0075a0001c0024t0003g0011others(52): Show | 55 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.3654-3126dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43750480 | |||||
| chr2:43750524
|
C | T | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3654-3095C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750524 | ||||||
| chr2:43750782
|
G | A | 49 | a0001c0001t0002g0075a0001c0024t0003g0011a0001c0024t0003g0065others(46): Show | 49 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.3654-2837G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750782 | ||||||
| chr2:43750803
|
A | G | 2 | a0001c0002t0012g0226a0001c0002t0012g0232 | 2 | NA18747.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3654-2816A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750803 | ||||||
| chr2:43750881
|
C | A | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3654-2738C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43750881 | ||||||
| chr2:43751179
|
T | C | 12 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(9): Show | 12 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3654-2440T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751179 | ||||||
| chr2:43751207
|
C | T | 18 | a0001c0001t0002g0075a0002c0005t0002g0020a0002c0005t0002g0045others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.3654-2412C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751207 | ||||||
| chr2:43751419
|
G | T | 15 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150others(12): Show | 15 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3654-2200G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751419 | ||||||
| chr2:43751450
|
T | C | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3654-2169T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751450 | ||||||
| chr2:43751543
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3654-2076G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751543 | ||||||
| chr2:43751916
|
C | T | 18 | a0001c0001t0002g0075a0002c0005t0002g0020a0002c0005t0002g0045others(15): Show | 18 | HG01168.hp2 HG01975.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.3654-1703C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751916 | ||||||
| chr2:43751926
|
C | CTTTTTTT others(1): Show |
21 | a0001c0003t0002g0181a0003c0004t0002g0107a0003c0004t0002g0118others(18): Show | 21 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.3654-1685_3654-167 others(12): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43751926 | |||||
| chr2:43751926
|
CT | C | 5 | a0002c0005t0002g0054a0003c0004t0002g0100a0003c0004t0002g0116others(2): Show | 5 | HG01106.hp1 HG01891.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3654-1678delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43751926 | |||||
| chr2:43751927
|
T | TC | 3 | a0001c0001t0001g0085a0001c0001t0001g0222a0007c0035t0001g0168 | 3 | NA18955.hp1 NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3654-1692_3654-169 others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751927 | ||||||
| chr2:43751952
|
C | A | 1 | a0002c0016t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3654-1667C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751952 | ||||||
| chr2:43751977
|
T | A | 2 | a0002c0005t0011g0013a0002c0006t0011g0239 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3654-1642T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43751977 | ||||||
| chr2:43752057
|
G | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3654-1562G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752057 | ||||||
| chr2:43752071
|
C | A | 1 | a0003c0022t0002g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3654-1548C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752071 | ||||||
| chr2:43752092
|
C | G | 5 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3654-1527C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752092 | ||||||
| chr2:43752133
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3654-1486C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752133 | ||||||
| chr2:43752402
|
A | G | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3654-1217A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752402 | ||||||
| chr2:43752464
|
C | T | 1 | a0001c0002t0002g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3654-1155C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752464 | ||||||
| chr2:43752555
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3654-1064G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752555 | ||||||
| chr2:43752646
|
G | A | 1 | a0004c0038t0006g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3654-973G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752646 | ||||||
| chr2:43752878
|
T | C | 2 | a0001c0002t0012g0226a0001c0002t0012g0232 | 2 | NA18747.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3654-741T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43752878 | ||||||
| chr2:43753065
|
C | T | 9 | a0001c0002t0001g0243a0001c0003t0001g0076a0001c0003t0001g0154others(6): Show | 9 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.3654-554C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43753065 | ||||||
| chr2:43753104
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3654-515G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43753104 | ||||||
| chr2:43753297
|
A | G | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3654-322A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43753297 | ||||||
| chr2:43753335
|
A | G | 1 | a0001c0002t0002g0220 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3654-284A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43753335 | ||||||
| chr2:43753492
|
T | C | 32 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(29): Show | 32 | HG00438.hp1 HG01168.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.3654-127T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43753492 | ||||||
| chr2:43753538
|
T | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3654-81T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | chr2 | 43753538 | ||||||
| chr2:43753605
|
C | CT | 11 | a0002c0006t0004g0108a0003c0004t0002g0107a0003c0012t0004g0174others(8): Show | 11 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.3654-5dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 43753605 | |||||
| chr2:43753821
|
A | G | 2 | a0002c0005t0011g0013a0002c0006t0011g0239 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3795+61A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43753821 | ||||||
| chr2:43753898
|
A | T | 1 | a0001c0001t0002g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3795+138A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43753898 | ||||||
| chr2:43754027
|
G | T | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3795+267G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754027 | ||||||
| chr2:43754165
|
T | TAC | 18 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.3795+445_3795+446d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754165 | |||||
| chr2:43754165
|
TAC | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0041others(49): Show | 52 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.3795+445_3795+446d others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754165 | |||||
| chr2:43754165
|
TACAC | T | 3 | a0001c0003t0001g0199a0001c0007t0001g0019a0001c0030t0001g0215 | 3 | HG00140.hp1 HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3795+443_3795+446d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754165 | |||||
| chr2:43754165
|
TACACAC | T | 8 | a0001c0001t0001g0084a0001c0003t0001g0180a0001c0003t0001g0186others(5): Show | 8 | HG01346.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3795+441_3795+446d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754165 | |||||
| chr2:43754171
|
C | CACACACA others(156): Show |
3 | a0002c0005t0003g0012a0002c0005t0003g0083a0002c0005t0003g0143 | 3 | HG03130.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3795+438_3795+439i others(165): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754171 | |||||
| chr2:43754195
|
C | A | 1 | a0003c0044t0007g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3795+435C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754195 | ||||||
| chr2:43754195
|
C | CA | 17 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(14): Show | 17 | HG00438.hp1 HG01168.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.3795+436dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754195 | |||||
| chr2:43754195
|
C | CAA | 7 | a0001c0003t0002g0207a0002c0006t0002g0146a0002c0020t0002g0113others(4): Show | 7 | HG02622.hp2 HG02630.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.3795+436_3795+437i others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754195 | |||||
| chr2:43754196
|
ACAC | A | 6 | a0001c0043t0004g0247a0002c0005t0003g0002a0002c0023t0004g0159others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3795+437_3795+439d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754196 | ||||||
| chr2:43754197
|
C | A | 29 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(26): Show | 29 | HG00438.hp1 HG01168.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.3795+437C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754197 | ||||||
| chr2:43754197
|
C | CA | 11 | a0001c0003t0002g0181a0002c0005t0002g0020a0002c0005t0002g0056others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.3795+438dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754197 | |||||
| chr2:43754198
|
AC | A | 8 | a0001c0002t0002g0220a0001c0002t0002g0233a0001c0002t0009g0236others(5): Show | 8 | HG00639.hp1 HG01256.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.3795+439delC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754198 | ||||||
| chr2:43754198
|
ACAC | A | 3 | a0002c0005t0003g0069a0002c0006t0003g0163a0020c0046t0003g0165 | 3 | HG02922.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3795+439_3795+441d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754198 | ||||||
| chr2:43754199
|
C | A | 51 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(48): Show | 51 | HG00438.hp1 HG01074.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.3795+439C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754199 | ||||||
| chr2:43754199
|
C | CAA | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3795+440_3795+441i others(4): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754199 | |||||
| chr2:43754200
|
AC | A | 26 | a0001c0001t0002g0031a0001c0001t0002g0047a0001c0001t0002g0058others(23): Show | 26 | HG00597.hp2 HG01074.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.3795+441delC | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754200 | ||||||
| chr2:43754200
|
ACAC | A | 4 | a0002c0006t0003g0132a0002c0025t0004g0015a0002c0025t0004g0088others(1): Show | 4 | HG02132.hp2 HG02257.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3795+441_3795+443d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754200 | ||||||
| chr2:43754201
|
C | A | 84 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(81): Show | 84 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.3795+441C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754201 | ||||||
| chr2:43754203
|
C | A | 115 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(112): Show | 115 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.3795+443C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754203 | ||||||
| chr2:43754205
|
C | A | 121 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(118): Show | 121 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.3795+445C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754205 | ||||||
| chr2:43754205
|
C | CA | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3795+449dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754205 | |||||
| chr2:43754205
|
C | CAAAA | 9 | a0001c0024t0003g0011a0001c0024t0003g0065a0004c0010t0005g0092others(6): Show | 9 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3795+446_3795+449d others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754205 | |||||
| chr2:43754206
|
A | ACAC | 6 | a0002c0006t0004g0108a0003c0012t0004g0174a0003c0012t0004g0175others(3): Show | 6 | HG00738.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3795+446_3795+447i others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754206 | ||||||
| chr2:43754429
|
T | C | 11 | a0002c0006t0004g0108a0003c0004t0002g0107a0003c0012t0004g0174others(8): Show | 11 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.3795+669T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754429 | ||||||
| chr2:43754649
|
C | T | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3795+889C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754649 | ||||||
| chr2:43754727
|
G | T | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3795+967G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754727 | ||||||
| chr2:43754756
|
C | G | 1 | a0001c0051t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3795+996C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754756 | ||||||
| chr2:43754782
|
C | A | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3795+1022C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43754782 | ||||||
| chr2:43754869
|
C | CT | 28 | a0001c0001t0001g0040a0001c0003t0001g0180a0001c0024t0003g0011others(25): Show | 28 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.3795+1130dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754869 | |||||
| chr2:43754869
|
C | CTT | 103 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(100): Show | 103 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.3795+1129_3795+113 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754869 | |||||
| chr2:43754869
|
C | CTTT | 8 | a0001c0002t0009g0236a0002c0011t0008g0119a0002c0011t0008g0120others(5): Show | 8 | HG02027.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3795+1128_3795+113 others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754869 | |||||
| chr2:43754869
|
CT | C | 18 | a0001c0001t0001g0074a0001c0003t0001g0202a0001c0007t0001g0010others(15): Show | 18 | HG00738.hp1 HG00741.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3795+1130delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43754869 | |||||
| chr2:43755045
|
G | A | 1 | a0022c0056t0003g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3795+1285G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755045 | ||||||
| chr2:43755093
|
G | A | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3795+1333G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755093 | ||||||
| chr2:43755349
|
G | A | 11 | a0002c0006t0004g0108a0003c0004t0002g0107a0003c0012t0004g0174others(8): Show | 11 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.3795+1589G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755349 | ||||||
| chr2:43755440
|
C | G | 1 | a0002c0011t0008g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3796-1679C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755440 | ||||||
| chr2:43755498
|
C | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3796-1621C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755498 | ||||||
| chr2:43755585
|
T | C | 8 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(5): Show | 8 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3796-1534T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755585 | ||||||
| chr2:43755713
|
G | A | 1 | a0003c0004t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3796-1406G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43755713 | ||||||
| chr2:43756077
|
C | T | 2 | a0002c0005t0011g0013a0002c0006t0011g0239 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3796-1042C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756077 | ||||||
| chr2:43756150
|
T | A | 1 | a0001c0003t0001g0004 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3796-969T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756150 | ||||||
| chr2:43756196
|
T | C | 8 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(5): Show | 8 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3796-923T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756196 | ||||||
| chr2:43756213
|
CA | C | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3796-903delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43756213 | |||||
| chr2:43756217
|
G | T | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3796-902G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756217 | ||||||
| chr2:43756218
|
TAATGAG | T | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3796-897_3796-892d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43756218 | |||||
| chr2:43756254
|
G | A | 19 | a0003c0004t0002g0080a0003c0004t0002g0097a0003c0004t0002g0098others(16): Show | 19 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.3796-865G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756254 | ||||||
| chr2:43756264
|
CA | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3796-850delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr2 | 43756264 | |||||
| chr2:43756362
|
G | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3796-757G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756362 | ||||||
| chr2:43756418
|
G | C | 1 | a0005c0008t0003g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3796-701G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756418 | ||||||
| chr2:43756444
|
C | T | 5 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3796-675C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756444 | ||||||
| chr2:43756510
|
G | A | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3796-609G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756510 | ||||||
| chr2:43756543
|
A | G | 3 | a0002c0006t0002g0096a0002c0006t0002g0182a0002c0016t0002g0251 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3796-576A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756543 | ||||||
| chr2:43756559
|
C | T | 9 | a0003c0004t0002g0107a0003c0012t0004g0174a0003c0012t0004g0175others(6): Show | 9 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.3796-560C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756559 | ||||||
| chr2:43756664
|
C | G | 11 | a0002c0006t0004g0108a0003c0004t0002g0107a0003c0012t0004g0174others(8): Show | 11 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.3796-455C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756664 | ||||||
| chr2:43756670
|
G | A | 3 | a0001c0002t0002g0220a0001c0002t0002g0234a0001c0002t0002g0241 | 3 | HG01175.hp1 HG01256.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3796-449G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756670 | ||||||
| chr2:43756689
|
T | C | 5 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0173others(2): Show | 5 | HG01071.hp2 HG01257.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.3796-430T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756689 | ||||||
| chr2:43756694
|
T | A | 1 | a0002c0005t0011g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3796-425T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756694 | ||||||
| chr2:43756775
|
C | T | 1 | a0003c0013t0007g0131 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3796-344C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756775 | ||||||
| chr2:43756816
|
G | A | 22 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150others(19): Show | 22 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3796-303G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756816 | ||||||
| chr2:43756891
|
A | G | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3796-228A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756891 | ||||||
| chr2:43756892
|
T | C | 3 | a0001c0003t0001g0186a0007c0014t0001g0142a0017c0036t0001g0099 | 3 | HG01346.hp2 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3796-227T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756892 | ||||||
| chr2:43756919
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3796-200G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 25/29 | chr2 | 43756919 | ||||||
| chr2:43757392
|
G | A | 1 | a0005c0008t0002g0147 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3941+128G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43757392 | ||||||
| chr2:43757409
|
AT | A | 10 | a0002c0006t0004g0108a0003c0004t0002g0107a0003c0012t0004g0174others(7): Show | 10 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.3941+153delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 43757409 | |||||
| chr2:43757422
|
C | CT | 104 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(101): Show | 104 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.3941+173dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 43757422 | |||||
| chr2:43757486
|
C | G | 2 | a0002c0025t0004g0088a0019c0042t0015g0028 | 2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3941+222C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43757486 | ||||||
| chr2:43757763
|
TA | T | 100 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(97): Show | 100 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.3941+502delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 43757763 | |||||
| chr2:43757778
|
TA | T | 17 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.3941+523delA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 43757778 | |||||
| chr2:43757848
|
AAAT | A | 7 | a0001c0001t0001g0006a0001c0003t0001g0195a0001c0003t0001g0196others(4): Show | 7 | HG01981.hp2 HG02818.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.3941+587_3941+589d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 43757848 | |||||
| chr2:43757970
|
G | T | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3941+706G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43757970 | ||||||
| chr2:43758061
|
G | A | 1 | a0007c0014t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3941+797G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758061 | ||||||
| chr2:43758299
|
C | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3942-601C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758299 | ||||||
| chr2:43758378
|
G | C | 100 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(97): Show | 100 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.3942-522G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758378 | ||||||
| chr2:43758442
|
G | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3942-458G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758442 | ||||||
| chr2:43758613
|
G | A | 2 | a0002c0006t0002g0096a0002c0006t0002g0182 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3942-287G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758613 | ||||||
| chr2:43758687
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3942-213G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758687 | ||||||
| chr2:43758801
|
C | A | 103 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(100): Show | 103 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.3942-99C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758801 | ||||||
| chr2:43758804
|
A | G | 5 | a0002c0005t0002g0020a0002c0005t0002g0054a0002c0005t0002g0056others(2): Show | 5 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.3942-96A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 26/29 | chr2 | 43758804 | ||||||
| chr2:43759048
|
G | A | 3 | a0004c0010t0006g0206a0008c0017t0006g0162a0021c0052t0006g0144 | 3 | HG01884.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4071+19G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43759048 | ||||||
| chr2:43759240
|
T | G | 1 | a0003c0004t0002g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4071+211T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43759240 | ||||||
| chr2:43759591
|
C | G | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4071+562C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43759591 | ||||||
| chr2:43759751
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4071+722T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43759751 | ||||||
| chr2:43759824
|
T | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4071+795T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43759824 | ||||||
| chr2:43760061
|
G | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4071+1032G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760061 | ||||||
| chr2:43760113
|
A | G | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4071+1084A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760113 | ||||||
| chr2:43760184
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4071+1155T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760184 | ||||||
| chr2:43760355
|
T | TA | 50 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(47): Show | 50 | HG00438.hp1 HG00639.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.4071+1328dupA | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43760355 | |||||
| chr2:43760358
|
C | A | 3 | a0002c0005t0002g0056a0002c0016t0002g0091a0002c0025t0004g0088 | 3 | HG02717.hp1 NA18977.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.4071+1329C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760358 | ||||||
| chr2:43760359
|
C | CT | 70 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0046others(67): Show | 70 | HG00323.hp2 HG00597.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4071+1351dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43760359 | |||||
| chr2:43760359
|
C | CTT | 18 | a0001c0001t0014g0064a0001c0002t0009g0236a0001c0002t0009g0238others(15): Show | 18 | HG00597.hp2 HG00642.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.4071+1350_4071+135 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43760359 | |||||
| chr2:43760359
|
C | T | 50 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(47): Show | 50 | HG00438.hp1 HG00639.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.4071+1330C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760359 | ||||||
| chr2:43760359
|
CT | C | 5 | a0001c0001t0001g0205a0002c0011t0008g0119a0002c0011t0008g0120others(2): Show | 5 | HG01257.hp1 HG02109.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.4071+1351delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43760359 | |||||
| chr2:43760386
|
G | A | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4071+1357G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760386 | ||||||
| chr2:43760423
|
T | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4071+1394T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760423 | ||||||
| chr2:43760505
|
G | A | 4 | a0003c0004t0002g0107a0003c0022t0002g0140a0003c0022t0002g0164others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.4071+1476G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760505 | ||||||
| chr2:43760510
|
A | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4071+1481A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760510 | ||||||
| chr2:43760512
|
A | G | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4071+1483A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760512 | ||||||
| chr2:43760589
|
C | T | 9 | a0003c0004t0002g0107a0003c0012t0004g0174a0003c0012t0004g0175others(6): Show | 9 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.4071+1560C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760589 | ||||||
| chr2:43760747
|
C | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-1557C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43760747 | ||||||
| chr2:43760749
|
CTT | C | 25 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(22): Show | 25 | HG00438.hp1 HG01168.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.4072-1550_4072-154 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43760749 | |||||
| chr2:43761005
|
G | T | 162 | a0001c0001t0001g0006a0001c0001t0002g0017a0001c0001t0002g0030others(159): Show | 162 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.4072-1299G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761005 | ||||||
| chr2:43761006
|
G | GTA | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-1289_4072-128 others(6): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43761006 | |||||
| chr2:43761221
|
G | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-1083G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761221 | ||||||
| chr2:43761351
|
T | C | 3 | a0002c0023t0004g0246a0002c0025t0004g0088a0019c0042t0015g0028 | 3 | HG02132.hp2 NA19012.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4072-953T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761351 | ||||||
| chr2:43761385
|
T | C | 98 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(95): Show | 98 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.4072-919T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761385 | ||||||
| chr2:43761410
|
C | CT | 6 | a0001c0001t0001g0026a0001c0001t0001g0049a0003c0013t0007g0131others(3): Show | 6 | HG02486.hp1 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4072-875dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43761410 | |||||
| chr2:43761410
|
C | CTTT | 5 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.4072-877_4072-875d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43761410 | |||||
| chr2:43761410
|
CT | C | 38 | a0001c0001t0001g0074a0001c0001t0014g0063a0001c0001t0014g0064others(35): Show | 38 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.4072-875delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43761410 | |||||
| chr2:43761435
|
A | G | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-869A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761435 | ||||||
| chr2:43761507
|
T | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-797T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761507 | ||||||
| chr2:43761700
|
A | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-604A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761700 | ||||||
| chr2:43761717
|
G | A | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-587G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761717 | ||||||
| chr2:43761762
|
A | G | 2 | a0001c0002t0012g0226a0001c0002t0012g0232 | 2 | NA18747.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.4072-542A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761762 | ||||||
| chr2:43761800
|
T | C | 6 | a0001c0043t0004g0247a0002c0023t0004g0159a0002c0023t0004g0246others(3): Show | 6 | HG01261.hp2 HG02132.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4072-504T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761800 | ||||||
| chr2:43761902
|
T | A | 2 | a0001c0001t0014g0063a0001c0001t0014g0064 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4072-402T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761902 | ||||||
| chr2:43761962
|
C | CT | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-340dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43761962 | |||||
| chr2:43761991
|
A | G | 6 | a0001c0002t0001g0243a0001c0003t0001g0154a0001c0003t0001g0155others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.4072-313A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43761991 | ||||||
| chr2:43762081
|
A | G | 1 | a0007c0014t0001g0167 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4072-223A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43762081 | ||||||
| chr2:43762088
|
T | C | 7 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4072-216T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43762088 | ||||||
| chr2:43762128
|
G | A | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.4072-176G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43762128 | ||||||
| chr2:43762137
|
C | T | 1 | a0018c0041t0003g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4072-167C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43762137 | ||||||
| chr2:43762173
|
C | T | 1 | a0021c0052t0006g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4072-131C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43762173 | ||||||
| chr2:43762225
|
TACATG | T | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4072-74_4072-70del others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr2 | 43762225 | |||||
| chr2:43762259
|
T | C | 2 | a0005c0008t0001g0153a0007c0035t0001g0168 | 2 | NA18947.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.4072-45T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 27/29 | chr2 | 43762259 | ||||||
| chr2:43762402
|
C | T | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+12C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762402 | ||||||
| chr2:43762496
|
G | A | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+106G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762496 | ||||||
| chr2:43762546
|
C | T | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+156C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762546 | ||||||
| chr2:43762549
|
T | C | 1 | a0023c0031t0016g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4158+159T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762549 | ||||||
| chr2:43762588
|
C | T | 1 | a0001c0003t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4158+198C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762588 | ||||||
| chr2:43762801
|
G | A | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+411G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762801 | ||||||
| chr2:43762817
|
C | G | 94 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(91): Show | 94 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.4158+427C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762817 | ||||||
| chr2:43762880
|
C | T | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+490C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762880 | ||||||
| chr2:43762891
|
T | G | 1 | a0001c0001t0002g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4158+501T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762891 | ||||||
| chr2:43762911
|
G | C | 1 | a0002c0011t0008g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4158+521G>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762911 | ||||||
| chr2:43762964
|
G | A | 1 | a0003c0037t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4158+574G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762964 | ||||||
| chr2:43762981
|
T | A | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+591T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43762981 | ||||||
| chr2:43763008
|
CAGA | C | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4158+622_4158+624d others(5): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763008 | |||||
| chr2:43763061
|
C | T | 11 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4158+671C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763061 | ||||||
| chr2:43763202
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4158+812A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763202 | ||||||
| chr2:43763274
|
A | G | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.4158+884A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763274 | ||||||
| chr2:43763364
|
T | C | 77 | a0001c0003t0002g0181a0001c0024t0003g0011a0001c0024t0003g0065others(74): Show | 77 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.4159-864T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763364 | ||||||
| chr2:43763410
|
T | C | 28 | a0001c0024t0003g0011a0001c0024t0003g0065a0001c0043t0004g0247others(25): Show | 28 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.4159-818T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763410 | ||||||
| chr2:43763428
|
A | AT | 8 | a0001c0001t0001g0006a0001c0003t0001g0195a0001c0003t0001g0196others(5): Show | 8 | HG01981.hp2 HG02818.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.4159-791dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763428 | |||||
| chr2:43763428
|
AT | A | 31 | a0002c0006t0004g0108a0003c0004t0002g0080a0003c0004t0002g0097others(28): Show | 31 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.4159-791delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763428 | |||||
| chr2:43763580
|
C | A | 21 | a0001c0002t0002g0200a0001c0003t0002g0181a0001c0018t0002g0149others(18): Show | 21 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4159-648C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763580 | ||||||
| chr2:43763586
|
A | AT | 13 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0014g0063others(10): Show | 13 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.4159-623dupT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763586 | |||||
| chr2:43763586
|
A | ATTTTT | 6 | a0001c0003t0002g0181a0004c0010t0006g0135a0004c0010t0006g0206others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4159-627_4159-623d others(7): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763586 | |||||
| chr2:43763586
|
A | ATTTTTT | 5 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4159-628_4159-623d others(8): Show |
PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763586 | |||||
| chr2:43763586
|
AT | A | 28 | a0001c0001t0002g0086a0001c0003t0001g0179a0001c0024t0003g0011others(25): Show | 28 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.4159-623delT | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr2 | 43763586 | |||||
| chr2:43763615
|
T | G | 18 | a0001c0003t0002g0181a0003c0013t0007g0131a0003c0013t0007g0133others(15): Show | 18 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.4159-613T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763615 | ||||||
| chr2:43763642
|
G | A | 3 | a0002c0005t0011g0013a0002c0006t0011g0239a0002c0047t0002g0014 | 3 | HG02451.hp2 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4159-586G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763642 | ||||||
| chr2:43763689
|
C | T | 24 | a0002c0005t0011g0013a0002c0006t0002g0096a0002c0006t0002g0182others(21): Show | 24 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.4159-539C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763689 | ||||||
| chr2:43763690
|
G | A | 31 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0042others(28): Show | 31 | HG00438.hp1 HG01168.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.4159-538G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763690 | ||||||
| chr2:43763757
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4159-471A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763757 | ||||||
| chr2:43763874
|
G | A | 14 | a0001c0003t0002g0181a0004c0010t0005g0092a0004c0010t0005g0094others(11): Show | 14 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4159-354G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763874 | ||||||
| chr2:43763992
|
T | A | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4159-236T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43763992 | ||||||
| chr2:43764038
|
G | A | 17 | a0001c0043t0004g0247a0002c0006t0004g0108a0002c0023t0004g0159others(14): Show | 17 | HG00738.hp1 HG01243.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.4159-190G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764038 | ||||||
| chr2:43764111
|
G | A | 4 | a0003c0004t0002g0100a0003c0004t0002g0116a0003c0004t0002g0248others(1): Show | 4 | HG01106.hp1 HG01891.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.4159-117G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764111 | ||||||
| chr2:43764116
|
A | G | 3 | a0002c0011t0008g0119a0002c0011t0008g0120a0002c0011t0008g0145 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4159-112A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764116 | ||||||
| chr2:43764166
|
A | T | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4159-62A>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764166 | ||||||
| chr2:43764167
|
T | A | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4159-61T>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764167 | ||||||
| chr2:43764171
|
C | T | 148 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0031others(145): Show | 148 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.4159-57C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764171 | ||||||
| chr2:43764218
|
A | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.4159-10A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 28/29 | chr2 | 43764218 | ||||||
| chr2:43764393
|
T | G | 1 | a0001c0002t0002g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4296+28T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764393 | ||||||
| chr2:43764471
|
T | G | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4296+106T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764471 | ||||||
| chr2:43764524
|
A | C | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4296+159A>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764524 | ||||||
| chr2:43764560
|
T | C | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4296+195T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764560 | ||||||
| chr2:43764561
|
G | T | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4296+196G>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764561 | ||||||
| chr2:43764563
|
T | G | 1 | a0019c0042t0015g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4296+198T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764563 | ||||||
| chr2:43764624
|
A | G | 1 | a0001c0002t0002g0228 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4296+259A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764624 | ||||||
| chr2:43764705
|
C | T | 13 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(10): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4296+340C>T | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764705 | ||||||
| chr2:43764714
|
T | G | 13 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(10): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4296+349T>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764714 | ||||||
| chr2:43764978
|
C | A | 13 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(10): Show | 13 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4297-435C>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43764978 | ||||||
| chr2:43765045
|
AG | A | 7 | a0004c0010t0005g0092a0004c0010t0005g0094a0004c0010t0005g0095others(4): Show | 7 | HG00642.hp1 HG01099.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4297-365delG | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr2 | 43765045 | |||||
| chr2:43765203
|
A | G | 4 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4297-210A>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43765203 | ||||||
| chr2:43765310
|
T | C | 17 | a0003c0013t0007g0131a0003c0013t0007g0133a0003c0013t0007g0134others(14): Show | 17 | HG00642.hp1 HG01099.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.4297-103T>C | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43765310 | ||||||
| chr2:43765313
|
G | A | 3 | a0001c0002t0002g0200a0001c0018t0002g0149a0001c0018t0002g0150 | 3 | HG02886.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4297-100G>A | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43765313 | ||||||
| chr2:43765390
|
C | G | 3 | a0003c0004t0010g0102a0003c0004t0010g0136a0003c0004t0010g0139 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.4297-23C>G | PLEKHH2 | ENSG00000152527.14 | transcript | ENST00000282406.9 | protein_coding | 29/29 | chr2 | 43765390 |