Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23035 |
|---|---|
| ensemblid | ENSG00000040199.18 |
| hgncid | 29149 |
| symbol | PHLPP2 |
| name | PH domain and leucine rich repeat protein phosphatase 2 |
| refseq_nuc | NM_015020.3 |
| refseq_prot | NP_055835.2 |
| ensembl_nuc | ENST00000568954.5 |
| ensembl_prot | ENSP00000457991.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 71644924 |
| end | 71724701 |
| strand | - |
| ver | v1.2 |
| region | chr16:71644924-71724701 |
| region5000 | chr16:71639924-71729701 |
| regionname0 | PHLPP2_chr16_71644924_71724701 |
| regionname5000 | PHLPP2_chr16_71639924_71729701 |
| 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 | 1323 | 244 | 76 | 31 | 96 | 7 | 32 | 77 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002 | 0/0 | 1323 | 28 | 3 | 11 | 6 | 3 | 5 | 5 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0003 | 0/0 | 1323 | 23 | 6 | 13 | 1 | 0 | 3 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0004 | 0/0 | 1323 | 14 | 1 | 8 | 5 | 0 | 0 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0005 | 0/0 | 1323 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0006 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0007 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0008 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0009 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0010 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0011 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0012 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0013 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0014 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0015 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| 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 | 3972 | 158 | 66 | 24 | 51 | 6 | 10 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0002 | 0/0 | 3972 | 51 | 0 | 5 | 31 | 0 | 15 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0003 | 0/0 | 3972 | 26 | 3 | 10 | 6 | 3 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0004 | 0/0 | 3972 | 23 | 6 | 13 | 1 | 0 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0005 | 0/0 | 3972 | 18 | 0 | 2 | 11 | 1 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0006 | 0/0 | 3972 | 14 | 1 | 8 | 5 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0007 | 0/0 | 3972 | 9 | 9 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0008 | 0/0 | 3972 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0009 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0010 | 0/0 | 3972 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0011 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0012 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0013 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0014 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0015 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0016 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0017 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0018 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0019 | 0/1 | 3972 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0020 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0021 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0022 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0023 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0024 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0025 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0026 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| c0027 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| 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 | 0/0 | 4345 | 91 | 2 | 21 | 56 | 3 | 9 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0002 | 0/0 | 4336 | 87 | 6 | 21 | 40 | 2 | 18 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0003 | 0/1 | 4336 | 42 | 15 | 13 | 4 | 3 | 6 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0004 | 1/0 | 4346 | 34 | 22 | 8 | 3 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0005 | 0/0 | 4345 | 16 | 15 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0006 | 0/0 | 4345 | 12 | 12 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0007 | 0/0 | 4336 | 7 | 7 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0008 | 0/0 | 4336 | 5 | 0 | 0 | 0 | 0 | 5 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0009 | 0/0 | 4336 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0010 | 0/0 | 4345 | 3 | 3 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0011 | 0/0 | 4332 | 2 | 0 | 0 | 2 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0012 | 0/0 | 4345 | 2 | 2 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0013 | 0/0 | 4336 | 2 | 0 | 0 | 2 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0014 | 0/0 | 4345 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0015 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0016 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0017 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0018 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0019 | 0/0 | 4336 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0020 | 0/0 | 4336 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0021 | 0/0 | 4336 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0022 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0023 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0024 | 0/0 | 4346 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0025 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0026 | 0/0 | 4337 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0027 | 0/0 | 4332 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0028 | 0/0 | 4346 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0029 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| t0030 | 0/0 | 4336 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| 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 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0302 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| 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 | 3972 | 158 | 66 | 24 | 51 | 6 | 10 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002 | 0/0 | 3972 | 51 | 0 | 5 | 31 | 0 | 15 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0005 | 0/0 | 3972 | 18 | 0 | 2 | 11 | 1 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0007 | 0/0 | 3972 | 9 | 9 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0009 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0013 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0017 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0019 | 0/1 | 3972 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0021 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0024 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0026 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0003 | 0/0 | 3972 | 26 | 3 | 10 | 6 | 3 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0011 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0016 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0003c0004 | 0/0 | 3972 | 23 | 6 | 13 | 1 | 0 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0004c0006 | 0/0 | 3972 | 14 | 1 | 8 | 5 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0005c0008 | 0/0 | 3972 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0006c0010 | 0/0 | 3972 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0007c0015 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0008c0018 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0009c0012 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0010c0020 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0011c0014 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0012c0023 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0013c0022 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0014c0025 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0015c0027 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8316 | 67 | 1 | 11 | 46 | 3 | 6 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0003 | 0/0 | 8307 | 19 | 12 | 3 | 0 | 1 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0004 | 1/0 | 8317 | 34 | 22 | 8 | 3 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0005 | 0/0 | 8316 | 15 | 14 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0007 | 0/0 | 8307 | 7 | 7 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0010 | 0/0 | 8316 | 3 | 3 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0011 | 0/0 | 8303 | 2 | 0 | 0 | 2 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0012 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0014 | 0/0 | 8316 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0016 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0017 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0018 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0022 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0023 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0024 | 0/0 | 8317 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0026 | 0/0 | 8308 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0027 | 0/0 | 8303 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0001t0028 | 0/0 | 8317 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002t0002 | 0/0 | 8307 | 38 | 0 | 5 | 24 | 0 | 9 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002t0008 | 0/0 | 8307 | 5 | 0 | 0 | 0 | 0 | 5 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002t0009 | 0/0 | 8307 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002t0013 | 0/0 | 8307 | 2 | 0 | 0 | 2 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002t0015 | 0/0 | 8307 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0002t0020 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0005t0002 | 0/0 | 8307 | 18 | 0 | 2 | 11 | 1 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0007t0006 | 0/0 | 8316 | 9 | 9 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0009t0001 | 0/0 | 8316 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0013t0002 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0017t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0019t0003 | 0/1 | 8307 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0021t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0024t0005 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0001c0026t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0003t0002 | 0/0 | 8307 | 2 | 0 | 1 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0003t0003 | 0/0 | 8307 | 21 | 3 | 9 | 4 | 2 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0003t0021 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0003t0025 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0003t0029 | 0/0 | 8307 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0011t0002 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0002c0016t0003 | 0/0 | 8307 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0003c0004t0002 | 0/0 | 8307 | 22 | 6 | 13 | 1 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0003c0004t0019 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0004c0006t0001 | 0/0 | 8316 | 14 | 1 | 8 | 5 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0005c0008t0002 | 0/0 | 8307 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0006c0010t0001 | 0/0 | 8316 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0007c0015t0006 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0008c0018t0012 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0009c0012t0030 | 0/0 | 8307 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0010c0020t0001 | 0/0 | 8316 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0011c0014t0006 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0012c0023t0006 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0013c0022t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0014c0025t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| a0015c0027t0002 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | copy fasta | chr16 | 71639924 | 71729701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0302 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0011g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0014g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0017g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0018g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0022g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0023g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0024g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0026g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0027g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0028g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0008g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0008g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0015g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0020g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0007t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0009t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0009t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0013t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0017t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0019t0003g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0021t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0024t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0026t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0021g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0025g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0029g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0011t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0016t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0003c0004t0019g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0005c0008t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0005c0008t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0005c0008t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0005c0008t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0006c0010t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0006c0010t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0007c0015t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0008c0018t0012g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0009c0012t0030g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0010c0020t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0011c0014t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0012c0023t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0013c0022t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0014c0025t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0015c0027t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00140 | hp2 | a0002 | c0003 | t0003 | g0317 | EUR | GBR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00558 | hp2 | a0001 | c0026 | t0001 | g0100 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0254 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00639 | hp2 | a0001 | c0001 | t0024 | g0299 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00642 | hp1 | a0003 | c0004 | t0002 | g0228 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00642 | hp2 | a0006 | c0010 | t0001 | g0056 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0312 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0226 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG00741 | hp2 | a0003 | c0004 | t0002 | g0210 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01070 | hp2 | a0003 | c0004 | t0002 | g0219 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01071 | hp1 | a0001 | c0005 | t0002 | g0166 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01071 | hp2 | a0003 | c0004 | t0002 | g0220 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01081 | hp2 | a0006 | c0010 | t0001 | g0063 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01099 | hp1 | a0004 | c0006 | t0001 | g0054 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01106 | hp1 | a0002 | c0003 | t0003 | g0315 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01109 | hp2 | a0001 | c0005 | t0002 | g0171 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0244 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01169 | hp1 | a0002 | c0003 | t0003 | g0241 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01175 | hp1 | a0002 | c0003 | t0003 | g0313 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01192 | hp2 | a0002 | c0003 | t0003 | g0314 | AMR | PUR | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01255 | hp2 | a0003 | c0004 | t0002 | g0223 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01256 | hp1 | a0004 | c0006 | t0001 | g0088 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01256 | hp2 | a0002 | c0003 | t0003 | g0253 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01257 | hp1 | a0002 | c0003 | t0003 | g0243 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01257 | hp2 | a0003 | c0004 | t0002 | g0218 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01258 | hp1 | a0004 | c0006 | t0001 | g0076 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01258 | hp2 | a0003 | c0004 | t0002 | g0217 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01346 | hp1 | a0002 | c0003 | t0003 | g0311 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01346 | hp2 | a0009 | c0012 | t0030 | g0189 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01358 | hp1 | a0004 | c0006 | t0001 | g0060 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01358 | hp2 | a0002 | c0016 | t0003 | g0239 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0300 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0292 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0121 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01496 | hp1 | a0004 | c0006 | t0001 | g0091 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0291 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01515 | hp2 | a0001 | c0001 | t0027 | g0307 | EUR | IBS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01517 | hp2 | a0002 | c0003 | t0002 | g0240 | EUR | IBS | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0284 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01891 | hp2 | a0001 | c0007 | t0006 | g0158 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0296 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01934 | hp2 | a0002 | c0003 | t0002 | g0316 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01978 | hp1 | a0004 | c0006 | t0001 | g0073 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01981 | hp1 | a0004 | c0006 | t0001 | g0047 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01981 | hp2 | a0003 | c0004 | t0002 | g0211 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01993 | hp1 | a0003 | c0004 | t0002 | g0224 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02055 | hp2 | a0003 | c0004 | t0002 | g0269 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02071 | hp1 | a0004 | c0006 | t0001 | g0062 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02074 | hp1 | a0001 | c0021 | t0001 | g0033 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02083 | hp1 | a0014 | c0025 | t0001 | g0085 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02083 | hp2 | a0001 | c0005 | t0002 | g0169 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02148 | hp2 | a0003 | c0004 | t0002 | g0214 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02155 | hp2 | a0001 | c0001 | t0011 | g0107 | EAS | CDX | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02165 | hp1 | a0003 | c0004 | t0002 | g0272 | EAS | CDX | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02165 | hp2 | a0004 | c0006 | t0001 | g0089 | EAS | CDX | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02258 | hp1 | a0002 | c0003 | t0003 | g0318 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02258 | hp2 | a0001 | c0007 | t0006 | g0150 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02280 | hp1 | a0001 | c0001 | t0028 | g0288 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02293 | hp1 | a0004 | c0006 | t0001 | g0099 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02293 | hp2 | a0003 | c0004 | t0002 | g0229 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02300 | hp2 | a0003 | c0004 | t0002 | g0222 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02451 | hp1 | a0003 | c0004 | t0002 | g0268 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0274 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02523 | hp1 | a0001 | c0005 | t0002 | g0162 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0264 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0123 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02647 | hp2 | a0001 | c0001 | t0018 | g0126 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02683 | hp2 | a0003 | c0004 | t0002 | g0221 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02698 | hp1 | a0001 | c0002 | t0008 | g0209 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02698 | hp2 | a0001 | c0009 | t0001 | g0093 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02717 | hp1 | a0003 | c0004 | t0002 | g0270 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02738 | hp1 | a0001 | c0009 | t0001 | g0275 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02738 | hp2 | a0001 | c0002 | t0020 | g0139 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0262 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02818 | hp1 | a0002 | c0003 | t0003 | g0207 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0310 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02896 | hp1 | a0012 | c0023 | t0006 | g0160 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02922 | hp2 | a0003 | c0004 | t0002 | g0267 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02965 | hp1 | a0001 | c0007 | t0006 | g0208 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02970 | hp1 | a0011 | c0014 | t0006 | g0155 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03017 | hp1 | a0003 | c0004 | t0002 | g0216 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03017 | hp2 | a0015 | c0027 | t0002 | g0203 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03098 | hp1 | a0008 | c0018 | t0012 | g0265 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03130 | hp1 | a0007 | c0015 | t0006 | g0154 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03225 | hp2 | a0001 | c0001 | t0023 | g0273 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03239 | hp1 | a0003 | c0004 | t0019 | g0225 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03486 | hp1 | a0003 | c0004 | t0002 | g0263 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03490 | hp1 | a0002 | c0003 | t0003 | g0003 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03491 | hp2 | a0001 | c0002 | t0008 | g0001 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03492 | hp1 | a0002 | c0003 | t0003 | g0003 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03492 | hp2 | a0001 | c0002 | t0008 | g0001 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03540 | hp1 | a0001 | c0007 | t0006 | g0156 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03654 | hp1 | a0001 | c0005 | t0002 | g0116 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03669 | hp2 | a0001 | c0005 | t0002 | g0167 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0066 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03704 | hp1 | a0001 | c0013 | t0002 | g0186 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03710 | hp1 | a0001 | c0005 | t0002 | g0117 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | BEB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0184 | SAS | BEB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03834 | hp2 | a0010 | c0020 | t0001 | g0012 | SAS | BEB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03942 | hp1 | a0001 | c0002 | t0008 | g0143 | SAS | BEB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03942 | hp2 | a0002 | c0003 | t0021 | g0006 | SAS | BEB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG04199 | hp1 | a0001 | c0002 | t0008 | g0140 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG04199 | hp2 | a0001 | c0005 | t0002 | g0164 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG04204 | hp2 | a0002 | c0011 | t0002 | g0246 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0320 | SAS | STU | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | CHB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18747 | hp2 | a0001 | c0005 | t0002 | g0170 | EAS | CHB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18906 | hp1 | a0001 | c0007 | t0006 | g0151 | AFR | YRI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | YRI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18941 | hp2 | a0005 | c0008 | t0002 | g0213 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18948 | hp2 | a0001 | c0005 | t0002 | g0204 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18950 | hp1 | a0013 | c0022 | t0001 | g0032 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18959 | hp1 | a0001 | c0005 | t0002 | g0163 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18961 | hp2 | a0001 | c0002 | t0013 | g0023 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18966 | hp2 | a0001 | c0002 | t0009 | g0201 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18968 | hp1 | a0002 | c0003 | t0003 | g0236 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18971 | hp2 | a0002 | c0003 | t0003 | g0245 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18973 | hp2 | a0002 | c0003 | t0003 | g0235 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18978 | hp1 | a0004 | c0006 | t0001 | g0081 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18978 | hp2 | a0001 | c0002 | t0009 | g0148 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18982 | hp1 | a0001 | c0005 | t0002 | g0165 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18984 | hp2 | a0001 | c0005 | t0002 | g0172 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18985 | hp1 | a0001 | c0002 | t0013 | g0025 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18990 | hp1 | a0005 | c0008 | t0002 | g0230 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18992 | hp1 | a0005 | c0008 | t0002 | g0227 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18992 | hp2 | a0001 | c0005 | t0002 | g0137 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18994 | hp1 | a0002 | c0003 | t0025 | g0242 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19004 | hp2 | a0001 | c0005 | t0002 | g0168 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0095 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | LWK | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | LWK | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | LWK | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19043 | hp2 | a0001 | c0007 | t0006 | g0153 | AFR | LWK | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19054 | hp2 | a0002 | c0003 | t0029 | g0238 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19058 | hp2 | a0001 | c0005 | t0002 | g0138 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19060 | hp2 | a0001 | c0017 | t0001 | g0101 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19065 | hp1 | a0004 | c0006 | t0001 | g0098 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19066 | hp2 | a0001 | c0002 | t0009 | g0149 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19076 | hp1 | a0001 | c0002 | t0009 | g0202 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19078 | hp1 | a0001 | c0005 | t0002 | g0173 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19088 | hp1 | a0001 | c0002 | t0015 | g0022 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19091 | hp1 | a0004 | c0006 | t0001 | g0075 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19091 | hp2 | a0005 | c0008 | t0002 | g0215 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | YRI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19240 | hp2 | a0001 | c0007 | t0006 | g0152 | AFR | YRI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ASW | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20752 | hp1 | a0001 | c0005 | t0002 | g0266 | EUR | TSI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0247 | EUR | TSI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20805 | hp1 | a0002 | c0003 | t0003 | g0319 | EUR | TSI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20805 | hp2 | a0001 | c0001 | t0026 | g0298 | EUR | TSI | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0294 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01123 | hp2 | a0003 | c0004 | t0002 | g0212 | AMR | CLM | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02109 | hp2 | a0001 | c0007 | t0006 | g0157 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0118 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02559 | hp2 | a0002 | c0003 | t0003 | g0206 | AFR | ACB | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03471 | hp2 | a0001 | c0024 | t0005 | g0129 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | USA | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG06807 | hp2 | a0001 | c0007 | t0006 | g0159 | AFR | USA | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20300 | hp1 | a0004 | c0006 | t0001 | g0053 | AFR | USA | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA21309 | hp1 | a0003 | c0004 | t0002 | g0271 | AFR | LWK | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | LWK | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0019 | t0003 | g0237 | REF | REF | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0302 | REF | REF | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71648927
|
C | T | 2 | a0003a0005 | 27 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
missense_variant | MODERATE | c.3935G>A | p.Arg1312Gln | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 4314/8317 | 3935/3972 | 1312/1323 | chr16 | 71648927 | ||
| chr16:71649018
|
C | T | 1 | a0008 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.3844G>A | p.Val1282Ile | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 4223/8317 | 3844/3972 | 1282/1323 | chr16 | 71649018 | ||
| chr16:71649219
|
T | C | 1 | a0009 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.3643A>G | p.Met1215Val | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 4022/8317 | 3643/3972 | 1215/1323 | chr16 | 71649219 | ||
| chr16:71649647
|
G | C | 1 | a0007 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3215C>G | p.Ser1072Cys | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3594/8317 | 3215/3972 | 1072/1323 | chr16 | 71649647 | ||
| chr16:71649669
|
G | A | 1 | a0010 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.3193C>T | p.Pro1065Ser | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3572/8317 | 3193/3972 | 1065/1323 | chr16 | 71649669 | ||
| chr16:71649815
|
A | G | 1 | a0002 | 28 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(25): Show |
missense_variant | MODERATE | c.3047T>C | p.Leu1016Ser | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3426/8317 | 3047/3972 | 1016/1323 | chr16 | 71649815 | ||
| chr16:71649937
|
A | C | 1 | a0011 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2925T>G | p.Ile975Met | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3304/8317 | 2925/3972 | 975/1323 | chr16 | 71649937 | ||
| chr16:71652963
|
G | A | 1 | a0012 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.2644C>T | p.Pro882Ser | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/19 | 3023/8317 | 2644/3972 | 882/1323 | chr16 | 71652963 | ||
| chr16:71658321
|
G | C | 1 | a0006 | 2 | HG00642.hp2 HG01081.hp2 |
missense_variant | MODERATE | c.2191C>G | p.Pro731Ala | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/19 | 2570/8317 | 2191/3972 | 731/1323 | chr16 | 71658321 | ||
| chr16:71667332
|
T | C | 1 | a0005 | 4 | NA18941.hp2 NA18990.hp1 NA18992.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1630A>G | p.Ile544Val | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/19 | 2009/8317 | 1630/3972 | 544/1323 | chr16 | 71667332 | ||
| chr16:71679398
|
T | C | 1 | a0013 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.1028A>G | p.Asn343Ser | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 7/19 | 1407/8317 | 1028/3972 | 343/1323 | chr16 | 71679398 | ||
| chr16:71681895
|
T | C | 1 | a0014 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.746A>G | p.Gln249Arg | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/19 | 1125/8317 | 746/3972 | 249/1323 | chr16 | 71681895 | ||
| chr16:71690558
|
T | G | 1 | a0004 | 14 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(11): Show |
missense_variant | MODERATE | c.570A>C | p.Gln190His | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/19 | 949/8317 | 570/3972 | 190/1323 | chr16 | 71690558 | ||
| chr16:71702630
|
G | C | 1 | a0015 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.386C>G | p.Pro129Arg | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/19 | 765/8317 | 386/3972 | 129/1323 | chr16 | 71702630 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71648893
|
T | C | 8 | a0001c0002a0001c0005a0001c0013others(5): Show | 100 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(97): Show |
synonymous_variant | LOW | c.3969A>G | p.Leu1323Leu | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 4348/8317 | 3969/3972 | 1323/1323 | chr16 | 71648893 | ||
| chr16:71648914
|
C | T | 1 | a0001c0009 | 2 | HG02698.hp2 HG02738.hp1 |
synonymous_variant | LOW | c.3948G>A | p.Pro1316Pro | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 4327/8317 | 3948/3972 | 1316/1323 | chr16 | 71648914 | ||
| chr16:71649322
|
C | T | 1 | a0001c0017 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.3540G>A | p.Glu1180Glu | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3919/8317 | 3540/3972 | 1180/1323 | chr16 | 71649322 | ||
| chr16:71649547
|
G | A | 1 | a0001c0019 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.3315C>T | p.Gly1105Gly | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3694/8317 | 3315/3972 | 1105/1323 | chr16 | 71649547 | ||
| chr16:71649856
|
G | A | 1 | a0001c0013 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.3006C>T | p.His1002His | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3385/8317 | 3006/3972 | 1002/1323 | chr16 | 71649856 | ||
| chr16:71656621
|
C | T | 1 | a0002c0016 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.2340G>A | p.Thr780Thr | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/19 | 2719/8317 | 2340/3972 | 780/1323 | chr16 | 71656621 | ||
| chr16:71658692
|
G | A | 1 | a0001c0021 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.2109C>T | p.Ile703Ile | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 14/19 | 2488/8317 | 2109/3972 | 703/1323 | chr16 | 71658692 | ||
| chr16:71669349
|
A | G | 4 | a0001c0007a0007c0015a0011c0014others(1): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
synonymous_variant | LOW | c.1554T>C | p.Pro518Pro | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/19 | 1933/8317 | 1554/3972 | 518/1323 | chr16 | 71669349 | ||
| chr16:71676525
|
G | A | 1 | a0001c0005 | 18 | HG01071.hp1 HG01109.hp2 HG02083.hp2 others(15): Show |
synonymous_variant | LOW | c.1393C>T | p.Leu465Leu | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/19 | 1772/8317 | 1393/3972 | 465/1323 | chr16 | 71676525 | ||
| chr16:71678883
|
A | G | 6 | a0001c0002a0001c0005a0001c0013others(3): Show | 73 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(70): Show |
synonymous_variant | LOW | c.1140T>C | p.Phe380Phe | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/19 | 1519/8317 | 1140/3972 | 380/1323 | chr16 | 71678883 | ||
| chr16:71679517
|
G | A | 2 | a0001c0024a0012c0023 | 2 | HG02896.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.909C>T | p.Gly303Gly | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 7/19 | 1288/8317 | 909/3972 | 303/1323 | chr16 | 71679517 | ||
| chr16:71684521
|
G | A | 1 | a0001c0026 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.690C>T | p.Phe230Phe | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/19 | 1069/8317 | 690/3972 | 230/1323 | chr16 | 71684521 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71645029
|
T | C | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(13): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*3861A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3861 | chr16 | 71645029 | |||||
| chr16:71645120
|
G | A | 4 | a0001c0007t0006a0007c0015t0006a0011c0014t0006others(1): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3770C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3770 | chr16 | 71645120 | |||||
| chr16:71645124
|
G | T | 8 | a0001c0001t0003a0001c0001t0007a0001c0019t0003others(5): Show | 52 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3766C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3766 | chr16 | 71645124 | |||||
| chr16:71645154
|
C | T | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(47): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*3736G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3736 | chr16 | 71645154 | |||||
| chr16:71645266
|
T | C | 1 | a0001c0001t0028 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3624A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3624 | chr16 | 71645266 | |||||
| chr16:71645301
|
C | T | 12 | a0001c0001t0001a0001c0001t0011a0001c0001t0014others(9): Show | 94 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*3589G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3589 | chr16 | 71645301 | |||||
| chr16:71645362
|
G | A | 1 | a0001c0001t0017 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3528C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3528 | chr16 | 71645362 | |||||
| chr16:71645619
|
T | C | 4 | a0001c0007t0006a0007c0015t0006a0011c0014t0006others(1): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3271A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 3271 | chr16 | 71645619 | |||||
| chr16:71646099
|
C | T | 47 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(44): Show | 282 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2791G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2791 | chr16 | 71646099 | |||||
| chr16:71646171
|
C | G | 1 | a0002c0003t0021 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2719G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2719 | chr16 | 71646171 | |||||
| chr16:71646172
|
C | G | 2 | a0001c0001t0022a0001c0001t0023 | 2 | HG02451.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2718G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2718 | chr16 | 71646172 | |||||
| chr16:71646189
|
T | C | 1 | a0001c0001t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2701A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2701 | chr16 | 71646189 | |||||
| chr16:71646327
|
TTTTGGTA others(7): Show |
T | 1 | a0001c0001t0027 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549_*2562delTAGG others(10): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2549 | chr16 | 71646327 | |||||
| chr16:71646337
|
G | A | 1 | a0001c0002t0020 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2553C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2553 | chr16 | 71646337 | |||||
| chr16:71646345
|
C | G | 1 | a0001c0001t0016 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2545G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2545 | chr16 | 71646345 | |||||
| chr16:71646527
|
G | C | 1 | a0001c0002t0008 | 5 | HG02698.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2363C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2363 | chr16 | 71646527 | |||||
| chr16:71646563
|
C | T | 1 | a0003c0004t0019 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2327G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2327 | chr16 | 71646563 | |||||
| chr16:71646681
|
TTTCA | T | 24 | a0001c0001t0003a0001c0001t0007a0001c0001t0026others(21): Show | 155 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*2205_*2208delTGAA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2205 | chr16 | 71646681 | |||||
| chr16:71646741
|
C | A | 1 | a0001c0001t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2149G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2149 | chr16 | 71646741 | |||||
| chr16:71646839
|
C | T | 1 | a0001c0002t0009 | 4 | NA18966.hp2 NA18978.hp2 NA19066.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2051G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2051 | chr16 | 71646839 | |||||
| chr16:71646886
|
G | A | 1 | a0001c0001t0010 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 2004 | chr16 | 71646886 | |||||
| chr16:71646941
|
AATGACAC others(6): Show |
A | 1 | a0001c0001t0011 | 2 | HG02155.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1936_*1948delATGC others(9): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1936 | chr16 | 71646941 | |||||
| chr16:71647139
|
T | C | 1 | a0001c0001t0018 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1751A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1751 | chr16 | 71647139 | |||||
| chr16:71647250
|
G | A | 8 | a0001c0001t0003a0001c0001t0007a0001c0019t0003others(5): Show | 52 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1640C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1640 | chr16 | 71647250 | |||||
| chr16:71647359
|
CTTATG | C | 24 | a0001c0001t0003a0001c0001t0007a0001c0001t0026others(21): Show | 155 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1526_*1530delCATA others(1): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1526 | chr16 | 71647359 | |||||
| chr16:71647547
|
A | G | 2 | a0001c0002t0013a0001c0002t0015 | 3 | NA18961.hp2 NA18985.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1343T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1343 | chr16 | 71647547 | |||||
| chr16:71647604
|
G | A | 1 | a0009c0012t0030 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1286 | chr16 | 71647604 | |||||
| chr16:71647612
|
A | G | 45 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(42): Show | 280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*1278T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1278 | chr16 | 71647612 | |||||
| chr16:71647679
|
C | G | 49 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(46): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1211G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1211 | chr16 | 71647679 | |||||
| chr16:71647701
|
G | A | 1 | a0001c0002t0013 | 2 | NA18961.hp2 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1189C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1189 | chr16 | 71647701 | |||||
| chr16:71647813
|
C | A | 1 | a0001c0001t0007 | 7 | HG01884.hp1 HG02965.hp2 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1077G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 1077 | chr16 | 71647813 | |||||
| chr16:71648432
|
A | G | 1 | a0001c0001t0024 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 458 | chr16 | 71648432 | |||||
| chr16:71648604
|
TA | T | 48 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(45): Show | 285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*285delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 285 | chr16 | 71648604 | |||||
| chr16:71648629
|
G | A | 1 | a0002c0003t0029 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 261 | chr16 | 71648629 | |||||
| chr16:71648679
|
G | A | 1 | a0009c0012t0030 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 211 | chr16 | 71648679 | |||||
| chr16:71648687
|
G | A | 4 | a0001c0007t0006a0007c0015t0006a0011c0014t0006others(1): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*203C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 203 | chr16 | 71648687 | |||||
| chr16:71648793
|
A | C | 1 | a0001c0001t0014 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*97T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 19/19 | 97 | chr16 | 71648793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71650053
|
G | A | 1 | a0001c0002t0002g0192 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2818-9C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71650053 | ||||||
| chr16:71650455
|
T | A | 1 | a0001c0002t0002g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2818-411A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71650455 | ||||||
| chr16:71650616
|
C | T | 1 | a0003c0004t0002g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2818-572G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71650616 | ||||||
| chr16:71650974
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2818-930T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71650974 | ||||||
| chr16:71651067
|
C | T | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2818-1023G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651067 | ||||||
| chr16:71651338
|
C | CA | 7 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0252others(4): Show | 7 | HG01361.hp1 HG02486.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2818-1295dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651338 | ||||||
| chr16:71651424
|
C | T | 163 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(160): Show | 166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.2817+1366G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651424 | ||||||
| chr16:71651441
|
A | G | 7 | a0002c0003t0003g0311a0002c0003t0003g0312a0002c0003t0003g0313others(4): Show | 7 | HG00735.hp1 HG01106.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.2817+1349T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651441 | ||||||
| chr16:71651542
|
A | G | 1 | a0003c0004t0002g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2817+1248T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651542 | ||||||
| chr16:71651760
|
C | G | 1 | a0001c0005t0002g0169 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2817+1030G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651760 | ||||||
| chr16:71651914
|
A | T | 1 | a0002c0003t0003g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2817+876T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651914 | ||||||
| chr16:71651954
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2817+836T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71651954 | ||||||
| chr16:71652116
|
T | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2817+674A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71652116 | ||||||
| chr16:71652151
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(110): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2817+639T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71652151 | ||||||
| chr16:71652171
|
A | C | 1 | a0001c0007t0006g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2817+619T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71652171 | ||||||
| chr16:71652449
|
A | T | 1 | a0002c0003t0003g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2817+341T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71652449 | ||||||
| chr16:71652605
|
G | C | 4 | a0003c0004t0002g0217a0003c0004t0002g0218a0003c0004t0002g0219others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817+185C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 18/18 | chr16 | 71652605 | ||||||
| chr16:71653099
|
CT | C | 237 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(234): Show | 240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.2586-79delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653099 | ||||||
| chr16:71653307
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2586-286C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653307 | ||||||
| chr16:71653558
|
G | A | 1 | a0001c0002t0002g0187 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2586-537C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653558 | ||||||
| chr16:71653562
|
G | C | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0277others(7): Show | 10 | HG00738.hp2 HG01891.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2586-541C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653562 | ||||||
| chr16:71653870
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2586-849C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653870 | ||||||
| chr16:71653965
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2586-944C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653965 | ||||||
| chr16:71653988
|
G | A | 1 | a0002c0003t0003g0317 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2586-967C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653988 | ||||||
| chr16:71654107
|
A | C | 2 | a0001c0001t0012g0262a0008c0018t0012g0265 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2586-1086T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654107 | ||||||
| chr16:71654152
|
A | G | 285 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(282): Show | 288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2585+1088T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654152 | ||||||
| chr16:71654204
|
G | GA | 153 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(150): Show | 155 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.2585+1035dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654204 | ||||||
| chr16:71654204
|
G | GAA | 43 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0031others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.2585+1034_2585+103 others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654204 | ||||||
| chr16:71654204
|
GAAAAAAA others(4): Show |
G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2585+1025_2585+103 others(15): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654204 | ||||||
| chr16:71654217
|
A | C | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2585+1023T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654217 | ||||||
| chr16:71654222
|
A | AC | 3 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0110 | 3 | HG00735.hp2 HG01169.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2585+1017_2585+101 others(5): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654222 | ||||||
| chr16:71654286
|
CCT | C | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0277others(7): Show | 10 | HG00738.hp2 HG01891.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2585+952_2585+953d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654286 | ||||||
| chr16:71654311
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0161 | 3 | HG00741.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2585+929G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654311 | ||||||
| chr16:71654520
|
G | A | 1 | a0001c0001t0003g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2585+720C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654520 | ||||||
| chr16:71654558
|
A | G | 1 | a0001c0001t0004g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2585+682T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654558 | ||||||
| chr16:71654641
|
C | T | 68 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(65): Show | 70 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2585+599G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654641 | ||||||
| chr16:71654719
|
T | C | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0277others(7): Show | 10 | HG00738.hp2 HG01891.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2585+521A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654719 | ||||||
| chr16:71654744
|
G | C | 1 | a0001c0001t0005g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2585+496C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654744 | ||||||
| chr16:71654806
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2585+434A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71654806 | ||||||
| chr16:71655074
|
G | A | 280 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(277): Show | 283 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.2585+166C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71655074 | ||||||
| chr16:71655503
|
C | CT | 21 | a0001c0001t0003g0258a0001c0001t0004g0285a0001c0001t0004g0289others(18): Show | 22 | HG00639.hp2 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.2391-70dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655503 | ||||||
| chr16:71655660
|
G | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2391-226C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655660 | ||||||
| chr16:71655723
|
C | T | 1 | a0001c0013t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2391-289G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655723 | ||||||
| chr16:71655765
|
C | T | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2391-331G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655765 | ||||||
| chr16:71655780
|
G | A | 1 | a0014c0025t0001g0085 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2391-346C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655780 | ||||||
| chr16:71655790
|
A | G | 285 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(282): Show | 288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2391-356T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655790 | ||||||
| chr16:71655795
|
C | T | 2 | a0001c0001t0003g0231a0001c0001t0003g0232 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2391-361G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655795 | ||||||
| chr16:71655862
|
A | T | 1 | a0004c0006t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2391-428T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655862 | ||||||
| chr16:71655866
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0014g0066 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2391-432T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655866 | ||||||
| chr16:71655906
|
C | G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2391-472G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71655906 | ||||||
| chr16:71656089
|
AC | A | 69 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(66): Show | 71 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.2390+481delG | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656089 | ||||||
| chr16:71656097
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2390+474A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656097 | ||||||
| chr16:71656127
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(277): Show | 283 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.2390+444G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656127 | ||||||
| chr16:71656150
|
T | G | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2390+421A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656150 | ||||||
| chr16:71656277
|
T | C | 1 | a0001c0021t0001g0033 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2390+294A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656277 | ||||||
| chr16:71656303
|
G | A | 6 | a0001c0005t0002g0137a0001c0005t0002g0138a0001c0005t0002g0162others(3): Show | 6 | HG02083.hp2 HG02523.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.2390+268C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656303 | ||||||
| chr16:71656369
|
T | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2390+202A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 16/18 | chr16 | 71656369 | ||||||
| chr16:71656892
|
G | A | 3 | a0001c0001t0004g0287a0001c0001t0004g0290a0001c0001t0028g0288 | 3 | HG01884.hp2 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2280-211C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71656892 | ||||||
| chr16:71657013
|
G | A | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2280-332C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657013 | ||||||
| chr16:71657139
|
C | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2280-458G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657139 | ||||||
| chr16:71657204
|
A | G | 164 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(161): Show | 167 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(164): Show |
intron_variant | MODIFIER | c.2280-523T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657204 | ||||||
| chr16:71657232
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041 | 3 | NA18954.hp2 NA18959.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2280-551G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657232 | ||||||
| chr16:71657238
|
C | T | 1 | a0001c0001t0017g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2280-557G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657238 | ||||||
| chr16:71657253
|
T | A | 2 | a0001c0005t0002g0164a0001c0005t0002g0167 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2280-572A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657253 | ||||||
| chr16:71657392
|
C | CT | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0277others(7): Show | 10 | HG00738.hp2 HG01255.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2280-712dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657392 | ||||||
| chr16:71657420
|
A | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2280-739T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657420 | ||||||
| chr16:71657426
|
G | A | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2280-745C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657426 | ||||||
| chr16:71657434
|
G | A | 31 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(28): Show | 32 | HG00423.hp1 HG01070.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.2280-753C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657434 | ||||||
| chr16:71657474
|
A | C | 1 | a0001c0001t0017g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2279+759T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657474 | ||||||
| chr16:71657544
|
G | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2279+689C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657544 | ||||||
| chr16:71657683
|
C | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2279+550G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657683 | ||||||
| chr16:71657736
|
G | A | 1 | a0001c0005t0002g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2279+497C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657736 | ||||||
| chr16:71657839
|
C | T | 1 | a0001c0001t0005g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2279+394G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657839 | ||||||
| chr16:71657974
|
A | C | 1 | a0001c0002t0002g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2279+259T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71657974 | ||||||
| chr16:71658067
|
T | C | 1 | a0001c0005t0002g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2279+166A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71658067 | ||||||
| chr16:71658072
|
C | T | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2279+161G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71658072 | ||||||
| chr16:71658116
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2279+117A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71658116 | ||||||
| chr16:71658120
|
C | G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2279+113G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 15/18 | chr16 | 71658120 | ||||||
| chr16:71658369
|
A | G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.2149-6T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 14/18 | chr16 | 71658369 | ||||||
| chr16:71658479
|
T | C | 1 | a0001c0002t0002g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2149-116A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 14/18 | chr16 | 71658479 | ||||||
| chr16:71658520
|
A | C | 1 | a0001c0002t0002g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2148+133T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 14/18 | chr16 | 71658520 | ||||||
| chr16:71658540
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(110): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2148+113T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 14/18 | chr16 | 71658540 | ||||||
| chr16:71658644
|
C | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0090others(2): Show | 5 | HG00438.hp1 HG02155.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.2148+9G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 14/18 | chr16 | 71658644 | ||||||
| chr16:71659137
|
T | C | 49 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 49 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1986-322A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659137 | ||||||
| chr16:71659190
|
T | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(91): Show | 94 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1986-375A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659190 | ||||||
| chr16:71659247
|
AT | A | 270 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(267): Show | 273 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.1986-433delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659247 | ||||||
| chr16:71659533
|
G | T | 53 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(50): Show | 54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1986-718C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659533 | ||||||
| chr16:71659546
|
C | T | 1 | a0001c0005t0002g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1986-731G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659546 | ||||||
| chr16:71659814
|
C | T | 1 | a0001c0002t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1986-999G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659814 | ||||||
| chr16:71659870
|
C | G | 3 | a0002c0003t0003g0241a0002c0003t0003g0243a0002c0003t0003g0244 | 3 | HG01168.hp1 HG01169.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1986-1055G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659870 | ||||||
| chr16:71659966
|
A | G | 1 | a0001c0001t0005g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1986-1151T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659966 | ||||||
| chr16:71660019
|
T | G | 1 | a0001c0001t0004g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1986-1204A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660019 | ||||||
| chr16:71660181
|
T | C | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1986-1366A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660181 | ||||||
| chr16:71660188
|
T | C | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1986-1373A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660188 | ||||||
| chr16:71660308
|
T | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1986-1493A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660308 | ||||||
| chr16:71660372
|
C | CA | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(106): Show | 111 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.1986-1558dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660372 | ||||||
| chr16:71660372
|
C | CAA | 24 | a0001c0001t0001g0052a0001c0001t0005g0020a0001c0001t0010g0007others(21): Show | 24 | HG00423.hp1 HG01071.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1986-1559_1986-155 others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660372 | ||||||
| chr16:71660372
|
CA | C | 30 | a0001c0001t0001g0040a0001c0001t0001g0065a0001c0001t0001g0072others(27): Show | 30 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1986-1558delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660372 | ||||||
| chr16:71660421
|
AT | A | 70 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(67): Show | 71 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1986-1607delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660421 | ||||||
| chr16:71660421
|
ATT | A | 79 | a0001c0001t0001g0069a0001c0001t0001g0087a0001c0002t0002g0002others(76): Show | 81 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.1986-1608_1986-160 others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660421 | ||||||
| chr16:71660421
|
ATTT | A | 107 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(104): Show | 107 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1986-1609_1986-160 others(7): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660421 | ||||||
| chr16:71660640
|
G | A | 1 | a0002c0003t0003g0243 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1986-1825C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660640 | ||||||
| chr16:71660732
|
C | G | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1986-1917G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660732 | ||||||
| chr16:71660936
|
G | T | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1986-2121C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660936 | ||||||
| chr16:71661007
|
C | G | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1986-2192G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661007 | ||||||
| chr16:71661067
|
C | CT | 18 | a0001c0001t0004g0290a0001c0001t0022g0274a0001c0002t0002g0002others(15): Show | 19 | HG01070.hp1 HG01168.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1986-2253dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661067 | ||||||
| chr16:71661067
|
CT | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1986-2253delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661067 | ||||||
| chr16:71661127
|
C | T | 53 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(50): Show | 54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1986-2312G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661127 | ||||||
| chr16:71661131
|
A | G | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1986-2316T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661131 | ||||||
| chr16:71661239
|
T | G | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1986-2424A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661239 | ||||||
| chr16:71661359
|
C | T | 2 | a0001c0002t0002g0178a0001c0002t0002g0196 | 2 | HG01978.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1985+2540G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661359 | ||||||
| chr16:71661471
|
A | T | 1 | a0002c0003t0029g0238 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1985+2428T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661471 | ||||||
| chr16:71661657
|
G | C | 38 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(35): Show | 39 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1985+2242C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661657 | ||||||
| chr16:71661977
|
C | T | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1985+1922G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71661977 | ||||||
| chr16:71662074
|
G | A | 1 | a0001c0001t0004g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1985+1825C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662074 | ||||||
| chr16:71662117
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(91): Show | 94 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1985+1782G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662117 | ||||||
| chr16:71662129
|
G | C | 70 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(67): Show | 72 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.1985+1770C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662129 | ||||||
| chr16:71662154
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1985+1745C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662154 | ||||||
| chr16:71662230
|
G | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1985+1669C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662230 | ||||||
| chr16:71662230
|
G | C | 1 | a0001c0005t0002g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1985+1669C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662230 | ||||||
| chr16:71662250
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1985+1649A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662250 | ||||||
| chr16:71662302
|
T | A | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1985+1597A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662302 | ||||||
| chr16:71662343
|
T | A | 1 | a0001c0002t0002g0178 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1985+1556A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662343 | ||||||
| chr16:71662581
|
G | A | 1 | a0001c0001t0004g0280 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1985+1318C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662581 | ||||||
| chr16:71662736
|
G | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1985+1163C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662736 | ||||||
| chr16:71662817
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1985+1082C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662817 | ||||||
| chr16:71662879
|
GT | G | 280 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(277): Show | 283 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1985+1019delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662879 | ||||||
| chr16:71662949
|
G | A | 1 | a0001c0024t0005g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1985+950C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71662949 | ||||||
| chr16:71663036
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1985+863G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663036 | ||||||
| chr16:71663063
|
T | C | 1 | a0001c0001t0004g0300 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1985+836A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663063 | ||||||
| chr16:71663085
|
G | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1985+814C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663085 | ||||||
| chr16:71663112
|
T | G | 6 | a0001c0001t0004g0291a0001c0001t0004g0293a0001c0001t0004g0294others(3): Show | 6 | HG01123.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1985+787A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663112 | ||||||
| chr16:71663136
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1985+763G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663136 | ||||||
| chr16:71663223
|
T | C | 99 | a0001c0001t0026g0298a0001c0002t0002g0002a0001c0002t0002g0024others(96): Show | 101 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.1985+676A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663223 | ||||||
| chr16:71663355
|
C | T | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1985+544G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663355 | ||||||
| chr16:71663419
|
T | G | 1 | a0002c0011t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1985+480A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663419 | ||||||
| chr16:71663555
|
A | G | 1 | a0001c0002t0002g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1985+344T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663555 | ||||||
| chr16:71663603
|
A | C | 2 | a0002c0003t0003g0245a0002c0003t0029g0238 | 2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1985+296T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663603 | ||||||
| chr16:71663782
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1985+117C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663782 | ||||||
| chr16:71663802
|
G | A | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1985+97C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663802 | ||||||
| chr16:71663849
|
T | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1985+50A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71663849 | ||||||
| chr16:71664369
|
T | A | 151 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.1785-270A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71664369 | ||||||
| chr16:71664630
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1785-531A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71664630 | ||||||
| chr16:71664751
|
A | G | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1785-652T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71664751 | ||||||
| chr16:71664898
|
C | G | 1 | a0003c0004t0002g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1785-799G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71664898 | ||||||
| chr16:71665127
|
G | A | 1 | a0001c0002t0008g0143 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1785-1028C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71665127 | ||||||
| chr16:71665279
|
C | T | 1 | a0005c0008t0002g0227 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1785-1180G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71665279 | ||||||
| chr16:71665385
|
T | C | 28 | a0001c0002t0002g0226a0003c0004t0002g0210a0003c0004t0002g0211others(25): Show | 28 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1785-1286A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71665385 | ||||||
| chr16:71665695
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1784+1483C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71665695 | ||||||
| chr16:71665983
|
C | T | 1 | a0001c0002t0002g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1784+1195G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71665983 | ||||||
| chr16:71666057
|
C | T | 1 | a0003c0004t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1784+1121G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666057 | ||||||
| chr16:71666193
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1784+985A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666193 | ||||||
| chr16:71666310
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1784+868C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666310 | ||||||
| chr16:71666314
|
G | C | 2 | a0002c0003t0003g0241a0002c0003t0003g0244 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1784+864C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666314 | ||||||
| chr16:71666352
|
C | CA | 4 | a0001c0002t0002g0191a0001c0005t0002g0163a0001c0005t0002g0165others(1): Show | 4 | NA18959.hp1 NA18982.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+825dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666352 | ||||||
| chr16:71666601
|
G | T | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784+577C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666601 | ||||||
| chr16:71666695
|
T | C | 1 | a0001c0002t0002g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1784+483A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666695 | ||||||
| chr16:71666801
|
G | T | 27 | a0003c0004t0002g0210a0003c0004t0002g0211a0003c0004t0002g0212others(24): Show | 27 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1784+377C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71666801 | ||||||
| chr16:71667030
|
T | C | 1 | a0001c0002t0009g0148 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1784+148A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71667030 | ||||||
| chr16:71667063
|
G | T | 1 | a0002c0003t0021g0006 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1784+115C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71667063 | ||||||
| chr16:71667084
|
T | G | 1 | a0001c0002t0002g0177 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1784+94A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 12/18 | chr16 | 71667084 | ||||||
| chr16:71667345
|
G | A | 283 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.1629-12C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71667345 | ||||||
| chr16:71667371
|
T | C | 1 | a0001c0002t0020g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1629-38A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71667371 | ||||||
| chr16:71667423
|
T | A | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1629-90A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71667423 | ||||||
| chr16:71667511
|
C | A | 1 | a0001c0009t0001g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1629-178G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71667511 | ||||||
| chr16:71667775
|
C | T | 6 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1629-442G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71667775 | ||||||
| chr16:71668140
|
G | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1629-807C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668140 | ||||||
| chr16:71668160
|
C | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1629-827G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668160 | ||||||
| chr16:71668364
|
C | T | 2 | a0001c0002t0002g0183a0001c0002t0002g0184 | 2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1628+911G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668364 | ||||||
| chr16:71668365
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1628+910C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668365 | ||||||
| chr16:71668394
|
C | T | 1 | a0009c0012t0030g0189 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1628+881G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668394 | ||||||
| chr16:71668415
|
C | CA | 34 | a0001c0001t0003g0011a0001c0001t0003g0248a0001c0001t0003g0249others(31): Show | 34 | HG00423.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1628+859dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668415 | ||||||
| chr16:71668415
|
C | CAA | 6 | a0001c0001t0003g0247a0001c0001t0003g0252a0001c0001t0012g0262others(3): Show | 7 | HG01175.hp1 HG01361.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1628+858_1628+859d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668415 | ||||||
| chr16:71668415
|
CA | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(97): Show | 100 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1628+859delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668415 | ||||||
| chr16:71668717
|
C | T | 170 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(167): Show | 173 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(170): Show |
intron_variant | MODIFIER | c.1628+558G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668717 | ||||||
| chr16:71668830
|
A | T | 1 | a0001c0001t0005g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1628+445T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71668830 | ||||||
| chr16:71669072
|
C | T | 151 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.1628+203G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71669072 | ||||||
| chr16:71669229
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1628+46G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71669229 | ||||||
| chr16:71669272
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02148.hp1 | splice_region_variant&intron_variant | LOW | c.1628+3A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 11/18 | chr16 | 71669272 | ||||||
| chr16:71669449
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1533-79A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71669449 | ||||||
| chr16:71669533
|
T | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.1533-163A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71669533 | ||||||
| chr16:71669703
|
T | G | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1533-333A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71669703 | ||||||
| chr16:71669794
|
C | G | 1 | a0001c0001t0004g0303 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1533-424G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71669794 | ||||||
| chr16:71669826
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(110): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1533-456T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71669826 | ||||||
| chr16:71669984
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1533-614A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71669984 | ||||||
| chr16:71670135
|
G | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1533-765C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670135 | ||||||
| chr16:71670194
|
C | T | 27 | a0003c0004t0002g0210a0003c0004t0002g0211a0003c0004t0002g0212others(24): Show | 27 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1533-824G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670194 | ||||||
| chr16:71670319
|
T | C | 283 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.1533-949A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670319 | ||||||
| chr16:71670433
|
T | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533-1063A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670433 | ||||||
| chr16:71670608
|
ATAGT | A | 71 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(68): Show | 73 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1533-1242_1533-123 others(8): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670608 | ||||||
| chr16:71670693
|
A | AACACACA others(15): Show |
1 | a0001c0001t0001g0084 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1533-1324_1533-132 others(26): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670693 | ||||||
| chr16:71670693
|
A | ATAACACA others(15): Show |
1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1533-1324_1533-132 others(26): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670693 | ||||||
| chr16:71670695
|
A | AACACACA others(5): Show |
15 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0003g0011others(12): Show | 15 | HG01109.hp1 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533-1337_1533-132 others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(7): Show |
17 | a0001c0001t0003g0010a0001c0001t0007g0013a0001c0001t0007g0014others(14): Show | 17 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1533-1339_1533-132 others(18): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(9): Show |
23 | a0001c0001t0001g0046a0001c0001t0003g0252a0001c0002t0002g0147others(20): Show | 24 | HG00423.hp1 HG00609.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1533-1341_1533-132 others(20): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(11): Show |
58 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0003g0248others(55): Show | 58 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1533-1343_1533-132 others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(13): Show |
66 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0029others(63): Show | 68 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1533-1345_1533-132 others(24): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(15): Show |
23 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0041others(20): Show | 23 | HG00621.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1533-1347_1533-132 others(26): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(17): Show |
38 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0040others(35): Show | 38 | HG00140.hp1 HG00733.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1533-1349_1533-132 others(28): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(19): Show |
12 | a0001c0001t0001g0031a0001c0001t0001g0079a0001c0001t0001g0103others(9): Show | 12 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.1533-1351_1533-132 others(30): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(21): Show |
9 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0045others(6): Show | 9 | HG02280.hp2 HG03195.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-1326_1533-132 others(32): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(23): Show |
3 | a0001c0001t0005g0120a0001c0001t0005g0128a0001c0001t0016g0123 | 3 | HG02630.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1533-1326_1533-132 others(34): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(25): Show |
3 | a0001c0001t0005g0121a0001c0001t0005g0127a0001c0001t0005g0130 | 3 | HG01433.hp2 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1533-1326_1533-132 others(36): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(27): Show |
3 | a0001c0001t0005g0124a0001c0001t0005g0131a0001c0001t0005g0134 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1533-1326_1533-132 others(38): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(29): Show |
1 | a0001c0001t0018g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1533-1326_1533-132 others(40): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | AACACACA others(11): Show |
1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1533-1326_1533-132 others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | ACACACAC others(10): Show |
1 | a0001c0002t0002g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1533-1326_1533-132 others(21): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | ACACACAC others(16): Show |
1 | a0001c0026t0001g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1533-1326_1533-132 others(27): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | ACACACAC others(18): Show |
2 | a0001c0001t0001g0026a0001c0001t0014g0066 | 2 | HG03688.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1533-1326_1533-132 others(29): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670695
|
A | C | 2 | a0001c0001t0001g0084a0001c0001t0012g0262 | 2 | HG00558.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1533-1325T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | ||||||
| chr16:71670701
|
C | CACACACA others(11): Show |
1 | a0001c0019t0003g0237 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1533-1332_1533-133 others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670701 | ||||||
| chr16:71670762
|
T | C | 1 | a0001c0002t0002g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1533-1392A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670762 | ||||||
| chr16:71671263
|
G | A | 1 | a0003c0004t0002g0228 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1532+999C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671263 | ||||||
| chr16:71671290
|
T | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1532+972A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671290 | ||||||
| chr16:71671312
|
T | C | 282 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(279): Show | 285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): Show |
intron_variant | MODIFIER | c.1532+950A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671312 | ||||||
| chr16:71671323
|
G | C | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1532+939C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671323 | ||||||
| chr16:71671655
|
C | T | 1 | a0001c0013t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1532+607G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671655 | ||||||
| chr16:71671728
|
T | C | 299 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(296): Show | 302 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.1532+534A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671728 | ||||||
| chr16:71671871
|
G | A | 54 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(51): Show | 55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1532+391C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671871 | ||||||
| chr16:71671912
|
T | TCAAA | 55 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(52): Show | 56 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1532+346_1532+349d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671912 | ||||||
| chr16:71671912
|
TCAAA | T | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1532+346_1532+349d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671912 | ||||||
| chr16:71671930
|
A | G | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1532+332T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671930 | ||||||
| chr16:71671953
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1532+309A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671953 | ||||||
| chr16:71671976
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1532+286G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671976 | ||||||
| chr16:71672005
|
C | T | 14 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(11): Show | 14 | HG00733.hp2 HG01361.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1532+257G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71672005 | ||||||
| chr16:71672035
|
T | C | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1532+227A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71672035 | ||||||
| chr16:71672484
|
C | A | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1472-162G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71672484 | ||||||
| chr16:71672533
|
C | A | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0277others(7): Show | 10 | HG00738.hp2 HG01891.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1472-211G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71672533 | ||||||
| chr16:71672579
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1472-257C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71672579 | ||||||
| chr16:71672646
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1472-324G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71672646 | ||||||
| chr16:71673103
|
TTA | T | 4 | a0001c0001t0005g0125a0001c0001t0005g0127a0001c0001t0005g0128others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472-783_1472-782d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673103 | ||||||
| chr16:71673104
|
T | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1472-782A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673104 | ||||||
| chr16:71673385
|
C | A | 1 | a0001c0005t0002g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1472-1063G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673385 | ||||||
| chr16:71673411
|
T | A | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1472-1089A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673411 | ||||||
| chr16:71673485
|
G | A | 70 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(67): Show | 72 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.1472-1163C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673485 | ||||||
| chr16:71673495
|
T | C | 54 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(51): Show | 55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1472-1173A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673495 | ||||||
| chr16:71673605
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1472-1283C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673605 | ||||||
| chr16:71673733
|
T | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1472-1411A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673733 | ||||||
| chr16:71673867
|
G | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1472-1545C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71673867 | ||||||
| chr16:71674078
|
CT | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(105): Show | 108 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1472-1757delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674078 | ||||||
| chr16:71674140
|
T | C | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1472-1818A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674140 | ||||||
| chr16:71674290
|
G | C | 1 | a0001c0001t0011g0107 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1472-1968C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674290 | ||||||
| chr16:71674382
|
C | CT | 132 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(129): Show | 135 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.1472-2061dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674382 | ||||||
| chr16:71674382
|
CT | C | 7 | a0001c0001t0001g0034a0001c0001t0004g0310a0001c0001t0005g0121others(4): Show | 7 | HG01433.hp2 HG01515.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472-2061delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674382 | ||||||
| chr16:71674580
|
C | CA | 71 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(68): Show | 73 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1471+1866dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674580 | ||||||
| chr16:71674674
|
C | T | 151 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.1471+1773G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674674 | ||||||
| chr16:71674683
|
T | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1471+1764A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674683 | ||||||
| chr16:71674719
|
G | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1471+1728C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674719 | ||||||
| chr16:71674767
|
T | G | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1471+1680A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674767 | ||||||
| chr16:71675264
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(110): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1471+1183T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675264 | ||||||
| chr16:71675503
|
A | T | 1 | a0009c0012t0030g0189 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1471+944T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675503 | ||||||
| chr16:71675539
|
T | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1471+908A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675539 | ||||||
| chr16:71675676
|
G | C | 151 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.1471+771C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675676 | ||||||
| chr16:71675787
|
G | A | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1471+660C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675787 | ||||||
| chr16:71675875
|
C | G | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1471+572G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675875 | ||||||
| chr16:71675967
|
C | T | 1 | a0001c0001t0005g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1471+480G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71675967 | ||||||
| chr16:71676015
|
T | C | 2 | a0001c0001t0003g0231a0001c0001t0003g0232 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1471+432A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71676015 | ||||||
| chr16:71676306
|
G | A | 1 | a0001c0005t0002g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1471+141C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71676306 | ||||||
| chr16:71676407
|
G | A | 2 | a0001c0005t0002g0164a0001c0005t0002g0167 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1471+40C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71676407 | ||||||
| chr16:71676665
|
C | T | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1269-16G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71676665 | ||||||
| chr16:71676743
|
T | C | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1269-94A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71676743 | ||||||
| chr16:71676913
|
A | C | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1269-264T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71676913 | ||||||
| chr16:71677117
|
T | TAC | 283 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.1269-469_1269-468i others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677117 | ||||||
| chr16:71677453
|
C | CATAT | 4 | a0001c0001t0004g0021a0001c0001t0004g0277a0001c0001t0004g0278others(1): Show | 4 | HG00738.hp2 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1269-808_1269-805d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
C | CATATATA others(3): Show |
1 | a0001c0001t0004g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1269-814_1269-805d others(12): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
C | CATATATA others(7): Show |
2 | a0001c0001t0004g0281a0001c0001t0004g0283 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1269-818_1269-805d others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
C | CATATATA others(9): Show |
1 | a0001c0001t0004g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1269-820_1269-805d others(18): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CAT | C | 7 | a0001c0001t0004g0292a0001c0001t0004g0293a0001c0001t0004g0294others(4): Show | 7 | HG00639.hp2 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1269-806_1269-805d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATAT | C | 6 | a0001c0001t0004g0285a0001c0001t0004g0291a0001c0001t0004g0305others(3): Show | 6 | HG01496.hp2 HG01515.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1269-808_1269-805d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATAT | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0287a0001c0001t0004g0303others(2): Show | 6 | HG01884.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1269-810_1269-805d others(8): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(1): Show |
C | 8 | a0001c0001t0001g0092a0001c0001t0004g0286a0001c0001t0004g0290others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1269-812_1269-805d others(10): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(3): Show |
C | 39 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0042others(36): Show | 39 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1269-814_1269-805d others(12): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(5): Show |
C | 74 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(71): Show | 74 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1269-816_1269-805d others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1269-818_1269-805d others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(9): Show |
C | 19 | a0001c0002t0002g0264a0001c0005t0002g0137a0001c0005t0002g0138others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1269-820_1269-805d others(18): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(11): Show |
C | 89 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(86): Show | 91 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.1269-822_1269-805d others(20): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(13): Show |
C | 53 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(50): Show | 54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1269-824_1269-805d others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677453
|
CATATATA others(15): Show |
C | 2 | a0002c0003t0003g0245a0002c0003t0029g0238 | 2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1269-826_1269-805d others(24): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677453 | ||||||
| chr16:71677533
|
G | GT | 54 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(51): Show | 55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1269-885dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677533 | ||||||
| chr16:71677570
|
G | T | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1269-921C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677570 | ||||||
| chr16:71677588
|
G | A | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1269-939C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677588 | ||||||
| chr16:71677639
|
A | C | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1269-990T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677639 | ||||||
| chr16:71677844
|
A | G | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1268+911T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677844 | ||||||
| chr16:71678051
|
G | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1268+704C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678051 | ||||||
| chr16:71678339
|
C | T | 2 | a0001c0002t0002g0176a0001c0013t0002g0186 | 2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1268+416G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678339 | ||||||
| chr16:71678418
|
G | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1268+337C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678418 | ||||||
| chr16:71678559
|
G | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1268+196C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678559 | ||||||
| chr16:71678589
|
G | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1268+166C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678589 | ||||||
| chr16:71678608
|
C | G | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0277others(7): Show | 10 | HG00738.hp2 HG01891.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1268+147G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678608 | ||||||
| chr16:71678670
|
T | C | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1268+85A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678670 | ||||||
| chr16:71678690
|
A | G | 1 | a0005c0008t0002g0213 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1268+65T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71678690 | ||||||
| chr16:71679087
|
A | G | 1 | a0001c0001t0005g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1038-102T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 7/18 | chr16 | 71679087 | ||||||
| chr16:71679129
|
C | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1038-144G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 7/18 | chr16 | 71679129 | ||||||
| chr16:71679158
|
C | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1038-173G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 7/18 | chr16 | 71679158 | ||||||
| chr16:71679246
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1037+143C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 7/18 | chr16 | 71679246 | ||||||
| chr16:71679619
|
A | G | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.891-84T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71679619 | ||||||
| chr16:71679751
|
G | A | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-216C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71679751 | ||||||
| chr16:71679892
|
C | T | 1 | a0001c0013t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.891-357G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71679892 | ||||||
| chr16:71680007
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.891-472G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680007 | ||||||
| chr16:71680008
|
G | A | 98 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(95): Show | 100 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(97): Show |
intron_variant | MODIFIER | c.891-473C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680008 | ||||||
| chr16:71680040
|
G | A | 163 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(160): Show | 166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.891-505C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680040 | ||||||
| chr16:71680216
|
C | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(112): Show | 115 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.891-681G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680216 | ||||||
| chr16:71680318
|
G | A | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.891-783C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680318 | ||||||
| chr16:71680531
|
A | G | 4 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.891-996T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680531 | ||||||
| chr16:71680647
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.890+1104C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680647 | ||||||
| chr16:71680661
|
T | C | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.890+1090A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680661 | ||||||
| chr16:71680998
|
A | C | 9 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0255others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.890+753T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71680998 | ||||||
| chr16:71681163
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.890+588G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681163 | ||||||
| chr16:71681197
|
G | T | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.890+554C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681197 | ||||||
| chr16:71681228
|
G | A | 13 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(10): Show | 13 | HG00733.hp2 HG01884.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.890+523C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681228 | ||||||
| chr16:71681298
|
T | C | 1 | a0001c0002t0002g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.890+453A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681298 | ||||||
| chr16:71681351
|
G | A | 3 | a0002c0003t0003g0241a0002c0003t0003g0243a0002c0003t0003g0244 | 3 | HG01168.hp1 HG01169.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.890+400C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681351 | ||||||
| chr16:71681440
|
C | T | 1 | a0002c0003t0003g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.890+311G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681440 | ||||||
| chr16:71681442
|
T | G | 2 | a0001c0005t0002g0116a0001c0005t0002g0117 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.890+309A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681442 | ||||||
| chr16:71681443
|
C | G | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.890+308G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681443 | ||||||
| chr16:71681475
|
C | T | 283 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.890+276G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681475 | ||||||
| chr16:71681532
|
A | G | 3 | a0001c0005t0002g0163a0001c0005t0002g0165a0001c0005t0002g0173 | 3 | NA18959.hp1 NA18982.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.890+219T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681532 | ||||||
| chr16:71681705
|
T | A | 1 | a0001c0005t0002g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.890+46A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 6/18 | chr16 | 71681705 | ||||||
| chr16:71681949
|
T | C | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.736-44A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71681949 | ||||||
| chr16:71682012
|
G | GA | 306 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(303): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.736-108dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682012 | ||||||
| chr16:71682165
|
G | T | 1 | a0001c0001t0010g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.736-260C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682165 | ||||||
| chr16:71682183
|
C | A | 28 | a0002c0003t0003g0320a0003c0004t0002g0210a0003c0004t0002g0211others(25): Show | 28 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.736-278G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682183 | ||||||
| chr16:71682218
|
G | GT | 32 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0064others(29): Show | 32 | HG00609.hp2 HG00741.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.736-314dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682218 | ||||||
| chr16:71682218
|
GT | G | 23 | a0001c0001t0001g0111a0001c0001t0004g0281a0001c0001t0004g0283others(20): Show | 23 | HG00621.hp2 HG00642.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.736-314delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682218 | ||||||
| chr16:71682219
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.736-314A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682219 | ||||||
| chr16:71682224
|
T | C | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.736-319A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682224 | ||||||
| chr16:71682235
|
T | G | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.736-330A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682235 | ||||||
| chr16:71682281
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.736-376C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682281 | ||||||
| chr16:71682454
|
A | G | 4 | a0001c0002t0002g0145a0001c0002t0002g0188a0001c0002t0002g0190others(1): Show | 4 | NA18962.hp1 NA18977.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-549T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682454 | ||||||
| chr16:71682508
|
G | A | 1 | a0001c0005t0002g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.736-603C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682508 | ||||||
| chr16:71682621
|
A | G | 29 | a0001c0002t0002g0226a0002c0003t0003g0320a0003c0004t0002g0210others(26): Show | 29 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.736-716T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682621 | ||||||
| chr16:71682724
|
C | G | 1 | a0001c0002t0002g0185 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.736-819G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682724 | ||||||
| chr16:71682846
|
T | C | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.736-941A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682846 | ||||||
| chr16:71682927
|
G | T | 283 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.736-1022C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682927 | ||||||
| chr16:71682973
|
C | G | 1 | a0001c0002t0002g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.736-1068G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682973 | ||||||
| chr16:71682982
|
C | G | 22 | a0002c0003t0002g0240a0002c0003t0002g0316a0002c0003t0003g0003others(19): Show | 23 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.736-1077G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71682982 | ||||||
| chr16:71683018
|
C | G | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.736-1113G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683018 | ||||||
| chr16:71683129
|
C | T | 151 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.736-1224G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683129 | ||||||
| chr16:71683169
|
C | CA | 10 | a0001c0001t0001g0082a0001c0001t0007g0013a0001c0001t0007g0014others(7): Show | 10 | HG01884.hp1 HG02965.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-1265dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683169 | ||||||
| chr16:71683239
|
T | C | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.735+1237A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683239 | ||||||
| chr16:71683311
|
A | G | 14 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(11): Show | 14 | HG00733.hp2 HG01175.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+1165T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683311 | ||||||
| chr16:71683391
|
C | A | 2 | a0001c0001t0010g0007a0001c0001t0010g0008 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.735+1085G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683391 | ||||||
| chr16:71683397
|
C | A | 2 | a0001c0001t0010g0007a0001c0001t0010g0008 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.735+1079G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683397 | ||||||
| chr16:71683413
|
C | T | 7 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0084others(4): Show | 7 | HG00558.hp1 HG00609.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+1063G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683413 | ||||||
| chr16:71683481
|
G | A | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.735+995C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683481 | ||||||
| chr16:71683502
|
G | A | 2 | a0001c0001t0005g0135a0001c0001t0023g0273 | 2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.735+974C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683502 | ||||||
| chr16:71683502
|
G | C | 110 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(107): Show | 110 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.735+974C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683502 | ||||||
| chr16:71683538
|
T | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 6 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+938A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683538 | ||||||
| chr16:71683649
|
C | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.735+827G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683649 | ||||||
| chr16:71683797
|
T | A | 1 | a0002c0011t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.735+679A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683797 | ||||||
| chr16:71683862
|
C | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(113): Show | 116 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.735+614G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683862 | ||||||
| chr16:71683940
|
G | A | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.735+536C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683940 | ||||||
| chr16:71683946
|
C | CT | 116 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(113): Show | 116 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.735+529dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71683946 | ||||||
| chr16:71684117
|
GAGGTACT others(4): Show |
G | 1 | a0001c0001t0005g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735+348_735+358del others(11): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684117 | ||||||
| chr16:71684125
|
C | CT | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.735+350dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684125 | ||||||
| chr16:71684130
|
T | A | 1 | a0001c0001t0005g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735+346A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684130 | ||||||
| chr16:71684316
|
G | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.735+160C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684316 | ||||||
| chr16:71684393
|
T | A | 2 | a0001c0001t0010g0007a0001c0001t0010g0008 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.735+83A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684393 | ||||||
| chr16:71684395
|
G | C | 1 | a0004c0006t0001g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.735+81C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684395 | ||||||
| chr16:71684406
|
G | A | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.735+70C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684406 | ||||||
| chr16:71684463
|
C | T | 288 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(285): Show | 291 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.735+13G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 5/18 | chr16 | 71684463 | ||||||
| chr16:71684686
|
C | A | 9 | a0001c0002t0002g0145a0001c0002t0002g0174a0001c0002t0002g0188others(6): Show | 9 | NA18951.hp2 NA18962.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.610-85G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71684686 | ||||||
| chr16:71684701
|
T | C | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610-100A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71684701 | ||||||
| chr16:71684992
|
T | C | 30 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0067others(27): Show | 30 | HG00438.hp1 HG00558.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.610-391A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71684992 | ||||||
| chr16:71685054
|
G | A | 1 | a0014c0025t0001g0085 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.610-453C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685054 | ||||||
| chr16:71685110
|
G | A | 70 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(67): Show | 72 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.610-509C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685110 | ||||||
| chr16:71685112
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.610-511C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685112 | ||||||
| chr16:71685198
|
G | A | 7 | a0003c0004t0002g0211a0003c0004t0002g0214a0003c0004t0002g0222others(4): Show | 7 | HG01255.hp2 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-597C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685198 | ||||||
| chr16:71685234
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.610-633C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685234 | ||||||
| chr16:71685306
|
G | C | 2 | a0001c0001t0004g0306a0001c0001t0027g0307 | 2 | HG01515.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.610-705C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685306 | ||||||
| chr16:71685332
|
A | G | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610-731T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685332 | ||||||
| chr16:71685450
|
C | T | 52 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(49): Show | 53 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.610-849G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685450 | ||||||
| chr16:71685785
|
G | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.610-1184C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685785 | ||||||
| chr16:71685785
|
G | C | 9 | a0001c0002t0002g0145a0001c0002t0002g0174a0001c0002t0002g0188others(6): Show | 9 | NA18951.hp2 NA18962.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.610-1184C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685785 | ||||||
| chr16:71685792
|
C | A | 3 | a0001c0002t0009g0148a0001c0002t0009g0149a0001c0002t0009g0201 | 3 | NA18966.hp2 NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.610-1191G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685792 | ||||||
| chr16:71685795
|
T | C | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.610-1194A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71685795 | ||||||
| chr16:71686016
|
G | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(106): Show | 109 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.610-1415C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686016 | ||||||
| chr16:71686092
|
C | T | 13 | a0001c0002t0002g0184a0001c0007t0006g0150a0001c0007t0006g0151others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.610-1491G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686092 | ||||||
| chr16:71686117
|
C | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.610-1516G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686117 | ||||||
| chr16:71686175
|
G | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.610-1574C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686175 | ||||||
| chr16:71686183
|
T | C | 1 | a0002c0003t0003g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.610-1582A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686183 | ||||||
| chr16:71686284
|
C | T | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.610-1683G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686284 | ||||||
| chr16:71686339
|
A | T | 1 | a0004c0006t0001g0098 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.610-1738T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686339 | ||||||
| chr16:71686434
|
A | G | 99 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(96): Show | 101 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.610-1833T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686434 | ||||||
| chr16:71686620
|
C | T | 281 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(278): Show | 284 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.610-2019G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686620 | ||||||
| chr16:71686641
|
C | T | 1 | a0002c0003t0003g0320 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.610-2040G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686641 | ||||||
| chr16:71686668
|
T | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.610-2067A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686668 | ||||||
| chr16:71686771
|
C | CTT | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.610-2172_610-2171d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686771 | ||||||
| chr16:71686785
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0074 | 2 | HG00733.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.610-2184C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71686785 | ||||||
| chr16:71687018
|
T | G | 14 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(11): Show | 14 | HG00733.hp2 HG01361.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.610-2417A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687018 | ||||||
| chr16:71687042
|
T | C | 2 | a0001c0001t0010g0007a0001c0001t0010g0008 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.610-2441A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687042 | ||||||
| chr16:71687117
|
T | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.610-2516A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687117 | ||||||
| chr16:71687129
|
G | T | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.610-2528C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687129 | ||||||
| chr16:71687273
|
CT | C | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.610-2673delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687273 | ||||||
| chr16:71687489
|
T | A | 1 | a0001c0001t0003g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.610-2888A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687489 | ||||||
| chr16:71687497
|
T | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.610-2896A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687497 | ||||||
| chr16:71687525
|
C | T | 1 | a0001c0001t0004g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.610-2924G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687525 | ||||||
| chr16:71687610
|
G | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.609+2909C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687610 | ||||||
| chr16:71687657
|
T | C | 2 | a0001c0001t0004g0306a0001c0001t0027g0307 | 2 | HG01515.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.609+2862A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687657 | ||||||
| chr16:71687719
|
T | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.609+2800A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687719 | ||||||
| chr16:71687765
|
A | G | 2 | a0001c0001t0005g0132a0001c0001t0005g0133 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.609+2754T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687765 | ||||||
| chr16:71687789
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.609+2730C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687789 | ||||||
| chr16:71687860
|
T | C | 1 | a0001c0001t0005g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.609+2659A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71687860 | ||||||
| chr16:71688004
|
G | T | 69 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0136others(66): Show | 71 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.609+2515C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688004 | ||||||
| chr16:71688134
|
T | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.609+2385A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688134 | ||||||
| chr16:71688275
|
T | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.609+2244A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688275 | ||||||
| chr16:71688284
|
T | C | 1 | a0002c0003t0002g0316 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.609+2235A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688284 | ||||||
| chr16:71688306
|
C | T | 151 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.609+2213G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688306 | ||||||
| chr16:71688608
|
G | GT | 26 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257others(23): Show | 26 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.609+1910dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688608 | ||||||
| chr16:71688608
|
G | GTT | 103 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(100): Show | 103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.609+1909_609+1910d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688608 | ||||||
| chr16:71688608
|
G | GTTT | 11 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0001g0052others(8): Show | 11 | HG01515.hp1 HG02071.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.609+1908_609+1910d others(5): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688608 | ||||||
| chr16:71689186
|
G | C | 287 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(284): Show | 290 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.609+1333C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689186 | ||||||
| chr16:71689199
|
G | A | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.609+1320C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689199 | ||||||
| chr16:71689211
|
T | C | 1 | a0002c0003t0021g0006 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.609+1308A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689211 | ||||||
| chr16:71689278
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.609+1241G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689278 | ||||||
| chr16:71689385
|
C | CT | 33 | a0001c0001t0001g0052a0001c0001t0001g0108a0001c0001t0004g0277others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.609+1133dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689385 | ||||||
| chr16:71689385
|
CT | C | 48 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0003g0011others(45): Show | 49 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.609+1133delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689385 | ||||||
| chr16:71689385
|
CTT | C | 13 | a0001c0007t0006g0151a0001c0007t0006g0152a0001c0007t0006g0153others(10): Show | 13 | HG01169.hp1 HG01192.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.609+1132_609+1133d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689385 | ||||||
| chr16:71689385
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0002t0002g0183 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.609+1120_609+1133d others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689385 | ||||||
| chr16:71689530
|
T | C | 1 | a0003c0004t0002g0228 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.609+989A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689530 | ||||||
| chr16:71689641
|
G | A | 2 | a0003c0004t0002g0217a0003c0004t0002g0218 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.609+878C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689641 | ||||||
| chr16:71689858
|
A | G | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.609+661T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689858 | ||||||
| chr16:71690019
|
T | C | 1 | a0003c0004t0002g0228 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.609+500A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690019 | ||||||
| chr16:71690093
|
T | C | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.609+426A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690093 | ||||||
| chr16:71690171
|
G | A | 2 | a0001c0001t0005g0132a0001c0001t0005g0133 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.609+348C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690171 | ||||||
| chr16:71690187
|
C | A | 281 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(278): Show | 284 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.609+332G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690187 | ||||||
| chr16:71690188
|
G | A | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.609+331C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690188 | ||||||
| chr16:71690207
|
T | C | 1 | a0001c0026t0001g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.609+312A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690207 | ||||||
| chr16:71690466
|
T | C | 53 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(50): Show | 54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.609+53A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71690466 | ||||||
| chr16:71690740
|
C | A | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-31G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71690740 | ||||||
| chr16:71691052
|
G | C | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-343C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691052 | ||||||
| chr16:71691212
|
G | C | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-503C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691212 | ||||||
| chr16:71691267
|
G | A | 1 | a0001c0001t0004g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.419-558C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691267 | ||||||
| chr16:71691312
|
T | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.419-603A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691312 | ||||||
| chr16:71691387
|
G | A | 14 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(11): Show | 14 | HG01433.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.419-678C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691387 | ||||||
| chr16:71691460
|
C | CAAAT | 2 | a0001c0001t0023g0273a0002c0003t0003g0003 | 3 | HG03225.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.419-755_419-752dup others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691460 | ||||||
| chr16:71691460
|
CAAAT | C | 52 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0105others(49): Show | 53 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.419-755_419-752del others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691460 | ||||||
| chr16:71691460
|
CAAATAAA others(1): Show |
C | 54 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0048others(51): Show | 54 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.419-759_419-752del others(8): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691460 | ||||||
| chr16:71691460
|
CAAATAAA others(5): Show |
C | 46 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(43): Show | 46 | HG00741.hp1 HG01175.hp2 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.419-763_419-752del others(12): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691460 | ||||||
| chr16:71691460
|
CAAATAAA others(9): Show |
C | 50 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0042others(47): Show | 50 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.419-767_419-752del others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691460 | ||||||
| chr16:71691460
|
CAAATAAA others(13): Show |
C | 95 | a0001c0001t0001g0044a0001c0002t0002g0002a0001c0002t0002g0024others(92): Show | 97 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.419-771_419-752del others(20): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691460 | ||||||
| chr16:71691610
|
T | G | 30 | a0001c0002t0002g0145a0001c0002t0002g0188a0001c0002t0002g0190others(27): Show | 31 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.419-901A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691610 | ||||||
| chr16:71691719
|
G | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.419-1010C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71691719 | ||||||
| chr16:71692015
|
G | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.419-1306C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692015 | ||||||
| chr16:71692099
|
T | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.419-1390A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692099 | ||||||
| chr16:71692138
|
C | T | 113 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(110): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.419-1429G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692138 | ||||||
| chr16:71692233
|
C | T | 54 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(51): Show | 55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.419-1524G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692233 | ||||||
| chr16:71692301
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.419-1592G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692301 | ||||||
| chr16:71692321
|
G | T | 15 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(12): Show | 15 | HG01433.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.419-1612C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692321 | ||||||
| chr16:71692654
|
A | C | 2 | a0004c0006t0001g0060a0004c0006t0001g0091 | 2 | HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.419-1945T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692654 | ||||||
| chr16:71692822
|
G | GTT | 284 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.419-2115_419-2114d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692822 | ||||||
| chr16:71692837
|
T | A | 1 | a0003c0004t0002g0214 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.419-2128A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692837 | ||||||
| chr16:71692838
|
A | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(113): Show | 116 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.419-2129T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71692838 | ||||||
| chr16:71693020
|
G | C | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-2311C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693020 | ||||||
| chr16:71693040
|
C | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(113): Show | 116 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.419-2331G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693040 | ||||||
| chr16:71693072
|
C | T | 162 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(159): Show | 165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.419-2363G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693072 | ||||||
| chr16:71693081
|
A | G | 1 | a0001c0002t0002g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.419-2372T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693081 | ||||||
| chr16:71693082
|
A | G | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.419-2373T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693082 | ||||||
| chr16:71693106
|
T | C | 1 | a0002c0003t0003g0317 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.419-2397A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693106 | ||||||
| chr16:71693129
|
A | C | 1 | a0001c0002t0002g0191 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.419-2420T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693129 | ||||||
| chr16:71693220
|
G | A | 1 | a0004c0006t0001g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.419-2511C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693220 | ||||||
| chr16:71693274
|
G | A | 13 | a0001c0005t0002g0117a0001c0007t0006g0150a0001c0007t0006g0151others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.419-2565C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693274 | ||||||
| chr16:71693293
|
G | C | 1 | a0001c0001t0004g0290 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.419-2584C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693293 | ||||||
| chr16:71693387
|
C | G | 69 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0141others(66): Show | 71 | HG00423.hp1 HG00738.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.419-2678G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693387 | ||||||
| chr16:71693542
|
A | T | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-2833T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693542 | ||||||
| chr16:71693668
|
A | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(118): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.419-2959T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693668 | ||||||
| chr16:71693939
|
T | G | 1 | a0001c0005t0002g0167 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.419-3230A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693939 | ||||||
| chr16:71693959
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(114): Show | 117 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.419-3250G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71693959 | ||||||
| chr16:71694003
|
G | A | 2 | a0002c0003t0003g0245a0002c0003t0029g0238 | 2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.419-3294C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694003 | ||||||
| chr16:71694055
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(107): Show | 110 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.419-3346C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694055 | ||||||
| chr16:71694108
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.419-3399G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694108 | ||||||
| chr16:71694197
|
TAATAA | T | 150 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(147): Show | 153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.419-3493_419-3489d others(7): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694197 | ||||||
| chr16:71694324
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-3615C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694324 | ||||||
| chr16:71694392
|
C | G | 150 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(147): Show | 153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.419-3683G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694392 | ||||||
| chr16:71694409
|
C | T | 128 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(125): Show | 128 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.419-3700G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694409 | ||||||
| chr16:71694499
|
C | G | 1 | a0003c0004t0002g0223 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.419-3790G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694499 | ||||||
| chr16:71694570
|
A | G | 1 | a0001c0002t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.419-3861T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694570 | ||||||
| chr16:71694844
|
G | C | 1 | a0001c0001t0004g0290 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.419-4135C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694844 | ||||||
| chr16:71694848
|
G | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.419-4139C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71694848 | ||||||
| chr16:71695063
|
G | C | 1 | a0001c0001t0005g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.419-4354C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695063 | ||||||
| chr16:71695075
|
G | A | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.419-4366C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695075 | ||||||
| chr16:71695134
|
A | T | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.419-4425T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695134 | ||||||
| chr16:71695216
|
T | A | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-4507A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695216 | ||||||
| chr16:71695483
|
C | T | 1 | a0001c0001t0014g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.419-4774G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695483 | ||||||
| chr16:71695647
|
T | G | 1 | a0015c0027t0002g0203 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.419-4938A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695647 | ||||||
| chr16:71695712
|
GA | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(106): Show | 109 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.419-5004delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695712 | ||||||
| chr16:71695905
|
G | C | 1 | a0001c0001t0027g0307 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.419-5196C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695905 | ||||||
| chr16:71695922
|
T | C | 306 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(303): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.419-5213A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695922 | ||||||
| chr16:71695923
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.419-5214C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71695923 | ||||||
| chr16:71696020
|
G | C | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.419-5311C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696020 | ||||||
| chr16:71696058
|
C | T | 1 | a0001c0021t0001g0033 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.419-5349G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696058 | ||||||
| chr16:71696137
|
G | A | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.419-5428C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696137 | ||||||
| chr16:71696153
|
C | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.419-5444G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696153 | ||||||
| chr16:71696647
|
C | CA | 8 | a0001c0001t0001g0059a0001c0001t0004g0281a0001c0001t0004g0283others(5): Show | 8 | HG01433.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-5939dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696647 | ||||||
| chr16:71696683
|
T | C | 164 | a0001c0001t0001g0161a0001c0001t0003g0010a0001c0001t0003g0011others(161): Show | 167 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(164): Show |
intron_variant | MODIFIER | c.418+5915A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696683 | ||||||
| chr16:71696936
|
A | G | 1 | a0001c0005t0002g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.418+5662T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696936 | ||||||
| chr16:71696998
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.418+5600G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71696998 | ||||||
| chr16:71697127
|
GGCACCAC others(188): Show |
G | 1 | a0001c0005t0002g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.418+5276_418+5470d others(2): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697127 | ||||||
| chr16:71697172
|
C | CAATA | 15 | a0001c0001t0004g0284a0001c0001t0004g0285a0001c0001t0004g0290others(12): Show | 15 | HG01099.hp2 HG01123.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.418+5422_418+5425d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697172 | ||||||
| chr16:71697172
|
C | CAATAAAT others(1): Show |
5 | a0001c0001t0004g0004a0001c0001t0004g0286a0001c0001t0004g0305others(2): Show | 6 | HG01515.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.418+5418_418+5425d others(10): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697172 | ||||||
| chr16:71697172
|
C | CAATAAAT others(5): Show |
1 | a0001c0001t0004g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.418+5414_418+5425d others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697172 | ||||||
| chr16:71697172
|
CAATA | C | 3 | a0001c0001t0010g0009a0001c0001t0022g0274a0001c0001t0023g0273 | 3 | HG02451.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.418+5422_418+5425d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697172 | ||||||
| chr16:71697200
|
AAATAAAT others(8): Show |
A | 1 | a0014c0025t0001g0085 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.418+5383_418+5397d others(17): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697200 | ||||||
| chr16:71697212
|
AAAT | A | 146 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.418+5383_418+5385d others(5): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697212 | ||||||
| chr16:71697215
|
T | A | 1 | a0001c0002t0002g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.418+5383A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697215 | ||||||
| chr16:71697215
|
T | TA | 100 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0112others(97): Show | 102 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.418+5382dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697215 | ||||||
| chr16:71697215
|
T | TAAATA | 18 | a0001c0001t0001g0044a0001c0001t0001g0161a0001c0001t0005g0020others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.418+5382_418+5383i others(7): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697215 | ||||||
| chr16:71697215
|
T | TAAATAAA others(2): Show |
8 | a0001c0002t0002g0144a0001c0005t0002g0162a0001c0005t0002g0163others(5): Show | 8 | HG02083.hp2 HG02523.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.418+5382_418+5383i others(11): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697215 | ||||||
| chr16:71697215
|
T | TAAATAAA others(6): Show |
1 | a0001c0005t0002g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.418+5382_418+5383i others(15): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697215 | ||||||
| chr16:71697228
|
A | G | 5 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+5370T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697228 | ||||||
| chr16:71697486
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.418+5112C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697486 | ||||||
| chr16:71697559
|
T | C | 1 | a0001c0001t0017g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.418+5039A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697559 | ||||||
| chr16:71697582
|
T | C | 306 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(303): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.418+5016A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697582 | ||||||
| chr16:71697584
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0074 | 2 | HG00733.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.418+5014A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697584 | ||||||
| chr16:71697816
|
TC | T | 51 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0046others(48): Show | 51 | HG00438.hp1 HG00558.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.418+4781delG | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697816 | ||||||
| chr16:71697817
|
C | T | 231 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(228): Show | 234 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.418+4781G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697817 | ||||||
| chr16:71697848
|
A | AT | 121 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(118): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.418+4749dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697848 | ||||||
| chr16:71697848
|
A | ATT | 10 | a0001c0001t0001g0041a0001c0001t0001g0161a0001c0001t0005g0121others(7): Show | 10 | HG00741.hp1 HG01099.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.418+4748_418+4749d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697848 | ||||||
| chr16:71697848
|
AT | A | 29 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(26): Show | 30 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.418+4749delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697848 | ||||||
| chr16:71697941
|
G | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 6 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+4657C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697941 | ||||||
| chr16:71697941
|
G | T | 1 | a0001c0001t0017g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.418+4657C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697941 | ||||||
| chr16:71697949
|
A | G | 1 | a0001c0001t0004g0300 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.418+4649T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71697949 | ||||||
| chr16:71698143
|
G | A | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0015others(4): Show | 7 | HG01884.hp1 HG02965.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+4455C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698143 | ||||||
| chr16:71698290
|
C | T | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.418+4308G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698290 | ||||||
| chr16:71698364
|
A | G | 306 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(303): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.418+4234T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698364 | ||||||
| chr16:71698418
|
A | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.418+4180T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698418 | ||||||
| chr16:71698442
|
G | A | 163 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(160): Show | 166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.418+4156C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698442 | ||||||
| chr16:71698587
|
A | C | 1 | a0001c0001t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+4011T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698587 | ||||||
| chr16:71698610
|
G | A | 5 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+3988C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698610 | ||||||
| chr16:71698866
|
C | G | 1 | a0003c0004t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.418+3732G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698866 | ||||||
| chr16:71698892
|
C | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.418+3706G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71698892 | ||||||
| chr16:71699044
|
T | C | 6 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+3554A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699044 | ||||||
| chr16:71699166
|
G | A | 1 | a0001c0005t0002g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.418+3432C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699166 | ||||||
| chr16:71699250
|
T | C | 1 | a0003c0004t0002g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+3348A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699250 | ||||||
| chr16:71699397
|
G | A | 3 | a0001c0002t0002g0183a0001c0002t0002g0184a0001c0013t0002g0186 | 3 | HG03654.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.418+3201C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699397 | ||||||
| chr16:71699520
|
C | T | 3 | a0001c0005t0002g0163a0001c0005t0002g0165a0001c0005t0002g0173 | 3 | NA18959.hp1 NA18982.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.418+3078G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699520 | ||||||
| chr16:71699544
|
C | A | 1 | a0001c0002t0002g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.418+3054G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699544 | ||||||
| chr16:71699561
|
C | T | 1 | a0004c0006t0001g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.418+3037G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699561 | ||||||
| chr16:71699676
|
C | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.418+2922G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699676 | ||||||
| chr16:71699676
|
C | G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.418+2922G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699676 | ||||||
| chr16:71699785
|
C | A | 1 | a0001c0001t0004g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.418+2813G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699785 | ||||||
| chr16:71699791
|
G | T | 1 | a0003c0004t0019g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.418+2807C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699791 | ||||||
| chr16:71699939
|
T | A | 2 | a0002c0003t0003g0245a0002c0003t0029g0238 | 2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.418+2659A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71699939 | ||||||
| chr16:71700001
|
C | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0090others(2): Show | 5 | HG00438.hp1 HG02155.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+2597G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700001 | ||||||
| chr16:71700133
|
G | A | 319 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(316): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.418+2465C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700133 | ||||||
| chr16:71700279
|
C | T | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+2319G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700279 | ||||||
| chr16:71700280
|
G | A | 1 | a0001c0001t0005g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.418+2318C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700280 | ||||||
| chr16:71700305
|
T | C | 34 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(31): Show | 34 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.418+2293A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700305 | ||||||
| chr16:71700414
|
A | T | 1 | a0002c0003t0003g0319 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.418+2184T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700414 | ||||||
| chr16:71700519
|
C | CT | 97 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0031others(94): Show | 100 | HG00438.hp2 HG00621.hp1 HG00741.hp1 others(97): Show |
intron_variant | MODIFIER | c.418+2078dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700519 | ||||||
| chr16:71700519
|
C | CTT | 10 | a0001c0001t0017g0118a0001c0002t0002g0145a0001c0002t0002g0147others(7): Show | 10 | HG00423.hp1 HG02486.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.418+2077_418+2078d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700519 | ||||||
| chr16:71700519
|
CT | C | 21 | a0001c0001t0005g0130a0001c0001t0005g0134a0001c0001t0010g0009others(18): Show | 21 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+2078delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700519 | ||||||
| chr16:71700595
|
G | A | 1 | a0001c0002t0002g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.418+2003C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71700595 | ||||||
| chr16:71701062
|
G | A | 1 | a0001c0021t0001g0033 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.418+1536C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701062 | ||||||
| chr16:71701092
|
C | T | 1 | a0001c0005t0002g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.418+1506G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701092 | ||||||
| chr16:71701139
|
GACCATCC others(10): Show |
G | 7 | a0003c0004t0002g0211a0003c0004t0002g0214a0003c0004t0002g0222others(4): Show | 7 | HG01255.hp2 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+1442_418+1458d others(19): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701139 | ||||||
| chr16:71701189
|
T | C | 1 | a0001c0002t0002g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.418+1409A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701189 | ||||||
| chr16:71701242
|
A | T | 2 | a0001c0001t0003g0231a0001c0001t0003g0232 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.418+1356T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701242 | ||||||
| chr16:71701265
|
CATCT | C | 57 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0036others(54): Show | 58 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.418+1329_418+1332d others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701265 | ||||||
| chr16:71701265
|
CATCTATC others(1): Show |
C | 119 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0043others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.418+1325_418+1332d others(10): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701265 | ||||||
| chr16:71701265
|
CATCTATC others(5): Show |
C | 79 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0034others(76): Show | 80 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.418+1321_418+1332d others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701265 | ||||||
| chr16:71701265
|
CATCTATC others(9): Show |
C | 34 | a0001c0001t0001g0161a0001c0001t0004g0306a0001c0001t0010g0007others(31): Show | 35 | HG00741.hp1 HG01071.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+1317_418+1332d others(18): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701265 | ||||||
| chr16:71701265
|
CATCTATC others(13): Show |
C | 1 | a0003c0004t0002g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.418+1313_418+1332d others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701265 | ||||||
| chr16:71701296
|
CTATCTAT others(13): Show |
C | 1 | a0001c0001t0005g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.418+1282_418+1301d others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701296 | ||||||
| chr16:71701300
|
CTATCTAT others(9): Show |
C | 4 | a0001c0001t0001g0084a0001c0001t0005g0130a0001c0001t0005g0134others(1): Show | 4 | HG00558.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+1282_418+1297d others(18): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701300 | ||||||
| chr16:71701304
|
CTATCTAT others(5): Show |
C | 1 | a0003c0004t0002g0229 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.418+1282_418+1293d others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701304 | ||||||
| chr16:71701316
|
A | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00621.hp1 HG01175.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+1282T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701316 | ||||||
| chr16:71701320
|
C | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00621.hp1 HG01175.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+1278G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701320 | ||||||
| chr16:71701327
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00621.hp1 HG01175.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+1271G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701327 | ||||||
| chr16:71701339
|
CCTA | C | 312 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(309): Show | 315 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(312): Show |
intron_variant | MODIFIER | c.418+1256_418+1258d others(5): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701339 | ||||||
| chr16:71701342
|
A | AC | 6 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 7 | HG00621.hp1 HG01175.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+1255dupG | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701342 | ||||||
| chr16:71701391
|
A | G | 4 | a0001c0002t0008g0001a0001c0002t0008g0140a0001c0002t0008g0143others(1): Show | 5 | HG02698.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+1207T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701391 | ||||||
| chr16:71701601
|
A | G | 1 | a0001c0005t0002g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.418+997T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701601 | ||||||
| chr16:71701703
|
C | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.418+895G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701703 | ||||||
| chr16:71701762
|
G | GT | 299 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(296): Show | 302 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.418+835_418+836ins others(1): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71701762 | ||||||
| chr16:71702049
|
G | A | 1 | a0003c0004t0002g0229 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.418+549C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71702049 | ||||||
| chr16:71702195
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0087 | 2 | HG00621.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.418+403A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71702195 | ||||||
| chr16:71702415
|
T | A | 1 | a0004c0006t0001g0088 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.418+183A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71702415 | ||||||
| chr16:71702456
|
G | C | 13 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(10): Show | 13 | HG00733.hp2 HG01884.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.418+142C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71702456 | ||||||
| chr16:71702799
|
G | GTATTTT | 284 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.285-74_285-69dupAA others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71702799 | ||||||
| chr16:71703261
|
T | C | 69 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0141others(66): Show | 71 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.285-530A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703261 | ||||||
| chr16:71703289
|
G | A | 1 | a0002c0003t0003g0319 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.285-558C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703289 | ||||||
| chr16:71703415
|
A | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285-684T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703415 | ||||||
| chr16:71703453
|
C | G | 1 | a0001c0005t0002g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.285-722G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703453 | ||||||
| chr16:71703502
|
TA | T | 163 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(160): Show | 166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.285-772delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703502 | ||||||
| chr16:71703631
|
T | C | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.285-900A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703631 | ||||||
| chr16:71703743
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.285-1012A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703743 | ||||||
| chr16:71703756
|
T | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(112): Show | 115 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.285-1025A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703756 | ||||||
| chr16:71703821
|
C | T | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-1090G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703821 | ||||||
| chr16:71703953
|
G | A | 1 | a0001c0001t0005g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.285-1222C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703953 | ||||||
| chr16:71703967
|
G | A | 5 | a0003c0004t0002g0210a0003c0004t0002g0217a0003c0004t0002g0218others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-1236C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703967 | ||||||
| chr16:71704045
|
G | A | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.285-1314C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704045 | ||||||
| chr16:71704047
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-1316C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704047 | ||||||
| chr16:71704049
|
G | A | 1 | a0001c0005t0002g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.285-1318C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704049 | ||||||
| chr16:71704094
|
G | A | 1 | a0001c0002t0020g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.285-1363C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704094 | ||||||
| chr16:71704259
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-1528C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704259 | ||||||
| chr16:71704265
|
G | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-1534C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704265 | ||||||
| chr16:71704307
|
C | CA | 74 | a0001c0001t0003g0010a0001c0001t0003g0261a0001c0001t0005g0135others(71): Show | 76 | HG00423.hp1 HG00558.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.285-1577dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704307 | ||||||
| chr16:71704307
|
C | CAA | 106 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(103): Show | 106 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.285-1578_285-1577d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704307 | ||||||
| chr16:71704307
|
C | CAAA | 18 | a0001c0001t0001g0080a0001c0001t0005g0120a0001c0001t0005g0131others(15): Show | 18 | HG01258.hp1 HG01891.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.285-1579_285-1577d others(5): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704307 | ||||||
| chr16:71704307
|
C | CAAAAAAA others(6): Show |
1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-1589_285-1577d others(15): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704307 | ||||||
| chr16:71704307
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-1577_285-1576i others(21): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704307 | ||||||
| chr16:71704307
|
C | CAAAAACA others(5): Show |
1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.285-1577_285-1576i others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704307 | ||||||
| chr16:71704655
|
C | T | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-1924G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704655 | ||||||
| chr16:71704835
|
G | A | 1 | a0001c0002t0002g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.285-2104C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704835 | ||||||
| chr16:71704906
|
A | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0006c0010t0001g0056others(1): Show | 4 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-2175T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704906 | ||||||
| chr16:71704953
|
G | C | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.285-2222C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704953 | ||||||
| chr16:71704972
|
G | T | 1 | a0004c0006t0001g0088 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.285-2241C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71704972 | ||||||
| chr16:71705019
|
A | G | 1 | a0002c0003t0021g0006 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.285-2288T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705019 | ||||||
| chr16:71705073
|
T | C | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285-2342A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705073 | ||||||
| chr16:71705179
|
G | A | 5 | a0003c0004t0002g0210a0003c0004t0002g0217a0003c0004t0002g0218others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-2448C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705179 | ||||||
| chr16:71705264
|
C | T | 1 | a0001c0001t0016g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.285-2533G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705264 | ||||||
| chr16:71705360
|
G | C | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.285-2629C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705360 | ||||||
| chr16:71705472
|
T | G | 1 | a0001c0005t0002g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.285-2741A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705472 | ||||||
| chr16:71705745
|
C | T | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-3014G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705745 | ||||||
| chr16:71705746
|
A | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(117): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.285-3015T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705746 | ||||||
| chr16:71705803
|
C | A | 1 | a0001c0001t0004g0293 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.285-3072G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705803 | ||||||
| chr16:71705866
|
A | T | 2 | a0001c0001t0004g0309a0001c0001t0004g0310 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.285-3135T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705866 | ||||||
| chr16:71705973
|
T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0109a0001c0017t0001g0101others(1): Show | 4 | HG00558.hp2 NA18948.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-3242A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71705973 | ||||||
| chr16:71706146
|
A | G | 7 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(4): Show | 7 | HG00733.hp2 HG01175.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-3415T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706146 | ||||||
| chr16:71706268
|
G | GCTATGTC | 70 | a0001c0001t0017g0118a0001c0002t0002g0002a0001c0002t0002g0024others(67): Show | 72 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.285-3538_285-3537i others(9): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706268 | ||||||
| chr16:71706270
|
C | A | 70 | a0001c0001t0017g0118a0001c0002t0002g0002a0001c0002t0002g0024others(67): Show | 72 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.285-3539G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706270 | ||||||
| chr16:71706309
|
C | T | 2 | a0001c0001t0022g0274a0001c0001t0023g0273 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.285-3578G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706309 | ||||||
| chr16:71706385
|
A | C | 3 | a0001c0001t0004g0021a0001c0001t0005g0020a0008c0018t0012g0265 | 3 | HG02647.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.285-3654T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706385 | ||||||
| chr16:71706531
|
C | A | 1 | a0001c0001t0004g0021 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.285-3800G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706531 | ||||||
| chr16:71706574
|
G | A | 284 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.285-3843C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706574 | ||||||
| chr16:71706925
|
T | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-4194A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706925 | ||||||
| chr16:71706946
|
A | AT | 7 | a0001c0001t0004g0285a0001c0001t0004g0306a0001c0001t0004g0308others(4): Show | 7 | HG01515.hp2 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-4216dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706946 | ||||||
| chr16:71706946
|
AT | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0031others(70): Show | 74 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.285-4216delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706946 | ||||||
| chr16:71706946
|
ATT | A | 37 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp1 HG00741.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.285-4217_285-4216d others(4): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706946 | ||||||
| chr16:71706946
|
ATTT | A | 144 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(141): Show | 147 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.285-4218_285-4216d others(5): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71706946 | ||||||
| chr16:71707138
|
G | T | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.285-4407C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71707138 | ||||||
| chr16:71707146
|
G | A | 8 | a0001c0001t0004g0276a0001c0001t0004g0277a0001c0001t0004g0278others(5): Show | 8 | HG00738.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.285-4415C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71707146 | ||||||
| chr16:71707411
|
G | C | 1 | a0012c0023t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.285-4680C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71707411 | ||||||
| chr16:71707485
|
G | A | 1 | a0001c0002t0002g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.285-4754C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71707485 | ||||||
| chr16:71707581
|
T | C | 1 | a0001c0001t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.285-4850A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71707581 | ||||||
| chr16:71707721
|
C | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(107): Show | 110 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.285-4990G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71707721 | ||||||
| chr16:71708025
|
C | T | 54 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(51): Show | 55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.285-5294G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708025 | ||||||
| chr16:71708097
|
C | G | 162 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(159): Show | 165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.285-5366G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708097 | ||||||
| chr16:71708485
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0078others(1): Show | 4 | NA18973.hp1 NA18977.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-5754G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708485 | ||||||
| chr16:71708495
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.285-5764G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708495 | ||||||
| chr16:71708496
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-5765C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708496 | ||||||
| chr16:71708536
|
A | C | 1 | a0001c0001t0003g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.285-5805T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708536 | ||||||
| chr16:71708558
|
G | A | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.285-5827C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708558 | ||||||
| chr16:71708574
|
C | G | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.285-5843G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708574 | ||||||
| chr16:71708629
|
T | C | 1 | a0001c0001t0017g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284+5883A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708629 | ||||||
| chr16:71708778
|
T | C | 1 | a0001c0005t0002g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.284+5734A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708778 | ||||||
| chr16:71708826
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.284+5686C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708826 | ||||||
| chr16:71708894
|
T | C | 1 | a0001c0019t0003g0237 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284+5618A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708894 | ||||||
| chr16:71708969
|
A | AT | 76 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(73): Show | 77 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.284+5542dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708969 | ||||||
| chr16:71708977
|
A | T | 1 | a0001c0001t0007g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.284+5535T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708977 | ||||||
| chr16:71709266
|
T | C | 27 | a0002c0003t0002g0240a0002c0003t0002g0316a0002c0003t0003g0003others(24): Show | 28 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.284+5246A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709266 | ||||||
| chr16:71709307
|
G | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+5205C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709307 | ||||||
| chr16:71709313
|
A | G | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.284+5199T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709313 | ||||||
| chr16:71709314
|
G | A | 1 | a0001c0005t0002g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284+5198C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709314 | ||||||
| chr16:71709517
|
C | T | 1 | a0002c0003t0003g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.284+4995G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709517 | ||||||
| chr16:71709697
|
G | A | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.284+4815C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709697 | ||||||
| chr16:71709752
|
G | A | 1 | a0001c0002t0002g0185 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.284+4760C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709752 | ||||||
| chr16:71709908
|
A | G | 1 | a0003c0004t0002g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284+4604T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71709908 | ||||||
| chr16:71710060
|
G | A | 2 | a0001c0001t0004g0309a0001c0001t0004g0310 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.284+4452C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710060 | ||||||
| chr16:71710081
|
C | T | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.284+4431G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710081 | ||||||
| chr16:71710460
|
C | T | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.284+4052G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710460 | ||||||
| chr16:71710497
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.284+4015C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710497 | ||||||
| chr16:71710723
|
G | C | 1 | a0001c0013t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.284+3789C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710723 | ||||||
| chr16:71710936
|
T | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+3576A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710936 | ||||||
| chr16:71710979
|
G | A | 1 | a0001c0002t0002g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284+3533C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71710979 | ||||||
| chr16:71711159
|
G | A | 24 | a0002c0003t0002g0240a0002c0003t0002g0316a0002c0003t0003g0003others(21): Show | 25 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.284+3353C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711159 | ||||||
| chr16:71711287
|
C | T | 2 | a0001c0001t0005g0121a0001c0001t0005g0122 | 2 | HG01433.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.284+3225G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711287 | ||||||
| chr16:71711317
|
G | A | 3 | a0002c0003t0003g0235a0002c0003t0003g0236a0002c0003t0003g0254 | 3 | HG00609.hp2 NA18968.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.284+3195C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711317 | ||||||
| chr16:71711498
|
G | T | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.284+3014C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711498 | ||||||
| chr16:71711588
|
A | T | 190 | a0001c0001t0001g0161a0001c0001t0003g0010a0001c0001t0003g0011others(187): Show | 194 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(191): Show |
intron_variant | MODIFIER | c.284+2924T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711588 | ||||||
| chr16:71711615
|
C | T | 191 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(188): Show | 195 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(192): Show |
intron_variant | MODIFIER | c.284+2897G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711615 | ||||||
| chr16:71711806
|
G | A | 67 | a0001c0001t0001g0161a0001c0002t0002g0002a0001c0002t0002g0024others(64): Show | 69 | HG00423.hp1 HG00741.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.284+2706C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711806 | ||||||
| chr16:71711845
|
C | T | 54 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(51): Show | 55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.284+2667G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711845 | ||||||
| chr16:71711871
|
G | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.284+2641C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711871 | ||||||
| chr16:71711935
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.284+2577C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711935 | ||||||
| chr16:71712613
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.284+1899C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71712613 | ||||||
| chr16:71712890
|
G | A | 1 | a0001c0001t0004g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.284+1622C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71712890 | ||||||
| chr16:71713018
|
C | T | 7 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(4): Show | 7 | HG00733.hp2 HG01175.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+1494G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713018 | ||||||
| chr16:71713114
|
C | G | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.284+1398G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713114 | ||||||
| chr16:71713209
|
G | A | 1 | a0001c0005t0002g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.284+1303C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713209 | ||||||
| chr16:71713227
|
T | C | 1 | a0001c0001t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.284+1285A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713227 | ||||||
| chr16:71713388
|
A | T | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0015others(4): Show | 7 | HG01884.hp1 HG02965.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+1124T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713388 | ||||||
| chr16:71713577
|
T | C | 2 | a0003c0004t0002g0219a0003c0004t0002g0220 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.284+935A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713577 | ||||||
| chr16:71713632
|
C | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.284+880G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713632 | ||||||
| chr16:71713912
|
T | C | 1 | a0001c0005t0002g0173 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.284+600A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713912 | ||||||
| chr16:71713923
|
C | CA | 84 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(81): Show | 85 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.284+588dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713923 | ||||||
| chr16:71713940
|
C | CT | 8 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0080others(5): Show | 8 | HG00642.hp2 HG02738.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+571dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713940 | ||||||
| chr16:71713945
|
C | CT | 10 | a0001c0001t0004g0021a0001c0001t0004g0276a0001c0001t0004g0285others(7): Show | 10 | HG01515.hp2 HG02055.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+566dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713945 | ||||||
| chr16:71713945
|
C | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.284+567G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713945 | ||||||
| chr16:71714004
|
A | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.284+508T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71714004 | ||||||
| chr16:71714282
|
A | T | 1 | a0001c0002t0002g0187 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.284+230T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71714282 | ||||||
| chr16:71714836
|
G | A | 17 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(14): Show | 17 | HG01433.hp2 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6-35C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71714836 | ||||||
| chr16:71715033
|
C | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(316): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.-6-232G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715033 | ||||||
| chr16:71715062
|
A | G | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-6-261T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715062 | ||||||
| chr16:71715130
|
C | T | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6-329G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715130 | ||||||
| chr16:71715258
|
T | G | 22 | a0001c0001t0004g0004a0001c0001t0004g0276a0001c0001t0004g0277others(19): Show | 23 | HG00738.hp2 HG01515.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6-457A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715258 | ||||||
| chr16:71715294
|
G | A | 16 | a0001c0002t0002g0024a0001c0002t0002g0145a0001c0002t0002g0146others(13): Show | 16 | HG01346.hp2 NA18747.hp1 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-493C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715294 | ||||||
| chr16:71715364
|
G | C | 67 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0141others(64): Show | 69 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-6-563C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715364 | ||||||
| chr16:71715450
|
C | T | 22 | a0001c0001t0004g0004a0001c0001t0004g0276a0001c0001t0004g0277others(19): Show | 23 | HG00738.hp2 HG01515.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6-649G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715450 | ||||||
| chr16:71715457
|
C | T | 1 | a0001c0002t0002g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-6-656G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715457 | ||||||
| chr16:71715473
|
C | G | 1 | a0001c0001t0010g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6-672G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715473 | ||||||
| chr16:71715522
|
C | CA | 22 | a0001c0001t0004g0004a0001c0001t0004g0276a0001c0001t0004g0277others(19): Show | 23 | HG00738.hp2 HG01515.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6-722dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715522 | ||||||
| chr16:71715773
|
T | C | 36 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(33): Show | 36 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-972A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715773 | ||||||
| chr16:71715823
|
C | CA | 25 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0161others(22): Show | 26 | HG00738.hp2 HG00741.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.-6-1023dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715823 | ||||||
| chr16:71715823
|
CA | C | 157 | a0001c0001t0001g0109a0001c0001t0003g0010a0001c0001t0003g0011others(154): Show | 160 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(157): Show |
intron_variant | MODIFIER | c.-6-1023delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715823 | ||||||
| chr16:71715831
|
A | C | 2 | a0002c0003t0003g0206a0002c0003t0003g0207 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-6-1030T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715831 | ||||||
| chr16:71715833
|
A | C | 3 | a0001c0001t0004g0021a0001c0001t0005g0020a0001c0001t0005g0121 | 3 | HG01433.hp2 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-6-1032T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715833 | ||||||
| chr16:71715836
|
A | C | 4 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-1035T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715836 | ||||||
| chr16:71715837
|
A | C | 5 | a0003c0004t0002g0210a0003c0004t0002g0217a0003c0004t0002g0218others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-1036T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715837 | ||||||
| chr16:71715839
|
A | C | 1 | a0001c0001t0004g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-6-1038T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715839 | ||||||
| chr16:71715839
|
AC | A | 7 | a0001c0002t0002g0197a0003c0004t0002g0263a0003c0004t0002g0267others(4): Show | 7 | HG02165.hp1 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-1039delG | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715839 | ||||||
| chr16:71715840
|
C | A | 26 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0161others(23): Show | 27 | HG00738.hp2 HG00741.hp1 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.-6-1039G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715840 | ||||||
| chr16:71715853
|
G | A | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-6-1052C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715853 | ||||||
| chr16:71715896
|
T | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-1095A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715896 | ||||||
| chr16:71715913
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0104others(1): Show | 4 | HG00438.hp1 NA19003.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-1112A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715913 | ||||||
| chr16:71715991
|
C | CA | 26 | a0001c0001t0001g0105a0001c0001t0004g0004a0001c0001t0004g0276others(23): Show | 27 | HG00609.hp2 HG00738.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6-1191dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715991 | ||||||
| chr16:71716008
|
C | A | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-1207G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716008 | ||||||
| chr16:71716056
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-6-1255G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716056 | ||||||
| chr16:71716188
|
C | G | 1 | a0001c0001t0022g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-6-1387G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716188 | ||||||
| chr16:71716325
|
C | T | 1 | a0002c0003t0003g0320 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-6-1524G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716325 | ||||||
| chr16:71716412
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-6-1611C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716412 | ||||||
| chr16:71716431
|
T | C | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6-1630A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716431 | ||||||
| chr16:71716649
|
A | T | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-1848T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716649 | ||||||
| chr16:71716650
|
A | G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-1849T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716650 | ||||||
| chr16:71716922
|
A | G | 196 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0003g0010others(193): Show | 200 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(197): Show |
intron_variant | MODIFIER | c.-6-2121T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716922 | ||||||
| chr16:71717093
|
G | A | 170 | a0001c0001t0001g0161a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 173 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(170): Show |
intron_variant | MODIFIER | c.-6-2292C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71717093 | ||||||
| chr16:71717204
|
T | C | 2 | a0001c0001t0004g0303a0001c0001t0004g0304 | 2 | NA18954.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-6-2403A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71717204 | ||||||
| chr16:71717639
|
G | C | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-2838C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71717639 | ||||||
| chr16:71717751
|
C | T | 12 | a0001c0007t0006g0150a0001c0007t0006g0151a0001c0007t0006g0152others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-2950G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71717751 | ||||||
| chr16:71717818
|
T | C | 1 | a0001c0001t0011g0107 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-6-3017A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71717818 | ||||||
| chr16:71717896
|
G | A | 1 | a0002c0003t0003g0320 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-6-3095C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71717896 | ||||||
| chr16:71718198
|
T | C | 22 | a0001c0001t0004g0004a0001c0001t0004g0276a0001c0001t0004g0277others(19): Show | 23 | HG00738.hp2 HG01515.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6-3397A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718198 | ||||||
| chr16:71718254
|
T | C | 7 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(4): Show | 7 | HG00733.hp2 HG01175.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-3453A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718254 | ||||||
| chr16:71718302
|
G | A | 22 | a0001c0001t0004g0004a0001c0001t0004g0276a0001c0001t0004g0277others(19): Show | 23 | HG00738.hp2 HG01515.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6-3501C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718302 | ||||||
| chr16:71718370
|
G | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-3569C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718370 | ||||||
| chr16:71718380
|
C | A | 50 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0141others(47): Show | 52 | HG00423.hp1 HG01070.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-6-3579G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718380 | ||||||
| chr16:71718390
|
C | A | 50 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0141others(47): Show | 52 | HG00423.hp1 HG01070.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-6-3589G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718390 | ||||||
| chr16:71718441
|
G | A | 151 | a0001c0001t0001g0161a0001c0001t0003g0010a0001c0001t0003g0011others(148): Show | 154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-6-3640C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718441 | ||||||
| chr16:71718496
|
C | T | 1 | a0004c0006t0001g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6-3695G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718496 | ||||||
| chr16:71718579
|
C | CA | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-3779dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718579 | ||||||
| chr16:71718594
|
C | A | 9 | a0001c0002t0002g0002a0001c0002t0002g0147a0001c0002t0002g0198others(6): Show | 10 | HG00423.hp1 HG01070.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-3793G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718594 | ||||||
| chr16:71718660
|
G | A | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6-3859C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718660 | ||||||
| chr16:71718673
|
C | G | 69 | a0001c0001t0001g0161a0001c0002t0002g0002a0001c0002t0002g0024others(66): Show | 71 | HG00423.hp1 HG00741.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.-6-3872G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718673 | ||||||
| chr16:71718694
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-6-3893G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718694 | ||||||
| chr16:71718695
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-6-3894C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718695 | ||||||
| chr16:71718831
|
G | A | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-6-4030C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718831 | ||||||
| chr16:71718885
|
G | T | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-6-4084C>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71718885 | ||||||
| chr16:71719011
|
C | A | 163 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(160): Show | 166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.-6-4210G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719011 | ||||||
| chr16:71719199
|
C | T | 7 | a0003c0004t0002g0263a0003c0004t0002g0267a0003c0004t0002g0268others(4): Show | 7 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-4398G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719199 | ||||||
| chr16:71719210
|
A | G | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-6-4409T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719210 | ||||||
| chr16:71719258
|
G | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 6 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-4457C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719258 | ||||||
| chr16:71719294
|
G | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 6 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-4493C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719294 | ||||||
| chr16:71719422
|
C | A | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-4621G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719422 | ||||||
| chr16:71719443
|
G | C | 34 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(31): Show | 34 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-6-4642C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719443 | ||||||
| chr16:71719612
|
T | C | 1 | a0001c0001t0004g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+4717A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719612 | ||||||
| chr16:71719646
|
G | C | 1 | a0015c0027t0002g0203 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-7+4683C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719646 | ||||||
| chr16:71719651
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-7+4678A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719651 | ||||||
| chr16:71719673
|
A | C | 2 | a0002c0003t0003g0206a0002c0003t0003g0207 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-7+4656T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719673 | ||||||
| chr16:71719713
|
T | TA | 69 | a0001c0001t0001g0161a0001c0002t0002g0002a0001c0002t0002g0024others(66): Show | 71 | HG00423.hp1 HG00741.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7+4615dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719713 | ||||||
| chr16:71719887
|
G | A | 1 | a0002c0003t0003g0253 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-7+4442C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719887 | ||||||
| chr16:71719888
|
C | A | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+4441G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719888 | ||||||
| chr16:71719945
|
A | G | 1 | a0003c0004t0002g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-7+4384T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719945 | ||||||
| chr16:71719956
|
C | T | 7 | a0003c0004t0002g0263a0003c0004t0002g0267a0003c0004t0002g0268others(4): Show | 7 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+4373G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719956 | ||||||
| chr16:71719964
|
A | AT | 15 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(12): Show | 15 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7+4364dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATT | 122 | a0001c0001t0001g0161a0001c0001t0003g0011a0001c0001t0003g0232others(119): Show | 125 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.-7+4363_-7+4364dup others(2): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTT | 34 | a0001c0001t0003g0010a0001c0001t0003g0231a0001c0001t0003g0255others(31): Show | 34 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-7+4362_-7+4364dup others(3): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTT | 6 | a0001c0001t0004g0004a0001c0001t0004g0286a0001c0001t0004g0287others(3): Show | 7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+4359_-7+4364dup others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-7+4355_-7+4364dup others(10): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0004g0285a0001c0001t0004g0309a0001c0001t0004g0310others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+4354_-7+4364dup others(11): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0027g0307 | 3 | HG01515.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-7+4353_-7+4364dup others(12): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG01169.hp2 NA18948.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-7+4352_-7+4364dup others(13): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(7): Show |
30 | a0001c0001t0001g0036a0001c0001t0001g0082a0001c0001t0001g0083others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-7+4351_-7+4364dup others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(8): Show |
38 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(35): Show | 38 | HG00438.hp1 HG00438.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.-7+4350_-7+4364dup others(15): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(9): Show |
15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 15 | HG01106.hp2 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7+4349_-7+4364dup others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(10): Show |
14 | a0001c0001t0001g0114a0001c0001t0005g0121a0001c0001t0005g0122others(11): Show | 14 | HG00140.hp1 HG01433.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+4348_-7+4364dup others(17): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(11): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG00621.hp1 HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-7+4347_-7+4364dup others(18): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0042 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-7+4346_-7+4364dup others(19): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0005g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7+4344_-7+4364dup others(21): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0005g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-7+4343_-7+4364dup others(22): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0026 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-7+4341_-7+4364dup others(24): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7+4364_-7+4365ins others(25): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(21): Show |
3 | a0001c0001t0004g0281a0001c0001t0004g0282a0001c0001t0004g0283 | 3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-7+4364_-7+4365ins others(28): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(22): Show |
1 | a0001c0001t0004g0280 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7+4364_-7+4365ins others(29): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(24): Show |
1 | a0001c0001t0004g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-7+4364_-7+4365ins others(31): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(32): Show |
1 | a0001c0001t0004g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-7+4364_-7+4365ins others(39): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719964
|
A | ATTTTTTT others(33): Show |
2 | a0001c0001t0004g0276a0001c0001t0004g0277 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-7+4364_-7+4365ins others(40): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719964 | ||||||
| chr16:71719988
|
T | TTTTTTTT others(9): Show |
1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-7+4340_-7+4341ins others(16): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719988 | ||||||
| chr16:71719994
|
G | A | 5 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+4335C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71719994 | ||||||
| chr16:71720115
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | NA18954.hp2 NA18959.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+4214C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720115 | ||||||
| chr16:71720137
|
T | C | 75 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(72): Show | 76 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-7+4192A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720137 | ||||||
| chr16:71720172
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-7+4157A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720172 | ||||||
| chr16:71720261
|
G | A | 1 | a0001c0007t0006g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-7+4068C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720261 | ||||||
| chr16:71720544
|
C | G | 1 | a0001c0001t0004g0291 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+3785G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720544 | ||||||
| chr16:71720609
|
A | T | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-7+3720T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720609 | ||||||
| chr16:71720710
|
C | T | 1 | a0001c0001t0023g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-7+3619G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720710 | ||||||
| chr16:71720740
|
T | C | 1 | a0002c0003t0003g0254 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-7+3589A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720740 | ||||||
| chr16:71720808
|
T | C | 165 | a0001c0001t0001g0161a0001c0001t0003g0010a0001c0001t0003g0011others(162): Show | 168 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(165): Show |
intron_variant | MODIFIER | c.-7+3521A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720808 | ||||||
| chr16:71720841
|
G | A | 1 | a0001c0002t0008g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7+3488C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720841 | ||||||
| chr16:71720875
|
GA | G | 94 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(91): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-7+3453delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71720875 | ||||||
| chr16:71721027
|
T | A | 1 | a0003c0004t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7+3302A>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721027 | ||||||
| chr16:71721148
|
C | G | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7+3181G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721148 | ||||||
| chr16:71721195
|
A | C | 32 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0002t0002g0226others(29): Show | 32 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7+3134T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721195 | ||||||
| chr16:71721313
|
T | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+3016A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721313 | ||||||
| chr16:71721375
|
C | G | 289 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(286): Show | 292 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.-7+2954G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721375 | ||||||
| chr16:71721388
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7+2941A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721388 | ||||||
| chr16:71721405
|
G | A | 7 | a0003c0004t0002g0263a0003c0004t0002g0267a0003c0004t0002g0268others(4): Show | 7 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+2924C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721405 | ||||||
| chr16:71721420
|
T | C | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+2909A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721420 | ||||||
| chr16:71721483
|
A | G | 34 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(31): Show | 34 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-7+2846T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721483 | ||||||
| chr16:71721491
|
C | T | 16 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(13): Show | 16 | HG00438.hp2 HG01515.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7+2838G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721491 | ||||||
| chr16:71721528
|
G | C | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+2801C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721528 | ||||||
| chr16:71721613
|
A | C | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-7+2716T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721613 | ||||||
| chr16:71721671
|
GA | G | 274 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(271): Show | 277 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.-7+2657delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721671 | ||||||
| chr16:71721769
|
A | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(90): Show | 93 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-7+2560T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721769 | ||||||
| chr16:71721770
|
C | A | 1 | a0003c0004t0002g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7+2559G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721770 | ||||||
| chr16:71721949
|
T | C | 73 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0231others(70): Show | 74 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.-7+2380A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721949 | ||||||
| chr16:71721950
|
C | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-7+2379G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721950 | ||||||
| chr16:71721994
|
A | G | 4 | a0001c0002t0002g0024a0001c0002t0013g0023a0001c0002t0013g0025others(1): Show | 4 | NA18941.hp1 NA18961.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+2335T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721994 | ||||||
| chr16:71722020
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7+2309A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722020 | ||||||
| chr16:71722057
|
C | G | 2 | a0001c0001t0004g0021a0001c0001t0005g0020 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7+2272G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722057 | ||||||
| chr16:71722068
|
T | G | 7 | a0003c0004t0002g0263a0003c0004t0002g0267a0003c0004t0002g0268others(4): Show | 7 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+2261A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722068 | ||||||
| chr16:71722301
|
G | A | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7+2028C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722301 | ||||||
| chr16:71722713
|
G | A | 7 | a0003c0004t0002g0263a0003c0004t0002g0267a0003c0004t0002g0268others(4): Show | 7 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+1616C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722713 | ||||||
| chr16:71722832
|
A | C | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0015others(4): Show | 7 | HG01884.hp1 HG02965.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+1497T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722832 | ||||||
| chr16:71722942
|
C | G | 306 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(303): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.-7+1387G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71722942 | ||||||
| chr16:71723023
|
C | A | 1 | a0001c0002t0002g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-7+1306G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723023 | ||||||
| chr16:71723058
|
T | G | 1 | a0008c0018t0012g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+1271A>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723058 | ||||||
| chr16:71723089
|
C | G | 1 | a0010c0020t0001g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-7+1240G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723089 | ||||||
| chr16:71723112
|
G | A | 6 | a0003c0004t0002g0267a0003c0004t0002g0268a0003c0004t0002g0269others(3): Show | 6 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+1217C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723112 | ||||||
| chr16:71723221
|
G | A | 1 | a0003c0004t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+1108C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723221 | ||||||
| chr16:71723334
|
G | C | 1 | a0001c0005t0002g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-7+995C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723334 | ||||||
| chr16:71723345
|
G | A | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-7+984C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723345 | ||||||
| chr16:71723380
|
G | A | 6 | a0003c0004t0002g0267a0003c0004t0002g0268a0003c0004t0002g0269others(3): Show | 6 | HG02055.hp2 HG02165.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+949C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723380 | ||||||
| chr16:71723484
|
C | G | 284 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.-7+845G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723484 | ||||||
| chr16:71723492
|
A | G | 284 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.-7+837T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723492 | ||||||
| chr16:71723547
|
G | A | 5 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+782C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723547 | ||||||
| chr16:71723710
|
C | G | 3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-7+619G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723710 | ||||||
| chr16:71723716
|
TCCGCTTG others(9): Show |
T | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-7+597_-7+612delGC others(14): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723716 | ||||||
| chr16:71723733
|
C | CCGCTCGC others(1): Show |
3 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009 | 3 | HG02257.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-7+588_-7+595dupAG others(6): Show |
PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723733 | ||||||
| chr16:71723910
|
C | A | 1 | a0001c0009t0001g0275 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-7+419G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723910 | ||||||
| chr16:71724036
|
C | G | 284 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.-7+293G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71724036 | ||||||
| chr16:71724039
|
C | A | 5 | a0001c0001t0004g0306a0001c0001t0004g0308a0001c0001t0004g0309others(2): Show | 5 | HG01515.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+290G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71724039 | ||||||
| chr16:71724107
|
C | T | 1 | a0002c0003t0021g0006 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-7+222G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71724107 | ||||||
| chr16:71724165
|
G | C | 10 | a0002c0003t0002g0316a0002c0003t0003g0311a0002c0003t0003g0312others(7): Show | 10 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+164C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71724165 | ||||||
| chr16:71724195
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-7+134T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71724195 | ||||||
| chr16:71724326
|
C | A | 1 | a0002c0003t0003g0320 | 1 | HG04228.hp2 | splice_region_variant&intron_variant | LOW | c.-7+3G>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71724326 |