Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0002 | 0/0 | 1323 | 28 | 3 | 11 | 6 | 3 | 5 | 5 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0003 | 0/0 | 1323 | 23 | 6 | 13 | 1 | 0 | 3 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0004 | 0/0 | 1323 | 14 | 1 | 8 | 5 | 0 | 0 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0005 | 0/0 | 1323 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0006 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0007 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0008 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0009 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0010 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0011 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0012 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0013 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0014 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| a0015 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | MKRNG others(1318): Show |
chr16 | 71639924 | 71729701 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3969 | 158 | 66 | 24 | 51 | 6 | 10 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0002 | 0/0 | 3969 | 51 | 0 | 5 | 31 | 0 | 15 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0005 | 0/0 | 3969 | 18 | 0 | 2 | 11 | 1 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0007 | 0/0 | 3969 | 9 | 9 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0009 | 0/0 | 3969 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0013 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0017 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0019 | 0/1 | 3969 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0021 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0024 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0001c0026 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0002c0003 | 0/0 | 3969 | 26 | 3 | 10 | 6 | 3 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0002c0011 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0002c0016 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0003c0004 | 0/0 | 3969 | 23 | 6 | 13 | 1 | 0 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0004c0006 | 0/0 | 3969 | 14 | 1 | 8 | 5 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0005c0008 | 0/0 | 3969 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0006c0010 | 0/0 | 3969 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0007c0012 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0008c0025 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0009c0023 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0010c0014 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0011c0027 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0012c0018 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0013c0015 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0014c0020 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
chr16 | 71639924 | 71729701 | ||
| a0015c0022 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | ATGAA others(3964): Show |
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 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0003 | 0/0 | 8307 | 19 | 12 | 3 | 0 | 1 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0004 | 1/0 | 8317 | 34 | 22 | 8 | 3 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8312): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0005 | 0/0 | 8316 | 15 | 14 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0007 | 0/0 | 8307 | 7 | 7 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0010 | 0/0 | 8316 | 3 | 3 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0011 | 0/0 | 8303 | 2 | 0 | 0 | 2 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8298): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0012 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0014 | 0/0 | 8316 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0016 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0017 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0018 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0021 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0022 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0023 | 0/0 | 8317 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8312): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0025 | 0/0 | 8308 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8303): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0026 | 0/0 | 8303 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8298): Show |
chr16 | 71639924 | 71729701 |
| a0001c0001t0027 | 0/0 | 8317 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8312): Show |
chr16 | 71639924 | 71729701 |
| a0001c0002t0002 | 0/0 | 8307 | 39 | 0 | 5 | 24 | 0 | 10 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0002t0008 | 0/0 | 8307 | 5 | 0 | 0 | 0 | 0 | 5 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0002t0009 | 0/0 | 8307 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0002t0013 | 0/0 | 8307 | 2 | 0 | 0 | 2 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0002t0015 | 0/0 | 8307 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0005t0002 | 0/0 | 8307 | 18 | 0 | 2 | 11 | 1 | 4 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0007t0006 | 0/0 | 8316 | 9 | 9 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0009t0001 | 0/0 | 8316 | 2 | 0 | 0 | 0 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0013t0002 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0017t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0019t0003 | 0/1 | 8307 | 1 | 0 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0001c0021t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0024t0005 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0001c0026t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0002c0003t0002 | 0/0 | 8307 | 2 | 0 | 1 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0002c0003t0003 | 0/0 | 8307 | 21 | 3 | 9 | 4 | 2 | 3 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0002c0003t0020 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0002c0003t0024 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8303): Show |
chr16 | 71639924 | 71729701 |
| a0002c0003t0028 | 0/0 | 8307 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0002c0011t0002 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0002c0016t0003 | 0/0 | 8307 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0003c0004t0002 | 0/0 | 8307 | 22 | 6 | 13 | 1 | 0 | 2 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0003c0004t0019 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0004c0006t0001 | 0/0 | 8316 | 14 | 1 | 8 | 5 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0005c0008t0002 | 0/0 | 8307 | 4 | 0 | 0 | 4 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0006c0010t0001 | 0/0 | 8316 | 2 | 0 | 2 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0007c0012t0029 | 0/0 | 8307 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0008c0025t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0009c0023t0006 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0010c0014t0006 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0011c0027t0002 | 0/0 | 8307 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8302): Show |
chr16 | 71639924 | 71729701 |
| a0012c0018t0012 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0013c0015t0006 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0014c0020t0001 | 0/0 | 8316 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| a0015c0022t0001 | 0/0 | 8316 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | GCACA others(8311): Show |
chr16 | 71639924 | 71729701 |
| actghapid | grch38/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 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0001g0099 | 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 | 1/0 | 1 | 0 | 0 | 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 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0011g0097 | 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 |
| a0001c0001t0021g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0022g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0023g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0025g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0026g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0001t0027g0288 | 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 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| 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 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0001c0005t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0009t0001g0095 | 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 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0002g0317 | 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 |
| a0002c0003t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0242 | 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 |
| a0002c0003t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0002c0003t0020g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0024g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0002c0003t0028g0238 | 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 |
| a0004c0006t0001g0050 | 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 |
| a0004c0006t0001g0068 | 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 |
| a0004c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0004c0006t0001g0093 | 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 |
| a0007c0012t0029g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0008c0025t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0009c0023t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0010c0014t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0011c0027t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0012c0018t0012g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0013c0015t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0014c0020t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| a0015c0022t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0318 | 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 | t0023 | 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 | g0069 | 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 | g0167 | 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 | g0180 | 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 | g0302 | 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 | g0240 | 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 | g0242 | 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 | g0070 | 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 | g0244 | 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 | a0007 | c0012 | t0029 | 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 | g0301 | 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 | t0026 | 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 | g0241 | 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 | g0317 | AMR | PEL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG01978 | hp1 | a0004 | c0006 | t0001 | g0068 | 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 | a0008 | c0025 | t0001 | g0085 | EAS | KHV | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02083 | hp2 | a0001 | c0005 | t0002 | g0168 | 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 | g0316 | 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 | t0027 | 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 | g0093 | 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 | t0021 | 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 | g0276 | 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 | g0095 | 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 | g0181 | 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 | t0002 | 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 | g0277 | 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 | a0009 | 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 | g0013 | AFR | ESN | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG02970 | hp1 | a0010 | 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 | a0011 | c0027 | t0002 | g0203 | SAS | PJL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03098 | hp1 | a0012 | c0018 | t0012 | g0265 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03130 | hp1 | a0013 | 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 | g0018 | 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 | g0016 | AFR | MSL | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | 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 | g0015 | 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 | g0071 | 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 | g0017 | 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 | g0169 | 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 | g0182 | 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 | g0179 | 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 | g0051 | 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 | a0014 | 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 | t0020 | 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 | a0015 | 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 | g0098 | 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 | g0040 | 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 | g0072 | 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 | g0094 | 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 | g0041 | 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 | g0053 | 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 | t0024 | g0243 | 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 | g0099 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19004 | hp2 | a0001 | c0005 | t0002 | g0166 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0097 | 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 | g0039 | 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 | g0052 | EAS | JPT | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| NA19054 | hp2 | a0002 | c0003 | t0028 | 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 | g0092 | 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 | g0096 | 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 | g0073 | 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 | g0074 | 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 | t0025 | 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 | g0050 | 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 | a0001 | c0019 | t0003 | g0237 | REF | REF | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0300 | REF | REF | PHLPP2_chr16_71639924_71729701 | PHLPP2 | chr16 | 71639924 | 71729701 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71648927 | C | T | 2 | a0003 a0005 |
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 | a0012 | 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 | a0007 | 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 | a0013 | 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 | a0014 | 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 | a0010 | 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 | a0009 | 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 | a0015 | 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 | a0008 | 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 | a0011 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71648893 | T | C | 8 | a0001c0002 a0001c0005 a0001c0013 others(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 | |||
| chr16:71649856 | 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 | a0001c0007 a0009c0023 a0010c0014 others(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 | a0001c0002 a0001c0005 a0001c0013 others(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 | a0001c0024 a0009c0023 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71645029 | T | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(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 | a0001c0007t0006 a0009c0023t0006 a0010c0014t0006 others(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 | 7 | a0001c0001t0003 a0001c0001t0007 a0002c0003t0003 others(4): Show |
51 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(48): 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 | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(45): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): 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 | a0001c0001t0027 | 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 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(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 | a0001c0007t0006 a0009c0023t0006 a0010c0014t0006 others(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 | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
281 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(278): 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 | a0002c0003t0020 | 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 | a0001c0001t0021 a0001c0001t0022 |
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 | a0001c0001t0022 | 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 | a0001c0001t0026 | 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 | a0001c0002t0002 | 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 | 22 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0025 others(19): Show |
154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): 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 | a0001c0001t0022 | 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 | 7 | a0001c0001t0003 a0001c0001t0007 a0002c0003t0003 others(4): Show |
51 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(48): 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 | 22 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0025 others(19): Show |
154 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(151): 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 | a0001c0002t0013 a0001c0002t0015 |
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 | a0007c0012t0029 | 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 | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): 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 | 47 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(44): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0001c0001t0023 | 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 | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(43): Show |
284 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(281): 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 | a0002c0003t0028 | 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 | a0007c0012t0029 | 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 | a0001c0007t0006 a0009c0023t0006 a0010c0014t0006 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0252 others(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 | 162 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(159): Show |
165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): 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 | a0002c0003t0003g0311 a0002c0003t0003g0312 a0002c0003t0003g0313 others(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 | a0001c0005t0002g0168 | 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 | a0012c0018t0012g0265 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0003c0004t0002g0217 a0003c0004t0002g0218 a0003c0004t0002g0219 others(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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(233): Show |
239 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.2586-79delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 17/18 | chr16 | 71653099 | |||||||
| chr16:71653307 | G | A | 1 | a0001c0001t0022g0273 | 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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0001t0022g0273 | 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 | a0002c0003t0003g0318 | 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 | a0001c0001t0012g0262 a0012c0018t0012g0265 |
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 | 284 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(281): Show |
287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): 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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0110 |
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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0161 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | 279 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(276): Show |
282 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(279): 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 | a0001c0001t0003g0258 a0001c0001t0004g0285 a0001c0001t0004g0289 others(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 | a0001c0001t0021g0274 | 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 | a0008c0025t0001g0085 | 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 | 284 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(281): Show |
287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): 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 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
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 | a0004c0006t0001g0068 | 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 | a0001c0001t0001g0113 a0001c0001t0014g0066 |
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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0001c0001t0001g0041 | 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 | 279 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(276): Show |
282 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(279): 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 | a0001c0005t0002g0137 a0001c0005t0002g0138 a0001c0005t0002g0162 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0004g0287 a0001c0001t0004g0290 a0001c0001t0027g0288 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 163 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(160): Show |
166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0005t0002g0164 a0001c0005t0002g0169 |
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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0012c0018t0012g0265 | 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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0182 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 269 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.1986-433delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71659247 | |||||||
| chr16:71659533 | G | T | 52 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(49): Show |
53 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(50): 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 | a0002c0003t0003g0240 a0002c0003t0003g0242 a0002c0003t0003g0244 |
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 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 108 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(105): Show |
110 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.1986-1558dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 13/18 | chr16 | 71660372 | |||||||
| chr16:71660372 | C | CAA | 24 | a0001c0001t0001g0051 a0001c0001t0005g0020 a0001c0001t0010g0007 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0074 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0002c0003t0003g0244 | 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 | a0001c0001t0022g0273 | 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 | a0001c0001t0004g0290 a0001c0001t0021g0274 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 52 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(49): Show |
53 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(50): 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0021g0274 | 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 | a0001c0002t0002g0178 a0001c0002t0002g0196 |
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 | a0002c0003t0028g0238 | 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0004g0302 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0001c0001t0021g0274 | 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 | a0001c0001t0022g0273 | 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 | 279 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(276): Show |
282 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(279): 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 | a0001c0001t0004g0301 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0004g0291 a0001c0001t0004g0293 a0001c0001t0004g0294 others(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 | a0001c0001t0025g0298 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0002c0003t0003g0245 a0002c0003t0028g0238 |
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 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 150 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): 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 | a0001c0002t0002g0226 a0003c0004t0002g0210 a0003c0004t0002g0211 others(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 | a0001c0002t0002g0180 | 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 | a0001c0001t0022g0273 | 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 | a0002c0003t0003g0240 a0002c0003t0003g0242 |
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 | a0001c0002t0002g0191 a0001c0005t0002g0163 a0001c0005t0002g0165 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0003c0004t0002g0210 a0003c0004t0002g0211 a0003c0004t0002g0212 others(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 | a0002c0003t0020g0006 | 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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0001c0002t0002g0139 | 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0009t0001g0095 | 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0022g0273 | 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 | a0001c0002t0002g0183 a0001c0002t0002g0184 |
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 | a0007c0012t0029g0189 | 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 | a0001c0001t0003g0011 a0001c0001t0003g0248 a0001c0001t0003g0249 others(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 | 5 | a0001c0001t0003g0247 a0001c0001t0003g0252 a0001c0001t0012g0262 others(2): Show |
6 | HG01175.hp1 HG01361.hp1 HG02809.hp2 others(3): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 169 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(166): Show |
172 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(169): 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 | 150 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): 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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0002t0002g0179 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0003c0004t0002g0210 a0003c0004t0002g0211 a0003c0004t0002g0212 others(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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0003g0011 others(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 | a0001c0001t0003g0010 a0001c0001t0007g0013 a0001c0001t0007g0014 others(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 | a0001c0001t0001g0046 a0001c0001t0003g0252 a0001c0002t0002g0139 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0003g0248 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0045 others(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 | a0001c0001t0005g0120 a0001c0001t0005g0128 a0001c0001t0016g0123 |
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 | a0001c0001t0005g0121 a0001c0001t0005g0127 a0001c0001t0005g0130 |
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 | a0001c0001t0005g0124 a0001c0001t0005g0131 a0001c0001t0005g0134 |
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 | a0001c0001t0001g0026 a0001c0001t0014g0066 |
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 | a0001c0001t0001g0084 a0001c0001t0012g0262 |
2 | HG00558.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1533-1325T>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71670695 | |||||||
| chr16:71670762 | T | C | 1 | a0001c0002t0002g0180 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | 281 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(278): Show |
284 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(281): 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 | a0001c0001t0022g0273 | 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 | 298 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(295): Show |
301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.1532+534A>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671728 | |||||||
| chr16:71671871 | G | A | 53 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(50): Show |
54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1532+391C>T | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 10/18 | chr16 | 71671871 | |||||||
| chr16:71671912 | T | TCAAA | 54 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(51): Show |
55 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(52): 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | 13 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(10): Show |
13 | HG00733.hp2 HG01361.hp1 HG01884.hp1 others(10): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0005g0125 a0001c0001t0005g0127 a0001c0001t0005g0128 others(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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | 53 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(50): Show |
54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): 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 | a0001c0001t0001g0099 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 131 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(128): Show |
134 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.1472-2061dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 9/18 | chr16 | 71674382 | |||||||
| chr16:71674382 | CT | C | 7 | a0001c0001t0001g0034 a0001c0001t0004g0310 a0001c0001t0005g0121 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | 150 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): 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 | a0001c0001t0022g0273 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0007c0012t0029g0189 | 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 | 150 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): 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 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0009c0023t0006g0160 | 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 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
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 | a0001c0005t0002g0164 a0001c0005t0002g0169 |
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 | a0001c0001t0021g0274 | 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0022g0273 | 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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0278 others(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 | a0001c0001t0004g0281 a0001c0001t0004g0283 |
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 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(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 | a0001c0001t0004g0285 a0001c0001t0004g0291 a0001c0001t0004g0305 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0287 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0094 a0001c0001t0004g0286 a0001c0001t0004g0290 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | a0001c0002t0002g0264 a0001c0005t0002g0137 a0001c0005t0002g0138 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | 52 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(49): Show |
53 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(50): 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 | a0002c0003t0003g0245 a0002c0003t0028g0238 |
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 | 53 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(50): Show |
54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1269-885dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 8/18 | chr16 | 71677533 | |||||||
| chr16:71677570 | G | T | 12 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0001c0001t0022g0273 | 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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0002t0002g0176 a0001c0013t0002g0186 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0021g0274 | 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 | a0001c0001t0004g0021 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0012c0018t0012g0265 | 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 | a0012c0018t0012g0265 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | 162 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(159): Show |
165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0233 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0255 others(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 | a0001c0001t0001g0051 | 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 | 12 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(9): Show |
12 | HG00733.hp2 HG01884.hp1 HG02602.hp1 others(9): 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 | a0002c0003t0003g0240 a0002c0003t0003g0242 a0002c0003t0003g0244 |
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 | a0002c0003t0003g0316 | 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 | a0001c0005t0002g0116 a0001c0005t0002g0117 |
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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0001c0005t0002g0163 a0001c0005t0002g0165 a0001c0005t0002g0173 |
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 | a0001c0001t0022g0273 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(302): Show |
309 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(306): 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 | a0002c0003t0003g0320 a0003c0004t0002g0210 a0003c0004t0002g0211 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0111 a0001c0001t0004g0281 a0001c0001t0004g0283 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0145 a0001c0002t0002g0188 a0001c0002t0002g0190 others(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 | a0001c0002t0002g0226 a0002c0003t0003g0320 a0003c0004t0002g0210 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
285 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(282): 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 | a0002c0003t0002g0241 a0002c0003t0002g0317 a0002c0003t0003g0003 others(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 | 150 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): 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 | a0001c0001t0001g0082 a0001c0001t0007g0013 a0001c0001t0007g0014 others(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 | a0001c0001t0022g0273 | 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 | 13 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(10): Show |
13 | HG00733.hp2 HG01175.hp1 HG01884.hp1 others(10): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 |
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 | a0001c0001t0010g0007 a0001c0001t0010g0008 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0005g0135 a0001c0001t0022g0273 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0286 a0001c0001t0004g0287 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 |
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 | a0004c0006t0001g0093 | 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 | 287 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(284): Show |
290 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(287): 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 | a0001c0002t0002g0145 a0001c0002t0002g0174 a0001c0002t0002g0188 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0067 others(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 | a0008c0025t0001g0085 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0001c0001t0001g0051 | 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 | a0003c0004t0002g0211 a0003c0004t0002g0214 a0003c0004t0002g0222 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0004g0306 a0001c0001t0026g0307 |
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 | 51 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(48): Show |
52 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(49): 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 | a0001c0001t0021g0274 | 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 | a0001c0002t0002g0145 a0001c0002t0002g0174 a0001c0002t0002g0188 others(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 | a0001c0002t0009g0148 a0001c0002t0009g0149 a0001c0002t0009g0201 |
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 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0002t0002g0184 a0001c0007t0006g0150 a0001c0007t0006g0151 others(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 | a0001c0001t0021g0274 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0021g0274 | 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 | a0004c0006t0001g0092 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | 280 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
283 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(280): 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0069 |
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 | 13 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(10): Show |
13 | HG00733.hp2 HG01361.hp1 HG01884.hp1 others(10): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0004g0306 a0001c0001t0026g0307 |
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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0005g0132 a0001c0001t0005g0133 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0136 others(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 | a0012c0018t0012g0265 | 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 | a0002c0003t0002g0317 | 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 | 150 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.609+2213G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688306 | |||||||
| chr16:71688608 | G | GT | 25 | a0001c0001t0003g0255 a0001c0001t0003g0256 a0001c0001t0003g0257 others(22): Show |
25 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.609+1910dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71688608 | |||||||
| chr16:71688608 | G | GTT | 103 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | 286 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(283): Show |
289 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(286): 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 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0002c0003t0020g0006 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0004g0276 others(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 | 47 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0003g0011 others(44): Show |
48 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.609+1133delA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 4/18 | chr16 | 71689385 | |||||||
| chr16:71689385 | CTT | C | 13 | a0001c0007t0006g0151 a0001c0007t0006g0152 a0001c0007t0006g0153 others(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 | a0003c0004t0002g0217 a0003c0004t0002g0218 |
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 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0001c0001t0005g0132 a0001c0001t0005g0133 |
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 | 280 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
283 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(280): 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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | 52 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(49): Show |
53 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(50): 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 | a0009c0023t0006g0160 | 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 | a0009c0023t0006g0160 | 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 | a0009c0023t0006g0160 | 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 | a0012c0018t0012g0265 | 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 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(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 | a0001c0001t0022g0273 a0002c0003t0003g0003 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0087 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | a0001c0002t0002g0145 a0001c0002t0002g0188 a0001c0002t0002g0190 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 53 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(50): Show |
54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): 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 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(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 | a0004c0006t0001g0060 a0004c0006t0001g0091 |
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 | 283 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 161 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(158): Show |
164 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(161): 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0002c0003t0003g0318 | 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 | a0004c0006t0001g0093 | 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 | a0001c0005t0002g0117 a0001c0007t0006g0150 a0001c0007t0006g0151 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0139 others(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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0005t0002g0169 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0002c0003t0003g0245 a0002c0003t0028g0238 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0094 | 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 | 149 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(146): Show |
152 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(149): 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 | 149 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(146): Show |
152 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(149): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0001c0001t0021g0274 | 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 | a0009c0023t0006g0160 | 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 | a0011c0027t0002g0203 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0026g0307 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(302): Show |
309 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(306): 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 | a0001c0001t0022g0273 | 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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0012c0018t0012g0265 | 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 | a0001c0001t0001g0059 a0001c0001t0004g0281 a0001c0001t0004g0283 others(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 | 163 | a0001c0001t0001g0161 a0001c0001t0003g0010 a0001c0001t0003g0011 others(160): Show |
166 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(163): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0290 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0286 a0001c0001t0004g0305 others(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 | a0001c0001t0010g0009 a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0008c0025t0001g0085 | 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 | 145 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(143): 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 | a0001c0002t0002g0179 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0161 a0001c0001t0005g0020 others(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 | a0001c0002t0002g0144 a0001c0005t0002g0162 a0001c0005t0002g0163 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0001t0001g0099 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(302): Show |
309 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(306): 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 | a0001c0001t0001g0067 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(227): Show |
233 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(230): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0161 a0001c0001t0005g0121 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0286 a0001c0001t0004g0287 others(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 | a0001c0001t0004g0301 | 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 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(302): Show |
309 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(306): 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 | a0012c0018t0012g0265 | 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 | 162 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(159): Show |
165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0002t0002g0183 a0001c0002t0002g0184 a0001c0013t0002g0186 |
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 | a0001c0005t0002g0163 a0001c0005t0002g0165 a0001c0005t0002g0173 |
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 | a0012c0018t0012g0265 | 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 | a0002c0003t0003g0245 a0002c0003t0028g0238 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0090 others(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 | |||||||
| chr16:71700279 | C | T | 5 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0001c0001t0017g0118 a0001c0002t0002g0139 a0001c0002t0002g0145 others(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 | a0001c0001t0005g0130 a0001c0001t0005g0134 a0001c0001t0010g0009 others(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 | a0003c0004t0002g0211 a0003c0004t0002g0214 a0003c0004t0002g0222 others(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 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | 78 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(75): Show |
79 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(76): 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 | a0001c0001t0001g0161 a0001c0001t0004g0306 a0001c0001t0010g0007 others(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 | a0001c0001t0001g0084 a0001c0001t0005g0130 a0001c0001t0005g0134 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | 311 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(308): Show |
314 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(311): 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 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0002t0008g0001 a0001c0002t0008g0140 a0001c0002t0008g0143 others(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 | 298 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(295): Show |
301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): 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 | a0001c0001t0001g0005 a0001c0001t0001g0087 |
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 | 12 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(9): Show |
12 | HG00733.hp2 HG01884.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.418+142C>G | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 3/18 | chr16 | 71702456 | |||||||
| chr16:71702799 | G | GTATTTT | 283 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0139 others(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 | 162 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(159): Show |
165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.285-772delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71703502 | |||||||
| chr16:71703631 | T | C | 2 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0022g0273 | 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 | a0003c0004t0002g0210 a0003c0004t0002g0217 a0003c0004t0002g0218 others(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 | a0001c0001t0021g0274 | 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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0139 | 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 | a0012c0018t0012g0265 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0261 a0001c0001t0005g0135 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0080 a0001c0001t0005g0120 a0001c0001t0005g0131 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0022g0273 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0006c0010t0001g0056 others(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 | a0009c0023t0006g0160 | 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 | a0002c0003t0020g0006 | 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 | a0003c0004t0002g0210 a0003c0004t0002g0217 a0003c0004t0002g0218 others(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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0001c0001t0022g0273 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0004g0309 a0001c0001t0004g0310 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0017t0001g0101 others(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 | 6 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(3): Show |
6 | HG00733.hp2 HG01175.hp1 HG02602.hp1 others(3): 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 | a0001c0001t0017g0118 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | a0001c0001t0017g0118 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | a0001c0001t0021g0274 a0001c0001t0022g0273 |
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 | a0001c0001t0004g0021 a0001c0001t0005g0020 a0012c0018t0012g0265 |
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 | 283 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): 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 | a0012c0018t0012g0265 | 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 | a0001c0001t0004g0285 a0001c0001t0004g0306 a0001c0001t0004g0308 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | 143 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(140): Show |
146 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(143): 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 | a0001c0001t0004g0276 a0001c0001t0004g0277 a0001c0001t0004g0278 others(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 | a0009c0023t0006g0160 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 53 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(50): Show |
54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.285-5294G>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708025 | |||||||
| chr16:71708097 | C | G | 161 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(158): Show |
164 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(161): 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 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0078 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | |||||||
| chr16:71708969 | A | AT | 75 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(72): Show |
76 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.284+5542dupA | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71708969 | |||||||
| chr16:71708977 | A | T | 1 | a0001c0001t0007g0018 | 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 | a0002c0003t0002g0241 a0002c0003t0002g0317 a0002c0003t0003g0003 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0004g0309 a0001c0001t0004g0310 |
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 | a0001c0001t0022g0273 | 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 | a0001c0001t0022g0273 | 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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0002c0003t0002g0241 a0002c0003t0002g0317 a0002c0003t0003g0003 others(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 | a0001c0001t0005g0121 a0001c0001t0005g0122 |
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 | a0002c0003t0003g0235 a0002c0003t0003g0236 a0002c0003t0003g0254 |
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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | 189 | a0001c0001t0001g0161 a0001c0001t0003g0010 a0001c0001t0003g0011 others(186): Show |
193 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(190): Show |
intron_variant | MODIFIER | c.284+2924T>A | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71711588 | |||||||
| chr16:71711615 | C | T | 190 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(187): Show |
194 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(191): 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 | a0001c0001t0001g0161 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | 53 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(50): Show |
54 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(51): 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 | a0001c0001t0022g0273 | 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 | a0001c0001t0022g0273 | 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 | a0001c0001t0004g0302 | 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 | 6 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(3): Show |
6 | HG00733.hp2 HG01175.hp1 HG02602.hp1 others(3): 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(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 | a0003c0004t0002g0219 a0003c0004t0002g0220 |
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 | a0012c0018t0012g0265 | 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 | 83 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(80): Show |
84 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.284+588dupT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 2/18 | chr16 | 71713923 | |||||||
| chr16:71713940 | C | CT | 8 | a0001c0001t0001g0055 a0001c0001t0001g0078 a0001c0001t0001g0080 others(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 | a0001c0001t0004g0021 a0001c0001t0004g0277 a0001c0001t0004g0285 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(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 | |||||||
| chr16:71715062 | 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0002t0002g0024 a0001c0002t0002g0145 a0001c0002t0002g0146 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0139 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0161 others(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 | 156 | a0001c0001t0001g0109 a0001c0001t0003g0010 a0001c0001t0003g0011 others(153): Show |
159 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(156): Show |
intron_variant | MODIFIER | c.-6-1023delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71715823 | |||||||
| chr16:71715831 | A | C | 2 | a0002c0003t0003g0206 a0002c0003t0003g0207 |
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 | a0001c0001t0004g0021 a0001c0001t0005g0020 a0001c0001t0005g0121 |
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 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0233 others(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 | a0003c0004t0002g0210 a0003c0004t0002g0217 a0003c0004t0002g0218 others(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 | a0001c0002t0002g0197 a0003c0004t0002g0263 a0003c0004t0002g0267 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0161 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0004 a0001c0001t0004g0276 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0021g0274 | 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 | a0001c0001t0022g0273 | 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 | a0012c0018t0012g0265 | 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 | a0012c0018t0012g0265 | 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 | 195 | a0001c0001t0001g0045 a0001c0001t0001g0161 a0001c0001t0003g0010 others(192): Show |
199 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(196): Show |
intron_variant | MODIFIER | c.-6-2121T>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71716922 | |||||||
| chr16:71717093 | G | A | 169 | a0001c0001t0001g0161 a0001c0001t0003g0010 a0001c0001t0003g0011 others(166): Show |
172 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(169): 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 | a0001c0001t0004g0303 a0001c0001t0004g0304 |
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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0007t0006g0150 a0001c0007t0006g0151 a0001c0007t0006g0152 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | 6 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(3): Show |
6 | HG00733.hp2 HG01175.hp1 HG02602.hp1 others(3): 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 | a0001c0001t0004g0004 a0001c0001t0004g0276 a0001c0001t0004g0277 others(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 | a0012c0018t0012g0265 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0139 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0024 a0001c0002t0002g0139 others(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 | 150 | a0001c0001t0001g0161 a0001c0001t0003g0010 a0001c0001t0003g0011 others(147): Show |
153 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(150): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0147 a0001c0002t0002g0198 others(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 | a0001c0001t0022g0273 | 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 | a0001c0001t0001g0161 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | 162 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(159): Show |
165 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(162): 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 | a0003c0004t0002g0263 a0003c0004t0002g0267 a0003c0004t0002g0268 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0004g0004 a0001c0001t0004g0286 a0001c0001t0004g0287 others(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 | a0001c0001t0004g0004 a0001c0001t0004g0286 a0001c0001t0004g0287 others(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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0011c0027t0002g0203 | 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 | a0002c0003t0003g0206 a0002c0003t0003g0207 |
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 | a0001c0001t0001g0161 a0001c0002t0002g0002 a0001c0002t0002g0024 others(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 | a0012c0018t0012g0265 | 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 | a0003c0004t0002g0263 a0003c0004t0002g0267 a0003c0004t0002g0268 others(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 | a0001c0001t0004g0294 a0001c0001t0004g0295 a0001c0001t0004g0296 others(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 | a0001c0001t0001g0161 a0001c0001t0003g0011 a0001c0001t0003g0232 others(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 | 33 | a0001c0001t0003g0010 a0001c0001t0003g0231 a0001c0001t0003g0255 others(30): Show |
33 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(30): 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 | a0001c0001t0004g0004 a0001c0001t0004g0286 a0001c0001t0004g0287 others(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 | a0001c0001t0004g0285 a0001c0001t0004g0309 a0001c0001t0004g0310 others(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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0026g0307 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0114 a0001c0001t0005g0121 a0001c0001t0005g0122 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0042 |
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 | a0001c0001t0004g0281 a0001c0001t0004g0282 a0001c0001t0004g0283 |
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 | a0001c0001t0004g0276 a0001c0001t0004g0277 |
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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | 74 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(71): Show |
75 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(72): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0022g0273 | 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 | 164 | a0001c0001t0001g0161 a0001c0001t0003g0010 a0001c0001t0003g0011 others(161): Show |
167 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(164): 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0002t0002g0226 others(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 | a0012c0018t0012g0265 | 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 | 288 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(285): Show |
291 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(288): 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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0003c0004t0002g0263 a0003c0004t0002g0267 a0003c0004t0002g0268 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | a0012c0018t0012g0265 | 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | 273 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(270): Show |
276 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.-7+2657delT | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71721671 | |||||||
| chr16:71721769 | A | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | 72 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0231 others(69): Show |
73 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(70): 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 | a0001c0001t0003g0010 a0001c0001t0003g0011 |
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 | a0001c0002t0002g0024 a0001c0002t0013g0023 a0001c0002t0013g0025 others(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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0001c0001t0004g0021 a0001c0001t0005g0020 |
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 | a0003c0004t0002g0263 a0003c0004t0002g0267 a0003c0004t0002g0268 others(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 | a0003c0004t0002g0263 a0003c0004t0002g0267 a0003c0004t0002g0268 others(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 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(302): Show |
309 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(306): 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 | a0012c0018t0012g0265 | 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 | a0014c0020t0001g0012 | 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 | a0003c0004t0002g0267 a0003c0004t0002g0268 a0003c0004t0002g0269 others(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 | a0003c0004t0002g0267 a0003c0004t0002g0268 a0003c0004t0002g0269 others(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 | 283 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.-7+845G>C | PHLPP2 | ENSG00000040199.18 | transcript | ENST00000568954.5 | protein_coding | 1/18 | chr16 | 71723484 | |||||||
| chr16:71723492 | A | G | 283 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): 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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0011 |
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 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
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 | 283 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(283): 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 | a0001c0001t0004g0306 a0001c0001t0004g0308 a0001c0001t0004g0309 others(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 | a0002c0003t0020g0006 | 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 | a0002c0003t0002g0317 a0002c0003t0003g0311 a0002c0003t0003g0312 others(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 |