Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5571 |
| ensemblid | ENSG00000181929.13 |
| hgncid | 9385 |
| symbol | PRKAG1 |
| name | protein kinase AMP-activated non-catalytic subunit gamma 1 |
| refseq_nuc | NM_002733.5 |
| refseq_prot | NP_002724.1 |
| ensembl_nuc | ENST00000548065.7 |
| ensembl_prot | ENSP00000447433.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 49002274 |
| end | 49018776 |
| strand | - |
| ver | v1.2 |
| region | chr12:49002274-49018776 |
| region5000 | chr12:48997274-49023776 |
| regionname0 | PRKAG1_chr12_49002274_49018776 |
| regionname5000 | PRKAG1_chr12_48997274_49023776 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 331 | 311 | 82 | 46 | 142 | 11 | 28 | 104 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | METVI others(326): Show |
chr12 | 48997274 | 49023776 |
| a0002 | 0/0 | 331 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | METVI others(326): Show |
chr12 | 48997274 | 49023776 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 993 | 310 | 82 | 46 | 141 | 11 | 28 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | ATGGA others(988): Show |
chr12 | 48997274 | 49023776 | ||
| a0001c0003 | 0/0 | 993 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | ATGGA others(988): Show |
chr12 | 48997274 | 49023776 | ||
| a0002c0002 | 0/0 | 993 | 3 | 0 | 2 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | ATGGA others(988): Show |
chr12 | 48997274 | 49023776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1657 | 291 | 65 | 46 | 140 | 11 | 27 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1652): Show |
chr12 | 48997274 | 49023776 |
| a0001c0001t0002 | 0/0 | 1657 | 11 | 11 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1652): Show |
chr12 | 48997274 | 49023776 |
| a0001c0001t0003 | 0/0 | 1657 | 6 | 6 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1652): Show |
chr12 | 48997274 | 49023776 |
| a0001c0001t0004 | 0/0 | 1687 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1682): Show |
chr12 | 48997274 | 49023776 |
| a0001c0001t0005 | 0/0 | 1657 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1652): Show |
chr12 | 48997274 | 49023776 |
| a0001c0003t0001 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1652): Show |
chr12 | 48997274 | 49023776 |
| a0002c0002t0001 | 0/0 | 1657 | 3 | 0 | 2 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | CCTAA others(1652): Show |
chr12 | 48997274 | 49023776 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 25 | 4 | 6 | 13 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 3 | 9 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0003 | 0/0 | 12 | 1 | 1 | 10 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0004 | 0/0 | 12 | 1 | 0 | 11 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 3 | 6 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0008 | 0/0 | 7 | 1 | 3 | 1 | 0 | 2 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0009 | 0/0 | 7 | 1 | 2 | 0 | 0 | 4 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0010 | 0/0 | 7 | 5 | 1 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0015 | 0/1 | 5 | 1 | 3 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0067 | EUR | GBR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | USA | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0015 | REF | REF | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | PRKAG1_chr12_48997274_49023776 | PRKAG1 | chr12 | 48997274 | 49023776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49005349 | G | C | 1 | a0002 | 3 | HG00099.hp2 HG01243.hp1 HG01243.hp2 |
missense_variant | MODERATE | c.266C>G | p.Thr89Ser | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 5/12 | 302/1657 | 266/996 | 89/331 | chr12 | 49005349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49005752 | C | T | 1 | a0001c0003 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.159G>A | p.Thr53Thr | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 3/12 | 195/1657 | 159/996 | 53/331 | chr12 | 49005752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49002545 | A | AGGGCCAA others(23): Show |
1 | a0001c0001t0004 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*324_*353dupCCTCAC others(24): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 12/12 | 353 | chr12 | 49002545 | ||||||
| chr12:49002565 | G | A | 1 | a0001c0001t0002 | 11 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*334C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 12/12 | 334 | chr12 | 49002565 | ||||||
| chr12:49002700 | T | C | 1 | a0001c0001t0005 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 12/12 | 199 | chr12 | 49002700 | ||||||
| chr12:49002747 | C | G | 1 | a0001c0001t0003 | 6 | HG02257.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*152G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 12/12 | 152 | chr12 | 49002747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49003086 | C | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0085 |
3 | HG02886.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.888+58G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 11/11 | chr12 | 49003086 | |||||||
| chr12:49003508 | G | GC | 13 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0063 others(10): Show |
17 | HG01074.hp2 HG01106.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.741+49dupG | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 10/11 | chr12 | 49003508 | |||||||
| chr12:49003508 | GC | G | 40 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0022 others(37): Show |
55 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.741+49delG | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 10/11 | chr12 | 49003508 | |||||||
| chr12:49003510 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.741+48G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 10/11 | chr12 | 49003510 | |||||||
| chr12:49003516 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.741+42G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 10/11 | chr12 | 49003516 | |||||||
| chr12:49003518 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.741+40G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 10/11 | chr12 | 49003518 | |||||||
| chr12:49003683 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.703+74C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 9/11 | chr12 | 49003683 | |||||||
| chr12:49003940 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.538-18T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 8/11 | chr12 | 49003940 | |||||||
| chr12:49004093 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.538-171G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 8/11 | chr12 | 49004093 | |||||||
| chr12:49004230 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.537+277A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 8/11 | chr12 | 49004230 | |||||||
| chr12:49004806 | A | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0086 others(9): Show |
14 | HG02451.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.410+158T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004806 | |||||||
| chr12:49004813 | C | CTG | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0019 others(9): Show |
39 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.410+149_410+150dup others(2): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | CTGTG | 20 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(17): Show |
42 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.410+147_410+150dup others(4): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | CTGTGTG | 19 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0029 others(16): Show |
34 | HG00733.hp1 HG01261.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.410+145_410+150dup others(6): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | CTGTGTGT others(1): Show |
15 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0036 others(12): Show |
24 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.410+143_410+150dup others(8): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | CTGTGTGT others(3): Show |
10 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0033 others(7): Show |
19 | HG01109.hp1 HG02015.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+141_410+150dup others(10): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | CTGTGTGT others(5): Show |
4 | a0001c0001t0001g0062 a0001c0001t0001g0073 a0001c0001t0001g0079 others(1): Show |
4 | HG03927.hp2 NA18974.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+139_410+150dup others(12): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.410+137_410+150dup others(14): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.410+151G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | CTG | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(15): Show |
28 | HG00558.hp2 HG01071.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.410+149_410+150del others(2): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | CTGTG | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(7): Show |
27 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+147_410+150del others(4): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | CTGTGTG | C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0034 others(13): Show |
23 | HG00099.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.410+145_410+150del others(6): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | CTGTGTGT others(1): Show |
C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
17 | HG00099.hp1 HG01167.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.410+143_410+150del others(8): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.410+141_410+150del others(10): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004813 | CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0002g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.410+133_410+150del others(18): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004813 | |||||||
| chr12:49004821 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.410+143C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004821 | |||||||
| chr12:49004823 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.410+141C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004823 | |||||||
| chr12:49004861 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.410+103C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004861 | |||||||
| chr12:49004896 | T | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0003g0018 others(3): Show |
8 | HG02257.hp1 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.410+68A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 7/11 | chr12 | 49004896 | |||||||
| chr12:49005079 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
136 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.355+41C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 6/11 | chr12 | 49005079 | |||||||
| chr12:49005180 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310-15T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 5/11 | chr12 | 49005180 | |||||||
| chr12:49005604 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.169-61C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 3/11 | chr12 | 49005604 | |||||||
| chr12:49005946 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.59-94T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49005946 | |||||||
| chr12:49005980 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-128A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49005980 | |||||||
| chr12:49006376 | A | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0139 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-524T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49006376 | |||||||
| chr12:49006419 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.59-567A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49006419 | |||||||
| chr12:49006432 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.59-580T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49006432 | |||||||
| chr12:49006692 | G | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0045 |
4 | HG01167.hp2 HG01169.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-840C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49006692 | |||||||
| chr12:49006722 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
156 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.59-870T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49006722 | |||||||
| chr12:49006977 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.59-1125A>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49006977 | |||||||
| chr12:49007011 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.59-1159G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007011 | |||||||
| chr12:49007236 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.59-1384C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007236 | |||||||
| chr12:49007267 | ACAGAGTG others(7): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59-1429_59-1416del others(14): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007267 | |||||||
| chr12:49007286 | CA | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0042 others(5): Show |
10 | HG01346.hp2 HG02896.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-1435delT | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007286 | |||||||
| chr12:49007286 | CAA | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
144 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.59-1436_59-1435del others(2): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007286 | |||||||
| chr12:49007380 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59-1528T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007380 | |||||||
| chr12:49007518 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0045 |
4 | HG01167.hp2 HG01169.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-1666T>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007518 | |||||||
| chr12:49007696 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59-1844T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007696 | |||||||
| chr12:49007859 | C | CT | 25 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0046 others(22): Show |
29 | HG00609.hp1 HG01346.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-2008dupA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007859 | |||||||
| chr12:49007988 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0070 |
3 | HG01261.hp2 HG02683.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.59-2136A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007988 | |||||||
| chr12:49007992 | T | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
18 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-2140A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49007992 | |||||||
| chr12:49008319 | C | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.59-2467G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008319 | |||||||
| chr12:49008516 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
165 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.59-2664C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008516 | |||||||
| chr12:49008541 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.59-2689G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008541 | |||||||
| chr12:49008610 | G | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.59-2758C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008610 | |||||||
| chr12:49008618 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59-2766C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008618 | |||||||
| chr12:49008619 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59-2767T>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008619 | |||||||
| chr12:49008625 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.59-2773C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008625 | |||||||
| chr12:49008779 | T | G | 1 | a0001c0001t0001g0030 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.59-2927A>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49008779 | |||||||
| chr12:49009058 | A | C | 1 | a0001c0001t0001g0057 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.59-3206T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49009058 | |||||||
| chr12:49009120 | C | CT | 21 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0049 others(18): Show |
29 | HG01891.hp2 HG02109.hp2 HG02165.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3269dupA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49009120 | |||||||
| chr12:49009120 | CT | C | 12 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0043 others(9): Show |
14 | HG02451.hp2 HG02647.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3269delA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49009120 | |||||||
| chr12:49009498 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.58+3564A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49009498 | |||||||
| chr12:49010069 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18945.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.58+2993C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010069 | |||||||
| chr12:49010161 | C | A | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG01167.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+2901G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010161 | |||||||
| chr12:49010325 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+2737G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010325 | |||||||
| chr12:49010624 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.58+2438A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010624 | |||||||
| chr12:49010674 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18945.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.58+2388A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010674 | |||||||
| chr12:49010848 | CT | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0078 others(3): Show |
8 | HG00735.hp2 HG01261.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+2213delA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010848 | |||||||
| chr12:49010906 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.58+2156G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49010906 | |||||||
| chr12:49011027 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
11 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+2035C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011027 | |||||||
| chr12:49011134 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0032 others(7): Show |
17 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+1928G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011134 | |||||||
| chr12:49011191 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.58+1871T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011191 | |||||||
| chr12:49011202 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58+1860A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011202 | |||||||
| chr12:49011691 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+1371G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011691 | |||||||
| chr12:49011697 | G | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG01167.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+1365C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011697 | |||||||
| chr12:49011698 | G | A | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0002g0039 others(8): Show |
13 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+1364C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011698 | |||||||
| chr12:49011708 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0136 |
2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.58+1354C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011708 | |||||||
| chr12:49011731 | T | C | 4 | a0001c0001t0001g0050 a0001c0001t0002g0158 a0001c0001t0002g0159 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1331A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011731 | |||||||
| chr12:49011815 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.58+1247C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011815 | |||||||
| chr12:49011817 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.58+1245G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011817 | |||||||
| chr12:49011818 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.58+1244A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011818 | |||||||
| chr12:49011841 | CG | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0085 |
3 | HG02886.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.58+1220delC | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011841 | |||||||
| chr12:49011863 | C | CCTT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
165 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.58+1196_58+1198dup others(3): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011863 | |||||||
| chr12:49011887 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58+1175A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011887 | |||||||
| chr12:49011960 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
141 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.58+1102T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011960 | |||||||
| chr12:49011960 | A | T | 13 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(10): Show |
15 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+1102T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49011960 | |||||||
| chr12:49012001 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58+1061C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012001 | |||||||
| chr12:49012063 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58+999C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012063 | |||||||
| chr12:49012132 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.58+930G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012132 | |||||||
| chr12:49012353 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58+709C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012353 | |||||||
| chr12:49012378 | C | CT | 15 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0052 others(12): Show |
22 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+683dupA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012378 | |||||||
| chr12:49012400 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58+662C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012400 | |||||||
| chr12:49012440 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.58+622G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 2/11 | chr12 | 49012440 | |||||||
| chr12:49013243 | C | CT | 22 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(19): Show |
26 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-134dupA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013243 | |||||||
| chr12:49013279 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.10-169A>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013279 | |||||||
| chr12:49013583 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.10-473T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013583 | |||||||
| chr12:49013650 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10-540G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013650 | |||||||
| chr12:49013686 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0091 |
8 | HG02109.hp2 HG02723.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.10-576C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013686 | |||||||
| chr12:49013752 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.10-642A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013752 | |||||||
| chr12:49013994 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0054 others(9): Show |
14 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.10-884G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49013994 | |||||||
| chr12:49014085 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | NA18952.hp1 NA18959.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-975A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014085 | |||||||
| chr12:49014125 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
155 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.10-1015G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014125 | |||||||
| chr12:49014169 | C | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.10-1059G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014169 | |||||||
| chr12:49014175 | C | T | 4 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0156 others(1): Show |
6 | HG02559.hp1 HG02922.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-1065G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014175 | |||||||
| chr12:49014183 | C | A | 10 | a0001c0001t0001g0049 a0001c0001t0002g0039 a0001c0001t0002g0040 others(7): Show |
12 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.10-1073G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014183 | |||||||
| chr12:49014621 | C | G | 1 | a0002c0002t0001g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10-1511G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014621 | |||||||
| chr12:49014645 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.10-1535C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014645 | |||||||
| chr12:49014657 | A | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
164 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.10-1547T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014657 | |||||||
| chr12:49014801 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.10-1691G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014801 | |||||||
| chr12:49014918 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.10-1808T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49014918 | |||||||
| chr12:49015514 | T | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
18 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.10-2404A>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015514 | |||||||
| chr12:49015536 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0005g0144 |
6 | HG01175.hp2 HG01433.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-2426A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015536 | |||||||
| chr12:49015561 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.10-2451T>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015561 | |||||||
| chr12:49015567 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02896.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.10-2457A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015567 | |||||||
| chr12:49015720 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.10-2610G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015720 | |||||||
| chr12:49015767 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0042 others(1): Show |
7 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.10-2657C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015767 | |||||||
| chr12:49015812 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.10-2702C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015812 | |||||||
| chr12:49015875 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.10-2765G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015875 | |||||||
| chr12:49015948 | CTT | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
145 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.9+2782_9+2783delAA | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49015948 | |||||||
| chr12:49016006 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.9+2726G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49016006 | |||||||
| chr12:49016394 | T | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
18 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.9+2338A>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49016394 | |||||||
| chr12:49016900 | C | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
11 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+1832G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49016900 | |||||||
| chr12:49017002 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.9+1730G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017002 | |||||||
| chr12:49017363 | C | CCAT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
156 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.9+1368_9+1369insAT others(1): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017363 | |||||||
| chr12:49017827 | G | T | 1 | a0001c0001t0001g0021 | 2 | NA18978.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.9+905C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017827 | |||||||
| chr12:49017838 | G | A | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG01167.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+894C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017838 | |||||||
| chr12:49017858 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+874C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017858 | |||||||
| chr12:49017859 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9+873A>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017859 | |||||||
| chr12:49017860 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+872C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017860 | |||||||
| chr12:49017863 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+869G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017863 | |||||||
| chr12:49017864 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+868G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017864 | |||||||
| chr12:49017866 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+866C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017866 | |||||||
| chr12:49017872 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+860G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017872 | |||||||
| chr12:49017876 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.9+856G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017876 | |||||||
| chr12:49017876 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+856G>C | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017876 | |||||||
| chr12:49017877 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+855C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017877 | |||||||
| chr12:49017881 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+851G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017881 | |||||||
| chr12:49017884 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+848G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017884 | |||||||
| chr12:49017887 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+845A>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017887 | |||||||
| chr12:49017888 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+844T>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017888 | |||||||
| chr12:49017889 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+843C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017889 | |||||||
| chr12:49017892 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+840C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017892 | |||||||
| chr12:49017903 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+829G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017903 | |||||||
| chr12:49017904 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+828G>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017904 | |||||||
| chr12:49017907 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+825C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017907 | |||||||
| chr12:49017910 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+822C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017910 | |||||||
| chr12:49017911 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+821C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017911 | |||||||
| chr12:49017913 | AAGAGTTA others(7): Show |
A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+805_9+818delGGCA others(10): Show |
PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017913 | |||||||
| chr12:49017915 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.9+817C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017915 | |||||||
| chr12:49017929 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+803C>A | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017929 | |||||||
| chr12:49017938 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+794G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017938 | |||||||
| chr12:49017940 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9+792G>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017940 | |||||||
| chr12:49017951 | A | C | 1 | a0001c0001t0002g0039 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.9+781T>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49017951 | |||||||
| chr12:49018236 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.9+496C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49018236 | |||||||
| chr12:49018587 | G | A | 8 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0156 others(5): Show |
10 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.9+145C>T | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49018587 | |||||||
| chr12:49018679 | G | C | 9 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0155 others(6): Show |
11 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+53C>G | PRKAG1 | ENSG00000181929.13 | transcript | ENST00000548065.7 | protein_coding | 1/11 | chr12 | 49018679 |