Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5528 |
| ensemblid | ENSG00000112640.16 |
| hgncid | 9312 |
| symbol | PPP2R5D |
| name | protein phosphatase 2 regulatory subunit B'delta |
| refseq_nuc | NM_006245.4 |
| refseq_prot | NP_006236.1 |
| ensembl_nuc | ENST00000485511.6 |
| ensembl_prot | ENSP00000417963.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 42984570 |
| end | 43012342 |
| strand | + |
| ver | v1.2 |
| region | chr6:42984570-43012342 |
| region5000 | chr6:42979570-43017342 |
| regionname0 | PPP2R5D_chr6_42984570_43012342 |
| regionname5000 | PPP2R5D_chr6_42979570_43017342 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1806 | 305 | 92 | 64 | 108 | 10 | 29 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | ATGCC others(1801): Show |
chr6 | 42979570 | 43017342 | ||
| a0001c0002 | 0/0 | 1806 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | ATGCC others(1801): Show |
chr6 | 42979570 | 43017342 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2973 | 280 | 77 | 57 | 107 | 10 | 27 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0002 | 0/0 | 2973 | 9 | 7 | 2 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0003 | 0/0 | 2961 | 6 | 0 | 4 | 0 | 0 | 2 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2956): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0004 | 0/0 | 2973 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0005 | 0/0 | 2973 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0006 | 0/0 | 2973 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0007 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0008 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0001t0009 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| a0001c0002t0001 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | GCAGC others(2968): Show |
chr6 | 42979570 | 43017342 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 6 | 1 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0002 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 3 | 0 | 2 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 4 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00597 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0136 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0198 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0230 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | YRI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | LWK | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | USA | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0229 | REF | REF | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0141 | REF | REF | PPP2R5D_chr6_42979570_43017342 | PPP2R5D | chr6 | 42979570 | 43017342 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43006915 | G | A | 1 | a0001c0002 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.327G>A | p.Ser109Ser | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 4/16 | 435/2973 | 327/1809 | 109/602 | chr6 | 43006915 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43011403 | T | A | 1 | a0001c0001t0005 | 2 | HG02145.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 117 | chr6 | 43011403 | ||||||
| chr6:43011559 | C | T | 1 | a0001c0001t0009 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 273 | chr6 | 43011559 | ||||||
| chr6:43011671 | T | C | 1 | a0001c0001t0007 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 385 | chr6 | 43011671 | ||||||
| chr6:43011742 | CAGAGTAG others(5): Show |
C | 1 | a0001c0001t0003 | 6 | HG01069.hp1 HG01099.hp1 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*457_*468delAGAGTA others(6): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 457 | chr6 | 43011742 | ||||||
| chr6:43012052 | A | C | 1 | a0001c0001t0002 | 9 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*766A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 766 | chr6 | 43012052 | ||||||
| chr6:43012101 | A | G | 1 | a0001c0001t0006 | 2 | HG02109.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*815A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 815 | chr6 | 43012101 | ||||||
| chr6:43012116 | C | T | 1 | a0001c0001t0004 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*830C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 830 | chr6 | 43012116 | ||||||
| chr6:43012195 | G | A | 1 | a0001c0001t0008 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 909 | chr6 | 43012195 | ||||||
| chr6:43012224 | G | T | 1 | a0001c0001t0005 | 2 | HG02145.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*938G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 16/16 | 938 | chr6 | 43012224 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:42984835 | C | G | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01891.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27+131C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42984835 | |||||||
| chr6:42984915 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27+211C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42984915 | |||||||
| chr6:42984916 | CCCCACAT others(3): Show |
C | 1 | a0001c0001t0001g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27+215_27+224delCA others(8): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 42984916 | ||||||
| chr6:42984963 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.27+259A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42984963 | |||||||
| chr6:42985048 | C | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG00735.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.27+344C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42985048 | |||||||
| chr6:42985177 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.27+473C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42985177 | |||||||
| chr6:42985653 | G | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
36 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.27+949G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42985653 | |||||||
| chr6:42985775 | C | CT | 33 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(30): Show |
39 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.27+1090dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 42985775 | ||||||
| chr6:42985775 | C | CTT | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0235 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+1089_27+1090dup others(2): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 42985775 | ||||||
| chr6:42985775 | CT | C | 13 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
13 | HG01069.hp1 HG01070.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+1090delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 42985775 | ||||||
| chr6:42985781 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+1077T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42985781 | |||||||
| chr6:42985844 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.27+1140C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42985844 | |||||||
| chr6:42985938 | C | T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+1234C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42985938 | |||||||
| chr6:42986126 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27+1422G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986126 | |||||||
| chr6:42986390 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.27+1686A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986390 | |||||||
| chr6:42986449 | T | G | 1 | a0001c0001t0001g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27+1745T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986449 | |||||||
| chr6:42986451 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.27+1747G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986451 | |||||||
| chr6:42986691 | G | A | 42 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(39): Show |
48 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.27+1987G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986691 | |||||||
| chr6:42986754 | C | T | 42 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(39): Show |
48 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.27+2050C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986754 | |||||||
| chr6:42986794 | C | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+2090C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986794 | |||||||
| chr6:42986826 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.27+2122G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42986826 | |||||||
| chr6:42986968 | G | GC | 9 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0191 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+2265dupC | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 42986968 | ||||||
| chr6:42987014 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27+2310G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987014 | |||||||
| chr6:42987138 | G | T | 14 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
14 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.27+2434G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987138 | |||||||
| chr6:42987243 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0183 a0001c0001t0001g0239 |
4 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-2368A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987243 | |||||||
| chr6:42987323 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.28-2288G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987323 | |||||||
| chr6:42987363 | C | T | 42 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(39): Show |
48 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.28-2248C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987363 | |||||||
| chr6:42987401 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.28-2210C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987401 | |||||||
| chr6:42987449 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.28-2162C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987449 | |||||||
| chr6:42987633 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.28-1978A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987633 | |||||||
| chr6:42987654 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-1957G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987654 | |||||||
| chr6:42987786 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
133 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.28-1825C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987786 | |||||||
| chr6:42987962 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.28-1649G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42987962 | |||||||
| chr6:42988011 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(82): Show |
101 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.28-1600T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42988011 | |||||||
| chr6:42988020 | GGGTTAGT others(4): Show |
G | 1 | a0001c0001t0001g0059 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.28-1590_28-1580del others(11): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42988020 | |||||||
| chr6:42988115 | A | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.28-1496A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42988115 | |||||||
| chr6:42988579 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.28-1032C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42988579 | |||||||
| chr6:42988725 | CTCCAGGA others(9): Show |
C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-885_28-870delTC others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42988725 | |||||||
| chr6:42988951 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.28-660C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42988951 | |||||||
| chr6:42989008 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(50): Show |
72 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.28-603C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989008 | |||||||
| chr6:42989117 | C | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.28-494C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989117 | |||||||
| chr6:42989130 | G | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(35): Show |
44 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.28-481G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989130 | |||||||
| chr6:42989177 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.28-434G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989177 | |||||||
| chr6:42989283 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.28-328T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989283 | |||||||
| chr6:42989291 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.28-320T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989291 | |||||||
| chr6:42989461 | C | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
10 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-150C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989461 | |||||||
| chr6:42989511 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.28-100A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 1/15 | chr6 | 42989511 | |||||||
| chr6:42989755 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | NA18973.hp2 NA18992.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.105+67G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42989755 | |||||||
| chr6:42989897 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.105+209C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42989897 | |||||||
| chr6:42989968 | CA | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+285delA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42989968 | ||||||
| chr6:42989973 | A | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | NA18980.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.105+285A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42989973 | |||||||
| chr6:42990005 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+317G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990005 | |||||||
| chr6:42990139 | G | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+451G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990139 | |||||||
| chr6:42990176 | A | T | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.105+488A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990176 | |||||||
| chr6:42990226 | C | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(35): Show |
44 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.105+538C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990226 | |||||||
| chr6:42990276 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(42): Show |
64 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.105+588G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990276 | |||||||
| chr6:42990346 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.105+658A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990346 | |||||||
| chr6:42990350 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.105+662T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990350 | |||||||
| chr6:42990512 | G | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+824G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990512 | |||||||
| chr6:42990553 | A | AG | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0198 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+865_105+866ins others(1): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990553 | |||||||
| chr6:42990699 | C | CT | 17 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0035 others(14): Show |
19 | HG02071.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+1038dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42990699 | ||||||
| chr6:42990699 | C | CTT | 37 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(34): Show |
43 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.105+1037_105+1038d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42990699 | ||||||
| chr6:42990699 | C | CTTT | 11 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0212 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.105+1036_105+1038d others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42990699 | ||||||
| chr6:42990699 | CT | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.105+1038delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42990699 | ||||||
| chr6:42990699 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.105+1029_105+1038d others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42990699 | ||||||
| chr6:42990903 | T | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.105+1215T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990903 | |||||||
| chr6:42990945 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.105+1257C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42990945 | |||||||
| chr6:42991032 | T | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1344T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42991032 | |||||||
| chr6:42991162 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(109): Show |
137 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.105+1474T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42991162 | |||||||
| chr6:42991196 | GAC | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+1513_105+1514d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42991196 | ||||||
| chr6:42991335 | A | G | 10 | a0001c0001t0001g0209 a0001c0001t0002g0052 a0001c0001t0002g0201 others(7): Show |
10 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.105+1647A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42991335 | |||||||
| chr6:42991482 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.105+1794T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42991482 | |||||||
| chr6:42991849 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.105+2161C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42991849 | |||||||
| chr6:42992028 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.105+2340T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992028 | |||||||
| chr6:42992098 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 |
3 | HG03654.hp1 HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.105+2410C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992098 | |||||||
| chr6:42992099 | GC | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0191 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.105+2414delC | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42992099 | ||||||
| chr6:42992181 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA19003.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.105+2493T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992181 | |||||||
| chr6:42992281 | G | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+2593G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992281 | |||||||
| chr6:42992311 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.105+2623G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992311 | |||||||
| chr6:42992333 | ACAGATGT others(4): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.105+2648_105+2658d others(13): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42992333 | ||||||
| chr6:42992337 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.105+2649A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992337 | |||||||
| chr6:42992348 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(43): Show |
65 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.105+2660C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992348 | |||||||
| chr6:42992715 | C | G | 1 | a0001c0001t0001g0016 | 2 | HG02056.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.105+3027C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992715 | |||||||
| chr6:42992728 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.105+3040C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992728 | |||||||
| chr6:42992779 | A | G | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+3091A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992779 | |||||||
| chr6:42992850 | A | C | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02145.hp2 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.105+3162A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992850 | |||||||
| chr6:42992912 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.105+3224G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42992912 | |||||||
| chr6:42993228 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
74 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.105+3540C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42993228 | |||||||
| chr6:42993297 | C | CA | 11 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0102 others(8): Show |
11 | HG00673.hp2 HG01081.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.105+3624dupA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42993297 | ||||||
| chr6:42993297 | CA | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(33): Show |
42 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.105+3624delA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42993297 | ||||||
| chr6:42993314 | A | T | 5 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0241 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+3626A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42993314 | |||||||
| chr6:42993326 | C | T | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+3638C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42993326 | |||||||
| chr6:42993363 | G | A | 9 | a0001c0001t0002g0052 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
9 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+3675G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42993363 | |||||||
| chr6:42993426 | G | C | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+3738G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42993426 | |||||||
| chr6:42993715 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0198 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4027A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42993715 | |||||||
| chr6:42994177 | C | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+4489C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994177 | |||||||
| chr6:42994182 | T | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.105+4494T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994182 | |||||||
| chr6:42994261 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.105+4573G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994261 | |||||||
| chr6:42994519 | G | GA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0037 others(16): Show |
27 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.105+4840dupA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42994519 | ||||||
| chr6:42994580 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.105+4892G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994580 | |||||||
| chr6:42994621 | A | ATGG | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
74 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.105+4936_105+4938d others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42994621 | ||||||
| chr6:42994684 | AATCCCAG others(6): Show |
A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0082 others(16): Show |
24 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.105+5005_105+5017d others(15): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42994684 | ||||||
| chr6:42994704 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.105+5016G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994704 | |||||||
| chr6:42994710 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(43): Show |
65 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.105+5022C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994710 | |||||||
| chr6:42994758 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.105+5070C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994758 | |||||||
| chr6:42994799 | CAAGAGCA others(22): Show |
C | 1 | a0001c0001t0001g0108 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.105+5114_105+5142d others(31): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42994799 | ||||||
| chr6:42994818 | C | CA | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(51): Show |
72 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.105+5147dupA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42994818 | ||||||
| chr6:42994894 | G | A | 1 | a0001c0001t0004g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.105+5206G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42994894 | |||||||
| chr6:42995126 | C | CT | 39 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(36): Show |
45 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.105+5459dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTT | 9 | a0001c0001t0001g0219 a0001c0001t0002g0052 a0001c0001t0002g0202 others(6): Show |
9 | HG01070.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+5457_105+5459d others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTCTTT others(4): Show |
2 | a0001c0001t0004g0175 a0001c0001t0004g0178 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.105+5441_105+5442i others(13): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTCTTT others(5): Show |
1 | a0001c0001t0004g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.105+5441_105+5442i others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0166 a0001c0001t0001g0240 |
3 | HG02922.hp1 HG03209.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.105+5448_105+5459d others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0056 others(1): Show |
10 | HG01081.hp2 HG01261.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.105+5447_105+5459d others(15): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0021 others(9): Show |
22 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.105+5446_105+5459d others(16): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(8): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0158 others(6): Show |
10 | HG01943.hp2 HG01952.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.105+5445_105+5459d others(17): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0150 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.105+5444_105+5459d others(18): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0001g0148 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+5443_105+5459d others(19): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG02572.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+5442_105+5459d others(20): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.105+5441_105+5459d others(21): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995126 | CT | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(12): Show |
15 | HG01074.hp1 HG02004.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.105+5459delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995126 | ||||||
| chr6:42995130 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG01109.hp1 HG02257.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.105+5442T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995130 | |||||||
| chr6:42995192 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.105+5504A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995192 | |||||||
| chr6:42995359 | T | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0222 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.105+5671T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995359 | |||||||
| chr6:42995433 | C | T | 48 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(45): Show |
54 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.105+5745C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995433 | |||||||
| chr6:42995504 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.105+5816G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995504 | |||||||
| chr6:42995557 | CT | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(97): Show |
125 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.105+5882delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995557 | ||||||
| chr6:42995567 | T | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
74 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.105+5879T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995567 | |||||||
| chr6:42995576 | G | A | 9 | a0001c0001t0002g0052 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
9 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+5888G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995576 | |||||||
| chr6:42995681 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+5993T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995681 | |||||||
| chr6:42995728 | CT | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.105+6051delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42995728 | ||||||
| chr6:42995746 | C | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+6058C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995746 | |||||||
| chr6:42995978 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.105+6290C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42995978 | |||||||
| chr6:42996005 | AT | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.105+6337delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42996005 | ||||||
| chr6:42996005 | ATT | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(44): Show |
66 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.105+6336_105+6337d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42996005 | ||||||
| chr6:42996086 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.105+6398C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996086 | |||||||
| chr6:42996178 | A | AAG | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.105+6491_105+6492d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42996178 | ||||||
| chr6:42996195 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.105+6507G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996195 | |||||||
| chr6:42996224 | G | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.105+6536G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996224 | |||||||
| chr6:42996370 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(30): Show |
39 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.105+6682C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996370 | |||||||
| chr6:42996391 | G | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0134 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.105+6703G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996391 | |||||||
| chr6:42996395 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.105+6707C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996395 | |||||||
| chr6:42996432 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.105+6744C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996432 | |||||||
| chr6:42996450 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.105+6762C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996450 | |||||||
| chr6:42996479 | T | A | 9 | a0001c0001t0002g0052 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
9 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+6791T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996479 | |||||||
| chr6:42996561 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0215 |
3 | HG00423.hp1 NA19003.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.105+6873C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996561 | |||||||
| chr6:42996672 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+6984C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996672 | |||||||
| chr6:42996731 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.105+7043A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42996731 | |||||||
| chr6:42997123 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.105+7435G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997123 | |||||||
| chr6:42997140 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.105+7452C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997140 | |||||||
| chr6:42997222 | C | T | 13 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(10): Show |
13 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+7534C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997222 | |||||||
| chr6:42997297 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0191 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.105+7609A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997297 | |||||||
| chr6:42997345 | A | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
34 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.105+7657A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997345 | |||||||
| chr6:42997352 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0140 |
5 | HG00140.hp1 HG01192.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+7664C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997352 | |||||||
| chr6:42997425 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.105+7737C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997425 | |||||||
| chr6:42997472 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.105+7784G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997472 | |||||||
| chr6:42997566 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0183 a0001c0001t0001g0239 |
4 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+7878A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997566 | |||||||
| chr6:42997573 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.105+7885G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997573 | |||||||
| chr6:42997655 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.105+7967G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997655 | |||||||
| chr6:42997658 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
74 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.105+7970C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997658 | |||||||
| chr6:42997768 | A | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+8080A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997768 | |||||||
| chr6:42997788 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.105+8100C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997788 | |||||||
| chr6:42997964 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.105+8276G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42997964 | |||||||
| chr6:42998011 | T | TAATATAT others(3): Show |
3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02970.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.105+8323_105+8324i others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998011 | |||||||
| chr6:42998011 | TTATTTAT others(3): Show |
T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
8 | HG01070.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8327_105+8336d others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998011 | ||||||
| chr6:42998011 | TTATTTAT others(7): Show |
T | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+8327_105+8340d others(16): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998011 | ||||||
| chr6:42998011 | TTATTTAT others(15): Show |
T | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.105+8327_105+8348d others(24): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998011 | ||||||
| chr6:42998011 | TTATTTAT others(19): Show |
T | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.105+8327_105+8352d others(28): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998011 | ||||||
| chr6:42998012 | T | A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(49): Show |
58 | HG00423.hp1 HG00609.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.105+8324T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998012 | |||||||
| chr6:42998015 | T | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
134 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.105+8327T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998015 | |||||||
| chr6:42998015 | T | TTA | 3 | a0001c0001t0001g0060 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | HG06807.hp1 NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.105+8369_105+8370d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | T | TTATA | 3 | a0001c0001t0001g0045 a0001c0001t0001g0070 a0001c0001t0001g0130 |
3 | HG01109.hp1 HG01496.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.105+8367_105+8370d others(6): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0103 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.105+8361_105+8370d others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.105+8357_105+8370d others(16): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | TTA | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0126 others(3): Show |
6 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+8369_105+8370d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | TTATA | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0065 a0001c0001t0001g0068 others(2): Show |
5 | HG01123.hp1 HG01358.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+8367_105+8370d others(6): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.105+8359_105+8370d others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | TTATATAT others(15): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.105+8349_105+8370d others(24): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998015 | TTATATAT others(17): Show |
T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0140 |
3 | HG00140.hp1 HG01192.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.105+8347_105+8370d others(26): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998015 | ||||||
| chr6:42998020 | T | A | 1 | a0001c0001t0002g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.105+8332T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998020 | |||||||
| chr6:42998022 | T | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01070.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+8334T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998022 | |||||||
| chr6:42998026 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+8338T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998026 | |||||||
| chr6:42998029 | ATATATAT others(40): Show |
A | 1 | a0001c0001t0004g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.105+8343_106-8386d others(49): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998029 | ||||||
| chr6:42998031 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.105+8345_105+8382d others(40): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998031 | ||||||
| chr6:42998031 | ATATATAT others(40): Show |
A | 2 | a0001c0001t0004g0175 a0001c0001t0004g0178 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.105+8345_106-8384d others(49): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998031 | ||||||
| chr6:42998032 | TATATATA others(18): Show |
T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0187 |
3 | HG02818.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.105+8345_105+8369d others(27): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998032 | |||||||
| chr6:42998033 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0013 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.105+8347_105+8373d others(29): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998033 | ||||||
| chr6:42998033 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.105+8347_105+8385d others(41): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998033 | ||||||
| chr6:42998034 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.105+8346T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998034 | |||||||
| chr6:42998035 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.105+8349_105+8371d others(25): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(17): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0003g0005 |
2 | HG02922.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.105+8349_105+8372d others(26): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0022 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.105+8349_105+8373d others(27): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(19): Show |
A | 2 | a0001c0001t0001g0056 a0001c0001t0005g0146 |
2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.105+8349_105+8374d others(28): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0005g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.105+8349_105+8375d others(29): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0009 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.105+8349_105+8384d others(38): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(31): Show |
A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0220 others(3): Show |
7 | HG01099.hp2 HG02683.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+8349_105+8386d others(40): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998035 | ATATATAT others(32): Show |
A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0223 others(1): Show |
4 | HG02615.hp2 HG02809.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8349_105+8387d others(41): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998035 | ||||||
| chr6:42998037 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.105+8351_105+8371d others(23): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(16): Show |
A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0211 a0001c0001t0001g0241 others(2): Show |
5 | HG00673.hp2 HG01099.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+8351_105+8373d others(25): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(17): Show |
A | 8 | a0001c0001t0001g0057 a0001c0001t0001g0150 a0001c0001t0001g0160 others(5): Show |
8 | HG01069.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8351_105+8374d others(26): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(18): Show |
A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0047 others(5): Show |
8 | HG01496.hp2 HG01952.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8351_105+8375d others(27): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(19): Show |
A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(18): Show |
33 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.105+8351_105+8376d others(28): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(20): Show |
A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG03704.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.105+8351_105+8377d others(29): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(29): Show |
A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0027 others(7): Show |
12 | HG00423.hp1 HG02015.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.105+8351_105+8386d others(38): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(31): Show |
A | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02145.hp2 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.105+8351_106-8387d others(40): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998037 | ATATATAT others(32): Show |
A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0222 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.105+8351_106-8386d others(41): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998037 | ||||||
| chr6:42998039 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.105+8351A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998039 | |||||||
| chr6:42998039 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0193 |
2 | HG02572.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.105+8353_105+8375d others(25): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998039 | ATATATAT others(17): Show |
A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0166 others(2): Show |
5 | HG01981.hp2 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+8353_105+8376d others(26): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998039 | ATATATAT others(18): Show |
A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0192 a0001c0001t0001g0197 |
3 | HG01891.hp2 HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.105+8353_105+8377d others(27): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998039 | ATATATAT others(19): Show |
A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0019 |
2 | HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.105+8353_105+8378d others(28): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998039 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.105+8353_105+8379d others(29): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998039 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0001g0009 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.105+8353_105+8387d others(37): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998039 | ATATATAT others(29): Show |
A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00609.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.105+8353_106-8387d others(38): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998039 | ||||||
| chr6:42998040 | TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.105+8353_105+8369d others(19): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998040 | |||||||
| chr6:42998041 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0209 |
2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.105+8355_105+8377d others(25): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998041 | ||||||
| chr6:42998042 | T | C | 6 | a0001c0001t0002g0052 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG00741.hp2 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+8354T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998042 | |||||||
| chr6:42998043 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.105+8357_105+8376d others(22): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998043 | ||||||
| chr6:42998044 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.105+8357_105+8369d others(15): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998044 | |||||||
| chr6:42998045 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0006g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105+8359_105+8371d others(15): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998045 | ||||||
| chr6:42998045 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.105+8359_105+8384d others(28): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998045 | ||||||
| chr6:42998046 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.105+8359_105+8369d others(13): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998046 | |||||||
| chr6:42998047 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0032 a0001c0001t0002g0052 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.105+8361_105+8371d others(13): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998047 | ||||||
| chr6:42998047 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.105+8361_105+8385d others(27): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998047 | ||||||
| chr6:42998048 | T | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02970.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.105+8360T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998048 | |||||||
| chr6:42998048 | TATATATA others(2): Show |
T | 3 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0204 |
3 | HG00741.hp2 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.105+8361_105+8369d others(11): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998048 | |||||||
| chr6:42998049 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0003g0078 a0001c0001t0006g0199 |
2 | HG01358.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.105+8363_105+8373d others(13): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998049 | ||||||
| chr6:42998049 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0007 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.105+8363_105+8376d others(16): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998049 | ||||||
| chr6:42998049 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0067 |
2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.105+8363_105+8377d others(17): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998049 | ||||||
| chr6:42998049 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105+8363_105+8379d others(19): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998049 | ||||||
| chr6:42998049 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.105+8363_105+8385d others(25): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998049 | ||||||
| chr6:42998049 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.105+8363_105+8386d others(26): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998049 | ||||||
| chr6:42998050 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.105+8362T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998050 | |||||||
| chr6:42998051 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.105+8363A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998051 | |||||||
| chr6:42998051 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.105+8365_105+8374d others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998051 | ||||||
| chr6:42998051 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.105+8365_105+8377d others(15): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998051 | ||||||
| chr6:42998052 | T | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG01070.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.105+8364T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998052 | |||||||
| chr6:42998052 | TATATA | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0076 a0001c0001t0009g0007 |
3 | HG00597.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.105+8365_105+8369d others(7): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998052 | |||||||
| chr6:42998053 | A | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0090 others(3): Show |
7 | HG00323.hp1 HG01243.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+8365A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998053 | |||||||
| chr6:42998054 | TATA | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0106 others(1): Show |
4 | HG01261.hp2 HG02965.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8367_105+8369d others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998054 | |||||||
| chr6:42998055 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.105+8368_105+8369i others(19): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998055 | ||||||
| chr6:42998055 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(9): Show |
15 | HG00323.hp1 HG00423.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.105+8367A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998055 | |||||||
| chr6:42998055 | ATAT | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(6): Show |
10 | HG00609.hp1 HG01361.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.105+8369_105+8371d others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998055 | ||||||
| chr6:42998055 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.105+8369_105+8380d others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998055 | ||||||
| chr6:42998055 | ATATTTTT others(11): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.105+8369_105+8386d others(20): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998055 | ||||||
| chr6:42998057 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0001 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.105+8370_105+8371i others(15): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998057 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.105+8370_105+8371i others(13): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998057 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.105+8370_105+8371i others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998057 | A | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(16): Show |
23 | HG00323.hp1 HG00423.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.105+8369A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998057 | |||||||
| chr6:42998057 | AT | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0063 others(9): Show |
12 | HG00544.hp1 HG00544.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.106-8371delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998057 | ATT | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
7 | HG01433.hp2 HG01952.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-8372_106-8371d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998057 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0003g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.106-8380_106-8371d others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998057 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.106-8382_106-8371d others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 42998057 | ||||||
| chr6:42998058 | T | TA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0093 others(3): Show |
6 | HG00639.hp1 HG02071.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+8370_105+8371i others(3): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998058 | |||||||
| chr6:42998058 | T | TATA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0110 a0001c0001t0001g0123 others(1): Show |
4 | HG00735.hp1 HG03225.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+8370_105+8371i others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998058 | |||||||
| chr6:42998059 | T | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
19 | HG00639.hp2 HG01070.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+8371T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998059 | |||||||
| chr6:42998060 | T | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(13): Show |
16 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.105+8372T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998060 | |||||||
| chr6:42998061 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0108 others(5): Show |
8 | HG02004.hp1 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8373T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998061 | |||||||
| chr6:42998062 | T | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0123 |
3 | HG01981.hp1 NA18971.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.105+8374T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998062 | |||||||
| chr6:42998063 | T | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8375T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998063 | |||||||
| chr6:42998064 | T | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0123 |
2 | HG01258.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.105+8376T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998064 | |||||||
| chr6:42998065 | T | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.105+8377T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998065 | |||||||
| chr6:42998069 | T | A | 1 | a0001c0001t0003g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.105+8381T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998069 | |||||||
| chr6:42998071 | T | A | 2 | a0001c0001t0001g0125 a0001c0001t0003g0088 |
2 | HG01109.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.105+8383T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998071 | |||||||
| chr6:42998097 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0125 |
2 | HG02132.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.106-8366C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998097 | |||||||
| chr6:42998101 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.106-8362G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998101 | |||||||
| chr6:42998116 | C | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.106-8347C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998116 | |||||||
| chr6:42998141 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(109): Show |
137 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.106-8322G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998141 | |||||||
| chr6:42998142 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.106-8321C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998142 | |||||||
| chr6:42998182 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02486.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-8281T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998182 | |||||||
| chr6:42998218 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.106-8245G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998218 | |||||||
| chr6:42998274 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.106-8189C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998274 | |||||||
| chr6:42998361 | C | T | 50 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(47): Show |
56 | HG00423.hp1 HG00609.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.106-8102C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998361 | |||||||
| chr6:42998439 | C | T | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-8024C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998439 | |||||||
| chr6:42998567 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.106-7896G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998567 | |||||||
| chr6:42998622 | G | T | 3 | a0001c0001t0004g0175 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.106-7841G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42998622 | |||||||
| chr6:42999126 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.106-7337G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999126 | |||||||
| chr6:42999160 | CAG | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-7302_106-7301d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999160 | |||||||
| chr6:42999362 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.106-7101A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999362 | |||||||
| chr6:42999462 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0124 |
2 | NA19004.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.106-7001A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999462 | |||||||
| chr6:42999575 | T | G | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-6888T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999575 | |||||||
| chr6:42999678 | A | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0198 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6785A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999678 | |||||||
| chr6:42999700 | G | A | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0049 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106-6763G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999700 | |||||||
| chr6:42999812 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106-6651C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999812 | |||||||
| chr6:42999831 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.106-6632G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999831 | |||||||
| chr6:42999974 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(43): Show |
65 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.106-6489C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 42999974 | |||||||
| chr6:43000001 | G | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(113): Show |
141 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.106-6462G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000001 | |||||||
| chr6:43000022 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106-6441G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000022 | |||||||
| chr6:43000029 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-6434A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000029 | |||||||
| chr6:43000080 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.106-6383C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000080 | |||||||
| chr6:43000081 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.106-6382G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000081 | |||||||
| chr6:43000117 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.106-6346G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000117 | |||||||
| chr6:43000156 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.106-6307G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000156 | |||||||
| chr6:43000225 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.106-6238C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000225 | |||||||
| chr6:43000236 | C | CT | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(18): Show |
23 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.106-6208dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT | 6 | a0001c0001t0001g0165 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-6214_106-6208d others(9): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(1): Show |
33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(30): Show |
50 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.106-6215_106-6208d others(10): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0148 others(10): Show |
15 | HG00597.hp2 HG01891.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.106-6216_106-6208d others(11): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0167 a0001c0001t0001g0192 a0001c0001t0001g0197 |
3 | HG02257.hp2 HG03579.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.106-6217_106-6208d others(12): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.106-6219_106-6208d others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0207 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.106-6222_106-6208d others(17): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(9): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0224 others(7): Show |
13 | HG00609.hp2 HG02015.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.106-6223_106-6208d others(18): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(10): Show |
9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0223 others(6): Show |
11 | HG00741.hp2 HG01099.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.106-6224_106-6208d others(19): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(11): Show |
8 | a0001c0001t0001g0053 a0001c0001t0001g0213 a0001c0001t0001g0220 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-6225_106-6208d others(20): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(12): Show |
7 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0215 others(4): Show |
8 | HG00423.hp1 HG02145.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-6226_106-6208d others(21): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(13): Show |
6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-6208_106-6207i others(22): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000236 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.106-6208_106-6207i others(23): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43000236 | ||||||
| chr6:43000350 | A | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.106-6113A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000350 | |||||||
| chr6:43000383 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.106-6080G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43000383 | |||||||
| chr6:43001214 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.106-5249A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001214 | |||||||
| chr6:43001262 | C | G | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-5201C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001262 | |||||||
| chr6:43001267 | G | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.106-5196G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001267 | |||||||
| chr6:43001434 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.106-5029C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001434 | |||||||
| chr6:43001435 | G | C | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-5028G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001435 | |||||||
| chr6:43001500 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.106-4963T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001500 | |||||||
| chr6:43001505 | A | G | 1 | a0001c0001t0001g0018 | 2 | NA18960.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.106-4958A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001505 | |||||||
| chr6:43001747 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0140 |
5 | HG00140.hp1 HG01192.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-4716C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001747 | |||||||
| chr6:43001774 | C | G | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106-4689C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001774 | |||||||
| chr6:43001835 | T | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.106-4628T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001835 | |||||||
| chr6:43001861 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.106-4602G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001861 | |||||||
| chr6:43001885 | C | CA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(48): Show |
70 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.106-4565dupA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43001885 | ||||||
| chr6:43001907 | T | C | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-4556T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001907 | |||||||
| chr6:43001935 | CA | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(95): Show |
123 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.106-4514delA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43001935 | ||||||
| chr6:43001937 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.106-4526A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001937 | |||||||
| chr6:43001939 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.106-4524A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43001939 | |||||||
| chr6:43002148 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.106-4315G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002148 | |||||||
| chr6:43002166 | C | CT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0119 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.106-4282dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43002166 | ||||||
| chr6:43002166 | CT | C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0113 others(15): Show |
19 | HG01891.hp2 HG02015.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.106-4282delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43002166 | ||||||
| chr6:43002220 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-4243A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002220 | |||||||
| chr6:43002257 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.106-4206G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002257 | |||||||
| chr6:43002265 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.106-4198G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002265 | |||||||
| chr6:43002405 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0060 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.106-4058C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002405 | |||||||
| chr6:43002452 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.106-4011C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002452 | |||||||
| chr6:43002452 | CGTGCCTG others(5): Show |
C | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-4008_106-3997d others(14): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43002452 | ||||||
| chr6:43002557 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3906C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002557 | |||||||
| chr6:43002643 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106-3820C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002643 | |||||||
| chr6:43002727 | A | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0089 a0001c0001t0001g0106 others(1): Show |
4 | HG01074.hp1 HG01261.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-3736A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002727 | |||||||
| chr6:43002769 | T | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.106-3694T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002769 | |||||||
| chr6:43002821 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.106-3642T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002821 | |||||||
| chr6:43002829 | T | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0060 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.106-3634T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002829 | |||||||
| chr6:43002864 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.106-3599G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002864 | |||||||
| chr6:43002954 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.106-3509T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43002954 | |||||||
| chr6:43003012 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
74 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.106-3451T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003012 | |||||||
| chr6:43003013 | G | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-3450G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003013 | |||||||
| chr6:43003107 | TG | T | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-3353delG | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43003107 | ||||||
| chr6:43003151 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.106-3312G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003151 | |||||||
| chr6:43003181 | G | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-3282G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003181 | |||||||
| chr6:43003587 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.106-2876C>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003587 | |||||||
| chr6:43003659 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.106-2804G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003659 | |||||||
| chr6:43003767 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-2696C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003767 | |||||||
| chr6:43003854 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106-2609C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003854 | |||||||
| chr6:43003895 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-2568C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003895 | |||||||
| chr6:43003993 | C | T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-2470C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003993 | |||||||
| chr6:43003998 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.106-2465G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43003998 | |||||||
| chr6:43004105 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0068 others(1): Show |
5 | HG00735.hp2 HG01123.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-2358G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004105 | |||||||
| chr6:43004157 | G | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2306G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004157 | |||||||
| chr6:43004164 | A | G | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-2299A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004164 | |||||||
| chr6:43004179 | G | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.106-2284G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004179 | |||||||
| chr6:43004317 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.106-2146T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004317 | |||||||
| chr6:43004506 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.106-1957A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004506 | |||||||
| chr6:43004569 | C | CT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(55): Show |
74 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.106-1876dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43004569 | ||||||
| chr6:43004569 | C | CTT | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0046 others(7): Show |
10 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.106-1877_106-1876d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43004569 | ||||||
| chr6:43004569 | C | CTTT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1878_106-1876d others(5): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43004569 | ||||||
| chr6:43004569 | CT | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(62): Show |
84 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.106-1876delT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43004569 | ||||||
| chr6:43004590 | G | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG01243.hp2 HG01255.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.106-1873G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004590 | |||||||
| chr6:43004648 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.106-1815G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004648 | |||||||
| chr6:43004650 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.106-1813C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004650 | |||||||
| chr6:43004759 | C | CT | 18 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0029 others(15): Show |
21 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.106-1690dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43004759 | ||||||
| chr6:43004764 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.106-1699T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004764 | |||||||
| chr6:43004874 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0198 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1589C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004874 | |||||||
| chr6:43004954 | T | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1509T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43004954 | |||||||
| chr6:43005066 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.106-1397T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005066 | |||||||
| chr6:43005141 | C | CT | 27 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(24): Show |
34 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.106-1306dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43005141 | ||||||
| chr6:43005234 | G | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0211 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-1229G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005234 | |||||||
| chr6:43005339 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.106-1124G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005339 | |||||||
| chr6:43005380 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.106-1083C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005380 | |||||||
| chr6:43005480 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.106-983A>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005480 | |||||||
| chr6:43005481 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG01192.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.106-982T>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005481 | |||||||
| chr6:43005567 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106-896A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005567 | |||||||
| chr6:43005626 | G | GT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0128 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.106-825dupT | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 43005626 | ||||||
| chr6:43005647 | G | A | 9 | a0001c0001t0002g0052 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
9 | HG00741.hp2 HG01070.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.106-816G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005647 | |||||||
| chr6:43005673 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.106-790G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005673 | |||||||
| chr6:43005827 | G | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG02896.hp2 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.106-636G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005827 | |||||||
| chr6:43005868 | C | G | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-595C>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005868 | |||||||
| chr6:43005873 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
74 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.106-590C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005873 | |||||||
| chr6:43005950 | T | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.106-513T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43005950 | |||||||
| chr6:43006049 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0198 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-414C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43006049 | |||||||
| chr6:43006066 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.106-397C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43006066 | |||||||
| chr6:43006097 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.106-366C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43006097 | |||||||
| chr6:43006296 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106-167G>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 2/15 | chr6 | 43006296 | |||||||
| chr6:43006767 | G | C | 4 | a0001c0001t0003g0040 a0001c0001t0003g0078 a0001c0001t0003g0086 others(1): Show |
4 | HG01069.hp1 HG01099.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+88G>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 3/15 | chr6 | 43006767 | |||||||
| chr6:43006771 | A | G | 50 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(47): Show |
56 | HG00423.hp1 HG00609.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.322+92A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 3/15 | chr6 | 43006771 | |||||||
| chr6:43007131 | CAG | C | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | NA18939.hp1 NA18939.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+22_522+23delAG | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 4/15 | chr6 | 43007131 | |||||||
| chr6:43007132 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.522+22A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 4/15 | chr6 | 43007132 | |||||||
| chr6:43007689 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.726+183A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 6/15 | chr6 | 43007689 | |||||||
| chr6:43007724 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.727-211C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 6/15 | chr6 | 43007724 | |||||||
| chr6:43007906 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(94): Show |
122 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.727-29T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 6/15 | chr6 | 43007906 | |||||||
| chr6:43008098 | CCTT | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0198 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+36_857+38delTC others(1): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr6 | 43008098 | ||||||
| chr6:43008175 | CAAGA | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
34 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.858-25_858-22delAA others(2): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 7/15 | chr6 | 43008175 | |||||||
| chr6:43008494 | T | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1026+19T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 9/15 | chr6 | 43008494 | |||||||
| chr6:43008760 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1080+14C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 10/15 | chr6 | 43008760 | |||||||
| chr6:43008807 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0122 |
2 | HG00544.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1080+61T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 10/15 | chr6 | 43008807 | |||||||
| chr6:43008814 | T | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1080+68T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 10/15 | chr6 | 43008814 | |||||||
| chr6:43008865 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1080+119T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 10/15 | chr6 | 43008865 | |||||||
| chr6:43009295 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1252-27C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 11/15 | chr6 | 43009295 | |||||||
| chr6:43009507 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1379+58A>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43009507 | |||||||
| chr6:43009535 | A | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(46): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1379+86A>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43009535 | |||||||
| chr6:43009559 | T | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0066 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1379+110T>G | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43009559 | |||||||
| chr6:43009605 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1379+156G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43009605 | |||||||
| chr6:43009941 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1379+492T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43009941 | |||||||
| chr6:43010068 | T | TA | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(44): Show |
66 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1380-390dupA | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr6 | 43010068 | ||||||
| chr6:43010090 | GAA | G | 56 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(53): Show |
62 | HG00423.hp1 HG00609.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1380-375_1380-374d others(4): Show |
PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr6 | 43010090 | ||||||
| chr6:43010271 | T | C | 5 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0241 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380-197T>C | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43010271 | |||||||
| chr6:43010330 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1380-138C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43010330 | |||||||
| chr6:43010332 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380-136G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 12/15 | chr6 | 43010332 | |||||||
| chr6:43010588 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
145 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1481+19G>A | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 13/15 | chr6 | 43010588 | |||||||
| chr6:43011086 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0163 |
3 | HG00673.hp2 HG04184.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1672-63C>T | PPP2R5D | ENSG00000112640.16 | transcript | ENST00000485511.6 | protein_coding | 15/15 | chr6 | 43011086 |