| geneid | 151987 |
|---|---|
| ensemblid | ENSG00000163605.16 |
| hgncid | 18296 |
| symbol | PPP4R2 |
| name | protein phosphatase 4 regulatory subunit 2 |
| refseq_nuc | NM_174907.4 |
| refseq_prot | NP_777567.1 |
| ensembl_nuc | ENST00000356692.10 |
| ensembl_prot | ENSP00000349124.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 72996811 |
| end | 73069198 |
| strand | + |
| ver | v1.2 |
| region | chr3:72996811-73069198 |
| region5000 | chr3:72991811-73074198 |
| regionname0 | PPP4R2_chr3_72996811_73069198 |
| regionname5000 | PPP4R2_chr3_72991811_73074198 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 351 | 92 | 48 | 159 | 8 | 42 | 132 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0002 | 0/0 | 417 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0003 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0004 | 0/0 | 413 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0005 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0006 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0007 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1254 | 243 | 71 | 41 | 98 | 6 | 25 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0002 | 0/0 | 1254 | 97 | 10 | 7 | 61 | 2 | 17 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0003 | 0/0 | 1254 | 10 | 10 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0004 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0005 | 0/0 | 1254 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0006 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0007 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0008 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0009 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0010 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| c0011 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3703 | 72 | 16 | 14 | 39 | 1 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0002 | 0/0 | 3704 | 37 | 1 | 7 | 22 | 2 | 5 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0003 | 0/0 | 3710 | 32 | 3 | 3 | 22 | 0 | 4 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0004 | 0/1 | 3710 | 25 | 8 | 7 | 5 | 2 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0005 | 0/0 | 3705 | 16 | 2 | 2 | 11 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0006 | 0/0 | 3716 | 11 | 0 | 1 | 8 | 1 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0007 | 0/0 | 3712 | 11 | 5 | 0 | 4 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0008 | 0/0 | 3714 | 10 | 0 | 4 | 3 | 1 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0009 | 0/0 | 3708 | 8 | 8 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0010 | 0/0 | 3712 | 8 | 0 | 0 | 6 | 1 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0011 | 0/0 | 3714 | 8 | 0 | 0 | 6 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0012 | 0/0 | 3710 | 7 | 7 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0013 | 0/0 | 3712 | 7 | 7 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0014 | 0/0 | 3707 | 6 | 3 | 1 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0015 | 0/0 | 3709 | 6 | 0 | 0 | 6 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0016 | 0/0 | 3703 | 5 | 5 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0017 | 0/0 | 3706 | 5 | 0 | 0 | 4 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0018 | 0/0 | 3708 | 5 | 4 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0019 | 0/0 | 3708 | 5 | 4 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0020 | 0/0 | 3719 | 4 | 0 | 0 | 4 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0021 | 0/0 | 3703 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0022 | 0/0 | 3704 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0023 | 0/0 | 3718 | 3 | 0 | 0 | 1 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0024 | 0/0 | 3712 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0025 | 0/0 | 3712 | 3 | 0 | 0 | 0 | 0 | 3 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0026 | 0/0 | 3712 | 3 | 1 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0027 | 0/0 | 3711 | 3 | 0 | 0 | 0 | 0 | 3 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0028 | 0/0 | 3701 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0029 | 0/0 | 3704 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0030 | 0/0 | 3712 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0031 | 0/0 | 3720 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0032 | 0/0 | 3724 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0033 | 0/0 | 3704 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0034 | 0/0 | 3708 | 2 | 1 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0035 | 0/0 | 3714 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0036 | 0/0 | 3716 | 2 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0037 | 0/0 | 3718 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0038 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0039 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0040 | 1/0 | 3704 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0041 | 0/0 | 3703 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0042 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0043 | 0/0 | 3707 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0044 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0045 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0046 | 0/0 | 3711 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0047 | 0/0 | 3703 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0048 | 0/0 | 3716 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0049 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0050 | 0/0 | 3722 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0051 | 0/0 | 3702 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0052 | 0/0 | 3710 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0053 | 0/0 | 3715 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0054 | 0/0 | 3714 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0055 | 0/0 | 3716 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0056 | 0/0 | 3716 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0057 | 0/0 | 3718 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0058 | 0/0 | 3718 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0059 | 0/0 | 3721 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0060 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0061 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0062 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0063 | 0/0 | 3713 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0064 | 0/0 | 3719 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0065 | 0/0 | 3703 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0066 | 0/0 | 3707 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0067 | 0/0 | 3704 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| t0068 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1254 | 243 | 71 | 41 | 98 | 6 | 25 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002 | 0/0 | 1254 | 97 | 10 | 7 | 61 | 2 | 17 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0003 | 0/0 | 1254 | 10 | 10 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0010 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0002c0005 | 0/0 | 1254 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0003c0004 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0004c0007 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0004c0011 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0005c0006 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0006c0008 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0007c0009 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4956 | 69 | 15 | 14 | 37 | 1 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0002 | 0/0 | 4957 | 37 | 1 | 7 | 22 | 2 | 5 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0003 | 0/0 | 4963 | 4 | 3 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0004 | 0/1 | 4963 | 25 | 8 | 7 | 5 | 2 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0005 | 0/0 | 4958 | 16 | 2 | 2 | 11 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0007 | 0/0 | 4965 | 11 | 5 | 0 | 4 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0008 | 0/0 | 4967 | 10 | 0 | 4 | 3 | 1 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0009 | 0/0 | 4961 | 8 | 8 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0014 | 0/0 | 4960 | 6 | 3 | 1 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0016 | 0/0 | 4956 | 5 | 5 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0017 | 0/0 | 4959 | 3 | 0 | 0 | 2 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0018 | 0/0 | 4961 | 4 | 3 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0019 | 0/0 | 4961 | 4 | 4 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0021 | 0/0 | 4956 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0022 | 0/0 | 4957 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0024 | 0/0 | 4965 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0025 | 0/0 | 4965 | 3 | 0 | 0 | 0 | 0 | 3 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0026 | 0/0 | 4965 | 2 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0028 | 0/0 | 4954 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0029 | 0/0 | 4957 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0034 | 0/0 | 4961 | 2 | 1 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0035 | 0/0 | 4967 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0036 | 0/0 | 4969 | 2 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0038 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0039 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0040 | 1/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0041 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0042 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0044 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0046 | 0/0 | 4964 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0047 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0051 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0054 | 0/0 | 4967 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0056 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0057 | 0/0 | 4971 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0058 | 0/0 | 4971 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0065 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0066 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0067 | 0/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0001t0068 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0003 | 0/0 | 4963 | 27 | 0 | 2 | 21 | 0 | 4 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0006 | 0/0 | 4969 | 11 | 0 | 1 | 8 | 1 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0010 | 0/0 | 4965 | 8 | 0 | 0 | 6 | 1 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0011 | 0/0 | 4967 | 8 | 0 | 0 | 6 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0013 | 0/0 | 4965 | 5 | 5 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0015 | 0/0 | 4962 | 6 | 0 | 0 | 6 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0019 | 0/0 | 4961 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0020 | 0/0 | 4972 | 4 | 0 | 0 | 4 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0023 | 0/0 | 4971 | 3 | 0 | 0 | 1 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0027 | 0/0 | 4964 | 3 | 0 | 0 | 0 | 0 | 3 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0030 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0031 | 0/0 | 4973 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0032 | 0/0 | 4977 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0033 | 0/0 | 4957 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0037 | 0/0 | 4971 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0049 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0050 | 0/0 | 4975 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0052 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0053 | 0/0 | 4968 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0055 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0059 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0060 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0061 | 0/0 | 4978 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0062 | 0/0 | 4982 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0063 | 0/0 | 4966 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0002t0064 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0003t0012 | 0/0 | 4963 | 7 | 7 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0003t0043 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0003t0045 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0003t0048 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0001c0010t0001 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0002c0005t0017 | 0/0 | 4959 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0003c0004t0013 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0004c0007t0003 | 0/0 | 4951 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0004c0011t0001 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0005c0006t0026 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0006c0008t0001 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| a0007c0009t0018 | 0/0 | 4961 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | copy fasta | chr3 | 72991811 | 73074198 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0017g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0017g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0021g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0021g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0021g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0022g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0022g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0022g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0024g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0024g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0025g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0025g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0025g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0026g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0026g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0028g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0028g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0029g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0029g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0034g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0034g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0035g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0035g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0036g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0036g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0038g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0039g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0040g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0041g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0042g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0044g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0046g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0047g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0051g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0054g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0056g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0057g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0058g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0065g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0066g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0067g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0068g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0019g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0023g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0023g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0023g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0027g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0027g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0027g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0030g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0030g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0031g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0031g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0032g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0032g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0033g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0033g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0037g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0037g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0049g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0050g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0052g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0053g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0055g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0059g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0060g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0061g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0062g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0063g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0064g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0043g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0045g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0048g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0010t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0002c0005t0017g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0002c0005t0017g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0003c0004t0013g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0003c0004t0013g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0004c0007t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0004c0011t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0005c0006t0026g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0006c0008t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0007c0009t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0314 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00099 | hp2 | a0001 | c0002 | t0006 | g0099 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0169 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00423 | hp1 | a0001 | c0002 | t0010 | g0081 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00438 | hp1 | a0001 | c0001 | t0029 | g0306 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00597 | hp1 | a0001 | c0002 | t0020 | g0019 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00609 | hp1 | a0004 | c0011 | t0001 | g0294 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00621 | hp1 | a0001 | c0002 | t0010 | g0089 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00621 | hp2 | a0001 | c0001 | t0047 | g0286 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00639 | hp1 | a0001 | c0002 | t0061 | g0053 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0151 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0145 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01069 | hp2 | a0001 | c0002 | t0032 | g0056 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0148 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01099 | hp2 | a0001 | c0001 | t0036 | g0191 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01109 | hp1 | a0001 | c0001 | t0057 | g0153 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01192 | hp1 | a0001 | c0002 | t0032 | g0044 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01243 | hp1 | a0001 | c0001 | t0018 | g0192 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0065 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01255 | hp1 | a0001 | c0001 | t0026 | g0184 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01346 | hp1 | a0001 | c0002 | t0006 | g0105 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0168 | EUR | IBS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | IBS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01884 | hp1 | a0001 | c0002 | t0033 | g0093 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0193 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01891 | hp1 | a0003 | c0004 | t0013 | g0357 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01952 | hp2 | a0001 | c0001 | t0058 | g0140 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01993 | hp2 | a0001 | c0002 | t0053 | g0218 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02015 | hp1 | a0001 | c0001 | t0041 | g0269 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02027 | hp2 | a0001 | c0002 | t0019 | g0075 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02055 | hp2 | a0001 | c0002 | t0030 | g0091 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02080 | hp1 | a0001 | c0001 | t0068 | g0336 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02080 | hp2 | a0001 | c0002 | t0062 | g0051 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02083 | hp1 | a0001 | c0001 | t0014 | g0334 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0143 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0103 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0112 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | CDX | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02257 | hp1 | a0001 | c0001 | t0024 | g0177 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02258 | hp1 | a0001 | c0001 | t0066 | g0196 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02280 | hp1 | a0001 | c0003 | t0043 | g0208 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0200 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0150 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0109 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02572 | hp2 | a0001 | c0001 | t0019 | g0118 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02602 | hp1 | a0001 | c0001 | t0036 | g0162 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02615 | hp1 | a0001 | c0001 | t0018 | g0195 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02615 | hp2 | a0001 | c0001 | t0044 | g0207 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0117 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02647 | hp1 | a0001 | c0001 | t0021 | g0204 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02647 | hp2 | a0001 | c0003 | t0012 | g0211 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0088 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0057 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02698 | hp2 | a0001 | c0002 | t0027 | g0030 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0203 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02723 | hp2 | a0001 | c0003 | t0012 | g0354 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0220 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02735 | hp2 | a0001 | c0001 | t0025 | g0167 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02738 | hp2 | a0001 | c0002 | t0027 | g0077 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02809 | hp1 | a0001 | c0002 | t0013 | g0094 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0190 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02886 | hp2 | a0001 | c0003 | t0012 | g0212 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0170 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02922 | hp1 | a0001 | c0002 | t0013 | g0090 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0202 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0116 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02965 | hp2 | a0001 | c0003 | t0012 | g0352 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0201 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02976 | hp1 | a0001 | c0002 | t0030 | g0092 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02976 | hp2 | a0001 | c0002 | t0033 | g0098 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0079 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03041 | hp1 | a0001 | c0001 | t0024 | g0173 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03041 | hp2 | a0001 | c0001 | t0021 | g0199 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0205 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0171 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03130 | hp2 | a0005 | c0006 | t0026 | g0175 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0114 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03209 | hp1 | a0001 | c0001 | t0051 | g0198 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03225 | hp1 | a0007 | c0009 | t0018 | g0197 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03225 | hp2 | a0001 | c0002 | t0013 | g0097 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03239 | hp2 | a0001 | c0002 | t0023 | g0067 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03453 | hp1 | a0003 | c0004 | t0013 | g0356 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03453 | hp2 | a0001 | c0002 | t0013 | g0095 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0194 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0183 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03491 | hp1 | a0001 | c0002 | t0023 | g0100 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03516 | hp1 | a0001 | c0001 | t0024 | g0174 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03516 | hp2 | a0001 | c0010 | t0001 | g0337 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03540 | hp2 | a0001 | c0003 | t0045 | g0209 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03654 | hp1 | a0001 | c0001 | t0054 | g0147 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03654 | hp2 | a0001 | c0001 | t0034 | g0144 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03688 | hp1 | a0001 | c0001 | t0028 | g0297 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0154 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03704 | hp1 | a0001 | c0002 | t0037 | g0084 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03704 | hp2 | a0001 | c0002 | t0011 | g0083 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03710 | hp1 | a0001 | c0001 | t0028 | g0350 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0040 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0146 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03831 | hp2 | a0001 | c0001 | t0017 | g0249 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03834 | hp1 | a0001 | c0001 | t0067 | g0257 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03834 | hp2 | a0001 | c0002 | t0011 | g0027 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0101 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04115 | hp1 | a0001 | c0002 | t0063 | g0104 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04115 | hp2 | a0001 | c0001 | t0025 | g0180 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0186 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04184 | hp2 | a0001 | c0002 | t0027 | g0029 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0152 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04199 | hp2 | a0001 | c0001 | t0026 | g0160 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04204 | hp1 | a0001 | c0002 | t0031 | g0034 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04204 | hp2 | a0001 | c0002 | t0055 | g0358 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18522 | hp1 | a0001 | c0001 | t0056 | g0185 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18612 | hp2 | a0001 | c0002 | t0010 | g0041 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0003 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18942 | hp1 | a0001 | c0002 | t0006 | g0020 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18943 | hp2 | a0001 | c0002 | t0059 | g0054 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18944 | hp2 | a0001 | c0002 | t0010 | g0009 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18945 | hp2 | a0001 | c0002 | t0060 | g0052 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18946 | hp1 | a0001 | c0001 | t0022 | g0304 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18946 | hp2 | a0001 | c0001 | t0065 | g0295 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18948 | hp2 | a0001 | c0002 | t0011 | g0035 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18950 | hp1 | a0001 | c0001 | t0017 | g0351 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18951 | hp1 | a0001 | c0002 | t0006 | g0021 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18953 | hp2 | a0001 | c0002 | t0015 | g0087 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18956 | hp2 | a0001 | c0002 | t0023 | g0018 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18959 | hp1 | a0001 | c0002 | t0006 | g0017 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18959 | hp2 | a0001 | c0002 | t0015 | g0016 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18961 | hp1 | a0001 | c0001 | t0029 | g0341 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18963 | hp2 | a0002 | c0005 | t0017 | g0349 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18964 | hp2 | a0001 | c0002 | t0037 | g0011 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18965 | hp2 | a0001 | c0002 | t0020 | g0012 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18966 | hp2 | a0001 | c0002 | t0050 | g0043 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18969 | hp2 | a0001 | c0002 | t0052 | g0071 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18970 | hp1 | a0001 | c0002 | t0011 | g0060 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18970 | hp2 | a0001 | c0001 | t0014 | g0335 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18971 | hp1 | a0002 | c0005 | t0017 | g0348 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18972 | hp2 | a0001 | c0002 | t0011 | g0032 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18974 | hp1 | a0001 | c0001 | t0022 | g0266 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18978 | hp2 | a0004 | c0007 | t0003 | g0010 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0296 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18982 | hp1 | a0001 | c0002 | t0015 | g0063 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18983 | hp1 | a0001 | c0002 | t0006 | g0023 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18984 | hp2 | a0001 | c0002 | t0020 | g0069 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18985 | hp2 | a0001 | c0002 | t0006 | g0014 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18990 | hp1 | a0001 | c0002 | t0031 | g0066 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18994 | hp1 | a0001 | c0001 | t0038 | g0251 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18994 | hp2 | a0001 | c0002 | t0015 | g0045 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18995 | hp2 | a0001 | c0002 | t0011 | g0039 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18998 | hp2 | a0006 | c0008 | t0001 | g0275 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19002 | hp1 | a0001 | c0002 | t0015 | g0059 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19002 | hp2 | a0001 | c0001 | t0042 | g0260 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0036 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19012 | hp2 | a0001 | c0002 | t0011 | g0028 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19030 | hp1 | a0001 | c0002 | t0013 | g0096 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19055 | hp1 | a0001 | c0002 | t0064 | g0050 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19056 | hp1 | a0001 | c0002 | t0015 | g0058 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19064 | hp1 | a0001 | c0002 | t0006 | g0013 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0229 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0042 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19070 | hp1 | a0001 | c0002 | t0020 | g0055 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19074 | hp2 | a0001 | c0002 | t0006 | g0022 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19076 | hp1 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19076 | hp2 | a0001 | c0001 | t0022 | g0347 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19077 | hp1 | a0001 | c0002 | t0010 | g0008 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19081 | hp2 | a0001 | c0001 | t0039 | g0263 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19082 | hp1 | a0001 | c0002 | t0011 | g0033 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19083 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19084 | hp2 | a0001 | c0002 | t0010 | g0074 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19240 | hp1 | a0001 | c0002 | t0049 | g0072 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19240 | hp2 | a0001 | c0003 | t0012 | g0355 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20129 | hp1 | a0001 | c0003 | t0012 | g0210 | AFR | ASW | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | ASW | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20805 | hp1 | a0001 | c0002 | t0010 | g0076 | EUR | TSI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0156 | EUR | TSI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20905 | hp1 | a0001 | c0002 | t0010 | g0078 | SAS | GIH | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20905 | hp2 | a0001 | c0001 | t0025 | g0176 | SAS | GIH | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02109 | hp1 | a0001 | c0003 | t0048 | g0214 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0113 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02486 | hp1 | a0001 | c0001 | t0035 | g0172 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02559 | hp2 | a0001 | c0003 | t0012 | g0353 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0120 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0189 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG06807 | hp2 | a0001 | c0001 | t0046 | g0206 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0106 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0119 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0139 | REF | REF | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0040 | g0321 | REF | REF | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72998089
|
G | A | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.47G>A | p.Arg16Lys | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/9 | 274/4957 | 47/1254 | 16/417 | chr3 | 72998089 | ||
| chr3:73064029
|
C | T | 1 | a0002 | 2 | NA18963.hp2 NA18971.hp1 |
missense_variant | MODERATE | c.521C>T | p.Pro174Leu | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/9 | 748/4957 | 521/1254 | 174/417 | chr3 | 73064029 | ||
| chr3:73065004
|
C | A | 1 | a0006 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.791C>A | p.Thr264Asn | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 8/9 | 1018/4957 | 791/1254 | 264/417 | chr3 | 73065004 | ||
| chr3:73065103
|
CAGAAGAG others(5): Show |
C | 1 | a0004 | 2 | HG00609.hp1 NA18978.hp2 |
disruptive_inframe_deletion | MODERATE | c.906_917delAGAGGATG others(4): Show |
p.Glu303_Glu306del | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 8/9 | 1133/4957 | 906/1254 | 302/417 | INFO_REALIGN_3_PRIME | chr3 | 73065103 | |
| chr3:73065399
|
T | G | 1 | a0007 | 1 | HG03225.hp1 | missense_variant&splice_region_variant | MODERATE | c.931T>G | p.Ser311Ala | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1158/4957 | 931/1254 | 311/417 | chr3 | 73065399 | ||
| chr3:73065589
|
C | A | 1 | a0003 | 2 | HG01891.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.1121C>A | p.Ser374Tyr | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1348/4957 | 1121/1254 | 374/417 | chr3 | 73065589 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:73064036
|
A | G | 1 | a0001c0003 | 10 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.528A>G | p.Pro176Pro | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/9 | 755/4957 | 528/1254 | 176/417 | chr3 | 73064036 | ||
| chr3:73064852
|
T | C | 2 | a0001c0002a0004c0007 | 98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
splice_region_variant&synonymous_variant | LOW | c.639T>C | p.Ser213Ser | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 8/9 | 866/4957 | 639/1254 | 213/417 | chr3 | 73064852 | ||
| chr3:73065545
|
A | G | 1 | a0001c0010 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1077A>G | p.Leu359Leu | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1304/4957 | 1077/1254 | 359/417 | chr3 | 73065545 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72996876
|
C | T | 1 | a0001c0001t0068 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/9 | 162 | chr3 | 72996876 | |||||
| chr3:72996911
|
C | G | 1 | a0001c0001t0067 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/9 | 127 | chr3 | 72996911 | |||||
| chr3:72996912
|
C | T | 1 | a0001c0001t0066 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/9 | 126 | chr3 | 72996912 | |||||
| chr3:73065784
|
A | G | 1 | a0001c0001t0065 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 62 | chr3 | 73065784 | |||||
| chr3:73065839
|
A | G | 1 | a0001c0002t0064 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 117 | chr3 | 73065839 | |||||
| chr3:73065859
|
C | G | 1 | a0001c0001t0066 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 137 | chr3 | 73065859 | |||||
| chr3:73065979
|
A | AT | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(38): Show | 176 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*272dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 273 | INFO_REALIGN_3_PRIME | chr3 | 73065979 | ||||
| chr3:73065979
|
A | ATT | 9 | a0001c0002t0015a0001c0002t0020a0001c0002t0027others(6): Show | 19 | HG00597.hp1 HG00639.hp1 HG02080.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*271_*272dupTT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 273 | INFO_REALIGN_3_PRIME | chr3 | 73065979 | ||||
| chr3:73066024
|
A | G | 49 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(46): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*302A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 302 | chr3 | 73066024 | |||||
| chr3:73066079
|
G | T | 1 | a0001c0001t0047 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*357G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 357 | chr3 | 73066079 | |||||
| chr3:73066231
|
T | TATAC | 3 | a0001c0001t0018a0001c0001t0066a0007c0009t0018 | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*520dupCATA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066231 | ||||
| chr3:73066239
|
C | CAT | 5 | a0001c0001t0005a0001c0001t0017a0001c0001t0042others(2): Show | 23 | HG00741.hp1 HG01346.hp2 HG01891.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*539_*540dupTA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(1): Show |
3 | a0001c0002t0013a0001c0002t0030a0003c0004t0013 | 9 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(5): Show |
1 | a0001c0002t0006 | 11 | HG00099.hp2 HG01346.hp1 HG02683.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(7): Show |
3 | a0001c0002t0020a0001c0002t0023a0001c0002t0064 | 8 | HG00597.hp1 HG03239.hp2 HG03491.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(9): Show |
3 | a0001c0002t0031a0001c0002t0049a0001c0002t0059 | 4 | HG04204.hp1 NA18943.hp2 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(11): Show |
2 | a0001c0002t0050a0001c0002t0060 | 2 | NA18945.hp2 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(13): Show |
2 | a0001c0002t0032a0001c0002t0061 | 3 | HG00639.hp1 HG01069.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATACATA others(17): Show |
1 | a0001c0002t0062 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATAT | 9 | a0001c0001t0009a0001c0001t0014a0001c0001t0019others(6): Show | 30 | HG01109.hp2 HG02027.hp2 HG02083.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*537_*540dupTATA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATATAT | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0024others(6): Show | 72 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*535_*540dupTATATA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATATATA others(1): Show |
7 | a0001c0001t0007a0001c0001t0025a0001c0001t0026others(4): Show | 28 | HG00423.hp1 HG00621.hp1 HG01255.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*533_*540dupTATATA others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATATATA others(3): Show |
4 | a0001c0001t0008a0001c0001t0054a0001c0002t0011others(1): Show | 20 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*531_*540dupTATATA others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATATATA others(5): Show |
4 | a0001c0001t0036a0001c0001t0056a0001c0002t0055others(1): Show | 5 | HG01099.hp2 HG02109.hp1 HG02602.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*529_*540dupTATATA others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
C | CATATATA others(7): Show |
3 | a0001c0001t0057a0001c0001t0058a0001c0002t0037 | 4 | HG01109.hp1 HG01952.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*540dupTATATA others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066239
|
CAT | C | 2 | a0001c0001t0028a0001c0001t0051 | 3 | HG03209.hp1 HG03688.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*539_*540delTA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 539 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | ||||
| chr3:73066635
|
T | C | 49 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(46): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*913T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 913 | chr3 | 73066635 | |||||
| chr3:73066693
|
C | G | 1 | a0001c0001t0022 | 3 | NA18946.hp1 NA18974.hp1 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*971C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 971 | chr3 | 73066693 | |||||
| chr3:73067221
|
G | T | 3 | a0001c0001t0018a0001c0001t0066a0007c0009t0018 | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1499G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1499 | chr3 | 73067221 | |||||
| chr3:73067286
|
C | G | 29 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(26): Show | 141 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1564C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1564 | chr3 | 73067286 | |||||
| chr3:73067377
|
A | G | 3 | a0001c0001t0016a0001c0001t0044a0001c0001t0046 | 7 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1655A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1655 | chr3 | 73067377 | |||||
| chr3:73067390
|
C | T | 4 | a0001c0001t0016a0001c0001t0021a0001c0001t0044others(1): Show | 10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1668C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1668 | chr3 | 73067390 | |||||
| chr3:73067439
|
GACTGTCA others(5): Show |
G | 1 | a0001c0001t0038 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1720_*1731delTGTC others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1720 | INFO_REALIGN_3_PRIME | chr3 | 73067439 | ||||
| chr3:73067565
|
A | T | 53 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(50): Show | 198 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1843A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1843 | chr3 | 73067565 | |||||
| chr3:73067693
|
T | G | 3 | a0001c0001t0018a0001c0001t0066a0007c0009t0018 | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1971T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1971 | chr3 | 73067693 | |||||
| chr3:73068369
|
G | GAT | 7 | a0001c0001t0024a0001c0001t0035a0001c0001t0039others(4): Show | 10 | HG02257.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2662_*2663dupAT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2664 | INFO_REALIGN_3_PRIME | chr3 | 73068369 | ||||
| chr3:73068371
|
T | G | 1 | a0001c0002t0030 | 2 | HG02055.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2649T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2649 | chr3 | 73068371 | |||||
| chr3:73068372
|
A | G | 1 | a0001c0001t0041 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2650A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2650 | chr3 | 73068372 | |||||
| chr3:73068495
|
A | G | 1 | a0001c0001t0054 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2773A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2773 | chr3 | 73068495 | |||||
| chr3:73068572
|
T | C | 1 | a0001c0001t0042 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2850T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2850 | chr3 | 73068572 | |||||
| chr3:73068684
|
C | T | 14 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(11): Show | 65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2962C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2962 | chr3 | 73068684 | |||||
| chr3:73068803
|
A | G | 1 | a0001c0001t0009 | 8 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3081A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3081 | chr3 | 73068803 | |||||
| chr3:73068830
|
T | C | 2 | a0001c0001t0025a0001c0001t0054 | 4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3108T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3108 | chr3 | 73068830 | |||||
| chr3:73068854
|
C | A | 1 | a0001c0001t0029 | 2 | HG00438.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3132C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3132 | chr3 | 73068854 | |||||
| chr3:73068932
|
AG | A | 68 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(65): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*3212delG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3212 | INFO_REALIGN_3_PRIME | chr3 | 73068932 | ||||
| chr3:73069070
|
C | A | 73 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(70): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*3348C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3348 | chr3 | 73069070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72997155
|
C | G | 1 | a0001c0002t0055g0358 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.34+84C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997155 | ||||||
| chr3:72997214
|
C | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.34+143C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997214 | ||||||
| chr3:72997221
|
C | T | 4 | a0001c0003t0012g0352a0001c0003t0012g0353a0001c0003t0012g0354others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+150C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997221 | ||||||
| chr3:72997275
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.34+204C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997275 | ||||||
| chr3:72997340
|
C | G | 1 | a0001c0001t0017g0351 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.34+269C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997340 | ||||||
| chr3:72997357
|
G | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.34+286G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997357 | ||||||
| chr3:72997376
|
C | T | 1 | a0001c0001t0028g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+305C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997376 | ||||||
| chr3:72997382
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.34+311C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997382 | ||||||
| chr3:72997389
|
C | T | 2 | a0002c0005t0017g0348a0002c0005t0017g0349 | 2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.34+318C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997389 | ||||||
| chr3:72997393
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(195): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.34+322T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997393 | ||||||
| chr3:72997410
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.34+339C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997410 | ||||||
| chr3:72997530
|
C | T | 1 | a0001c0003t0048g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.34+459C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997530 | ||||||
| chr3:72997580
|
C | T | 1 | a0001c0002t0006g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.35-497C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997580 | ||||||
| chr3:72997656
|
T | C | 1 | a0001c0001t0016g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.35-421T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997656 | ||||||
| chr3:72997843
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.35-234A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997843 | ||||||
| chr3:72997993
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-84A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997993 | ||||||
| chr3:72998008
|
A | G | 1 | a0001c0001t0036g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.35-69A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72998008 | ||||||
| chr3:72998177
|
T | C | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+19T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998177 | ||||||
| chr3:72998326
|
A | G | 11 | a0001c0001t0001g0213a0001c0003t0012g0210a0001c0003t0012g0211others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+168A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998326 | ||||||
| chr3:72998714
|
A | G | 1 | a0001c0001t0022g0347 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.116+556A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998714 | ||||||
| chr3:72998874
|
ACTT | A | 3 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346 | 3 | HG02451.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.116+720_116+722del others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 72998874 | |||||
| chr3:72998886
|
A | C | 68 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(65): Show | 68 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.116+728A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998886 | ||||||
| chr3:72999022
|
A | G | 97 | a0001c0001t0002g0102a0001c0002t0003g0024a0001c0002t0003g0025others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+864A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999022 | ||||||
| chr3:72999032
|
T | A | 1 | a0001c0001t0002g0216 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.116+874T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999032 | ||||||
| chr3:72999194
|
G | C | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.116+1036G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999194 | ||||||
| chr3:72999210
|
G | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+1052G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999210 | ||||||
| chr3:72999552
|
C | T | 1 | a0001c0001t0019g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116+1394C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999552 | ||||||
| chr3:72999697
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.116+1539T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999697 | ||||||
| chr3:72999709
|
T | C | 1 | a0001c0001t0002g0216 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.116+1551T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999709 | ||||||
| chr3:72999764
|
C | A | 1 | a0001c0001t0018g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116+1606C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999764 | ||||||
| chr3:72999771
|
G | A | 1 | a0001c0001t0021g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116+1613G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999771 | ||||||
| chr3:72999791
|
G | A | 1 | a0001c0002t0053g0218 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.116+1633G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999791 | ||||||
| chr3:72999842
|
A | G | 16 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.116+1684A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999842 | ||||||
| chr3:72999934
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+1776A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999934 | ||||||
| chr3:73000029
|
A | G | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+1871A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000029 | ||||||
| chr3:73000142
|
T | G | 5 | a0001c0001t0005g0006a0001c0001t0014g0003a0001c0001t0014g0004others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+1984T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000142 | ||||||
| chr3:73000282
|
C | A | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+2124C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000282 | ||||||
| chr3:73000400
|
G | T | 1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+2242G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000400 | ||||||
| chr3:73000593
|
T | C | 1 | a0001c0001t0004g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.116+2435T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000593 | ||||||
| chr3:73000604
|
C | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+2446C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000604 | ||||||
| chr3:73000755
|
T | C | 2 | a0001c0002t0010g0008a0001c0002t0010g0009 | 2 | NA18944.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.116+2597T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000755 | ||||||
| chr3:73000857
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+2699A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000857 | ||||||
| chr3:73000921
|
T | A | 7 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(4): Show | 7 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+2763T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000921 | ||||||
| chr3:73000948
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+2790A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000948 | ||||||
| chr3:73001183
|
A | G | 100 | a0001c0001t0002g0102a0001c0002t0003g0024a0001c0002t0003g0025others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.116+3025A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001183 | ||||||
| chr3:73001463
|
A | C | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+3305A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001463 | ||||||
| chr3:73001483
|
AG | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+3327delG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73001483 | |||||
| chr3:73001507
|
G | C | 2 | a0001c0003t0043g0208a0001c0003t0045g0209 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.116+3349G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001507 | ||||||
| chr3:73001550
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+3392G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001550 | ||||||
| chr3:73001582
|
A | G | 2 | a0001c0001t0007g0187a0001c0001t0007g0188 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.116+3424A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001582 | ||||||
| chr3:73001604
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+3446G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001604 | ||||||
| chr3:73001713
|
A | G | 1 | a0001c0001t0029g0341 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.116+3555A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001713 | ||||||
| chr3:73001763
|
T | C | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.116+3605T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001763 | ||||||
| chr3:73001791
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+3633A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001791 | ||||||
| chr3:73001798
|
A | T | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+3640A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001798 | ||||||
| chr3:73001803
|
G | A | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+3645G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001803 | ||||||
| chr3:73001804
|
T | G | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+3646T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001804 | ||||||
| chr3:73002014
|
C | A | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+3856C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002014 | ||||||
| chr3:73002027
|
AATC | A | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+3874_116+3876d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002027 | |||||
| chr3:73002050
|
C | G | 2 | a0001c0001t0044g0207a0001c0001t0046g0206 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.116+3892C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002050 | ||||||
| chr3:73002165
|
C | G | 1 | a0001c0001t0007g0186 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+4007C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002165 | ||||||
| chr3:73002223
|
A | G | 2 | a0001c0001t0026g0184a0001c0001t0056g0185 | 2 | HG01255.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+4065A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002223 | ||||||
| chr3:73002274
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.116+4116G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002274 | ||||||
| chr3:73002360
|
C | T | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+4202C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002360 | ||||||
| chr3:73002441
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+4283A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002441 | ||||||
| chr3:73002520
|
C | G | 1 | a0001c0001t0007g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.116+4362C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002520 | ||||||
| chr3:73002523
|
A | G | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.116+4365A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002523 | ||||||
| chr3:73002526
|
A | G | 1 | a0001c0001t0056g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.116+4368A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002526 | ||||||
| chr3:73002552
|
A | G | 2 | a0001c0001t0005g0006a0001c0001t0014g0007 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116+4394A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002552 | ||||||
| chr3:73002598
|
C | A | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+4440C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002598 | ||||||
| chr3:73002604
|
T | TTTTTC | 14 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(11): Show | 15 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+4476_116+4480d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002604 | |||||
| chr3:73002604
|
TTTTTC | T | 8 | a0001c0001t0001g0333a0001c0001t0007g0141a0001c0001t0014g0334others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.116+4476_116+4480d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002604 | |||||
| chr3:73002604
|
TTTTTCTT others(3): Show |
T | 3 | a0001c0001t0001g0338a0001c0001t0002g0339a0001c0010t0001g0337 | 3 | HG00609.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116+4471_116+4480d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002604 | |||||
| chr3:73002619
|
C | T | 5 | a0001c0001t0018g0192a0001c0001t0018g0194a0001c0001t0018g0195others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+4461C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002619 | ||||||
| chr3:73002624
|
C | T | 1 | a0001c0001t0018g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.116+4466C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002624 | ||||||
| chr3:73002629
|
C | CTTTTTT | 8 | a0001c0001t0004g0154a0001c0001t0007g0183a0001c0001t0007g0186others(5): Show | 8 | HG00741.hp2 HG01109.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | CTTTTTTT | 6 | a0001c0001t0004g0157a0001c0001t0004g0158a0001c0001t0004g0159others(3): Show | 6 | HG01123.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | CTTTTTTT others(1): Show |
17 | a0001c0001t0003g0108a0001c0001t0004g0126a0001c0001t0004g0127others(14): Show | 17 | HG01081.hp2 HG01255.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | CTTTTTTT others(2): Show |
15 | a0001c0001t0004g0132a0001c0001t0004g0168a0001c0001t0004g0169others(12): Show | 15 | HG00140.hp1 HG01517.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0003g0115a0001c0001t0004g0178a0001c0001t0009g0116others(2): Show | 5 | HG00735.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0179a0001c0001t0019g0120a0001c0001t0025g0180 | 3 | HG02886.hp1 HG03471.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.116+4475_116+4476i others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.116+4475_116+4476i others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
C | T | 6 | a0001c0001t0004g0181a0001c0001t0007g0182a0001c0001t0007g0188others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+4471C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002629 | ||||||
| chr3:73002629
|
CTTTTCTT others(11): Show |
C | 1 | a0001c0002t0003g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.116+4476_116+4493d others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002629
|
CTTTTCTT others(12): Show |
C | 95 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.116+4476_116+4494d others(21): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | |||||
| chr3:73002630
|
TTTTC | T | 9 | a0001c0001t0001g0213a0001c0001t0004g0142a0001c0001t0018g0192others(6): Show | 9 | HG01243.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+4476_116+4479d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002630 | |||||
| chr3:73002633
|
T | C | 1 | a0001c0003t0012g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.116+4475T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002633 | ||||||
| chr3:73002634
|
C | CT | 16 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(13): Show | 16 | HG01934.hp1 HG02027.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.116+4501dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002634
|
C | CTTTTCT | 6 | a0001c0001t0001g0227a0001c0001t0005g0228a0001c0001t0017g0229others(3): Show | 6 | HG01346.hp2 HG01361.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+4480_116+4481i others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002634
|
C | CTTTTCTT others(4): Show |
1 | a0001c0001t0001g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.116+4480_116+4481i others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002634
|
C | CTTTTCTT others(5): Show |
1 | a0001c0003t0048g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.116+4480_116+4481i others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002634
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.116+4492_116+4501d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002634
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0004g0139 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.116+4490_116+4501d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002634
|
C | T | 72 | a0001c0001t0003g0108a0001c0001t0003g0115a0001c0001t0004g0126others(69): Show | 72 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.116+4476C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002634 | ||||||
| chr3:73002634
|
CT | C | 10 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG01517.hp2 HG01891.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+4501delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | |||||
| chr3:73002703
|
G | A | 1 | a0001c0001t0058g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.116+4545G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002703 | ||||||
| chr3:73002711
|
G | A | 1 | a0001c0001t0005g0238 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.116+4553G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002711 | ||||||
| chr3:73002860
|
T | C | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+4702T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002860 | ||||||
| chr3:73002887
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.116+4729C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002887 | ||||||
| chr3:73002899
|
C | T | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+4741C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002899 | ||||||
| chr3:73003078
|
C | T | 7 | a0001c0001t0001g0219a0001c0001t0018g0192a0001c0001t0018g0193others(4): Show | 7 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+4920C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003078 | ||||||
| chr3:73003118
|
AT | A | 177 | a0001c0001t0002g0239a0001c0001t0003g0107a0001c0001t0003g0108others(174): Show | 177 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(174): Show |
intron_variant | MODIFIER | c.116+4973delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73003118 | |||||
| chr3:73003197
|
A | G | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+5039A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003197 | ||||||
| chr3:73003199
|
T | C | 84 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(81): Show | 84 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.116+5041T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003199 | ||||||
| chr3:73003217
|
GT | G | 156 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.116+5071delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73003217 | |||||
| chr3:73003248
|
G | A | 12 | a0001c0001t0004g0142a0001c0001t0004g0158a0001c0001t0004g0159others(9): Show | 12 | HG00735.hp2 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+5090G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003248 | ||||||
| chr3:73003288
|
C | T | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+5130C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003288 | ||||||
| chr3:73003363
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+5205C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003363 | ||||||
| chr3:73003398
|
A | G | 1 | a0001c0001t0008g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116+5240A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003398 | ||||||
| chr3:73003410
|
G | A | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+5252G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003410 | ||||||
| chr3:73003598
|
T | C | 87 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(84): Show | 87 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.116+5440T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003598 | ||||||
| chr3:73003614
|
C | A | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+5456C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003614 | ||||||
| chr3:73003692
|
G | GT | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5543dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73003692 | |||||
| chr3:73003697
|
T | G | 2 | a0001c0001t0007g0189a0001c0001t0051g0198 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.116+5539T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003697 | ||||||
| chr3:73003706
|
T | C | 1 | a0001c0001t0002g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.116+5548T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003706 | ||||||
| chr3:73003711
|
T | TG | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+5553_116+5554i others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003711 | ||||||
| chr3:73003712
|
T | G | 3 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0018g0194 | 3 | HG03486.hp1 NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.116+5554T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003712 | ||||||
| chr3:73003722
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5564A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003722 | ||||||
| chr3:73003729
|
T | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5571T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003729 | ||||||
| chr3:73003753
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+5595C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003753 | ||||||
| chr3:73003820
|
T | G | 5 | a0001c0001t0026g0160a0001c0001t0026g0184a0001c0001t0056g0185others(2): Show | 5 | HG01255.hp1 HG01952.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+5662T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003820 | ||||||
| chr3:73003897
|
T | A | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+5739T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003897 | ||||||
| chr3:73003903
|
A | T | 84 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(81): Show | 84 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.116+5745A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003903 | ||||||
| chr3:73004001
|
A | C | 3 | a0001c0002t0010g0008a0001c0002t0010g0009a0001c0002t0010g0089 | 3 | HG00621.hp1 NA18944.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.116+5843A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004001 | ||||||
| chr3:73004007
|
T | C | 1 | a0001c0001t0014g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116+5849T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004007 | ||||||
| chr3:73004087
|
C | T | 2 | a0001c0002t0003g0088a0001c0002t0003g0101 | 2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.116+5929C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004087 | ||||||
| chr3:73004102
|
T | C | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(350): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.116+5944T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004102 | ||||||
| chr3:73004104
|
G | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+5946G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004104 | ||||||
| chr3:73004125
|
T | C | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+5967T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004125 | ||||||
| chr3:73004127
|
C | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+5969C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004127 | ||||||
| chr3:73004182
|
CT | C | 179 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.116+6037delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004182 | |||||
| chr3:73004217
|
T | G | 1 | a0001c0001t0004g0129 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116+6059T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004217 | ||||||
| chr3:73004280
|
A | G | 11 | a0001c0001t0001g0213a0001c0003t0012g0210a0001c0003t0012g0211others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+6122A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004280 | ||||||
| chr3:73004316
|
T | C | 8 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(5): Show | 8 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+6158T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004316 | ||||||
| chr3:73004337
|
G | A | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+6179G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004337 | ||||||
| chr3:73004375
|
A | T | 1 | a0001c0002t0003g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.116+6217A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004375 | ||||||
| chr3:73004422
|
T | G | 1 | a0001c0001t0005g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.116+6264T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004422 | ||||||
| chr3:73004448
|
A | G | 67 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(64): Show | 67 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.116+6290A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004448 | ||||||
| chr3:73004480
|
G | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+6322G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004480 | ||||||
| chr3:73004499
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+6341C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004499 | ||||||
| chr3:73004500
|
G | A | 9 | a0001c0001t0016g0200a0001c0001t0016g0201a0001c0001t0016g0202others(6): Show | 9 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+6342G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004500 | ||||||
| chr3:73004736
|
A | G | 85 | a0001c0001t0002g0319a0001c0001t0003g0107a0001c0001t0003g0108others(82): Show | 85 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.116+6578A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004736 | ||||||
| chr3:73004793
|
A | C | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+6635A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004793 | ||||||
| chr3:73004793
|
A | G | 1 | a0001c0001t0002g0332 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.116+6635A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004793 | ||||||
| chr3:73004844
|
G | GGT | 18 | a0001c0001t0002g0248a0001c0001t0017g0249a0001c0002t0003g0024others(15): Show | 18 | HG00597.hp1 HG02922.hp1 HG03831.hp2 others(15): Show |
intron_variant | MODIFIER | c.116+6711_116+6712d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004844 | |||||
| chr3:73004844
|
G | GT | 3 | a0001c0002t0011g0083a0001c0002t0033g0098a0001c0002t0037g0084 | 3 | HG02976.hp2 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.116+6686_116+6687i others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004844 | ||||||
| chr3:73004846
|
T | G | 3 | a0001c0001t0066g0196a0003c0004t0013g0356a0003c0004t0013g0357 | 3 | HG01891.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+6688T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004846 | ||||||
| chr3:73004848
|
T | G | 4 | a0001c0001t0005g0006a0001c0001t0014g0003a0001c0001t0014g0004others(1): Show | 4 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+6690T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004848 | ||||||
| chr3:73004857
|
GTGTGTGT others(11): Show |
G | 84 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(81): Show | 84 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.116+6703_116+6720d others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004857 | |||||
| chr3:73004863
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0318 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.116+6709_116+6720d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004863 | |||||
| chr3:73004867
|
GTGTT | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(105): Show | 110 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.116+6725_116+6728d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004867 | |||||
| chr3:73004867
|
GTGTTTGT others(1): Show |
G | 10 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0250others(7): Show | 10 | HG00597.hp2 NA18612.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+6721_116+6728d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004867 | |||||
| chr3:73004867
|
GTGTTTGT others(5): Show |
G | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+6717_116+6728d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004867 | |||||
| chr3:73004869
|
GTT | G | 19 | a0001c0001t0001g0213a0001c0001t0001g0227a0001c0001t0001g0245others(16): Show | 19 | HG00438.hp2 HG01243.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.116+6713_116+6714d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004869 | |||||
| chr3:73004869
|
GTTTGTT | G | 3 | a0001c0001t0001g0244a0001c0002t0003g0082a0001c0002t0010g0081 | 3 | HG00423.hp1 NA19063.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.116+6713_116+6718d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004869 | |||||
| chr3:73004871
|
T | G | 86 | a0001c0001t0021g0199a0001c0002t0003g0024a0001c0002t0003g0025others(83): Show | 86 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.116+6713T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004871 | ||||||
| chr3:73004875
|
T | G | 98 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(95): Show | 98 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.116+6717T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004875 | ||||||
| chr3:73004879
|
T | G | 2 | a0001c0001t0018g0194a0001c0002t0003g0026 | 2 | HG00738.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.116+6721T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004879 | ||||||
| chr3:73004905
|
G | A | 1 | a0001c0002t0010g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.116+6747G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004905 | ||||||
| chr3:73004910
|
CATGTGTG others(47): Show |
C | 1 | a0001c0002t0019g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.116+6753_116+6806d others(56): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004910 | ||||||
| chr3:73004911
|
A | G | 184 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+6753A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004911 | ||||||
| chr3:73004923
|
T | G | 1 | a0001c0001t0007g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.116+6765T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004923 | ||||||
| chr3:73004923
|
T | TTGTGTG | 178 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.116+6767_116+6772d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | |||||
| chr3:73004923
|
TTGTGTGT others(19): Show |
T | 2 | a0001c0002t0030g0091a0001c0002t0030g0092 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.116+6773_116+6798d others(28): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | |||||
| chr3:73004923
|
TTGTGTGT others(21): Show |
T | 2 | a0001c0002t0013g0090a0001c0002t0033g0098 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116+6773_116+6800d others(30): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | |||||
| chr3:73004923
|
TTGTGTGT others(23): Show |
T | 2 | a0001c0002t0013g0094a0001c0002t0033g0093 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.116+6773_116+6802d others(32): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | |||||
| chr3:73004944
|
C | CGT | 8 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0320others(5): Show | 8 | HG00735.hp2 HG01952.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+6831_116+6832d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGT | C | 37 | a0001c0001t0001g0232a0001c0001t0001g0258a0001c0001t0001g0259others(34): Show | 37 | HG00741.hp2 HG01123.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.116+6831_116+6832d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGT | C | 64 | a0001c0001t0001g0308a0001c0001t0001g0312a0001c0001t0001g0340others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.116+6829_116+6832d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGT | C | 88 | a0001c0001t0001g0213a0001c0001t0001g0244a0001c0001t0001g0261others(85): Show | 88 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.116+6827_116+6832d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGTG others(1): Show |
C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(93): Show | 98 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.116+6825_116+6832d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGTG others(3): Show |
C | 17 | a0001c0001t0001g0217a0001c0001t0005g0238a0001c0001t0005g0256others(14): Show | 17 | HG01255.hp1 HG01884.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.116+6823_116+6832d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGTG others(5): Show |
C | 6 | a0001c0001t0018g0192a0001c0001t0018g0194a0001c0001t0018g0195others(3): Show | 6 | HG01243.hp1 HG02155.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+6821_116+6832d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGTG others(9): Show |
C | 3 | a0001c0001t0066g0196a0003c0004t0013g0356a0003c0004t0013g0357 | 3 | HG01891.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+6817_116+6832d others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0002t0003g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.116+6815_116+6832d others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004944
|
CGTGTGTG others(15): Show |
C | 1 | a0001c0001t0017g0229 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.116+6811_116+6832d others(24): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | |||||
| chr3:73004950
|
T | TGTGTGTG others(91): Show |
1 | a0001c0002t0010g0074 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.116+6818_116+6819i others(100): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004950 | |||||
| chr3:73004951
|
G | T | 1 | a0001c0001t0021g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.116+6793G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004951 | ||||||
| chr3:73004953
|
G | T | 12 | a0001c0001t0001g0213a0001c0001t0021g0199a0001c0001t0021g0205others(9): Show | 12 | HG02280.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+6795G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004953 | ||||||
| chr3:73004957
|
G | T | 7 | a0001c0001t0016g0200a0001c0001t0016g0201a0001c0001t0016g0202others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+6799G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004957 | ||||||
| chr3:73004977
|
G | T | 1 | a0001c0002t0019g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.116+6819G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004977 | ||||||
| chr3:73004985
|
GTGTGT | G | 4 | a0001c0001t0001g0325a0001c0001t0029g0306a0001c0002t0003g0031others(1): Show | 4 | HG00438.hp1 NA18971.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+6829_116+6833d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004985 | |||||
| chr3:73004991
|
T | G | 1 | a0001c0002t0033g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.116+6833T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004991 | ||||||
| chr3:73004999
|
G | A | 1 | a0001c0001t0021g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116+6841G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004999 | ||||||
| chr3:73005008
|
C | A | 4 | a0001c0001t0008g0150a0001c0001t0008g0151a0001c0001t0008g0152others(1): Show | 4 | HG00741.hp2 HG01109.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+6850C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005008 | ||||||
| chr3:73005061
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116+6903C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005061 | ||||||
| chr3:73005337
|
CT | C | 152 | a0001c0001t0002g0307a0001c0001t0003g0128a0001c0001t0004g0126others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.116+7194delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005337 | |||||
| chr3:73005337
|
CTT | C | 11 | a0001c0001t0004g0142a0001c0001t0004g0149a0001c0001t0004g0158others(8): Show | 11 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+7193_116+7194d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005337 | |||||
| chr3:73005370
|
C | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+7212C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005370 | ||||||
| chr3:73005393
|
G | A | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+7235G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005393 | ||||||
| chr3:73005480
|
A | G | 1 | a0001c0001t0017g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.116+7322A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005480 | ||||||
| chr3:73005620
|
C | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+7462C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005620 | ||||||
| chr3:73005623
|
C | T | 94 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(91): Show | 94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.116+7465C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005623 | ||||||
| chr3:73005711
|
G | C | 6 | a0001c0002t0013g0090a0001c0002t0013g0094a0001c0002t0030g0091others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+7553G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005711 | ||||||
| chr3:73005734
|
A | G | 7 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(4): Show | 7 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+7576A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005734 | ||||||
| chr3:73005761
|
G | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+7603G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005761 | ||||||
| chr3:73005806
|
T | C | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+7648T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005806 | ||||||
| chr3:73005825
|
T | A | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+7667T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005825 | ||||||
| chr3:73005833
|
C | CA | 8 | a0001c0001t0001g0232a0001c0001t0001g0258a0001c0001t0001g0265others(5): Show | 8 | HG01891.hp1 HG02155.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+7688dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | |||||
| chr3:73005833
|
C | CAAAAAAA others(2): Show |
92 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(89): Show | 92 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.116+7680_116+7688d others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | |||||
| chr3:73005833
|
C | CAAAAAAA others(3): Show |
21 | a0001c0001t0004g0168a0001c0001t0009g0111a0001c0001t0009g0112others(18): Show | 21 | HG00738.hp1 HG01192.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.116+7679_116+7688d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | |||||
| chr3:73005833
|
C | CAAAAAAA others(4): Show |
46 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(43): Show | 46 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.116+7678_116+7688d others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | |||||
| chr3:73005833
|
C | CAAAAAAA others(5): Show |
20 | a0001c0001t0004g0131a0001c0001t0004g0158a0001c0001t0004g0161others(17): Show | 20 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.116+7677_116+7688d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | |||||
| chr3:73005890
|
A | G | 1 | a0001c0002t0023g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.116+7732A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005890 | ||||||
| chr3:73005922
|
T | C | 4 | a0001c0002t0011g0028a0001c0002t0011g0032a0001c0002t0011g0033others(1): Show | 4 | NA18948.hp2 NA18972.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+7764T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005922 | ||||||
| chr3:73006036
|
C | T | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+7878C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006036 | ||||||
| chr3:73006096
|
G | A | 1 | a0001c0001t0054g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.116+7938G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006096 | ||||||
| chr3:73006106
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+7948G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006106 | ||||||
| chr3:73006190
|
A | AT | 30 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0231others(27): Show | 31 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.116+8059dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | |||||
| chr3:73006190
|
ATTTTTTT | A | 9 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+8053_116+8059d others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | |||||
| chr3:73006190
|
ATTTTTTT others(1): Show |
A | 60 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(57): Show | 60 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.116+8052_116+8059d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | |||||
| chr3:73006190
|
ATTTTTTT others(2): Show |
A | 33 | a0001c0002t0003g0088a0001c0002t0006g0013a0001c0002t0006g0014others(30): Show | 33 | HG00597.hp1 HG00639.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.116+8051_116+8059d others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | |||||
| chr3:73006190
|
ATTTTTTT others(3): Show |
A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+8050_116+8059d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | |||||
| chr3:73006190
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0007g0136 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.116+8049_116+8059d others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | |||||
| chr3:73006225
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.116+8067A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006225 | ||||||
| chr3:73006344
|
G | A | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+8186G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006344 | ||||||
| chr3:73006377
|
T | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+8219T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006377 | ||||||
| chr3:73006387
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+8229C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006387 | ||||||
| chr3:73006403
|
G | A | 1 | a0001c0002t0055g0358 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.116+8245G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006403 | ||||||
| chr3:73006668
|
G | T | 1 | a0001c0001t0004g0181 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.116+8510G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006668 | ||||||
| chr3:73006681
|
A | C | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+8523A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006681 | ||||||
| chr3:73006773
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+8615C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006773 | ||||||
| chr3:73006806
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+8648G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006806 | ||||||
| chr3:73006892
|
G | A | 9 | a0001c0001t0001g0308a0001c0001t0002g0216a0001c0001t0002g0248others(6): Show | 9 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+8734G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006892 | ||||||
| chr3:73006945
|
T | TG | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+8788dupG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006945 | |||||
| chr3:73007008
|
C | T | 1 | a0007c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116+8850C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007008 | ||||||
| chr3:73007072
|
T | C | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+8914T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007072 | ||||||
| chr3:73007187
|
A | G | 2 | a0001c0001t0005g0292a0001c0001t0005g0296 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.116+9029A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007187 | ||||||
| chr3:73007219
|
G | A | 6 | a0001c0001t0002g0240a0001c0001t0002g0305a0001c0001t0002g0328others(3): Show | 6 | NA18946.hp1 NA18974.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+9061G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007219 | ||||||
| chr3:73007226
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+9068A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007226 | ||||||
| chr3:73007227
|
A | G | 98 | a0001c0001t0005g0243a0001c0002t0003g0024a0001c0002t0003g0025others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.116+9069A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007227 | ||||||
| chr3:73007238
|
T | C | 1 | a0001c0001t0017g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.116+9080T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007238 | ||||||
| chr3:73007312
|
A | G | 1 | a0001c0001t0002g0310 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.116+9154A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007312 | ||||||
| chr3:73007332
|
A | G | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+9174A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007332 | ||||||
| chr3:73007347
|
G | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+9189G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007347 | ||||||
| chr3:73007397
|
T | C | 1 | a0001c0001t0008g0143 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.116+9239T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007397 | ||||||
| chr3:73007484
|
GT | G | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+9335delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73007484 | |||||
| chr3:73007568
|
GGGTTCAA others(7): Show |
G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+9420_116+9433d others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73007568 | |||||
| chr3:73007575
|
A | G | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+9417A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007575 | ||||||
| chr3:73007734
|
C | G | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+9576C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007734 | ||||||
| chr3:73007780
|
C | T | 1 | a0001c0001t0036g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.116+9622C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007780 | ||||||
| chr3:73007785
|
G | A | 2 | a0001c0001t0035g0171a0001c0001t0035g0172 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.116+9627G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007785 | ||||||
| chr3:73007834
|
G | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+9676G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007834 | ||||||
| chr3:73007861
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.116+9703T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007861 | ||||||
| chr3:73007928
|
ATTAC | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+9773_116+9776d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73007928 | |||||
| chr3:73007999
|
C | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+9841C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007999 | ||||||
| chr3:73008039
|
A | AC | 43 | a0001c0001t0001g0221a0001c0001t0001g0244a0001c0001t0001g0261others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.116+9888dupC | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73008039 | |||||
| chr3:73008055
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.116+9897C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008055 | ||||||
| chr3:73008114
|
G | GCTT | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+9957_116+9959d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73008114 | |||||
| chr3:73008163
|
C | T | 2 | a0001c0002t0006g0057a0001c0002t0006g0105 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.116+10005C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008163 | ||||||
| chr3:73008276
|
T | G | 1 | a0001c0002t0015g0087 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.116+10118T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008276 | ||||||
| chr3:73008295
|
G | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+10137G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008295 | ||||||
| chr3:73008296
|
T | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+10138T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008296 | ||||||
| chr3:73008299
|
A | G | 2 | a0001c0001t0002g0316a0001c0001t0002g0320 | 2 | HG02738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.116+10141A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008299 | ||||||
| chr3:73008499
|
T | G | 1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+10341T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008499 | ||||||
| chr3:73008535
|
G | C | 1 | a0001c0001t0001g0308 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.116+10377G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008535 | ||||||
| chr3:73008543
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+10385C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008543 | ||||||
| chr3:73008727
|
A | T | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+10569A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008727 | ||||||
| chr3:73008747
|
A | C | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+10589A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008747 | ||||||
| chr3:73008772
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.116+10614A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008772 | ||||||
| chr3:73008773
|
T | TAGAATGA others(76): Show |
1 | a0001c0001t0068g0336 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.116+10617_116+1069 others(87): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73008773 | |||||
| chr3:73008796
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0235others(8): Show | 12 | HG03516.hp2 NA18747.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.116+10638C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008796 | ||||||
| chr3:73008838
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+10680A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008838 | ||||||
| chr3:73009090
|
T | G | 51 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(48): Show | 51 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.116+10932T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009090 | ||||||
| chr3:73009095
|
T | G | 11 | a0001c0001t0001g0213a0001c0003t0012g0210a0001c0003t0012g0211others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+10937T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009095 | ||||||
| chr3:73009097
|
A | C | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+10939A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009097 | ||||||
| chr3:73009145
|
A | T | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+10987A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009145 | ||||||
| chr3:73009430
|
CAA | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+11274_116+1127 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73009430 | |||||
| chr3:73009559
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116+11401A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009559 | ||||||
| chr3:73009568
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+11410T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009568 | ||||||
| chr3:73009612
|
CTTCAGAT others(13): Show |
C | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+11455_116+1147 others(24): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009612 | ||||||
| chr3:73009676
|
G | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+11518G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009676 | ||||||
| chr3:73009699
|
C | T | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+11541C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009699 | ||||||
| chr3:73009750
|
C | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+11592C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009750 | ||||||
| chr3:73009980
|
A | G | 2 | a0001c0001t0008g0145a0001c0001t0008g0148 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.116+11822A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009980 | ||||||
| chr3:73010009
|
C | T | 1 | a0001c0002t0013g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116+11851C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010009 | ||||||
| chr3:73010183
|
G | T | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+12025G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010183 | ||||||
| chr3:73010232
|
G | GT | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+12082dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73010232 | |||||
| chr3:73010261
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.116+12103C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010261 | ||||||
| chr3:73010294
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0291 | 2 | NA19000.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.116+12136C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010294 | ||||||
| chr3:73010299
|
T | C | 1 | a0001c0002t0049g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.116+12141T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010299 | ||||||
| chr3:73010342
|
C | T | 1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+12184C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010342 | ||||||
| chr3:73010516
|
G | A | 2 | a0001c0002t0006g0099a0001c0002t0023g0100 | 2 | HG00099.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.116+12358G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010516 | ||||||
| chr3:73010564
|
CT | C | 181 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.116+12418delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73010564 | |||||
| chr3:73010618
|
G | A | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+12460G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010618 | ||||||
| chr3:73010702
|
G | A | 1 | a0001c0001t0021g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116+12544G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010702 | ||||||
| chr3:73010717
|
A | G | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.116+12559A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010717 | ||||||
| chr3:73010747
|
C | T | 3 | a0001c0002t0003g0048a0001c0002t0003g0049a0001c0002t0003g0080 | 3 | NA18979.hp1 NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.116+12589C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010747 | ||||||
| chr3:73010801
|
G | C | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+12643G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010801 | ||||||
| chr3:73010820
|
A | G | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+12662A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010820 | ||||||
| chr3:73010953
|
G | A | 1 | a0001c0002t0050g0043 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.116+12795G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010953 | ||||||
| chr3:73011005
|
A | G | 2 | a0001c0001t0005g0006a0001c0001t0014g0007 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116+12847A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011005 | ||||||
| chr3:73011025
|
C | CTGA | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+12868_116+1286 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73011025 | |||||
| chr3:73011056
|
C | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+12898C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011056 | ||||||
| chr3:73011186
|
G | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+13028G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011186 | ||||||
| chr3:73011306
|
C | A | 4 | a0001c0001t0025g0167a0001c0001t0025g0176a0001c0001t0025g0180others(1): Show | 4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+13148C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011306 | ||||||
| chr3:73011308
|
T | C | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.116+13150T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011308 | ||||||
| chr3:73011373
|
C | T | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+13215C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011373 | ||||||
| chr3:73011482
|
GA | G | 98 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.116+13335delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73011482 | |||||
| chr3:73011531
|
G | A | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+13373G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011531 | ||||||
| chr3:73011712
|
A | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0296 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.116+13554A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011712 | ||||||
| chr3:73011773
|
GT | G | 105 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(102): Show | 105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+13616delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011773 | ||||||
| chr3:73011776
|
T | C | 105 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(102): Show | 105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+13618T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011776 | ||||||
| chr3:73011818
|
A | G | 19 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(16): Show | 19 | HG00735.hp2 HG01928.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.116+13660A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011818 | ||||||
| chr3:73011933
|
T | C | 5 | a0001c0001t0002g0301a0001c0001t0002g0303a0001c0001t0002g0311others(2): Show | 5 | HG01081.hp1 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+13775T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011933 | ||||||
| chr3:73011953
|
C | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+13795C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011953 | ||||||
| chr3:73012023
|
T | G | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+13865T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012023 | ||||||
| chr3:73012279
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.116+14121G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012279 | ||||||
| chr3:73012323
|
G | A | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+14165G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012323 | ||||||
| chr3:73012328
|
C | T | 99 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.116+14170C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012328 | ||||||
| chr3:73012387
|
G | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+14229G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012387 | ||||||
| chr3:73012401
|
G | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+14243G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012401 | ||||||
| chr3:73012424
|
C | T | 2 | a0001c0001t0005g0238a0001c0001t0005g0298 | 2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.116+14266C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012424 | ||||||
| chr3:73012472
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0293a0001c0001t0001g0327 | 4 | NA18747.hp1 NA18972.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+14314T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012472 | ||||||
| chr3:73012549
|
C | A | 1 | a0001c0001t0001g0231 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.116+14391C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012549 | ||||||
| chr3:73012621
|
C | G | 105 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(102): Show | 105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+14463C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012621 | ||||||
| chr3:73012698
|
C | G | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116+14540C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012698 | ||||||
| chr3:73012768
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.116+14610G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012768 | ||||||
| chr3:73012902
|
C | CT | 23 | a0001c0001t0001g0231a0001c0001t0002g0242a0001c0001t0002g0299others(20): Show | 23 | HG01243.hp1 HG01884.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.116+14762dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73012902 | |||||
| chr3:73012902
|
CT | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0001g0343others(78): Show | 81 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.116+14762delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73012902 | |||||
| chr3:73012902
|
CTT | C | 23 | a0001c0001t0001g0213a0001c0001t0016g0106a0001c0001t0016g0200others(20): Show | 23 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+14761_116+1476 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73012902 | |||||
| chr3:73012953
|
A | T | 1 | a0001c0001t0008g0143 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.116+14795A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012953 | ||||||
| chr3:73012991
|
AGTCGTGT others(4): Show |
A | 1 | a0001c0001t0029g0341 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.116+14834_116+1484 others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012991 | ||||||
| chr3:73013027
|
C | A | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+14869C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013027 | ||||||
| chr3:73013041
|
C | T | 3 | a0001c0001t0019g0117a0001c0001t0019g0118a0001c0001t0019g0119 | 3 | HG02572.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116+14883C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013041 | ||||||
| chr3:73013142
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+14984A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013142 | ||||||
| chr3:73013431
|
A | C | 1 | a0001c0001t0009g0113 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.116+15273A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013431 | ||||||
| chr3:73013492
|
A | AAAAG | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+15337_116+1533 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73013492 | |||||
| chr3:73013589
|
A | G | 1 | a0001c0001t0017g0229 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.116+15431A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013589 | ||||||
| chr3:73013646
|
C | CT | 9 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(6): Show | 9 | HG01109.hp2 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+15500dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73013646 | |||||
| chr3:73013646
|
CT | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+15500delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73013646 | |||||
| chr3:73013729
|
C | T | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+15571C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013729 | ||||||
| chr3:73013779
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+15621C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013779 | ||||||
| chr3:73013798
|
C | T | 2 | a0001c0002t0003g0026a0001c0002t0010g0076 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.116+15640C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013798 | ||||||
| chr3:73013825
|
G | C | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+15667G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013825 | ||||||
| chr3:73013827
|
G | C | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+15669G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013827 | ||||||
| chr3:73013926
|
CCACCGCG others(470): Show |
C | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+15769_116+1624 others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013926 | ||||||
| chr3:73013936
|
C | T | 16 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.116+15778C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013936 | ||||||
| chr3:73014102
|
T | C | 2 | a0001c0002t0006g0057a0001c0002t0006g0105 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.116+15944T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014102 | ||||||
| chr3:73014236
|
T | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+16078T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014236 | ||||||
| chr3:73014470
|
A | G | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+16312A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014470 | ||||||
| chr3:73014686
|
G | GT | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+16537dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73014686 | |||||
| chr3:73014775
|
A | G | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+16617A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014775 | ||||||
| chr3:73014908
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0318 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.116+16750T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014908 | ||||||
| chr3:73014952
|
C | T | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+16794C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014952 | ||||||
| chr3:73014965
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.116+16807A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014965 | ||||||
| chr3:73015165
|
A | G | 6 | a0001c0001t0002g0240a0001c0001t0002g0305a0001c0001t0002g0328others(3): Show | 6 | NA18946.hp1 NA18974.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+17007A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015165 | ||||||
| chr3:73015216
|
G | A | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+17058G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015216 | ||||||
| chr3:73015226
|
G | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+17068G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015226 | ||||||
| chr3:73015234
|
C | T | 2 | a0001c0002t0003g0024a0001c0002t0003g0025 | 2 | NA19065.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.116+17076C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015234 | ||||||
| chr3:73015259
|
C | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+17101C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015259 | ||||||
| chr3:73015327
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.116+17169G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015327 | ||||||
| chr3:73015364
|
A | T | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116+17206A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015364 | ||||||
| chr3:73015372
|
T | A | 1 | a0001c0001t0007g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.116+17214T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015372 | ||||||
| chr3:73015481
|
CT | C | 176 | a0001c0001t0001g0323a0001c0001t0001g0343a0001c0001t0002g0216others(173): Show | 176 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.116+17340delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73015481 | |||||
| chr3:73015488
|
T | C | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+17330T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015488 | ||||||
| chr3:73015506
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 5 | HG00140.hp2 HG00738.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+17348C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015506 | ||||||
| chr3:73015594
|
G | C | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+17436G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015594 | ||||||
| chr3:73015598
|
C | G | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+17440C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015598 | ||||||
| chr3:73015648
|
T | G | 1 | a0001c0002t0023g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.116+17490T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015648 | ||||||
| chr3:73015757
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.116+17599C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015757 | ||||||
| chr3:73015777
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.116+17619A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015777 | ||||||
| chr3:73015878
|
T | C | 1 | a0001c0001t0058g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.116+17720T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015878 | ||||||
| chr3:73015888
|
T | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+17730T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015888 | ||||||
| chr3:73015965
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+17807A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015965 | ||||||
| chr3:73016019
|
G | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+17861G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016019 | ||||||
| chr3:73016073
|
A | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0262 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.116+17915A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016073 | ||||||
| chr3:73016081
|
C | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+17923C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016081 | ||||||
| chr3:73016125
|
T | C | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+17967T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016125 | ||||||
| chr3:73016184
|
C | G | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+18026C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016184 | ||||||
| chr3:73016186
|
G | A | 2 | a0001c0001t0004g0169a0001c0001t0036g0162 | 2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.116+18028G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016186 | ||||||
| chr3:73016226
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+18068A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016226 | ||||||
| chr3:73016272
|
CT | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+18124delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016272 | |||||
| chr3:73016334
|
T | C | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+18176T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016334 | ||||||
| chr3:73016418
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+18260T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016418 | ||||||
| chr3:73016427
|
C | T | 4 | a0001c0001t0002g0301a0001c0001t0002g0303a0001c0001t0002g0317others(1): Show | 4 | HG01928.hp1 HG01934.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+18269C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016427 | ||||||
| chr3:73016439
|
A | G | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+18281A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016439 | ||||||
| chr3:73016440
|
G | T | 10 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+18282G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016440 | ||||||
| chr3:73016459
|
G | C | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+18301G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016459 | ||||||
| chr3:73016729
|
G | GTTTC | 3 | a0001c0002t0006g0099a0001c0002t0010g0078a0001c0002t0055g0358 | 3 | HG00099.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.116+18574_116+1857 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016729 | |||||
| chr3:73016729
|
G | GTTTCT | 69 | a0001c0002t0003g0026a0001c0002t0003g0031a0001c0002t0003g0036others(66): Show | 69 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016729 | |||||
| chr3:73016729
|
G | GTTTCTT | 27 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(24): Show | 27 | HG00621.hp1 HG01069.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016729 | |||||
| chr3:73016731
|
T | TTC | 4 | a0001c0001t0008g0145a0001c0001t0008g0148a0001c0001t0025g0180others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016731 | |||||
| chr3:73016732
|
T | TC | 25 | a0001c0001t0003g0128a0001c0001t0004g0129a0001c0001t0004g0131others(22): Show | 25 | HG00735.hp2 HG01255.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016732 | ||||||
| chr3:73016733
|
A | C | 57 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(54): Show | 57 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.116+18575A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016733 | ||||||
| chr3:73016733
|
A | T | 130 | a0001c0001t0003g0128a0001c0001t0004g0129a0001c0001t0004g0131others(127): Show | 130 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.116+18575A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016733 | ||||||
| chr3:73016735
|
TTTTATTA others(71): Show |
T | 1 | a0001c0002t0023g0018 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.116+18581_116+1865 others(82): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016735 | |||||
| chr3:73016737
|
TTA | T | 3 | a0001c0002t0003g0042a0003c0004t0013g0356a0003c0004t0013g0357 | 3 | HG01891.hp1 HG03453.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.116+18581_116+1858 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016737 | |||||
| chr3:73016739
|
A | T | 181 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.116+18581A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016739 | ||||||
| chr3:73016741
|
TA | T | 10 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+18584delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016741 | ||||||
| chr3:73016742
|
A | T | 197 | a0001c0001t0001g0213a0001c0001t0003g0107a0001c0001t0003g0108others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.116+18584A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016742 | ||||||
| chr3:73016745
|
T | A | 15 | a0001c0001t0001g0247a0001c0001t0001g0276a0001c0001t0001g0333others(12): Show | 15 | HG02572.hp1 HG02630.hp2 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+18587T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016745 | ||||||
| chr3:73016775
|
C | T | 3 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0195 | 3 | HG01243.hp1 HG01884.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.116+18617C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016775 | ||||||
| chr3:73016776
|
A | G | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+18618A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016776 | ||||||
| chr3:73016813
|
C | CT | 29 | a0001c0001t0001g0213a0001c0001t0001g0244a0001c0001t0001g0293others(26): Show | 29 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.116+18677dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | |||||
| chr3:73016813
|
C | CTT | 79 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(76): Show | 79 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.116+18676_116+1867 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | |||||
| chr3:73016813
|
C | CTTT | 10 | a0001c0002t0003g0042a0001c0002t0003g0065a0001c0002t0006g0099others(7): Show | 10 | HG00099.hp2 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+18675_116+1867 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | |||||
| chr3:73016813
|
CT | C | 7 | a0001c0001t0001g0277a0001c0001t0001g0308a0001c0001t0001g0323others(4): Show | 7 | HG02129.hp1 NA18946.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+18677delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | |||||
| chr3:73016813
|
CTTTTT | C | 77 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(74): Show | 77 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.116+18673_116+1867 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | |||||
| chr3:73016817
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+18659T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016817 | ||||||
| chr3:73016818
|
T | C | 1 | a0001c0001t0002g0310 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.116+18660T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016818 | ||||||
| chr3:73017159
|
A | G | 1 | a0001c0001t0005g0330 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.116+19001A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017159 | ||||||
| chr3:73017345
|
A | T | 1 | a0001c0001t0067g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116+19187A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017345 | ||||||
| chr3:73017346
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+19188T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017346 | ||||||
| chr3:73017357
|
G | GT | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+19200dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73017357 | |||||
| chr3:73017411
|
C | G | 1 | a0001c0002t0055g0358 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.116+19253C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017411 | ||||||
| chr3:73017715
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0225others(19): Show | 23 | HG00621.hp2 HG00639.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+19557C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017715 | ||||||
| chr3:73017888
|
C | T | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+19730C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017888 | ||||||
| chr3:73017956
|
T | G | 1 | a0002c0005t0017g0349 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.116+19798T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017956 | ||||||
| chr3:73017967
|
A | G | 105 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(102): Show | 105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+19809A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017967 | ||||||
| chr3:73018023
|
C | T | 1 | a0001c0001t0004g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.116+19865C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018023 | ||||||
| chr3:73018066
|
A | T | 1 | a0001c0001t0036g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.116+19908A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018066 | ||||||
| chr3:73018172
|
T | A | 1 | a0001c0002t0010g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.116+20014T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018172 | ||||||
| chr3:73018187
|
C | A | 1 | a0001c0001t0004g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.116+20029C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018187 | ||||||
| chr3:73018201
|
C | T | 1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+20043C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018201 | ||||||
| chr3:73018317
|
C | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+20159C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018317 | ||||||
| chr3:73018357
|
C | T | 1 | a0001c0001t0068g0336 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.116+20199C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018357 | ||||||
| chr3:73018407
|
C | CGTTAT | 56 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(53): Show | 57 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.116+20290_116+2029 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | |||||
| chr3:73018407
|
C | CGTTATGT others(3): Show |
56 | a0001c0001t0001g0002a0001c0001t0001g0225a0001c0001t0001g0230others(53): Show | 57 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.116+20285_116+2029 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | |||||
| chr3:73018407
|
C | CGTTATGT others(8): Show |
43 | a0001c0001t0001g0213a0001c0001t0001g0235a0001c0001t0001g0250others(40): Show | 43 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.116+20280_116+2029 others(19): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | |||||
| chr3:73018407
|
C | CGTTATGT others(13): Show |
7 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0344others(4): Show | 7 | HG02451.hp2 NA18948.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+20275_116+2029 others(24): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | |||||
| chr3:73018407
|
C | CGTTATGT others(77): Show |
3 | a0001c0001t0004g0159a0001c0001t0004g0163a0001c0001t0004g0178 | 3 | HG00735.hp2 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.116+20292_116+2029 others(88): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | |||||
| chr3:73018407
|
CGTTATGT others(3): Show |
C | 1 | a0001c0001t0001g0308 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.116+20285_116+2029 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | |||||
| chr3:73018408
|
G | GTTATGTT others(66): Show |
1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+20292_116+2029 others(77): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018408 | |||||
| chr3:73018408
|
G | GTTATGTT others(72): Show |
2 | a0001c0001t0003g0128a0001c0001t0004g0158 | 2 | HG01975.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.116+20292_116+2029 others(83): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018408 | |||||
| chr3:73018448
|
GTTAT | G | 9 | a0001c0002t0003g0036a0001c0002t0003g0061a0001c0002t0003g0065others(6): Show | 9 | HG01243.hp2 HG03225.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.116+20295_116+2029 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018448 | |||||
| chr3:73018452
|
T | TG | 25 | a0001c0001t0003g0128a0001c0001t0004g0158a0001c0001t0004g0159others(22): Show | 25 | HG00735.hp2 HG01884.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATG | 34 | a0001c0001t0018g0194a0001c0001t0018g0195a0001c0002t0003g0024others(31): Show | 34 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(4): Show |
24 | a0001c0001t0018g0192a0001c0002t0003g0026a0001c0002t0003g0038others(21): Show | 24 | HG00099.hp2 HG00738.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(9): Show |
14 | a0001c0002t0003g0040a0001c0002t0003g0047a0001c0002t0003g0049others(11): Show | 14 | HG00423.hp1 HG01069.hp2 HG03710.hp2 others(11): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(14): Show |
4 | a0001c0002t0003g0031a0001c0002t0020g0069a0001c0002t0033g0093others(1): Show | 4 | HG01884.hp1 HG02976.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(25): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
1 | a0001c0001t0007g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(83): Show |
1 | a0001c0001t0004g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(93): Show |
1 | a0001c0001t0004g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(104): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(93): Show |
1 | a0001c0001t0004g0149 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(104): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(113): Show |
1 | a0001c0001t0025g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(124): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(77): Show |
1 | a0001c0001t0009g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(88): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(79): Show |
1 | a0001c0001t0004g0181 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(90): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(78): Show |
2 | a0001c0001t0008g0145a0001c0001t0008g0148 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
1 | a0001c0001t0008g0130 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(73): Show |
1 | a0001c0001t0004g0168 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
3 | a0001c0001t0004g0138a0001c0001t0008g0150a0001c0001t0024g0173 | 3 | HG02293.hp1 HG03041.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(93): Show |
2 | a0001c0001t0008g0143a0001c0001t0057g0153 | 2 | HG01109.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(104): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(103): Show |
1 | a0001c0001t0025g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(114): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(78): Show |
1 | a0001c0001t0034g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(67): Show |
1 | a0001c0001t0009g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(78): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(77): Show |
1 | a0001c0001t0003g0115 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(88): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(83): Show |
1 | a0001c0001t0004g0129 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
1 | a0001c0001t0004g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(68): Show |
1 | a0001c0001t0007g0186 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(79): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(78): Show |
2 | a0001c0001t0004g0126a0001c0001t0036g0191 | 2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(83): Show |
8 | a0001c0001t0004g0154a0001c0001t0004g0169a0001c0001t0007g0135others(5): Show | 8 | HG00140.hp1 HG00741.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
2 | a0001c0001t0007g0155a0001c0001t0008g0152 | 2 | HG02145.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(99): Show |
1 | a0001c0001t0054g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(110): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(67): Show |
3 | a0001c0001t0009g0110a0001c0001t0009g0112a0001c0001t0009g0114 | 3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(78): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(43): Show |
1 | a0001c0001t0024g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(54): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(63): Show |
1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(74): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(68): Show |
1 | a0001c0001t0026g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(79): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(83): Show |
2 | a0001c0001t0004g0131a0001c0001t0004g0164 | 2 | HG01978.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
2 | a0001c0001t0026g0184a0001c0001t0056g0185 | 2 | HG01255.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(63): Show |
2 | a0001c0001t0004g0161a0001c0001t0034g0170 | 2 | HG01081.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(74): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(68): Show |
1 | a0001c0001t0004g0139 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(79): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(73): Show |
1 | a0001c0001t0025g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(78): Show |
2 | a0001c0001t0004g0157a0001c0001t0008g0146 | 2 | HG01123.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(83): Show |
2 | a0001c0001t0035g0171a0001c0001t0035g0172 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(88): Show |
2 | a0001c0001t0008g0103a0001c0001t0024g0177 | 2 | HG02129.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(57): Show |
4 | a0001c0001t0009g0109a0001c0001t0009g0113a0001c0001t0009g0116others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(68): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTATGT others(62): Show |
1 | a0001c0001t0019g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(73): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(73): Show |
1 | a0001c0001t0058g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(78): Show |
5 | a0001c0001t0004g0132a0001c0001t0004g0165a0001c0001t0004g0166others(2): Show | 5 | HG01928.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(83): Show |
1 | a0001c0001t0004g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(88): Show |
3 | a0001c0001t0007g0182a0001c0001t0007g0188a0005c0006t0026g0175 | 3 | HG02818.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(73): Show |
1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(52): Show |
2 | a0001c0001t0003g0107a0001c0001t0019g0120 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(63): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(57): Show |
1 | a0001c0001t0019g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(68): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018452
|
T | TGTTTGTT others(62): Show |
1 | a0001c0001t0003g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(73): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | ||||||
| chr3:73018534
|
G | C | 1 | a0001c0002t0031g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.116+20376G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018534 | ||||||
| chr3:73018612
|
A | C | 15 | a0001c0001t0001g0308a0001c0001t0002g0216a0001c0001t0002g0239others(12): Show | 15 | HG00438.hp1 HG00609.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+20454A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018612 | ||||||
| chr3:73018647
|
C | G | 3 | a0001c0002t0013g0094a0001c0002t0033g0093a0001c0002t0033g0098 | 3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116+20489C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018647 | ||||||
| chr3:73018724
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0124 | 3 | HG00738.hp2 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.116+20566A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018724 | ||||||
| chr3:73018759
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0326 | 2 | NA18954.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.116+20601C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018759 | ||||||
| chr3:73018840
|
T | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+20682T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018840 | ||||||
| chr3:73018934
|
A | G | 1 | a0001c0002t0027g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.116+20776A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018934 | ||||||
| chr3:73019015
|
T | TG | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+20858dupG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73019015 | |||||
| chr3:73019054
|
C | T | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+20896C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019054 | ||||||
| chr3:73019322
|
C | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+21164C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019322 | ||||||
| chr3:73019580
|
G | T | 1 | a0001c0001t0001g0288 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.116+21422G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019580 | ||||||
| chr3:73019627
|
G | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115 | 3 | HG02055.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.116+21469G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019627 | ||||||
| chr3:73019660
|
A | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+21502A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019660 | ||||||
| chr3:73019669
|
C | T | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+21511C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019669 | ||||||
| chr3:73019778
|
G | GCT | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.116+21629_116+2163 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73019778 | |||||
| chr3:73019967
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.116+21809C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019967 | ||||||
| chr3:73020010
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0014g0334 | 2 | HG00438.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.116+21852A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020010 | ||||||
| chr3:73020227
|
G | T | 1 | a0001c0002t0037g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.116+22069G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020227 | ||||||
| chr3:73020330
|
A | G | 2 | a0001c0002t0006g0017a0001c0002t0006g0020 | 2 | NA18942.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.116+22172A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020330 | ||||||
| chr3:73020400
|
G | C | 1 | a0007c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116+22242G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020400 | ||||||
| chr3:73020514
|
C | G | 1 | a0001c0002t0003g0080 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.116+22356C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020514 | ||||||
| chr3:73020543
|
G | T | 67 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(64): Show | 67 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.116+22385G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020543 | ||||||
| chr3:73020545
|
C | T | 1 | a0001c0001t0035g0171 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116+22387C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020545 | ||||||
| chr3:73020588
|
T | A | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+22430T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020588 | ||||||
| chr3:73020672
|
T | TAAAAAAA others(3): Show |
2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+22524_116+2253 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73020672 | |||||
| chr3:73020672
|
T | TTAA | 7 | a0001c0001t0004g0142a0001c0001t0007g0189a0001c0001t0026g0160others(4): Show | 7 | HG01255.hp1 HG01952.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | ||||||
| chr3:73020672
|
T | TTAAA | 23 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(20): Show | 23 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | ||||||
| chr3:73020672
|
T | TTAAAA | 56 | a0001c0001t0003g0108a0001c0001t0003g0115a0001c0001t0004g0126others(53): Show | 56 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | ||||||
| chr3:73020672
|
T | TTAAAAA | 76 | a0001c0001t0003g0107a0001c0001t0008g0152a0001c0001t0009g0112others(73): Show | 76 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | ||||||
| chr3:73020672
|
T | TTAAAAAA | 15 | a0001c0002t0003g0036a0001c0002t0003g0082a0001c0002t0010g0008others(12): Show | 15 | HG00423.hp1 HG01192.hp1 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | ||||||
| chr3:73020672
|
T | TTAAAAAA others(1): Show |
4 | a0001c0002t0003g0088a0001c0002t0011g0033a0001c0002t0027g0030others(1): Show | 4 | HG02683.hp1 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | ||||||
| chr3:73020672
|
TA | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(82): Show | 87 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.116+22533delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73020672 | |||||
| chr3:73020691
|
A | AAAAAAAA others(3): Show |
2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+22533_116+2253 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020691 | ||||||
| chr3:73020869
|
A | G | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+22711A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020869 | ||||||
| chr3:73020907
|
G | C | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.116+22749G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020907 | ||||||
| chr3:73020948
|
A | G | 1 | a0001c0001t0025g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.116+22790A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020948 | ||||||
| chr3:73021093
|
A | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+22935A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021093 | ||||||
| chr3:73021110
|
T | G | 1 | a0001c0001t0008g0103 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.116+22952T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021110 | ||||||
| chr3:73021224
|
TA | T | 67 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(64): Show | 67 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.116+23075delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021224 | |||||
| chr3:73021232
|
AAT | A | 17 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.116+23075_116+2307 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021232 | ||||||
| chr3:73021232
|
AATTTTTT others(4): Show |
A | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+23075_116+2308 others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021232 | ||||||
| chr3:73021233
|
A | AT | 9 | a0001c0001t0001g0123a0001c0001t0001g0217a0001c0001t0001g0219others(6): Show | 9 | HG01361.hp1 HG01361.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.116+23092dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021233 | |||||
| chr3:73021233
|
A | T | 13 | a0001c0001t0002g0316a0001c0001t0004g0134a0001c0001t0004g0178others(10): Show | 13 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+23075A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021233 | ||||||
| chr3:73021250
|
T | G | 1 | a0001c0001t0007g0186 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+23092T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021250 | ||||||
| chr3:73021251
|
G | T | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+23093G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021251 | ||||||
| chr3:73021314
|
G | A | 1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+23156G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021314 | ||||||
| chr3:73021346
|
G | A | 216 | a0001c0001t0001g0213a0001c0001t0001g0333a0001c0001t0001g0340others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.116+23188G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021346 | ||||||
| chr3:73021527
|
C | T | 57 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(54): Show | 57 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.116+23369C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021527 | ||||||
| chr3:73021605
|
G | A | 1 | a0001c0003t0045g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.116+23447G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021605 | ||||||
| chr3:73021678
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+23520C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021678 | ||||||
| chr3:73021844
|
C | CTGTG | 5 | a0001c0001t0004g0129a0001c0001t0004g0131a0001c0001t0004g0132others(2): Show | 5 | HG01928.hp2 HG01934.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+23687_116+2368 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | |||||
| chr3:73021844
|
CTA | C | 15 | a0001c0001t0004g0142a0001c0001t0004g0158a0001c0001t0004g0159others(12): Show | 15 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+23690_116+2369 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | |||||
| chr3:73021844
|
CTATA | C | 3 | a0001c0001t0026g0160a0001c0001t0056g0185a0005c0006t0026g0175 | 3 | HG03130.hp2 HG04199.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.116+23688_116+2369 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | |||||
| chr3:73021844
|
CTATATG | C | 3 | a0001c0001t0025g0167a0001c0001t0025g0176a0001c0001t0025g0180 | 3 | HG02735.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.116+23688_116+2369 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | |||||
| chr3:73021846
|
A | G | 10 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(7): Show | 10 | HG01255.hp1 HG01928.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+23688A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021846 | ||||||
| chr3:73021848
|
A | ATG | 41 | a0001c0001t0001g0123a0001c0001t0001g0219a0001c0001t0001g0223others(38): Show | 41 | HG00609.hp1 HG01069.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.116+23722_116+2372 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | |||||
| chr3:73021848
|
A | ATGTG | 5 | a0001c0001t0001g0221a0001c0001t0002g0305a0001c0001t0002g0328others(2): Show | 5 | HG01433.hp2 HG04115.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+23720_116+2372 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | |||||
| chr3:73021848
|
A | ATGTGTGT others(5): Show |
2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+23712_116+2372 others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | |||||
| chr3:73021848
|
A | G | 28 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(25): Show | 28 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.116+23690A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021848 | ||||||
| chr3:73021848
|
ATG | A | 24 | a0001c0001t0001g0213a0001c0001t0001g0234a0001c0001t0001g0333others(21): Show | 24 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.116+23722_116+2372 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | |||||
| chr3:73021848
|
ATGTG | A | 22 | a0001c0001t0003g0108a0001c0001t0009g0109a0001c0001t0009g0110others(19): Show | 22 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.116+23720_116+2372 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | |||||
| chr3:73021850
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+23692G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021850 | ||||||
| chr3:73021880
|
G | A | 97 | a0001c0001t0001g0213a0001c0001t0003g0107a0001c0001t0003g0108others(94): Show | 97 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.116+23722G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021880 | ||||||
| chr3:73021880
|
G | GTA | 3 | a0001c0001t0004g0134a0001c0001t0007g0141a0001c0001t0008g0150 | 3 | HG02040.hp2 HG02293.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.116+23728_116+2372 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021880 | |||||
| chr3:73021882
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0123a0001c0001t0001g0124others(11): Show | 15 | HG00735.hp1 HG00738.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+23724A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021882 | ||||||
| chr3:73021886
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23728A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021886 | ||||||
| chr3:73021887
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23729T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021887 | ||||||
| chr3:73021888
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23730G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021888 | ||||||
| chr3:73021889
|
C | CAT | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0122others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.116+23742_116+2374 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021889 | |||||
| chr3:73021889
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23731C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021889 | ||||||
| chr3:73021900
|
A | AT | 46 | a0001c0001t0001g0232a0001c0001t0001g0258a0001c0001t0001g0277others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.116+23758dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021900 | |||||
| chr3:73021900
|
ATT | A | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+23757_116+2375 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021900 | |||||
| chr3:73021901
|
T | TA | 17 | a0001c0001t0001g0226a0001c0001t0001g0236a0001c0001t0001g0245others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.116+23743_116+2374 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021901 | ||||||
| chr3:73021901
|
T | TATA | 109 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(106): Show | 109 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.116+23743_116+2374 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021901 | ||||||
| chr3:73021901
|
T | TATATA | 4 | a0001c0001t0019g0117a0001c0001t0019g0118a0001c0001t0019g0119others(1): Show | 4 | HG02027.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+23743_116+2374 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021901 | ||||||
| chr3:73021902
|
T | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.116+23744T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021902 | ||||||
| chr3:73021903
|
T | A | 36 | a0001c0001t0001g0226a0001c0001t0001g0236a0001c0001t0001g0290others(33): Show | 36 | HG01975.hp1 HG02027.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.116+23745T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021903 | ||||||
| chr3:73021904
|
T | A | 56 | a0001c0001t0001g0213a0001c0001t0001g0288a0001c0001t0001g0342others(53): Show | 56 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.116+23746T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021904 | ||||||
| chr3:73021905
|
T | A | 10 | a0001c0001t0003g0108a0001c0001t0003g0115a0001c0001t0009g0111others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+23747T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021905 | ||||||
| chr3:73021906
|
T | A | 4 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0195others(1): Show | 4 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+23748T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021906 | ||||||
| chr3:73021923
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+23765A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021923 | ||||||
| chr3:73022062
|
A | C | 1 | a0001c0001t0034g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.116+23904A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022062 | ||||||
| chr3:73022232
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.116+24074G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022232 | ||||||
| chr3:73022245
|
C | G | 2 | a0001c0001t0001g0245a0001c0001t0014g0334 | 2 | HG00438.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.116+24087C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022245 | ||||||
| chr3:73022333
|
A | AT | 33 | a0001c0001t0004g0126a0001c0001t0004g0137a0001c0001t0004g0138others(30): Show | 33 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.116+24180dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022333 | |||||
| chr3:73022400
|
T | C | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+24242T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022400 | ||||||
| chr3:73022412
|
T | G | 1 | a0001c0001t0004g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.116+24254T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022412 | ||||||
| chr3:73022463
|
A | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+24305A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022463 | ||||||
| chr3:73022477
|
G | A | 1 | a0001c0002t0063g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.116+24319G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022477 | ||||||
| chr3:73022498
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+24340G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022498 | ||||||
| chr3:73022727
|
G | A | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.117-24459G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022727 | ||||||
| chr3:73022768
|
C | CT | 13 | a0001c0001t0001g0213a0001c0001t0001g0267a0001c0001t0016g0200others(10): Show | 13 | HG00423.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.117-24400dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022768 | |||||
| chr3:73022768
|
CT | C | 115 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0279others(112): Show | 115 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.117-24400delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022768 | |||||
| chr3:73022771
|
T | TC | 14 | a0001c0001t0004g0142a0001c0001t0004g0158a0001c0001t0004g0159others(11): Show | 14 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-24415_117-2441 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022771 | ||||||
| chr3:73022772
|
T | C | 74 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(71): Show | 74 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.117-24414T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022772 | ||||||
| chr3:73022773
|
T | C | 95 | a0001c0001t0007g0189a0001c0001t0034g0170a0001c0002t0003g0024others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.117-24413T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022773 | ||||||
| chr3:73022774
|
T | C | 2 | a0001c0002t0006g0015a0001c0002t0020g0012 | 2 | NA18965.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.117-24412T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022774 | ||||||
| chr3:73022884
|
TG | T | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-24300delG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022884 | |||||
| chr3:73023008
|
A | G | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-24178A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023008 | ||||||
| chr3:73023091
|
A | G | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.117-24095A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023091 | ||||||
| chr3:73023119
|
A | T | 1 | a0001c0001t0002g0329 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.117-24067A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023119 | ||||||
| chr3:73023170
|
C | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-24016C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023170 | ||||||
| chr3:73023171
|
T | G | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-24015T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023171 | ||||||
| chr3:73023181
|
CT | C | 184 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.117-23997delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73023181 | |||||
| chr3:73023189
|
T | G | 1 | a0001c0002t0055g0358 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.117-23997T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023189 | ||||||
| chr3:73023190
|
G | T | 1 | a0001c0002t0055g0358 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.117-23996G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023190 | ||||||
| chr3:73023213
|
C | G | 6 | a0001c0002t0013g0090a0001c0002t0013g0094a0001c0002t0030g0091others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-23973C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023213 | ||||||
| chr3:73023270
|
A | C | 1 | a0001c0001t0002g0272 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.117-23916A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023270 | ||||||
| chr3:73023294
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-23892A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023294 | ||||||
| chr3:73023296
|
T | TCTC | 185 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.117-23888_117-2388 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73023296 | |||||
| chr3:73023417
|
C | G | 1 | a0001c0001t0001g0284 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117-23769C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023417 | ||||||
| chr3:73023433
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117-23753G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023433 | ||||||
| chr3:73023475
|
A | G | 2 | a0001c0001t0009g0111a0001c0001t0009g0116 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117-23711A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023475 | ||||||
| chr3:73023551
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-23635A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023551 | ||||||
| chr3:73023912
|
C | G | 2 | a0001c0002t0003g0046a0001c0002t0003g0086 | 2 | NA18973.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.117-23274C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023912 | ||||||
| chr3:73024076
|
A | T | 2 | a0001c0001t0001g0267a0006c0008t0001g0275 | 2 | HG00423.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.117-23110A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024076 | ||||||
| chr3:73024078
|
G | T | 2 | a0001c0001t0001g0267a0006c0008t0001g0275 | 2 | HG00423.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.117-23108G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024078 | ||||||
| chr3:73024083
|
G | T | 2 | a0001c0001t0001g0267a0006c0008t0001g0275 | 2 | HG00423.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.117-23103G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024083 | ||||||
| chr3:73024188
|
A | T | 7 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(4): Show | 7 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-22998A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024188 | ||||||
| chr3:73024219
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-22967A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024219 | ||||||
| chr3:73024378
|
A | G | 19 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(16): Show | 19 | HG00735.hp2 HG01928.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.117-22808A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024378 | ||||||
| chr3:73024491
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0002g0309 | 2 | NA19005.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.117-22695T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024491 | ||||||
| chr3:73024498
|
C | T | 1 | a0001c0002t0006g0057 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.117-22688C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024498 | ||||||
| chr3:73024523
|
G | C | 1 | a0001c0002t0010g0076 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.117-22663G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024523 | ||||||
| chr3:73024552
|
A | C | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-22634A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024552 | ||||||
| chr3:73024646
|
C | A | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-22540C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024646 | ||||||
| chr3:73024728
|
A | G | 99 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-22458A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024728 | ||||||
| chr3:73024923
|
C | G | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-22263C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024923 | ||||||
| chr3:73024928
|
C | T | 5 | a0001c0001t0026g0160a0001c0001t0026g0184a0001c0001t0056g0185others(2): Show | 5 | HG01255.hp1 HG01952.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-22258C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024928 | ||||||
| chr3:73024972
|
T | C | 89 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(86): Show | 89 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.117-22214T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024972 | ||||||
| chr3:73025385
|
G | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-21801G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025385 | ||||||
| chr3:73025508
|
G | C | 99 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-21678G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025508 | ||||||
| chr3:73025591
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-21595A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025591 | ||||||
| chr3:73025612
|
A | G | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-21574A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025612 | ||||||
| chr3:73025757
|
A | G | 99 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-21429A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025757 | ||||||
| chr3:73025953
|
A | G | 14 | a0001c0001t0001g0217a0001c0001t0005g0233a0001c0001t0005g0238others(11): Show | 14 | HG00741.hp1 NA18941.hp2 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.117-21233A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025953 | ||||||
| chr3:73026202
|
C | G | 1 | a0001c0001t0002g0299 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.117-20984C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026202 | ||||||
| chr3:73026259
|
G | A | 66 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(63): Show | 66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.117-20927G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026259 | ||||||
| chr3:73026329
|
G | A | 1 | a0001c0001t0004g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.117-20857G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026329 | ||||||
| chr3:73026398
|
G | C | 1 | a0005c0006t0026g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.117-20788G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026398 | ||||||
| chr3:73026501
|
A | ATT | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-20685_117-2068 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026501 | ||||||
| chr3:73026661
|
A | G | 99 | a0001c0001t0002g0302a0001c0001t0067g0257a0001c0002t0003g0024others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-20525A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026661 | ||||||
| chr3:73026674
|
T | G | 34 | a0001c0001t0004g0126a0001c0001t0004g0134a0001c0001t0004g0137others(31): Show | 34 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.117-20512T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026674 | ||||||
| chr3:73026682
|
A | T | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-20504A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026682 | ||||||
| chr3:73026701
|
AT | A | 187 | a0001c0001t0001g0318a0001c0001t0003g0107a0001c0001t0003g0108others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-20476delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73026701 | |||||
| chr3:73026710
|
T | A | 1 | a0001c0001t0025g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117-20476T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026710 | ||||||
| chr3:73026743
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117-20443T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026743 | ||||||
| chr3:73026765
|
C | G | 1 | a0001c0001t0067g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117-20421C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026765 | ||||||
| chr3:73026827
|
A | G | 2 | a0001c0001t0002g0313a0001c0001t0068g0336 | 2 | HG02080.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.117-20359A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026827 | ||||||
| chr3:73026903
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-20283C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026903 | ||||||
| chr3:73026983
|
C | A | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-20203C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026983 | ||||||
| chr3:73027013
|
T | C | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-20173T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027013 | ||||||
| chr3:73027133
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-20053G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027133 | ||||||
| chr3:73027252
|
A | T | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-19934A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027252 | ||||||
| chr3:73027272
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.117-19914G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027272 | ||||||
| chr3:73027365
|
A | C | 4 | a0001c0001t0001g0217a0001c0001t0005g0238a0001c0001t0005g0298others(1): Show | 4 | NA18970.hp2 NA19011.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-19821A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027365 | ||||||
| chr3:73027393
|
T | C | 99 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-19793T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027393 | ||||||
| chr3:73027404
|
G | A | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-19782G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027404 | ||||||
| chr3:73027659
|
G | GGTGT | 4 | a0001c0002t0003g0073a0001c0002t0013g0096a0001c0002t0013g0097others(1): Show | 4 | HG02155.hp2 HG03225.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-19504_117-1950 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
G | GGTGTGT | 69 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0031others(66): Show | 69 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.117-19506_117-1950 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
G | GGTGTGTG others(1): Show |
18 | a0001c0002t0003g0026a0001c0002t0003g0065a0001c0002t0003g0079others(15): Show | 18 | HG00738.hp1 HG01243.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.117-19508_117-1950 others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
G | GGTGTGTG others(3): Show |
5 | a0001c0002t0013g0090a0001c0002t0013g0094a0001c0002t0015g0058others(2): Show | 5 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-19510_117-1950 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
G | GGTGTGTG others(5): Show |
1 | a0001c0002t0011g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.117-19512_117-1950 others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
GGT | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0213a0001c0001t0001g0215others(58): Show | 62 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.117-19502_117-1950 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
GGTGT | G | 87 | a0001c0001t0001g0323a0001c0001t0003g0128a0001c0001t0004g0126others(84): Show | 87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-19504_117-1950 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027659
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.117-19510_117-1950 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | |||||
| chr3:73027909
|
C | CT | 48 | a0001c0001t0001g0236a0001c0001t0001g0259a0001c0001t0003g0107others(45): Show | 48 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.117-19263dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027909 | |||||
| chr3:73027944
|
A | AT | 14 | a0001c0001t0001g0232a0001c0001t0001g0258a0001c0001t0001g0345others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-19226dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | |||||
| chr3:73027944
|
A | ATT | 91 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(88): Show | 91 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.117-19227_117-1922 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | |||||
| chr3:73027944
|
AT | A | 35 | a0001c0001t0001g0324a0001c0001t0001g0338a0001c0001t0003g0128others(32): Show | 35 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.117-19226delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | |||||
| chr3:73027944
|
ATT | A | 7 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-19227_117-1922 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | |||||
| chr3:73027970
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.117-19216G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027970 | ||||||
| chr3:73027971
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-19215G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027971 | ||||||
| chr3:73028014
|
T | C | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-19172T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028014 | ||||||
| chr3:73028028
|
A | G | 1 | a0001c0001t0017g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.117-19158A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028028 | ||||||
| chr3:73028063
|
C | G | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-19123C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028063 | ||||||
| chr3:73028118
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.117-19068G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028118 | ||||||
| chr3:73028194
|
TTGCAGTG others(7): Show |
T | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-18991_117-1897 others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028194 | ||||||
| chr3:73028196
|
G | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-18990G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028196 | ||||||
| chr3:73028256
|
CA | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(85): Show | 89 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.117-18911delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028256 | |||||
| chr3:73028256
|
CAA | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0213a0001c0001t0001g0215others(64): Show | 68 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.117-18912_117-1891 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028256 | |||||
| chr3:73028256
|
CAAA | C | 143 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(140): Show | 143 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.117-18913_117-1891 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028256 | |||||
| chr3:73028381
|
T | C | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-18805T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028381 | ||||||
| chr3:73028427
|
C | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-18759C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028427 | ||||||
| chr3:73028442
|
AGAT | A | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-18743_117-1874 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028442 | ||||||
| chr3:73028489
|
G | C | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-18697G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028489 | ||||||
| chr3:73028602
|
A | G | 1 | a0001c0002t0020g0069 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.117-18584A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028602 | ||||||
| chr3:73028648
|
C | G | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-18538C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028648 | ||||||
| chr3:73028673
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0293a0001c0001t0001g0327 | 4 | NA18747.hp1 NA18972.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-18513C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028673 | ||||||
| chr3:73028680
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-18506C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028680 | ||||||
| chr3:73028685
|
G | A | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-18501G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028685 | ||||||
| chr3:73028763
|
G | T | 1 | a0001c0001t0001g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117-18423G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028763 | ||||||
| chr3:73028788
|
T | G | 1 | a0001c0001t0025g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.117-18398T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028788 | ||||||
| chr3:73028846
|
AAGGAG | A | 10 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-18334_117-1833 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028846 | |||||
| chr3:73028876
|
A | G | 1 | a0007c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.117-18310A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028876 | ||||||
| chr3:73028881
|
T | C | 98 | a0001c0001t0024g0174a0001c0002t0003g0024a0001c0002t0003g0025others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.117-18305T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028881 | ||||||
| chr3:73028893
|
A | G | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-18293A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028893 | ||||||
| chr3:73028940
|
G | A | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-18246G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028940 | ||||||
| chr3:73028942
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(311): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.117-18244C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028942 | ||||||
| chr3:73029030
|
C | G | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117-18156C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029030 | ||||||
| chr3:73029527
|
TTGTC | T | 3 | a0001c0003t0012g0210a0001c0003t0012g0211a0001c0003t0012g0212 | 3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.117-17656_117-1765 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73029527 | |||||
| chr3:73029574
|
A | AAG | 88 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(85): Show | 88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-17611_117-1761 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73029574 | |||||
| chr3:73029608
|
A | G | 1 | a0001c0001t0038g0251 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.117-17578A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029608 | ||||||
| chr3:73029675
|
G | A | 1 | a0001c0002t0003g0046 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.117-17511G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029675 | ||||||
| chr3:73029741
|
T | G | 2 | a0001c0003t0043g0208a0001c0003t0045g0209 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-17445T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029741 | ||||||
| chr3:73029816
|
A | G | 1 | a0001c0001t0021g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117-17370A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029816 | ||||||
| chr3:73030292
|
A | G | 1 | a0001c0001t0016g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117-16894A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030292 | ||||||
| chr3:73030432
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117-16754A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030432 | ||||||
| chr3:73030596
|
G | C | 7 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(4): Show | 7 | NA18942.hp1 NA18951.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-16590G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030596 | ||||||
| chr3:73030612
|
A | AT | 33 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0235others(30): Show | 34 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.117-16559dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030612 | |||||
| chr3:73030612
|
A | ATT | 8 | a0001c0001t0025g0167a0001c0001t0025g0176a0001c0001t0026g0160others(5): Show | 8 | HG01255.hp1 HG01952.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.117-16560_117-1655 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030612 | |||||
| chr3:73030612
|
AT | A | 116 | a0001c0001t0001g0231a0001c0001t0003g0107a0001c0001t0003g0108others(113): Show | 116 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.117-16559delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030612 | |||||
| chr3:73030666
|
A | AT | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-16519dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030666 | |||||
| chr3:73030922
|
G | A | 6 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0014g0334others(3): Show | 6 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-16264G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030922 | ||||||
| chr3:73031055
|
A | G | 1 | a0001c0002t0027g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.117-16131A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031055 | ||||||
| chr3:73031180
|
G | C | 1 | a0001c0002t0011g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.117-16006G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031180 | ||||||
| chr3:73031297
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-15889T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031297 | ||||||
| chr3:73031489
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.117-15697C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031489 | ||||||
| chr3:73031553
|
GA | G | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-15626delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73031553 | |||||
| chr3:73031654
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-15532G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031654 | ||||||
| chr3:73031707
|
A | G | 1 | a0001c0002t0027g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.117-15479A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031707 | ||||||
| chr3:73031850
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0041g0269 | 2 | HG02015.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.117-15336C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031850 | ||||||
| chr3:73032005
|
A | G | 2 | a0001c0001t0008g0145a0001c0001t0008g0148 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.117-15181A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032005 | ||||||
| chr3:73032027
|
G | A | 2 | a0002c0005t0017g0348a0002c0005t0017g0349 | 2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.117-15159G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032027 | ||||||
| chr3:73032036
|
T | A | 82 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(79): Show | 82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.117-15150T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032036 | ||||||
| chr3:73032036
|
T | G | 127 | a0001c0001t0001g0213a0001c0001t0001g0279a0001c0001t0016g0106others(124): Show | 127 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.117-15150T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032036 | ||||||
| chr3:73032097
|
T | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-15089T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032097 | ||||||
| chr3:73032289
|
C | CT | 8 | a0001c0001t0018g0193a0001c0001t0018g0194a0001c0001t0034g0144others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-14884dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73032289 | |||||
| chr3:73032289
|
C | CTT | 94 | a0001c0001t0018g0192a0001c0001t0018g0195a0001c0002t0003g0024others(91): Show | 94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.117-14885_117-1488 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73032289 | |||||
| chr3:73032304
|
A | G | 1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.117-14882A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032304 | ||||||
| chr3:73032315
|
C | A | 5 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(2): Show | 5 | NA18951.hp1 NA18983.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-14871C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032315 | ||||||
| chr3:73032316
|
G | A | 1 | a0001c0001t0002g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117-14870G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032316 | ||||||
| chr3:73032395
|
TCTCCTGC others(6): Show |
T | 99 | a0001c0001t0001g0213a0001c0001t0003g0107a0001c0001t0003g0108others(96): Show | 99 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.117-14784_117-1477 others(17): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73032395 | |||||
| chr3:73032447
|
C | T | 1 | a0001c0002t0003g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.117-14739C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032447 | ||||||
| chr3:73032477
|
C | T | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117-14709C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032477 | ||||||
| chr3:73032685
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0289 | 2 | NA18947.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.117-14501A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032685 | ||||||
| chr3:73032732
|
G | T | 98 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(95): Show | 98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.117-14454G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032732 | ||||||
| chr3:73032807
|
A | G | 1 | a0001c0002t0023g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.117-14379A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032807 | ||||||
| chr3:73032826
|
T | C | 3 | a0001c0001t0001g0213a0001c0001t0021g0204a0001c0001t0021g0205 | 3 | HG02630.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.117-14360T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032826 | ||||||
| chr3:73033027
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-14159G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033027 | ||||||
| chr3:73033101
|
T | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0318 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.117-14085T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033101 | ||||||
| chr3:73033178
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-14008T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033178 | ||||||
| chr3:73033406
|
T | C | 1 | a0001c0001t0008g0103 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117-13780T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033406 | ||||||
| chr3:73033562
|
C | T | 94 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(91): Show | 94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.117-13624C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033562 | ||||||
| chr3:73033647
|
A | T | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-13539A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033647 | ||||||
| chr3:73033948
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.117-13238C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033948 | ||||||
| chr3:73034104
|
C | T | 188 | a0001c0001t0002g0314a0001c0001t0003g0107a0001c0001t0003g0108others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.117-13082C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034104 | ||||||
| chr3:73034114
|
T | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-13072T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034114 | ||||||
| chr3:73034135
|
GGTGT | G | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-13046_117-1304 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034135 | |||||
| chr3:73034377
|
G | C | 1 | a0001c0002t0023g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.117-12809G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034377 | ||||||
| chr3:73034402
|
G | A | 1 | a0001c0002t0011g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.117-12784G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034402 | ||||||
| chr3:73034749
|
A | T | 209 | a0001c0001t0001g0213a0001c0001t0002g0314a0001c0001t0003g0107others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.117-12437A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034749 | ||||||
| chr3:73034846
|
T | TA | 151 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0003g0128others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.117-12327dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034846 | |||||
| chr3:73034846
|
T | TAA | 25 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(22): Show | 25 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.117-12328_117-1232 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034846 | |||||
| chr3:73034846
|
TA | T | 17 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0244others(14): Show | 17 | HG00423.hp2 HG00597.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.117-12327delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034846 | |||||
| chr3:73035028
|
A | C | 5 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0223others(2): Show | 5 | HG01346.hp2 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-12158A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035028 | ||||||
| chr3:73035125
|
T | A | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-12061T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035125 | ||||||
| chr3:73035136
|
A | G | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-12050A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035136 | ||||||
| chr3:73035172
|
T | C | 3 | a0001c0001t0005g0006a0001c0001t0014g0004a0001c0001t0014g0007 | 3 | HG01109.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.117-12014T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035172 | ||||||
| chr3:73035305
|
T | G | 1 | a0001c0001t0009g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117-11881T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035305 | ||||||
| chr3:73035420
|
T | C | 1 | a0001c0002t0013g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.117-11766T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035420 | ||||||
| chr3:73035490
|
C | G | 3 | a0001c0002t0013g0094a0001c0002t0033g0093a0001c0002t0033g0098 | 3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.117-11696C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035490 | ||||||
| chr3:73035559
|
A | G | 1 | a0001c0002t0010g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.117-11627A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035559 | ||||||
| chr3:73035782
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.117-11404C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035782 | ||||||
| chr3:73035945
|
A | G | 2 | a0001c0001t0016g0106a0001c0001t0016g0201 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.117-11241A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035945 | ||||||
| chr3:73036407
|
C | T | 3 | a0001c0002t0013g0094a0001c0002t0033g0093a0001c0002t0033g0098 | 3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.117-10779C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036407 | ||||||
| chr3:73036471
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-10715A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036471 | ||||||
| chr3:73036835
|
A | G | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-10351A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036835 | ||||||
| chr3:73036860
|
A | G | 1 | a0001c0002t0003g0036 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.117-10326A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036860 | ||||||
| chr3:73036872
|
ATTG | A | 141 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(138): Show | 141 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.117-10311_117-1030 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73036872 | |||||
| chr3:73036972
|
T | C | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117-10214T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036972 | ||||||
| chr3:73036996
|
C | T | 1 | a0001c0001t0002g0313 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.117-10190C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036996 | ||||||
| chr3:73037014
|
A | G | 11 | a0001c0001t0001g0213a0001c0001t0016g0106a0001c0001t0016g0200others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.117-10172A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037014 | ||||||
| chr3:73037120
|
AT | A | 4 | a0001c0001t0002g0302a0001c0001t0002g0307a0001c0002t0013g0096others(1): Show | 4 | HG02015.hp2 HG03225.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-10058delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73037120 | |||||
| chr3:73037128
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.117-10058T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037128 | ||||||
| chr3:73037240
|
A | C | 3 | a0001c0001t0019g0117a0001c0001t0019g0118a0001c0001t0019g0119 | 3 | HG02572.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.117-9946A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037240 | ||||||
| chr3:73037327
|
A | G | 1 | a0001c0002t0020g0055 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.117-9859A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037327 | ||||||
| chr3:73037352
|
T | C | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-9834T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037352 | ||||||
| chr3:73037442
|
T | C | 1 | a0001c0001t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.117-9744T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037442 | ||||||
| chr3:73037456
|
C | G | 40 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(37): Show | 40 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.117-9730C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037456 | ||||||
| chr3:73037890
|
TTTTG | T | 8 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(5): Show | 8 | NA18942.hp1 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-9292_117-9289d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73037890 | |||||
| chr3:73037987
|
T | C | 2 | a0001c0002t0030g0091a0001c0002t0030g0092 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.117-9199T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037987 | ||||||
| chr3:73038238
|
A | G | 141 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(138): Show | 141 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.117-8948A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038238 | ||||||
| chr3:73038285
|
A | G | 1 | a0001c0002t0052g0071 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.117-8901A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038285 | ||||||
| chr3:73038292
|
T | C | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-8894T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038292 | ||||||
| chr3:73038345
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-8841A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038345 | ||||||
| chr3:73038469
|
C | T | 1 | a0001c0003t0048g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117-8717C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038469 | ||||||
| chr3:73038476
|
A | G | 2 | a0001c0001t0002g0271a0001c0001t0002g0274 | 2 | NA18971.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.117-8710A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038476 | ||||||
| chr3:73038684
|
G | A | 125 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(122): Show | 125 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.117-8502G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038684 | ||||||
| chr3:73039021
|
C | A | 2 | a0001c0001t0018g0192a0001c0001t0018g0195 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.117-8165C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039021 | ||||||
| chr3:73039288
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117-7898C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039288 | ||||||
| chr3:73039331
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-7855T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039331 | ||||||
| chr3:73039337
|
G | A | 141 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(138): Show | 141 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.117-7849G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039337 | ||||||
| chr3:73039408
|
C | T | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-7778C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039408 | ||||||
| chr3:73039481
|
G | A | 92 | a0001c0001t0004g0126a0001c0001t0004g0134a0001c0001t0004g0137others(89): Show | 92 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.117-7705G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039481 | ||||||
| chr3:73039539
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-7647G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039539 | ||||||
| chr3:73039554
|
G | C | 3 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0195 | 3 | HG01243.hp1 HG01884.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.117-7632G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039554 | ||||||
| chr3:73039598
|
T | G | 1 | a0001c0002t0037g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.117-7588T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039598 | ||||||
| chr3:73039692
|
G | A | 4 | a0001c0001t0008g0150a0001c0001t0008g0151a0001c0001t0008g0152others(1): Show | 4 | HG00741.hp2 HG01109.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-7494G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039692 | ||||||
| chr3:73039713
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-7473G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039713 | ||||||
| chr3:73039823
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.117-7363C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039823 | ||||||
| chr3:73039828
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-7358A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039828 | ||||||
| chr3:73039977
|
C | G | 1 | a0001c0001t0001g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117-7209C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039977 | ||||||
| chr3:73040032
|
A | G | 1 | a0001c0002t0049g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.117-7154A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040032 | ||||||
| chr3:73040351
|
C | T | 40 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(37): Show | 40 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.117-6835C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040351 | ||||||
| chr3:73040434
|
T | C | 147 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(144): Show | 147 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.117-6752T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040434 | ||||||
| chr3:73040499
|
A | ATTTTTTT | 73 | a0001c0002t0003g0024a0001c0002t0003g0026a0001c0002t0003g0031others(70): Show | 73 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.117-6674_117-6668d others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73040499 | |||||
| chr3:73040499
|
A | ATTTTTTT others(1): Show |
17 | a0001c0002t0003g0025a0001c0002t0003g0042a0001c0002t0003g0046others(14): Show | 17 | HG00639.hp1 HG02080.hp2 HG02922.hp1 others(14): Show |
intron_variant | MODIFIER | c.117-6675_117-6668d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73040499 | |||||
| chr3:73040499
|
AT | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(195): Show | 200 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.117-6668delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73040499 | |||||
| chr3:73040840
|
T | A | 148 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(145): Show | 148 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.117-6346T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040840 | ||||||
| chr3:73040901
|
A | C | 60 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(57): Show | 60 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.117-6285A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040901 | ||||||
| chr3:73041017
|
A | ATTT | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-6168_117-6167i others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73041017 | |||||
| chr3:73041022
|
T | C | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-6164T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041022 | ||||||
| chr3:73041073
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-6113A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041073 | ||||||
| chr3:73041124
|
A | G | 1 | a0001c0001t0003g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.117-6062A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041124 | ||||||
| chr3:73041198
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-5988C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041198 | ||||||
| chr3:73041255
|
A | G | 1 | a0001c0001t0028g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117-5931A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041255 | ||||||
| chr3:73041311
|
G | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-5875G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041311 | ||||||
| chr3:73041449
|
A | T | 1 | a0001c0001t0054g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.117-5737A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041449 | ||||||
| chr3:73041580
|
C | A | 5 | a0001c0001t0002g0239a0001c0001t0029g0306a0001c0001t0029g0341others(2): Show | 5 | HG00438.hp1 NA18747.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-5606C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041580 | ||||||
| chr3:73041736
|
TTAG | T | 4 | a0001c0001t0025g0167a0001c0001t0025g0176a0001c0001t0025g0180others(1): Show | 4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-5446_117-5444d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73041736 | |||||
| chr3:73041857
|
A | C | 149 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(146): Show | 149 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(146): Show |
intron_variant | MODIFIER | c.117-5329A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041857 | ||||||
| chr3:73041974
|
T | C | 1 | a0001c0002t0015g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.117-5212T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041974 | ||||||
| chr3:73042130
|
T | C | 1 | a0001c0002t0019g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117-5056T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042130 | ||||||
| chr3:73042176
|
T | G | 2 | a0001c0003t0043g0208a0001c0003t0045g0209 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-5010T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042176 | ||||||
| chr3:73042242
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-4944G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042242 | ||||||
| chr3:73042275
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-4911G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042275 | ||||||
| chr3:73042281
|
A | G | 1 | a0001c0002t0003g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.117-4905A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042281 | ||||||
| chr3:73042296
|
T | G | 97 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-4890T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042296 | ||||||
| chr3:73042335
|
C | T | 1 | a0001c0001t0018g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.117-4851C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042335 | ||||||
| chr3:73042361
|
C | CT | 9 | a0001c0002t0006g0015a0001c0002t0006g0022a0001c0002t0013g0090others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-4804dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | |||||
| chr3:73042361
|
CT | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(230): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.117-4804delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | |||||
| chr3:73042361
|
CTT | C | 56 | a0001c0001t0001g0213a0001c0001t0001g0318a0001c0001t0003g0128others(53): Show | 56 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.117-4805_117-4804d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | |||||
| chr3:73042361
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-4811_117-4804d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | |||||
| chr3:73042395
|
C | T | 2 | a0001c0001t0008g0145a0001c0001t0008g0148 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.117-4791C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042395 | ||||||
| chr3:73042426
|
G | A | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.117-4760G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042426 | ||||||
| chr3:73042686
|
A | C | 147 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(144): Show | 147 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.117-4500A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042686 | ||||||
| chr3:73042766
|
C | T | 4 | a0001c0003t0012g0352a0001c0003t0012g0353a0001c0003t0012g0354others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-4420C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042766 | ||||||
| chr3:73042958
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-4228A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042958 | ||||||
| chr3:73043102
|
T | TAGTG | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-4084_117-4083i others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043102 | ||||||
| chr3:73043206
|
G | A | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-3980G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043206 | ||||||
| chr3:73043300
|
G | GAAATT | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-3882_117-3878d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73043300 | |||||
| chr3:73043361
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.117-3825G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043361 | ||||||
| chr3:73043362
|
G | A | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.117-3824G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043362 | ||||||
| chr3:73043498
|
C | A | 1 | a0001c0001t0001g0345 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117-3688C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043498 | ||||||
| chr3:73043587
|
A | G | 2 | a0001c0001t0001g0333a0001c0001t0001g0340 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.117-3599A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043587 | ||||||
| chr3:73043636
|
A | T | 1 | a0001c0002t0013g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-3550A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043636 | ||||||
| chr3:73043643
|
G | T | 1 | a0001c0001t0018g0194 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.117-3543G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043643 | ||||||
| chr3:73043786
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-3400T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043786 | ||||||
| chr3:73043790
|
T | G | 210 | a0001c0001t0001g0213a0001c0001t0002g0316a0001c0001t0003g0107others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.117-3396T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043790 | ||||||
| chr3:73043837
|
C | G | 5 | a0001c0001t0005g0006a0001c0001t0014g0003a0001c0001t0014g0004others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-3349C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043837 | ||||||
| chr3:73043845
|
A | G | 2 | a0001c0001t0009g0109a0001c0001t0009g0112 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.117-3341A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043845 | ||||||
| chr3:73043961
|
G | C | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-3225G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043961 | ||||||
| chr3:73044220
|
T | TTTG | 167 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.117-2945_117-2943d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73044220 | |||||
| chr3:73044220
|
T | TTTGTTG | 9 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(6): Show | 9 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-2948_117-2943d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73044220 | |||||
| chr3:73044235
|
G | T | 10 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-2951G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044235 | ||||||
| chr3:73044337
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.117-2849C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044337 | ||||||
| chr3:73044418
|
C | T | 6 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0014g0334others(3): Show | 6 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-2768C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044418 | ||||||
| chr3:73044527
|
A | G | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.117-2659A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044527 | ||||||
| chr3:73044568
|
G | A | 181 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.117-2618G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044568 | ||||||
| chr3:73044570
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.117-2616A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044570 | ||||||
| chr3:73044582
|
T | G | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-2604T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044582 | ||||||
| chr3:73044598
|
C | G | 1 | a0001c0002t0053g0218 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.117-2588C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044598 | ||||||
| chr3:73044639
|
GT | G | 10 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-2541delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73044639 | |||||
| chr3:73044862
|
A | T | 1 | a0001c0002t0013g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-2324A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044862 | ||||||
| chr3:73044871
|
T | G | 150 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(147): Show | 150 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(147): Show |
intron_variant | MODIFIER | c.117-2315T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044871 | ||||||
| chr3:73044896
|
G | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-2290G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044896 | ||||||
| chr3:73044907
|
C | T | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117-2279C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044907 | ||||||
| chr3:73045047
|
C | G | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117-2139C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045047 | ||||||
| chr3:73045086
|
T | G | 2 | a0001c0001t0008g0145a0001c0001t0008g0148 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.117-2100T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045086 | ||||||
| chr3:73045111
|
G | T | 1 | a0001c0001t0002g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117-2075G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045111 | ||||||
| chr3:73045193
|
G | A | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-1993G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045193 | ||||||
| chr3:73045255
|
G | A | 1 | a0001c0001t0065g0295 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.117-1931G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045255 | ||||||
| chr3:73045295
|
A | G | 1 | a0001c0001t0041g0269 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.117-1891A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045295 | ||||||
| chr3:73045451
|
T | C | 5 | a0001c0001t0024g0173a0001c0001t0024g0174a0001c0001t0024g0177others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-1735T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045451 | ||||||
| chr3:73045526
|
A | AT | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(90): Show | 95 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.117-1644dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | |||||
| chr3:73045526
|
A | ATT | 142 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(139): Show | 142 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.117-1645_117-1644d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | |||||
| chr3:73045526
|
A | ATTTTTTT | 27 | a0001c0002t0006g0057a0001c0002t0006g0099a0001c0002t0006g0105others(24): Show | 27 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.117-1650_117-1644d others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | |||||
| chr3:73045526
|
AT | A | 9 | a0001c0001t0002g0237a0001c0002t0006g0013a0001c0002t0006g0014others(6): Show | 9 | HG01517.hp2 NA18942.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-1644delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | |||||
| chr3:73045747
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.117-1439G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045747 | ||||||
| chr3:73045749
|
A | T | 38 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(35): Show | 38 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.117-1437A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045749 | ||||||
| chr3:73045752
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.117-1434C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045752 | ||||||
| chr3:73045774
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.117-1412G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045774 | ||||||
| chr3:73045778
|
G | A | 1 | a0001c0002t0060g0052 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.117-1408G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045778 | ||||||
| chr3:73045804
|
C | T | 125 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(122): Show | 125 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.117-1382C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045804 | ||||||
| chr3:73045848
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.117-1338C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045848 | ||||||
| chr3:73045893
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-1293G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045893 | ||||||
| chr3:73045896
|
G | A | 1 | a0001c0002t0031g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.117-1290G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045896 | ||||||
| chr3:73045927
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-1259T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045927 | ||||||
| chr3:73045929
|
A | G | 1 | a0001c0001t0028g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117-1257A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045929 | ||||||
| chr3:73045948
|
C | T | 2 | a0001c0002t0003g0088a0001c0002t0003g0101 | 2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.117-1238C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045948 | ||||||
| chr3:73046031
|
A | G | 9 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0282others(6): Show | 9 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-1155A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046031 | ||||||
| chr3:73046109
|
A | G | 147 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(144): Show | 147 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.117-1077A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046109 | ||||||
| chr3:73046143
|
A | G | 1 | a0001c0001t0007g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.117-1043A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046143 | ||||||
| chr3:73046331
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-855C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046331 | ||||||
| chr3:73046363
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-823A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046363 | ||||||
| chr3:73046410
|
G | C | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-776G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046410 | ||||||
| chr3:73046416
|
G | A | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-770G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046416 | ||||||
| chr3:73046441
|
C | G | 38 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(35): Show | 38 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.117-745C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046441 | ||||||
| chr3:73046583
|
A | C | 2 | a0001c0003t0043g0208a0001c0003t0045g0209 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-603A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046583 | ||||||
| chr3:73046628
|
G | T | 1 | a0001c0002t0020g0012 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.117-558G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046628 | ||||||
| chr3:73046981
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.117-205T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046981 | ||||||
| chr3:73047047
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.117-139A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73047047 | ||||||
| chr3:73047052
|
G | A | 2 | a0001c0001t0004g0169a0001c0001t0036g0162 | 2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.117-134G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73047052 | ||||||
| chr3:73047440
|
A | ATAAT | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+85_287+86insAA others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73047440 | |||||
| chr3:73047642
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0338a0001c0010t0001g0337 | 3 | HG03098.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.287+286C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047642 | ||||||
| chr3:73047809
|
C | T | 16 | a0001c0001t0001g0326a0001c0001t0003g0107a0001c0001t0003g0108others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+453C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047809 | ||||||
| chr3:73047865
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+509C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047865 | ||||||
| chr3:73047908
|
G | A | 1 | a0001c0001t0004g0138 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.287+552G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047908 | ||||||
| chr3:73047950
|
C | T | 4 | a0001c0002t0013g0096a0001c0002t0013g0097a0003c0004t0013g0356others(1): Show | 4 | HG01891.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+594C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047950 | ||||||
| chr3:73047978
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0338 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.287+622G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047978 | ||||||
| chr3:73048130
|
C | T | 1 | a0001c0002t0003g0031 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.287+774C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048130 | ||||||
| chr3:73048381
|
C | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115 | 3 | HG02055.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.287+1025C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048381 | ||||||
| chr3:73048408
|
C | T | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+1052C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048408 | ||||||
| chr3:73048661
|
C | G | 169 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.287+1305C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048661 | ||||||
| chr3:73048693
|
G | A | 6 | a0001c0002t0013g0090a0001c0002t0013g0094a0001c0002t0030g0091others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+1337G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048693 | ||||||
| chr3:73048800
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.287+1444T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048800 | ||||||
| chr3:73048901
|
G | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+1545G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048901 | ||||||
| chr3:73048904
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.287+1548G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048904 | ||||||
| chr3:73048924
|
G | A | 1 | a0001c0001t0016g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287+1568G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048924 | ||||||
| chr3:73049096
|
G | GA | 13 | a0001c0001t0001g0223a0001c0001t0002g0102a0001c0001t0002g0299others(10): Show | 13 | HG00741.hp2 HG01123.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+1748dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73049096 | |||||
| chr3:73049144
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0258a0001c0001t0001g0344others(2): Show | 5 | HG02451.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1788C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049144 | ||||||
| chr3:73049175
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+1819G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049175 | ||||||
| chr3:73049237
|
G | A | 1 | a0001c0001t0004g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.287+1881G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049237 | ||||||
| chr3:73049240
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.287+1884T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049240 | ||||||
| chr3:73049368
|
G | A | 1 | a0003c0004t0013g0356 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.287+2012G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049368 | ||||||
| chr3:73049422
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+2066C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049422 | ||||||
| chr3:73049523
|
G | A | 2 | a0001c0002t0003g0024a0001c0002t0003g0025 | 2 | NA19065.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.287+2167G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049523 | ||||||
| chr3:73049572
|
G | C | 208 | a0001c0001t0001g0213a0001c0001t0003g0107a0001c0001t0003g0108others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.287+2216G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049572 | ||||||
| chr3:73049674
|
T | C | 1 | a0001c0001t0021g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287+2318T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049674 | ||||||
| chr3:73049724
|
G | A | 1 | a0001c0001t0017g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.287+2368G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049724 | ||||||
| chr3:73049780
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+2424T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049780 | ||||||
| chr3:73049929
|
A | G | 1 | a0001c0001t0054g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.287+2573A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049929 | ||||||
| chr3:73049995
|
C | T | 1 | a0001c0001t0054g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.287+2639C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049995 | ||||||
| chr3:73050128
|
A | G | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.287+2772A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050128 | ||||||
| chr3:73050256
|
C | T | 1 | a0001c0001t0004g0131 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.287+2900C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050256 | ||||||
| chr3:73050266
|
G | A | 1 | a0001c0002t0052g0071 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.287+2910G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050266 | ||||||
| chr3:73050421
|
CAT | C | 35 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.287+3066_287+3067d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050421 | ||||||
| chr3:73050440
|
A | G | 39 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(36): Show | 39 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.287+3084A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050440 | ||||||
| chr3:73050457
|
A | T | 148 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(145): Show | 148 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.287+3101A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050457 | ||||||
| chr3:73050459
|
A | G | 95 | a0001c0001t0004g0126a0001c0001t0004g0134a0001c0001t0004g0137others(92): Show | 95 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.287+3103A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050459 | ||||||
| chr3:73050569
|
C | G | 1 | a0001c0002t0011g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.287+3213C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050569 | ||||||
| chr3:73050654
|
A | G | 1 | a0007c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.287+3298A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050654 | ||||||
| chr3:73050701
|
C | G | 1 | a0001c0001t0002g0299 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.287+3345C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050701 | ||||||
| chr3:73050843
|
T | G | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+3487T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050843 | ||||||
| chr3:73050912
|
C | T | 3 | a0001c0001t0026g0160a0001c0001t0056g0185a0005c0006t0026g0175 | 3 | HG03130.hp2 HG04199.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.287+3556C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050912 | ||||||
| chr3:73051003
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+3647C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051003 | ||||||
| chr3:73051022
|
C | A | 1 | a0001c0001t0029g0341 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.287+3666C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051022 | ||||||
| chr3:73051049
|
C | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+3693C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051049 | ||||||
| chr3:73051110
|
T | C | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.287+3754T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051110 | ||||||
| chr3:73051310
|
C | G | 1 | a0001c0001t0004g0161 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.287+3954C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051310 | ||||||
| chr3:73051354
|
T | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+3998T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051354 | ||||||
| chr3:73051474
|
A | G | 357 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.287+4118A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051474 | ||||||
| chr3:73051539
|
T | C | 2 | a0001c0002t0003g0048a0001c0002t0003g0049 | 2 | NA18979.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.287+4183T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051539 | ||||||
| chr3:73051543
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+4187A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051543 | ||||||
| chr3:73051567
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.287+4211C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051567 | ||||||
| chr3:73051866
|
C | T | 1 | a0001c0002t0030g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.287+4510C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051866 | ||||||
| chr3:73051992
|
T | C | 1 | a0001c0001t0034g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.287+4636T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051992 | ||||||
| chr3:73051994
|
T | C | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.287+4638T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051994 | ||||||
| chr3:73052020
|
G | A | 10 | a0001c0003t0012g0210a0001c0003t0012g0211a0001c0003t0012g0212others(7): Show | 10 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+4664G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052020 | ||||||
| chr3:73052022
|
C | A | 1 | a0001c0001t0028g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.287+4666C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052022 | ||||||
| chr3:73052175
|
A | C | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.287+4819A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052175 | ||||||
| chr3:73052241
|
C | CT | 35 | a0001c0001t0009g0116a0001c0001t0034g0144a0001c0001t0036g0162others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.287+4889dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052241 | |||||
| chr3:73052241
|
C | CTT | 118 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(115): Show | 118 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.287+4888_287+4889d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052241 | |||||
| chr3:73052241
|
C | CTTT | 29 | a0001c0001t0004g0127a0001c0001t0004g0131a0001c0001t0004g0132others(26): Show | 29 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.287+4887_287+4889d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052241 | |||||
| chr3:73052246
|
C | T | 186 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+4890C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052246 | ||||||
| chr3:73052287
|
T | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+4931T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052287 | ||||||
| chr3:73052398
|
A | G | 1 | a0001c0003t0012g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.287+5042A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052398 | ||||||
| chr3:73052406
|
G | A | 7 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0282others(4): Show | 7 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+5050G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052406 | ||||||
| chr3:73052434
|
C | G | 39 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(36): Show | 39 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.287+5078C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052434 | ||||||
| chr3:73052583
|
TTTG | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+5231_287+5233d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052583 | |||||
| chr3:73052699
|
T | C | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.287+5343T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052699 | ||||||
| chr3:73052765
|
C | A | 1 | a0001c0001t0009g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+5409C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052765 | ||||||
| chr3:73052781
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287+5425A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052781 | ||||||
| chr3:73052862
|
A | G | 94 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(91): Show | 94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.287+5506A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052862 | ||||||
| chr3:73052900
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.287+5544G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052900 | ||||||
| chr3:73052990
|
C | T | 81 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(78): Show | 81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.287+5634C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052990 | ||||||
| chr3:73053061
|
T | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.287+5705T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053061 | ||||||
| chr3:73053081
|
C | T | 1 | a0001c0002t0027g0077 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.287+5725C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053081 | ||||||
| chr3:73053091
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.287+5735T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053091 | ||||||
| chr3:73053198
|
G | A | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.288-5839G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053198 | ||||||
| chr3:73053282
|
C | G | 1 | a0001c0002t0003g0061 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.288-5755C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053282 | ||||||
| chr3:73053318
|
G | A | 1 | a0004c0007t0003g0010 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.288-5719G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053318 | ||||||
| chr3:73053324
|
C | T | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-5713C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053324 | ||||||
| chr3:73053415
|
T | G | 2 | a0001c0003t0043g0208a0001c0003t0045g0209 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.288-5622T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053415 | ||||||
| chr3:73053574
|
A | G | 31 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(28): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.288-5463A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053574 | ||||||
| chr3:73053691
|
T | C | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-5346T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053691 | ||||||
| chr3:73053787
|
T | G | 5 | a0001c0001t0024g0173a0001c0001t0024g0174a0001c0001t0024g0177others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-5250T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053787 | ||||||
| chr3:73053801
|
C | T | 7 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(4): Show | 7 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-5236C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053801 | ||||||
| chr3:73053908
|
C | CA | 19 | a0001c0001t0001g0213a0001c0001t0001g0226a0001c0001t0001g0268others(16): Show | 19 | HG01109.hp2 HG02280.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.288-5113dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | |||||
| chr3:73053908
|
C | CAA | 54 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(51): Show | 54 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.288-5114_288-5113d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | |||||
| chr3:73053908
|
C | CAAA | 7 | a0001c0001t0007g0189a0001c0001t0018g0195a0001c0001t0051g0198others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-5115_288-5113d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | |||||
| chr3:73053908
|
C | CAAAA | 105 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(102): Show | 105 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.288-5116_288-5113d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | |||||
| chr3:73053908
|
C | CAAAAA | 20 | a0001c0001t0004g0126a0001c0001t0004g0138a0001c0001t0004g0149others(17): Show | 20 | HG00423.hp1 HG01255.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.288-5117_288-5113d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | |||||
| chr3:73054018
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-5019A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054018 | ||||||
| chr3:73054038
|
A | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-4999A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054038 | ||||||
| chr3:73054070
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.288-4967A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054070 | ||||||
| chr3:73054169
|
C | T | 2 | a0001c0002t0003g0048a0001c0002t0003g0049 | 2 | NA18979.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.288-4868C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054169 | ||||||
| chr3:73054206
|
C | T | 1 | a0001c0002t0003g0068 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.288-4831C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054206 | ||||||
| chr3:73054270
|
G | C | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.288-4767G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054270 | ||||||
| chr3:73054282
|
C | G | 1 | a0001c0002t0011g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.288-4755C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054282 | ||||||
| chr3:73054438
|
A | G | 5 | a0001c0001t0005g0006a0001c0001t0014g0003a0001c0001t0014g0004others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-4599A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054438 | ||||||
| chr3:73054540
|
TGTG | T | 5 | a0001c0001t0016g0106a0001c0001t0016g0200a0001c0001t0016g0201others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.288-4494_288-4492d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73054540 | |||||
| chr3:73054585
|
G | A | 4 | a0001c0001t0025g0167a0001c0001t0025g0176a0001c0001t0025g0180others(1): Show | 4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.288-4452G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054585 | ||||||
| chr3:73054614
|
C | CT | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0111others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.288-4414dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73054614 | |||||
| chr3:73054759
|
T | A | 1 | a0001c0001t0009g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.288-4278T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054759 | ||||||
| chr3:73054875
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.288-4162G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054875 | ||||||
| chr3:73054890
|
A | G | 2 | a0001c0001t0018g0192a0001c0001t0018g0195 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.288-4147A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054890 | ||||||
| chr3:73054958
|
A | G | 1 | a0001c0002t0003g0042 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.288-4079A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054958 | ||||||
| chr3:73055066
|
A | G | 1 | a0001c0002t0003g0061 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.288-3971A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055066 | ||||||
| chr3:73055135
|
C | G | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-3902C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055135 | ||||||
| chr3:73055226
|
G | A | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.288-3811G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055226 | ||||||
| chr3:73055417
|
C | CGT | 23 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(20): Show | 23 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.288-3583_288-3582d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGT | 11 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0258others(8): Show | 11 | HG01109.hp2 HG01255.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.288-3585_288-3582d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGTGT | 54 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(51): Show | 55 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.288-3587_288-3582d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGTGTG others(1): Show |
29 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0219others(26): Show | 29 | HG01123.hp1 HG01361.hp2 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.288-3589_288-3582d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGTGTG others(3): Show |
34 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0001g0343others(31): Show | 34 | HG00140.hp1 HG00609.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.288-3591_288-3582d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGTGTG others(5): Show |
12 | a0001c0001t0001g0213a0001c0001t0001g0265a0001c0001t0004g0134others(9): Show | 12 | HG01517.hp1 HG02083.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.288-3593_288-3582d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGTGTG others(7): Show |
7 | a0001c0001t0001g0250a0001c0001t0003g0107a0001c0001t0007g0136others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-3595_288-3582d others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
C | CGTGTGTG others(9): Show |
1 | a0001c0001t0008g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.288-3597_288-3582d others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
CGT | C | 17 | a0001c0001t0002g0102a0001c0001t0002g0301a0001c0001t0002g0302others(14): Show | 17 | HG01123.hp2 HG01928.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.288-3583_288-3582d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
CGTGT | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0217others(54): Show | 58 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.288-3585_288-3582d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0007g0155a0001c0001t0008g0146a0001c0001t0021g0199others(1): Show | 4 | HG01099.hp2 HG02145.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.288-3589_288-3582d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
CGTGTGTG others(5): Show |
C | 11 | a0001c0002t0003g0026a0001c0002t0003g0040a0001c0002t0003g0065others(8): Show | 11 | HG00738.hp1 HG01243.hp2 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.288-3593_288-3582d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055417
|
CGTGTGTG others(7): Show |
C | 88 | a0001c0001t0002g0311a0001c0002t0003g0024a0001c0002t0003g0025others(85): Show | 88 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.288-3595_288-3582d others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | |||||
| chr3:73055463
|
T | A | 1 | a0001c0001t0035g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.288-3574T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055463 | ||||||
| chr3:73055468
|
A | G | 1 | a0001c0001t0008g0103 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.288-3569A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055468 | ||||||
| chr3:73055575
|
A | AT | 11 | a0001c0001t0001g0213a0001c0003t0012g0210a0001c0003t0012g0211others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.288-3461dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055575 | |||||
| chr3:73055667
|
C | CT | 185 | a0001c0001t0001g0124a0001c0001t0001g0324a0001c0001t0002g0242others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.288-3358dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055667 | |||||
| chr3:73055667
|
C | CTT | 7 | a0001c0001t0008g0152a0001c0001t0009g0109a0001c0001t0019g0118others(4): Show | 7 | HG00738.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-3359_288-3358d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055667 | |||||
| chr3:73055667
|
CT | C | 11 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0282others(8): Show | 11 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.288-3358delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055667 | |||||
| chr3:73055724
|
C | T | 1 | a0001c0001t0035g0171 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.288-3313C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055724 | ||||||
| chr3:73055725
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(312): Show | 317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.288-3312A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055725 | ||||||
| chr3:73055730
|
C | A | 5 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-3307C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055730 | ||||||
| chr3:73055835
|
G | C | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.288-3202G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055835 | ||||||
| chr3:73055848
|
C | A | 1 | a0001c0001t0018g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.288-3189C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055848 | ||||||
| chr3:73055910
|
G | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.288-3127G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055910 | ||||||
| chr3:73056016
|
T | C | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.288-3021T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056016 | ||||||
| chr3:73056296
|
TAC | T | 35 | a0001c0001t0004g0126a0001c0001t0004g0134a0001c0001t0004g0137others(32): Show | 35 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.288-2739_288-2738d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73056296 | |||||
| chr3:73056357
|
A | G | 1 | a0001c0001t0008g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288-2680A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056357 | ||||||
| chr3:73056447
|
C | T | 7 | a0001c0003t0012g0210a0001c0003t0012g0211a0001c0003t0012g0212others(4): Show | 7 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-2590C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056447 | ||||||
| chr3:73056491
|
G | T | 1 | a0001c0002t0037g0011 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.288-2546G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056491 | ||||||
| chr3:73056543
|
GTGT | G | 35 | a0001c0001t0004g0126a0001c0001t0004g0134a0001c0001t0004g0137others(32): Show | 35 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.288-2490_288-2488d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73056543 | |||||
| chr3:73056599
|
GCTT | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-2434_288-2432d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73056599 | |||||
| chr3:73056862
|
A | G | 95 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.288-2175A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056862 | ||||||
| chr3:73056902
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.288-2135T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056902 | ||||||
| chr3:73057135
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.288-1902A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057135 | ||||||
| chr3:73057270
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.288-1767A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057270 | ||||||
| chr3:73057309
|
G | A | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.288-1728G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057309 | ||||||
| chr3:73057355
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.288-1682C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057355 | ||||||
| chr3:73057449
|
A | G | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.288-1588A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057449 | ||||||
| chr3:73057693
|
T | G | 1 | a0001c0001t0001g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.288-1344T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057693 | ||||||
| chr3:73057860
|
G | A | 6 | a0001c0001t0001g0343a0001c0001t0005g0006a0001c0001t0014g0003others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-1177G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057860 | ||||||
| chr3:73058101
|
CTTAAAAA others(2): Show |
C | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.288-933_288-925del others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73058101 | |||||
| chr3:73058128
|
G | A | 19 | a0001c0001t0003g0128a0001c0001t0004g0127a0001c0001t0004g0129others(16): Show | 19 | HG00735.hp2 HG01928.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.288-909G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058128 | ||||||
| chr3:73058130
|
T | A | 2 | a0001c0001t0008g0145a0001c0001t0008g0148 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.288-907T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058130 | ||||||
| chr3:73058137
|
T | C | 1 | a0001c0001t0007g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.288-900T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058137 | ||||||
| chr3:73058139
|
T | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-898T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058139 | ||||||
| chr3:73058143
|
A | C | 2 | a0001c0002t0013g0096a0001c0002t0013g0097 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.288-894A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058143 | ||||||
| chr3:73058249
|
A | G | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.288-788A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058249 | ||||||
| chr3:73058275
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.288-762A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058275 | ||||||
| chr3:73058486
|
A | G | 7 | a0001c0003t0012g0210a0001c0003t0012g0211a0001c0003t0012g0212others(4): Show | 7 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-551A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058486 | ||||||
| chr3:73058492
|
G | T | 1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.288-545G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058492 | ||||||
| chr3:73058515
|
T | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0223others(4): Show | 7 | HG01346.hp2 HG01358.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-522T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058515 | ||||||
| chr3:73058516
|
A | T | 102 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(99): Show | 102 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.288-521A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058516 | ||||||
| chr3:73058583
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-454A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058583 | ||||||
| chr3:73058617
|
A | T | 1 | a0001c0002t0062g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.288-420A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058617 | ||||||
| chr3:73058712
|
G | T | 7 | a0001c0003t0012g0210a0001c0003t0012g0211a0001c0003t0012g0212others(4): Show | 7 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-325G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058712 | ||||||
| chr3:73058820
|
AAAGG | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0338a0001c0010t0001g0337 | 3 | HG03098.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.288-212_288-209del others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73058820 | |||||
| chr3:73058836
|
G | GT | 8 | a0001c0001t0001g0245a0001c0001t0001g0291a0001c0001t0001g0318others(5): Show | 8 | HG00438.hp2 HG02258.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.288-194dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73058836 | |||||
| chr3:73058941
|
G | A | 95 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.288-96G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058941 | ||||||
| chr3:73058995
|
A | G | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-42A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058995 | ||||||
| chr3:73059166
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.381+36G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059166 | ||||||
| chr3:73059275
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+145A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059275 | ||||||
| chr3:73059295
|
A | G | 1 | a0001c0001t0017g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.381+165A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059295 | ||||||
| chr3:73059384
|
G | A | 1 | a0001c0010t0001g0337 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.381+254G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059384 | ||||||
| chr3:73059517
|
C | T | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.381+387C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059517 | ||||||
| chr3:73059528
|
C | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+398C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059528 | ||||||
| chr3:73059826
|
C | T | 83 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(80): Show | 83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.381+696C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059826 | ||||||
| chr3:73059922
|
G | C | 1 | a0001c0001t0005g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.381+792G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059922 | ||||||
| chr3:73059936
|
GA | G | 184 | a0001c0001t0002g0316a0001c0001t0003g0107a0001c0001t0003g0108others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+822delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 73059936 | |||||
| chr3:73060044
|
G | T | 1 | a0001c0001t0002g0314 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.381+914G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060044 | ||||||
| chr3:73060089
|
G | A | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.382-934G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060089 | ||||||
| chr3:73060240
|
C | A | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.382-783C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060240 | ||||||
| chr3:73060267
|
C | T | 1 | a0001c0002t0049g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382-756C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060267 | ||||||
| chr3:73060305
|
G | C | 6 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-718G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060305 | ||||||
| chr3:73060306
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.382-717C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060306 | ||||||
| chr3:73060335
|
A | G | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.382-688A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060335 | ||||||
| chr3:73060593
|
TGAGTCTC | T | 142 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(139): Show | 142 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.382-429_382-423del others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060593 | ||||||
| chr3:73060685
|
A | T | 2 | a0001c0001t0004g0169a0001c0001t0036g0162 | 2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.382-338A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060685 | ||||||
| chr3:73060740
|
G | A | 46 | a0001c0001t0018g0192a0001c0001t0018g0193a0001c0001t0018g0194others(43): Show | 46 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.382-283G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060740 | ||||||
| chr3:73060799
|
GA | G | 6 | a0001c0001t0001g0252a0001c0001t0002g0322a0001c0001t0004g0164others(3): Show | 6 | HG01433.hp1 HG01891.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-214delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 73060799 | |||||
| chr3:73060829
|
T | G | 1 | a0001c0001t0007g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-194T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060829 | ||||||
| chr3:73060925
|
G | A | 187 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.382-98G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060925 | ||||||
| chr3:73061015
|
T | A | 3 | a0001c0003t0012g0210a0001c0003t0012g0211a0001c0003t0012g0212 | 3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.382-8T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73061015 | ||||||
| chr3:73061134
|
C | T | 1 | a0001c0003t0012g0353 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.419+74C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061134 | ||||||
| chr3:73061366
|
G | A | 29 | a0001c0002t0006g0013a0001c0002t0006g0014a0001c0002t0006g0015others(26): Show | 29 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.419+306G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061366 | ||||||
| chr3:73061489
|
A | G | 1 | a0001c0002t0003g0036 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.419+429A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061489 | ||||||
| chr3:73061566
|
GTT | G | 4 | a0001c0001t0025g0167a0001c0001t0025g0176a0001c0001t0025g0180others(1): Show | 4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+508_419+509del others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73061566 | |||||
| chr3:73061634
|
A | T | 1 | a0001c0001t0058g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.419+574A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061634 | ||||||
| chr3:73061746
|
C | T | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.419+686C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061746 | ||||||
| chr3:73061750
|
C | G | 3 | a0001c0002t0013g0094a0001c0002t0033g0093a0001c0002t0033g0098 | 3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.419+690C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061750 | ||||||
| chr3:73061864
|
A | G | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.419+804A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061864 | ||||||
| chr3:73061902
|
A | G | 126 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(123): Show | 126 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.419+842A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061902 | ||||||
| chr3:73061996
|
G | A | 1 | a0001c0002t0013g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.419+936G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061996 | ||||||
| chr3:73062025
|
G | A | 3 | a0001c0002t0003g0048a0001c0002t0003g0049a0001c0002t0003g0080 | 3 | NA18979.hp1 NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.419+965G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062025 | ||||||
| chr3:73062217
|
T | C | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.419+1157T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062217 | ||||||
| chr3:73062274
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.419+1214A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062274 | ||||||
| chr3:73062291
|
C | T | 2 | a0003c0004t0013g0356a0003c0004t0013g0357 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.419+1231C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062291 | ||||||
| chr3:73062330
|
C | CA | 96 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.419+1271dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73062330 | |||||
| chr3:73062349
|
G | T | 2 | a0001c0002t0003g0042a0001c0002t0010g0074 | 2 | NA19067.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.419+1289G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062349 | ||||||
| chr3:73062352
|
T | TTGG | 5 | a0001c0002t0003g0026a0001c0002t0003g0040a0001c0002t0003g0065others(2): Show | 5 | HG00738.hp1 HG01243.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.419+1293_419+1295d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73062352 | |||||
| chr3:73062399
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.420-1274A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062399 | ||||||
| chr3:73062573
|
T | G | 1 | a0001c0002t0023g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.420-1100T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062573 | ||||||
| chr3:73062596
|
C | T | 2 | a0001c0001t0002g0302a0001c0001t0067g0257 | 2 | HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.420-1077C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062596 | ||||||
| chr3:73062658
|
A | G | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.420-1015A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062658 | ||||||
| chr3:73062728
|
T | G | 4 | a0001c0001t0002g0301a0001c0001t0002g0303a0001c0001t0002g0317others(1): Show | 4 | HG01928.hp1 HG01934.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-945T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062728 | ||||||
| chr3:73062749
|
C | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0258 | 2 | HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.420-924C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062749 | ||||||
| chr3:73062822
|
A | G | 226 | a0001c0001t0001g0213a0001c0001t0001g0245a0001c0001t0001g0265others(223): Show | 226 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.420-851A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062822 | ||||||
| chr3:73062847
|
C | T | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.420-826C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062847 | ||||||
| chr3:73062977
|
C | T | 1 | a0001c0001t0051g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.420-696C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062977 | ||||||
| chr3:73063034
|
A | G | 12 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.420-639A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063034 | ||||||
| chr3:73063044
|
T | C | 4 | a0001c0001t0001g0213a0001c0001t0021g0199a0001c0001t0021g0204others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-629T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063044 | ||||||
| chr3:73063226
|
C | T | 20 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(17): Show | 20 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.420-447C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063226 | ||||||
| chr3:73063227
|
A | G | 184 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.420-446A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063227 | ||||||
| chr3:73063262
|
G | A | 2 | a0001c0002t0003g0088a0001c0002t0003g0101 | 2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.420-411G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063262 | ||||||
| chr3:73063293
|
C | G | 1 | a0001c0001t0005g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.420-380C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063293 | ||||||
| chr3:73063318
|
T | TA | 17 | a0001c0001t0001g0226a0001c0001t0001g0323a0001c0001t0001g0343others(14): Show | 17 | HG02129.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.420-333dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063318 | |||||
| chr3:73063318
|
T | TAA | 9 | a0001c0001t0001g0213a0001c0003t0012g0210a0001c0003t0012g0211others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.420-334_420-333dup others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063318 | |||||
| chr3:73063318
|
TA | T | 9 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0232others(6): Show | 9 | HG01361.hp1 HG01975.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.420-333delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063318 | |||||
| chr3:73063338
|
A | AAAAG | 96 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(93): Show | 96 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.420-333_420-332ins others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063338 | |||||
| chr3:73063338
|
A | AAAG | 71 | a0001c0001t0003g0128a0001c0001t0004g0126a0001c0001t0004g0127others(68): Show | 71 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.420-334_420-332dup others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063338 | |||||
| chr3:73063338
|
A | AAG | 11 | a0001c0001t0004g0137a0001c0001t0004g0142a0001c0001t0008g0130others(8): Show | 11 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.420-334_420-333ins others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063338 | |||||
| chr3:73063338
|
A | G | 1 | a0001c0002t0052g0071 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.420-335A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063338 | ||||||
| chr3:73063768
|
T | TA | 184 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.494+22dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 73063768 | |||||
| chr3:73063805
|
A | T | 5 | a0001c0001t0024g0173a0001c0001t0024g0174a0001c0001t0024g0177others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+58A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 6/8 | chr3 | 73063805 | ||||||
| chr3:73063823
|
A | T | 188 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.494+76A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 6/8 | chr3 | 73063823 | ||||||
| chr3:73064377
|
C | G | 184 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.638+231C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/8 | chr3 | 73064377 | ||||||
| chr3:73064577
|
G | A | 15 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0115others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.639-275G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/8 | chr3 | 73064577 | ||||||
| chr3:73064746
|
C | G | 1 | a0001c0001t0068g0336 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.639-106C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/8 | chr3 | 73064746 |