Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 192111 |
| ensemblid | ENSG00000247077.8 |
| hgncid | 28763 |
| symbol | PGAM5 |
| name | PGAM family member 5, mitochondrial serine/threonine protein phosphatase |
| refseq_nuc | NM_001170543.2 |
| refseq_prot | NP_001164014.1 |
| ensembl_nuc | ENST00000498926.7 |
| ensembl_prot | ENSP00000438465.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 132710842 |
| end | 132722734 |
| strand | + |
| ver | v1.2 |
| region | chr12:132710842-132722734 |
| region5000 | chr12:132705842-132727734 |
| regionname0 | PGAM5_chr12_132710842_132722734 |
| regionname5000 | PGAM5_chr12_132705842_132727734 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 289 | 384 | 88 | 78 | 153 | 16 | 47 | 113 | PGAM5_chr12_132705842_132727734 | PGAM5 | MAFRQ others(284): Show |
chr12 | 132705842 | 132727734 |
| a0002 | 0/0 | 289 | 8 | 0 | 6 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | MAFRQ others(284): Show |
chr12 | 132705842 | 132727734 |
| a0003 | 0/0 | 289 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | MAFRQ others(284): Show |
chr12 | 132705842 | 132727734 |
| a0004 | 0/0 | 289 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | MAFRQ others(284): Show |
chr12 | 132705842 | 132727734 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 867 | 350 | 80 | 73 | 135 | 15 | 45 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0001c0002 | 0/0 | 867 | 24 | 0 | 5 | 16 | 1 | 2 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0001c0004 | 0/0 | 867 | 4 | 4 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0001c0005 | 0/0 | 867 | 3 | 3 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0001c0007 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0001c0008 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0001c0010 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0002c0003 | 0/0 | 867 | 8 | 0 | 6 | 0 | 2 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0003c0009 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 | ||
| a0004c0006 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | ATGGC others(862): Show |
chr12 | 132705842 | 132727734 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2811 | 99 | 7 | 16 | 70 | 1 | 5 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0002 | 1/0 | 2811 | 88 | 27 | 21 | 25 | 2 | 12 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0003 | 0/1 | 2810 | 66 | 8 | 16 | 24 | 5 | 12 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0004 | 0/0 | 2810 | 3 | 0 | 2 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0005 | 0/0 | 2809 | 20 | 2 | 5 | 1 | 6 | 6 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2804): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0006 | 0/0 | 2807 | 11 | 10 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2802): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0007 | 0/0 | 2812 | 10 | 6 | 2 | 1 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0008 | 0/0 | 2808 | 7 | 5 | 2 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2803): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0009 | 0/0 | 2809 | 5 | 5 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2804): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0010 | 0/0 | 2811 | 4 | 0 | 0 | 4 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0011 | 0/0 | 2811 | 4 | 2 | 0 | 0 | 0 | 2 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0012 | 0/0 | 2811 | 3 | 0 | 1 | 1 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0013 | 0/0 | 2807 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2802): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0014 | 0/0 | 2808 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2803): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0015 | 0/0 | 2809 | 2 | 0 | 0 | 0 | 0 | 2 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2804): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0017 | 0/0 | 2811 | 2 | 0 | 1 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0021 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2802): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0022 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0023 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0024 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0025 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0026 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0027 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0028 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0030 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0031 | 0/0 | 2810 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0032 | 0/0 | 2799 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2794): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0033 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0034 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0035 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0036 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0037 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0038 | 0/0 | 2809 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2804): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0039 | 0/0 | 2809 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2804): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0040 | 0/0 | 2810 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0044 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0045 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0001t0046 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0002t0004 | 0/0 | 2810 | 18 | 0 | 5 | 10 | 1 | 2 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0002t0016 | 0/0 | 2811 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0002t0029 | 0/0 | 2810 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0002t0041 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0002t0042 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0001c0002t0043 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| a0001c0004t0008 | 0/0 | 2808 | 3 | 3 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2803): Show |
chr12 | 132705842 | 132727734 |
| a0001c0004t0018 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2802): Show |
chr12 | 132705842 | 132727734 |
| a0001c0005t0009 | 0/0 | 2809 | 3 | 3 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2804): Show |
chr12 | 132705842 | 132727734 |
| a0001c0007t0004 | 0/0 | 2810 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0001c0008t0006 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2802): Show |
chr12 | 132705842 | 132727734 |
| a0001c0010t0002 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2806): Show |
chr12 | 132705842 | 132727734 |
| a0002c0003t0006 | 0/0 | 2807 | 6 | 0 | 5 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2802): Show |
chr12 | 132705842 | 132727734 |
| a0002c0003t0019 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2803): Show |
chr12 | 132705842 | 132727734 |
| a0002c0003t0020 | 0/0 | 2808 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2803): Show |
chr12 | 132705842 | 132727734 |
| a0003c0009t0003 | 0/0 | 2810 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2805): Show |
chr12 | 132705842 | 132727734 |
| a0004c0006t0007 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | GGGCG others(2807): Show |
chr12 | 132705842 | 132727734 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 3 | 16 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 6 | 6 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0004 | 0/0 | 12 | 0 | 6 | 1 | 0 | 5 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0005 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0008 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0015 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0036 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0003 | 0/1 | 13 | 1 | 4 | 5 | 2 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0007 | 0/0 | 9 | 2 | 2 | 2 | 0 | 3 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0023 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0007g0010 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0010g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0012g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0012g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0015g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0015g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0017g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0017g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0021g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0024g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0025g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0026g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0027g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0028g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0031g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0032g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0033g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0034g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0035g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0036g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0037g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0038g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0039g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0040g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0044g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0045g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0001t0046g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0016g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0016g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0029g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0041g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0042g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0002t0043g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0004t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0004t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0004t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0004t0018g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0005t0009g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0005t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0007t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0008t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0001c0010t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0002c0003t0006g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0002c0003t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0002c0003t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0002c0003t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0002c0003t0019g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0002c0003t0020g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0003c0009t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| a0004c0006t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0020 | EUR | GBR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0023 | EUR | GBR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0071 | EUR | GBR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00140 | hp2 | a0002 | c0003 | t0006 | g0027 | EUR | GBR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00280 | hp1 | a0001 | c0001 | t0034 | g0103 | EUR | FIN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00280 | hp2 | a0001 | c0002 | t0004 | g0219 | EUR | FIN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | FIN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0143 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0019 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00642 | hp1 | a0001 | c0001 | t0031 | g0013 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00733 | hp2 | a0002 | c0003 | t0006 | g0027 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG00741 | hp2 | a0001 | c0001 | t0032 | g0089 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0056 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01175 | hp1 | a0001 | c0001 | t0017 | g0206 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0053 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0140 | AMR | PUR | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01255 | hp2 | a0001 | c0001 | t0026 | g0001 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01261 | hp1 | a0001 | c0001 | t0036 | g0002 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01358 | hp2 | a0002 | c0003 | t0006 | g0027 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01433 | hp2 | a0002 | c0003 | t0019 | g0153 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | IBS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0023 | EUR | IBS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0046 | EUR | IBS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01516 | hp2 | a0002 | c0003 | t0020 | g0156 | EUR | IBS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0046 | EUR | IBS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0023 | EUR | IBS | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01928 | hp2 | a0002 | c0003 | t0006 | g0152 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01981 | hp2 | a0001 | c0001 | t0040 | g0179 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01993 | hp2 | a0002 | c0003 | t0006 | g0155 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0217 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02145 | hp1 | a0001 | c0004 | t0018 | g0164 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0176 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02148 | hp2 | a0002 | c0003 | t0006 | g0149 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CDX | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CDX | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02300 | hp1 | a0001 | c0001 | t0022 | g0002 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0168 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0198 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0068 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02896 | hp1 | a0001 | c0001 | t0014 | g0050 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0073 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0051 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02965 | hp1 | a0001 | c0001 | t0038 | g0113 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03017 | hp1 | a0001 | c0001 | t0035 | g0043 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03098 | hp1 | a0001 | c0001 | t0024 | g0165 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03139 | hp2 | a0001 | c0004 | t0008 | g0059 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03195 | hp1 | a0001 | c0001 | t0021 | g0139 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03195 | hp2 | a0001 | c0005 | t0009 | g0035 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03209 | hp2 | a0001 | c0005 | t0009 | g0035 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0145 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03516 | hp2 | a0001 | c0001 | t0039 | g0112 | AFR | ESN | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03654 | hp1 | a0001 | c0001 | t0012 | g0180 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0032 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03669 | hp1 | a0001 | c0001 | t0015 | g0076 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03688 | hp1 | a0003 | c0009 | t0003 | g0175 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03704 | hp2 | a0001 | c0001 | t0046 | g0060 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0067 | SAS | PJL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03831 | hp2 | a0001 | c0001 | t0030 | g0003 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0043 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03927 | hp1 | a0001 | c0001 | t0028 | g0018 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0066 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0064 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0072 | SAS | BEB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0197 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0019 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0075 | SAS | STU | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | YRI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | YRI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | YRI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | YRI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18941 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0048 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18947 | hp2 | a0001 | c0002 | t0029 | g0063 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18951 | hp1 | a0001 | c0001 | t0010 | g0120 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18956 | hp1 | a0001 | c0002 | t0042 | g0221 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18957 | hp2 | a0001 | c0001 | t0037 | g0116 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18959 | hp2 | a0001 | c0001 | t0025 | g0134 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18962 | hp2 | a0001 | c0001 | t0027 | g0123 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18964 | hp2 | a0001 | c0001 | t0023 | g0002 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18967 | hp1 | a0001 | c0007 | t0004 | g0144 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18973 | hp2 | a0001 | c0010 | t0002 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18979 | hp2 | a0001 | c0001 | t0045 | g0003 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18986 | hp2 | a0001 | c0002 | t0016 | g0138 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0214 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18992 | hp1 | a0001 | c0002 | t0004 | g0142 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18992 | hp2 | a0001 | c0002 | t0004 | g0220 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18998 | hp1 | a0001 | c0002 | t0016 | g0047 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18998 | hp2 | a0001 | c0001 | t0017 | g0170 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19000 | hp1 | a0001 | c0002 | t0043 | g0216 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0048 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19004 | hp2 | a0001 | c0002 | t0004 | g0218 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | LWK | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | LWK | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19043 | hp1 | a0001 | c0004 | t0008 | g0058 | AFR | LWK | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0047 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19077 | hp1 | a0001 | c0001 | t0012 | g0184 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19082 | hp1 | a0001 | c0001 | t0033 | g0005 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0215 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19084 | hp1 | a0001 | c0001 | t0044 | g0187 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19084 | hp2 | a0001 | c0002 | t0041 | g0167 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19087 | hp2 | a0004 | c0006 | t0007 | g0049 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19240 | hp1 | a0001 | c0008 | t0006 | g0150 | AFR | YRI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | YRI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ASW | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0032 | EUR | TSI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0211 | EUR | TSI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | GIH | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20905 | hp2 | a0001 | c0001 | t0015 | g0114 | SAS | GIH | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02486 | hp1 | a0001 | c0005 | t0009 | g0100 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0070 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0148 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG03471 | hp2 | a0001 | c0004 | t0008 | g0057 | AFR | MSL | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | USA | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0178 | AFR | USA | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | USA | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0222 | AFR | USA | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0151 | AFR | LWK | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | LWK | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0003 | REF | REF | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0036 | REF | REF | PGAM5_chr12_132705842_132727734 | PGAM5 | chr12 | 132705842 | 132727734 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132710938 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.62T>C | p.Val21Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 97/2811 | 62/870 | 21/289 | chr12 | 132710938 | |||
| chr12:132710940 | C | G | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.64C>G | p.Leu22Val | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 99/2811 | 64/870 | 22/289 | chr12 | 132710940 | |||
| chr12:132710941 | T | A | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.65T>A | p.Leu22His | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 100/2811 | 65/870 | 22/289 | chr12 | 132710941 | |||
| chr12:132710943 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.67T>C | p.Phe23Leu | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 102/2811 | 67/870 | 23/289 | chr12 | 132710943 | |||
| chr12:132710944 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.68T>C | p.Phe23Ser | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 103/2811 | 68/870 | 23/289 | chr12 | 132710944 | |||
| chr12:132710946 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.70T>C | p.Ser24Pro | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 105/2811 | 70/870 | 24/289 | chr12 | 132710946 | |||
| chr12:132710953 | T | A | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.77T>A | p.Val26Glu | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 112/2811 | 77/870 | 26/289 | chr12 | 132710953 | |||
| chr12:132710955 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.79G>C | p.Ala27Pro | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 114/2811 | 79/870 | 27/289 | chr12 | 132710955 | |||
| chr12:132710959 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.83T>C | p.Val28Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 118/2811 | 83/870 | 28/289 | chr12 | 132710959 | |||
| chr12:132710964 | A | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.88A>C | p.Lys30Gln | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 123/2811 | 88/870 | 30/289 | chr12 | 132710964 | |||
| chr12:132710968 | C | T | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.92C>T | p.Pro31Leu | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 127/2811 | 92/870 | 31/289 | chr12 | 132710968 | |||
| chr12:132710976 | G | T | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.100G>T | p.Gly34Cys | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 135/2811 | 100/870 | 34/289 | chr12 | 132710976 | |||
| chr12:132710979 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.103G>C | p.Gly35Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 138/2811 | 103/870 | 35/289 | chr12 | 132710979 | |||
| chr12:132710982 | G | A | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.106G>A | p.Asp36Asn | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 141/2811 | 106/870 | 36/289 | chr12 | 132710982 | |||
| chr12:132710989 | A | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.113A>C | p.Glu38Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 148/2811 | 113/870 | 38/289 | chr12 | 132710989 | |||
| chr12:132710994 | C | T | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.118C>T | p.Arg40Cys | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 153/2811 | 118/870 | 40/289 | chr12 | 132710994 | |||
| chr12:132710998 | C | T | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.122C>T | p.Pro41Leu | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 157/2811 | 122/870 | 41/289 | chr12 | 132710998 | |||
| chr12:132711003 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.127G>C | p.Glu43Gln | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 162/2811 | 127/870 | 43/289 | chr12 | 132711003 | |||
| chr12:132711004 | A | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.128A>C | p.Glu43Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 163/2811 | 128/870 | 43/289 | chr12 | 132711004 | |||
| chr12:132711005 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.129G>C | p.Glu43Asp | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 164/2811 | 129/870 | 43/289 | chr12 | 132711005 | |||
| chr12:132711006 | C | G | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.130C>G | p.Pro44Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 165/2811 | 130/870 | 44/289 | chr12 | 132711006 | |||
| chr12:132711015 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.139T>C | p.Trp47Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 174/2811 | 139/870 | 47/289 | chr12 | 132711015 | |||
| chr12:132711017 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.141G>C | p.Trp47Cys | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 176/2811 | 141/870 | 47/289 | chr12 | 132711017 | |||
| chr12:132711021 | G | A | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.145G>A | p.Gly49Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 180/2811 | 145/870 | 49/289 | chr12 | 132711021 | |||
| chr12:132711024 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.148G>C | p.Gly50Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 183/2811 | 148/870 | 50/289 | chr12 | 132711024 | |||
| chr12:132711027 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.151G>C | p.Ala51Pro | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 186/2811 | 151/870 | 51/289 | chr12 | 132711027 | |||
| chr12:132711037 | G | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.161G>C | p.Gly54Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 196/2811 | 161/870 | 54/289 | chr12 | 132711037 | |||
| chr12:132711039 | C | G | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.163C>G | p.Pro55Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 198/2811 | 163/870 | 55/289 | chr12 | 132711039 | |||
| chr12:132711040 | C | A | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.164C>A | p.Pro55His | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 199/2811 | 164/870 | 55/289 | chr12 | 132711040 | |||
| chr12:132711046 | T | C | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.170T>C | p.Val57Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 205/2811 | 170/870 | 57/289 | chr12 | 132711046 | |||
| chr12:132711055 | C | G | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.179C>G | p.Pro60Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 214/2811 | 179/870 | 60/289 | chr12 | 132711055 | |||
| chr12:132711057 | A | G | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.181A>G | p.Asn61Asp | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 216/2811 | 181/870 | 61/289 | chr12 | 132711057 | |||
| chr12:132711060 | T | G | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.184T>G | p.Trp62Gly | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 219/2811 | 184/870 | 62/289 | chr12 | 132711060 | |||
| chr12:132711063 | G | A | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.187G>A | p.Asp63Asn | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 222/2811 | 187/870 | 63/289 | chr12 | 132711063 | |||
| chr12:132717541 | A | C | 1 | a0003 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.473A>C | p.Asp158Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/6 | 508/2811 | 473/870 | 158/289 | chr12 | 132717541 | |||
| chr12:132717785 | A | G | 1 | a0002 | 8 | HG00140.hp2 HG00733.hp2 HG01358.hp2 others(5): Show |
missense_variant | MODERATE | c.572A>G | p.Lys191Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/6 | 607/2811 | 572/870 | 191/289 | chr12 | 132717785 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132710939 | G | C | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.63G>C | p.Val21Val | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 98/2811 | 63/870 | 21/289 | chr12 | 132710939 | |||
| chr12:132710942 | C | G | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.66C>G | p.Leu22Leu | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 101/2811 | 66/870 | 22/289 | chr12 | 132710942 | |||
| chr12:132710957 | G | C | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.81G>C | p.Ala27Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 116/2811 | 81/870 | 27/289 | chr12 | 132710957 | |||
| chr12:132710975 | A | C | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.99A>C | p.Ala33Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 134/2811 | 99/870 | 33/289 | chr12 | 132710975 | |||
| chr12:132710999 | G | T | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.123G>T | p.Pro41Pro | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 158/2811 | 123/870 | 41/289 | chr12 | 132710999 | |||
| chr12:132711029 | G | A | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.153G>A | p.Ala51Ala | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 188/2811 | 153/870 | 51/289 | chr12 | 132711029 | |||
| chr12:132711044 | T | C | 1 | a0004c0006 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.168T>C | p.Gly56Gly | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 203/2811 | 168/870 | 56/289 | chr12 | 132711044 | |||
| chr12:132714873 | T | C | 1 | a0001c0007 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.207T>C | p.Ser69Ser | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/6 | 242/2811 | 207/870 | 69/289 | chr12 | 132714873 | |||
| chr12:132717512 | G | A | 1 | a0001c0005 | 3 | HG02486.hp1 HG03195.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.444G>A | p.Ser148Ser | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/6 | 479/2811 | 444/870 | 148/289 | chr12 | 132717512 | |||
| chr12:132717524 | C | T | 1 | a0001c0010 | 1 | NA18973.hp2 | synonymous_variant | LOW | c.456C>T | p.Arg152Arg | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/6 | 491/2811 | 456/870 | 152/289 | chr12 | 132717524 | |||
| chr12:132717747 | C | T | 2 | a0001c0002 a0001c0007 |
25 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(22): Show |
synonymous_variant | LOW | c.534C>T | p.Gly178Gly | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/6 | 569/2811 | 534/870 | 178/289 | chr12 | 132717747 | |||
| chr12:132717995 | C | T | 1 | a0001c0008 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.594C>T | p.Tyr198Tyr | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/6 | 629/2811 | 594/870 | 198/289 | chr12 | 132717995 | |||
| chr12:132718076 | G | A | 1 | a0001c0004 | 4 | HG02145.hp1 HG03139.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.675G>A | p.Glu225Glu | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/6 | 710/2811 | 675/870 | 225/289 | chr12 | 132718076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132710858 | C | T | 1 | a0001c0001t0046 | 1 | HG03704.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-19C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | chr12 | 132710858 | |||||||
| chr12:132710873 | C | T | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(12): Show |
105 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(102): Show |
5_prime_UTR_variant | MODIFIER | c.-4C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/6 | 4 | chr12 | 132710873 | ||||||
| chr12:132720873 | A | G | 1 | a0001c0001t0010 | 4 | NA18941.hp1 NA18951.hp1 NA18952.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 45 | chr12 | 132720873 | ||||||
| chr12:132720874 | C | A | 1 | a0001c0001t0010 | 4 | NA18941.hp1 NA18951.hp1 NA18952.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 46 | chr12 | 132720874 | ||||||
| chr12:132720909 | A | C | 2 | a0001c0001t0009 a0001c0005t0009 |
8 | HG02109.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*81A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 81 | chr12 | 132720909 | ||||||
| chr12:132721055 | C | T | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02965.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*227C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 227 | chr12 | 132721055 | ||||||
| chr12:132721062 | C | T | 1 | a0001c0001t0037 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 234 | chr12 | 132721062 | ||||||
| chr12:132721089 | T | C | 8 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0021 others(5): Show |
24 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*261T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 261 | chr12 | 132721089 | ||||||
| chr12:132721170 | G | A | 1 | a0001c0004t0018 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 342 | chr12 | 132721170 | ||||||
| chr12:132721175 | G | T | 1 | a0001c0001t0036 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 347 | chr12 | 132721175 | ||||||
| chr12:132721270 | C | T | 1 | a0001c0001t0035 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 442 | chr12 | 132721270 | ||||||
| chr12:132721302 | T | C | 1 | a0001c0001t0022 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*474T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 474 | chr12 | 132721302 | ||||||
| chr12:132721335 | T | C | 14 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(11): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*507T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 507 | chr12 | 132721335 | ||||||
| chr12:132721380 | A | C | 1 | a0001c0001t0039 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 552 | chr12 | 132721380 | ||||||
| chr12:132721461 | G | A | 2 | a0001c0001t0014 a0001c0001t0015 |
4 | HG02896.hp1 HG02897.hp2 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*633G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 633 | chr12 | 132721461 | ||||||
| chr12:132721577 | G | A | 1 | a0001c0001t0040 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*749G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 749 | chr12 | 132721577 | ||||||
| chr12:132721629 | C | A | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(14): Show |
104 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*801C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 801 | chr12 | 132721629 | ||||||
| chr12:132721631 | C | G | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(14): Show |
104 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*803C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 803 | chr12 | 132721631 | ||||||
| chr12:132721652 | G | A | 1 | a0001c0001t0023 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*824G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 824 | chr12 | 132721652 | ||||||
| chr12:132721723 | G | A | 1 | a0001c0001t0024 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 895 | chr12 | 132721723 | ||||||
| chr12:132721823 | G | A | 9 | a0001c0001t0004 a0001c0001t0037 a0001c0002t0004 others(6): Show |
29 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*995G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 995 | chr12 | 132721823 | ||||||
| chr12:132721966 | AT | A | 5 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0038 others(2): Show |
14 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1141delT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1141 | INFO_REALIGN_3_PRIME | chr12 | 132721966 | |||||
| chr12:132722020 | C | T | 1 | a0001c0001t0045 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1192 | chr12 | 132722020 | ||||||
| chr12:132722047 | C | G | 1 | a0001c0001t0028 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1219C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1219 | chr12 | 132722047 | ||||||
| chr12:132722052 | TGGG | T | 8 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0021 others(5): Show |
24 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1227_*1229delGGG | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1227 | INFO_REALIGN_3_PRIME | chr12 | 132722052 | |||||
| chr12:132722116 | C | T | 1 | a0001c0001t0021 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1288C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1288 | chr12 | 132722116 | ||||||
| chr12:132722130 | C | T | 1 | a0001c0001t0034 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1302 | chr12 | 132722130 | ||||||
| chr12:132722187 | A | G | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(41): Show |
266 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*1359A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1359 | chr12 | 132722187 | ||||||
| chr12:132722216 | CTTTTATG others(5): Show |
C | 1 | a0001c0001t0032 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1389_*1400delTTTT others(8): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1389 | chr12 | 132722216 | ||||||
| chr12:132722229 | G | A | 1 | a0001c0001t0025 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1401 | chr12 | 132722229 | ||||||
| chr12:132722243 | G | GT | 4 | a0001c0001t0007 a0001c0001t0033 a0001c0002t0043 others(1): Show |
13 | HG01106.hp2 HG01993.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1425dupT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1426 | INFO_REALIGN_3_PRIME | chr12 | 132722243 | |||||
| chr12:132722244 | T | G | 4 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0014 others(1): Show |
14 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1416T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1416 | chr12 | 132722244 | ||||||
| chr12:132722253 | TG | T | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(16): Show |
127 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1426delG | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1426 | chr12 | 132722253 | ||||||
| chr12:132722254 | G | T | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(18): Show |
126 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1426G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1426 | chr12 | 132722254 | ||||||
| chr12:132722254 | GT | G | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0027 |
22 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1439delT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1439 | INFO_REALIGN_3_PRIME | chr12 | 132722254 | |||||
| chr12:132722254 | GTT | G | 6 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(3): Show |
31 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1438_*1439delTT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1438 | INFO_REALIGN_3_PRIME | chr12 | 132722254 | |||||
| chr12:132722255 | T | G | 11 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0017 others(8): Show |
114 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1427T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1427 | chr12 | 132722255 | ||||||
| chr12:132722255 | T | TG | 3 | a0001c0001t0024 a0001c0001t0026 a0001c0001t0036 |
3 | HG01255.hp2 HG01261.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1427_*1428insG | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1428 | chr12 | 132722255 | ||||||
| chr12:132722256 | T | G | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(21): Show |
134 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1428T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1428 | chr12 | 132722256 | ||||||
| chr12:132722469 | C | T | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02965.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1641C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1641 | chr12 | 132722469 | ||||||
| chr12:132722538 | A | G | 5 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0038 others(2): Show |
14 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1710A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1710 | chr12 | 132722538 | ||||||
| chr12:132722557 | AAT | A | 4 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(1): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1732_*1733delAT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 132722557 | |||||
| chr12:132722563 | CA | C | 3 | a0001c0001t0008 a0001c0001t0014 a0001c0004t0008 |
12 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1738delA | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1738 | INFO_REALIGN_3_PRIME | chr12 | 132722563 | |||||
| chr12:132722631 | T | G | 1 | a0001c0002t0041 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1803T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1803 | chr12 | 132722631 | ||||||
| chr12:132722632 | G | T | 1 | a0001c0002t0041 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1804G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1804 | chr12 | 132722632 | ||||||
| chr12:132722633 | T | G | 1 | a0001c0002t0041 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1805T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 6/6 | 1805 | chr12 | 132722633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132711068 | G | C | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | splice_donor_variant&intron_variant | HIGH | c.191+1G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711068 | |||||||
| chr12:132711070 | G | T | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.191+3G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711070 | |||||||
| chr12:132711072 | G | C | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.191+5G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711072 | |||||||
| chr12:132711074 | G | C | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.191+7G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711074 | |||||||
| chr12:132711078 | G | T | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.191+11G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711078 | |||||||
| chr12:132711081 | T | C | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.191+14T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711081 | |||||||
| chr12:132711083 | T | C | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.191+16T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711083 | |||||||
| chr12:132711096 | T | G | 1 | a0004c0006t0007g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.191+29T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711096 | |||||||
| chr12:132711135 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.191+68A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711135 | |||||||
| chr12:132711244 | G | A | 11 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+177G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711244 | |||||||
| chr12:132711321 | C | T | 14 | a0001c0001t0004g0019 a0001c0001t0011g0222 a0001c0002t0004g0019 others(11): Show |
17 | HG00280.hp2 HG00639.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.191+254C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711321 | |||||||
| chr12:132711389 | G | T | 3 | a0001c0004t0008g0057 a0001c0004t0008g0058 a0001c0004t0008g0059 |
3 | HG03139.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+322G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711389 | |||||||
| chr12:132711611 | C | T | 55 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0013 others(52): Show |
80 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.191+544C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711611 | |||||||
| chr12:132711723 | C | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0109 a0001c0001t0006g0110 others(14): Show |
20 | HG01109.hp2 HG01243.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.191+656C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711723 | |||||||
| chr12:132711752 | T | C | 5 | a0001c0001t0001g0115 a0001c0001t0002g0030 a0001c0001t0003g0169 others(2): Show |
6 | HG02129.hp1 HG02155.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+685T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711752 | |||||||
| chr12:132711767 | G | C | 1 | a0001c0001t0003g0171 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.191+700G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711767 | |||||||
| chr12:132711788 | G | GA | 14 | a0001c0001t0006g0024 a0001c0001t0006g0109 a0001c0001t0006g0110 others(11): Show |
17 | HG01243.hp1 HG02559.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.191+734dupA | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 132711788 | ||||||
| chr12:132711789 | A | G | 2 | a0001c0001t0006g0168 a0001c0002t0041g0167 |
2 | HG02723.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.191+722A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711789 | |||||||
| chr12:132711818 | A | C | 1 | a0001c0001t0002g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.191+751A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711818 | |||||||
| chr12:132711884 | G | C | 1 | a0001c0001t0003g0172 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.191+817G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711884 | |||||||
| chr12:132711896 | T | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(39): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.191+829T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711896 | |||||||
| chr12:132711977 | G | C | 2 | a0001c0002t0016g0138 a0001c0002t0041g0167 |
2 | NA18986.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.191+910G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132711977 | |||||||
| chr12:132712020 | A | G | 1 | a0001c0001t0002g0037 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.191+953A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712020 | |||||||
| chr12:132712159 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.191+1092A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712159 | |||||||
| chr12:132712188 | G | T | 2 | a0001c0001t0001g0166 a0001c0001t0024g0165 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.191+1121G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712188 | |||||||
| chr12:132712203 | C | T | 3 | a0001c0004t0008g0057 a0001c0004t0008g0058 a0001c0004t0008g0059 |
3 | HG03139.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+1136C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712203 | |||||||
| chr12:132712252 | C | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.191+1185C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712252 | |||||||
| chr12:132712574 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.191+1507A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712574 | |||||||
| chr12:132712648 | G | T | 1 | a0001c0001t0002g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.191+1581G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712648 | |||||||
| chr12:132712652 | C | T | 1 | a0001c0004t0018g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.191+1585C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712652 | |||||||
| chr12:132712933 | G | A | 2 | a0001c0002t0016g0138 a0001c0002t0041g0167 |
2 | NA18986.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.191+1866G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712933 | |||||||
| chr12:132712956 | G | A | 1 | a0001c0001t0037g0116 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.191+1889G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132712956 | |||||||
| chr12:132713010 | A | C | 1 | a0001c0001t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.192-1848A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713010 | |||||||
| chr12:132713406 | G | A | 93 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0013 others(90): Show |
125 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.192-1452G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713406 | |||||||
| chr12:132713496 | C | T | 14 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0154 others(11): Show |
16 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.192-1362C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713496 | |||||||
| chr12:132713663 | C | T | 2 | a0001c0001t0003g0209 a0001c0001t0003g0210 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.192-1195C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713663 | |||||||
| chr12:132713679 | T | C | 2 | a0001c0001t0006g0146 a0001c0001t0006g0147 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.192-1179T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713679 | |||||||
| chr12:132713800 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192-1058C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713800 | |||||||
| chr12:132713870 | T | C | 4 | a0001c0001t0006g0024 a0001c0001t0006g0109 a0001c0001t0006g0110 others(1): Show |
6 | HG02559.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-988T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713870 | |||||||
| chr12:132713902 | C | G | 1 | a0001c0001t0006g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.192-956C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713902 | |||||||
| chr12:132713999 | C | T | 1 | a0001c0001t0003g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192-859C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132713999 | |||||||
| chr12:132714059 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG01099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.192-799C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714059 | |||||||
| chr12:132714120 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.192-738C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714120 | |||||||
| chr12:132714121 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.192-737G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714121 | |||||||
| chr12:132714301 | G | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0032 a0001c0001t0005g0033 others(17): Show |
27 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.192-557G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714301 | |||||||
| chr12:132714391 | A | G | 7 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 others(4): Show |
7 | HG01175.hp1 HG01934.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-467A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714391 | |||||||
| chr12:132714632 | G | A | 2 | a0001c0002t0004g0214 a0001c0002t0004g0215 |
2 | NA18990.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.192-226G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714632 | |||||||
| chr12:132714824 | G | C | 1 | a0001c0001t0021g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.192-34G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 1/5 | chr12 | 132714824 | |||||||
| chr12:132715052 | A | T | 1 | a0001c0001t0008g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.370+16A>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715052 | |||||||
| chr12:132715093 | A | ATCC | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(187): Show |
331 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.370+59_370+60insCT others(1): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132715093 | ||||||
| chr12:132715096 | T | C | 1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.370+60T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715096 | |||||||
| chr12:132715097 | G | T | 1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.370+61G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715097 | |||||||
| chr12:132715137 | C | G | 2 | a0001c0001t0003g0046 a0001c0001t0003g0199 |
3 | HG01516.hp1 HG01517.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.370+101C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715137 | |||||||
| chr12:132715293 | G | A | 39 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0077 others(36): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.370+257G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715293 | |||||||
| chr12:132715350 | T | C | 2 | a0001c0001t0013g0148 a0001c0001t0013g0151 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.370+314T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715350 | |||||||
| chr12:132715369 | G | A | 89 | a0001c0001t0001g0038 a0001c0001t0001g0158 a0001c0001t0001g0159 others(86): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.370+333G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715369 | |||||||
| chr12:132715389 | G | A | 1 | a0002c0003t0006g0152 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.370+353G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715389 | |||||||
| chr12:132715439 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+403T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715439 | |||||||
| chr12:132715503 | G | A | 5 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(2): Show |
6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+467G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715503 | |||||||
| chr12:132715570 | C | A | 2 | a0001c0002t0004g0047 a0001c0002t0016g0047 |
2 | NA18998.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.370+534C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715570 | |||||||
| chr12:132715570 | C | CAAA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(143): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.370+546_370+548dup others(3): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132715570 | ||||||
| chr12:132715570 | C | CAAAA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG00741.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.370+545_370+548dup others(4): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132715570 | ||||||
| chr12:132715593 | C | T | 57 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(54): Show |
82 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.370+557C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715593 | |||||||
| chr12:132715597 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.370+561G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715597 | |||||||
| chr12:132715648 | G | T | 1 | a0001c0001t0003g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.370+612G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715648 | |||||||
| chr12:132715668 | C | T | 79 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(76): Show |
107 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.370+632C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715668 | |||||||
| chr12:132715677 | G | C | 1 | a0003c0009t0003g0175 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.370+641G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715677 | |||||||
| chr12:132715684 | G | C | 7 | a0001c0001t0006g0154 a0002c0003t0006g0027 a0002c0003t0006g0149 others(4): Show |
9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.370+648G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715684 | |||||||
| chr12:132715736 | G | A | 3 | a0001c0004t0008g0057 a0001c0004t0008g0058 a0001c0004t0008g0059 |
3 | HG03139.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.370+700G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715736 | |||||||
| chr12:132715848 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(53): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.370+812T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132715848 | |||||||
| chr12:132715878 | C | CA | 9 | a0001c0001t0002g0082 a0001c0001t0002g0086 a0001c0001t0008g0029 others(6): Show |
10 | HG01243.hp1 HG01975.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.370+853dupA | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132715878 | ||||||
| chr12:132715980 | TGCCTTGG others(3): Show |
T | 1 | a0001c0001t0001g0137 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.370+947_370+956del others(10): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132715980 | ||||||
| chr12:132716003 | G | GAATCACT others(9): Show |
1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+967_370+968ins others(16): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716003 | |||||||
| chr12:132716015 | G | A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG01891.hp1 HG01934.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.370+979G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716015 | |||||||
| chr12:132716019 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+983A>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716019 | |||||||
| chr12:132716026 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+990C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716026 | |||||||
| chr12:132716029 | G | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+993G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716029 | |||||||
| chr12:132716034 | C | A | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+998C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716034 | |||||||
| chr12:132716043 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1007T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716043 | |||||||
| chr12:132716051 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1015G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716051 | |||||||
| chr12:132716052 | G | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1016G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716052 | |||||||
| chr12:132716055 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1019T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716055 | |||||||
| chr12:132716056 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1020G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716056 | |||||||
| chr12:132716058 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1022G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716058 | |||||||
| chr12:132716059 | G | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1023G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716059 | |||||||
| chr12:132716060 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1024C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716060 | |||||||
| chr12:132716061 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1025A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716061 | |||||||
| chr12:132716073 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1037G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716073 | |||||||
| chr12:132716075 | T | A | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1039T>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716075 | |||||||
| chr12:132716082 | CGTCTGCT others(3): Show |
C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1047_370+1056d others(12): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716082 | |||||||
| chr12:132716083 | G | C | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.370+1047G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716083 | |||||||
| chr12:132716087 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.370+1051G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716087 | |||||||
| chr12:132716095 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1059G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716095 | |||||||
| chr12:132716099 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1063G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716099 | |||||||
| chr12:132716110 | T | G | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.370+1074T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716110 | |||||||
| chr12:132716159 | C | T | 72 | a0001c0001t0002g0099 a0001c0001t0003g0003 a0001c0001t0003g0007 others(69): Show |
101 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.370+1123C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716159 | |||||||
| chr12:132716223 | C | T | 3 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 |
3 | HG01109.hp2 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.370+1187C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716223 | |||||||
| chr12:132716331 | C | T | 2 | a0001c0001t0006g0146 a0001c0001t0006g0147 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.371-1108C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716331 | |||||||
| chr12:132716345 | A | G | 1 | a0001c0001t0034g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.371-1094A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716345 | |||||||
| chr12:132716375 | A | G | 2 | a0001c0001t0038g0113 a0001c0001t0039g0112 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.371-1064A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716375 | |||||||
| chr12:132716377 | A | G | 2 | a0001c0001t0038g0113 a0001c0001t0039g0112 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.371-1062A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716377 | |||||||
| chr12:132716381 | A | G | 2 | a0001c0001t0038g0113 a0001c0001t0039g0112 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.371-1058A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716381 | |||||||
| chr12:132716387 | A | AT | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0037 others(7): Show |
11 | HG00544.hp2 HG00673.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.371-1037dupT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132716387 | ||||||
| chr12:132716443 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.371-996C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716443 | |||||||
| chr12:132716445 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.371-994G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716445 | |||||||
| chr12:132716462 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0109 a0001c0001t0006g0111 others(14): Show |
21 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.371-977C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716462 | |||||||
| chr12:132716465 | G | A | 85 | a0001c0001t0001g0016 a0001c0001t0001g0121 a0001c0001t0002g0099 others(82): Show |
120 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.371-974G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716465 | |||||||
| chr12:132716518 | C | T | 1 | a0001c0001t0006g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.371-921C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716518 | |||||||
| chr12:132716521 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0161 others(5): Show |
12 | HG01192.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.371-918G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716521 | |||||||
| chr12:132716526 | G | C | 1 | a0001c0001t0006g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.371-913G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716526 | |||||||
| chr12:132716554 | T | TG | 3 | a0002c0003t0006g0027 a0002c0003t0006g0149 a0002c0003t0020g0156 |
5 | HG00140.hp2 HG00733.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-884dupG | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132716554 | ||||||
| chr12:132716618 | G | A | 77 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0013 others(74): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.371-821G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716618 | |||||||
| chr12:132716637 | C | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0120 |
4 | NA18941.hp1 NA18951.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-802C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716637 | |||||||
| chr12:132716698 | A | G | 75 | a0001c0001t0002g0099 a0001c0001t0003g0003 a0001c0001t0003g0007 others(72): Show |
105 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.371-741A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716698 | |||||||
| chr12:132716768 | C | T | 6 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0056 others(3): Show |
6 | HG01109.hp2 HG02717.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-671C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716768 | |||||||
| chr12:132716891 | C | G | 1 | a0001c0001t0021g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.371-548C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716891 | |||||||
| chr12:132716892 | T | G | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.371-547T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716892 | |||||||
| chr12:132716947 | CAA | C | 5 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(2): Show |
6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.371-491_371-490del others(2): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716947 | |||||||
| chr12:132716948 | A | C | 2 | a0001c0001t0003g0207 a0001c0001t0017g0206 |
2 | HG01175.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.371-491A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716948 | |||||||
| chr12:132716949 | A | C | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.371-490A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716949 | |||||||
| chr12:132716950 | G | A | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.371-489G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716950 | |||||||
| chr12:132716985 | A | T | 2 | a0001c0001t0003g0207 a0001c0001t0017g0206 |
2 | HG01175.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.371-454A>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132716985 | |||||||
| chr12:132717025 | C | T | 52 | a0001c0001t0002g0096 a0001c0001t0002g0099 a0001c0001t0003g0003 others(49): Show |
77 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.371-414C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717025 | |||||||
| chr12:132717108 | A | C | 1 | a0001c0002t0043g0216 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.371-331A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717108 | |||||||
| chr12:132717142 | G | C | 36 | a0001c0001t0002g0099 a0001c0001t0005g0020 a0001c0001t0005g0023 others(33): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.371-297G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717142 | |||||||
| chr12:132717240 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.371-199C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717240 | |||||||
| chr12:132717246 | G | C | 9 | a0001c0001t0005g0033 a0001c0001t0005g0064 a0001c0001t0005g0066 others(6): Show |
10 | HG00140.hp1 HG01361.hp2 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.371-193G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717246 | |||||||
| chr12:132717257 | C | A | 19 | a0001c0001t0005g0033 a0001c0001t0005g0064 a0001c0001t0005g0065 others(16): Show |
22 | HG00140.hp1 HG01361.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.371-182C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717257 | |||||||
| chr12:132717291 | C | CGTGTTTG others(15): Show |
1 | a0001c0001t0034g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.371-118_371-97dupC others(21): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717291 | ||||||
| chr12:132717299 | C | A | 5 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0014g0050 others(2): Show |
6 | HG02145.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.371-140C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717299 | |||||||
| chr12:132717303 | C | CGGAGGAG others(37): Show |
2 | a0001c0004t0008g0057 a0001c0004t0008g0058 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.371-126_371-83dupG others(43): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717303 | ||||||
| chr12:132717303 | C | CGGAGGAG others(191): Show |
1 | a0001c0004t0008g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.371-83_371-82insGG others(196): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717303 | ||||||
| chr12:132717313 | G | GGTGTTTG others(37): Show |
32 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
70 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.371-82_371-39dupCG others(42): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717313 | ||||||
| chr12:132717313 | G | GGTGTTTG others(81): Show |
2 | a0001c0001t0001g0122 a0001c0001t0027g0123 |
2 | NA18962.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.371-39_371-38insCG others(86): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717313 | ||||||
| chr12:132717313 | G | GGTGTTTG others(37): Show |
15 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(12): Show |
36 | HG00597.hp1 HG00673.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.371-119_371-118ins others(44): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717313 | ||||||
| chr12:132717313 | G | GGTGTTTG others(103): Show |
1 | a0001c0001t0001g0131 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.371-119_371-118ins others(110): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717313 | ||||||
| chr12:132717313 | GGTGTTTG others(37): Show |
G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0085 others(11): Show |
25 | HG00423.hp2 HG00738.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.371-82_371-39delCG others(42): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717313 | ||||||
| chr12:132717325 | C | CGGAGGAG others(103): Show |
2 | a0001c0001t0006g0157 a0001c0004t0018g0164 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.371-39_371-38insCG others(108): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717325 | ||||||
| chr12:132717325 | C | CGGAGGAG others(125): Show |
4 | a0001c0001t0006g0024 a0001c0001t0006g0109 a0001c0001t0006g0110 others(1): Show |
6 | HG02559.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-97_371-96insCG others(130): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717325 | ||||||
| chr12:132717335 | G | GGTGTTTG others(59): Show |
7 | a0001c0001t0006g0154 a0002c0003t0006g0027 a0002c0003t0006g0149 others(4): Show |
9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.371-39_371-38insCG others(64): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717335 | ||||||
| chr12:132717337 | T | G | 1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.371-102T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | chr12 | 132717337 | |||||||
| chr12:132717343 | AGGGTGGA others(15): Show |
A | 1 | a0001c0001t0039g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.371-92_371-71delTG others(20): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717343 | ||||||
| chr12:132717357 | C | CGTGTTTG others(59): Show |
2 | a0001c0001t0006g0146 a0001c0001t0006g0147 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.371-39_371-38insCG others(64): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 132717357 | ||||||
| chr12:132717577 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.496+13C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/5 | chr12 | 132717577 | |||||||
| chr12:132717606 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.496+42C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/5 | chr12 | 132717606 | |||||||
| chr12:132717645 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(49): Show |
96 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.497-65G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/5 | chr12 | 132717645 | |||||||
| chr12:132717702 | C | A | 5 | a0001c0001t0005g0069 a0001c0001t0009g0068 a0001c0001t0009g0073 others(2): Show |
6 | HG02486.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.497-8C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 3/5 | chr12 | 132717702 | |||||||
| chr12:132717811 | C | A | 1 | a0001c0001t0006g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.585+13C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717811 | |||||||
| chr12:132717812 | C | G | 1 | a0001c0001t0003g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.585+14C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717812 | |||||||
| chr12:132717867 | C | T | 2 | a0001c0001t0003g0192 a0001c0001t0003g0202 |
2 | HG00738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.585+69C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717867 | |||||||
| chr12:132717869 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.585+71C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717869 | |||||||
| chr12:132717885 | C | G | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.585+87C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717885 | |||||||
| chr12:132717887 | G | C | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.585+89G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717887 | |||||||
| chr12:132717888 | C | G | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.585+90C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717888 | |||||||
| chr12:132717906 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.586-81C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717906 | |||||||
| chr12:132717939 | G | C | 1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.586-48G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 4/5 | chr12 | 132717939 | |||||||
| chr12:132718142 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(38): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.719+22C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718142 | |||||||
| chr12:132718183 | A | G | 12 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(9): Show |
13 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.719+63A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718183 | |||||||
| chr12:132718212 | C | T | 1 | a0001c0001t0003g0188 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.719+92C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718212 | |||||||
| chr12:132718240 | G | GC | 50 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0003g0003 others(47): Show |
74 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.719+125dupC | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718240 | ||||||
| chr12:132718253 | C | T | 2 | a0001c0004t0008g0058 a0001c0004t0008g0059 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.719+133C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718253 | |||||||
| chr12:132718291 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.719+171C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718291 | |||||||
| chr12:132718358 | T | TGGTGTCC others(68): Show |
1 | a0001c0001t0008g0029 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.719+254_719+255ins others(75): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718358 | ||||||
| chr12:132718358 | T | TGGTGTCC others(220): Show |
1 | a0001c0001t0008g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.719+254_719+255ins others(227): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718358 | ||||||
| chr12:132718358 | T | TGGTGTCC others(159): Show |
1 | a0001c0001t0014g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.719+254_719+255ins others(166): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718358 | ||||||
| chr12:132718358 | T | TGGTGTCC others(158): Show |
1 | a0001c0001t0014g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.719+254_719+255ins others(165): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718358 | ||||||
| chr12:132718358 | TGGTGTCC others(177): Show |
T | 1 | a0001c0008t0006g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.719+278_719+461del | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718358 | ||||||
| chr12:132718361 | T | TGTCCTGG others(283): Show |
1 | a0001c0001t0008g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.719+254_719+255ins others(290): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718361 | ||||||
| chr12:132718361 | T | TGTCCTGG others(282): Show |
1 | a0001c0001t0008g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.719+254_719+255ins others(289): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718361 | ||||||
| chr12:132718361 | T | TGTCCTGG others(298): Show |
2 | a0001c0004t0008g0057 a0001c0004t0008g0059 |
2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.719+254_719+255ins others(305): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718361 | ||||||
| chr12:132718361 | T | TGTCCTGG others(298): Show |
1 | a0001c0004t0008g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.719+254_719+255ins others(305): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718361 | ||||||
| chr12:132718373 | GGTGCGTG others(56): Show |
G | 1 | a0001c0004t0018g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.719+257_719+319del others(63): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718373 | ||||||
| chr12:132718377 | C | G | 2 | a0001c0001t0008g0053 a0001c0001t0008g0055 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.719+257C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718377 | |||||||
| chr12:132718378 | G | A | 8 | a0001c0001t0006g0157 a0001c0001t0008g0029 a0001c0001t0008g0052 others(5): Show |
9 | HG02630.hp1 HG02717.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.719+258G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718378 | |||||||
| chr12:132718386 | T | TG | 8 | a0001c0001t0001g0012 a0001c0001t0001g0163 a0001c0001t0003g0190 others(5): Show |
8 | HG00423.hp1 HG01175.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.719+272dupG | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718386 | ||||||
| chr12:132718391 | G | GGTCCTGG others(84): Show |
1 | a0001c0001t0006g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.719+277_719+278ins others(91): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718391 | ||||||
| chr12:132718391 | G | GGTCCTGG others(178): Show |
1 | a0001c0001t0006g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.719+277_719+278ins others(185): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718391 | ||||||
| chr12:132718391 | G | GGTCCTGG others(115): Show |
4 | a0001c0001t0006g0024 a0001c0001t0006g0109 a0001c0001t0006g0110 others(1): Show |
5 | HG02559.hp1 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+277_719+278ins others(122): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718391 | ||||||
| chr12:132718391 | G | GGTCCTGG others(177): Show |
1 | a0001c0001t0006g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.719+277_719+278ins others(184): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718391 | ||||||
| chr12:132718391 | G | GT | 7 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0014g0050 others(4): Show |
8 | HG02630.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.719+271_719+272ins others(1): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718391 | |||||||
| chr12:132718391 | G | GTGTCCTG others(360): Show |
1 | a0001c0001t0006g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.719+271_719+272ins others(367): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718391 | |||||||
| chr12:132718391 | GGTCCTGA others(85): Show |
G | 1 | a0001c0001t0002g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.719+278_719+369del others(92): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718391 | ||||||
| chr12:132718398 | A | AGTGGGGT others(325): Show |
1 | a0001c0001t0003g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.719+301_719+302ins others(332): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718398 | ||||||
| chr12:132718398 | A | AGTGGGGT others(371): Show |
1 | a0001c0001t0003g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.719+315_719+316ins others(378): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718398 | ||||||
| chr12:132718398 | A | AGTGGGGT others(285): Show |
1 | a0001c0001t0002g0008 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.719+317_719+318ins others(292): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718398 | ||||||
| chr12:132718398 | A | G | 19 | a0001c0001t0005g0069 a0001c0001t0006g0024 a0001c0001t0006g0109 others(16): Show |
22 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.719+278A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718398 | |||||||
| chr12:132718402 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.719+282G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718402 | |||||||
| chr12:132718407 | C | G | 1 | a0001c0001t0005g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.719+287C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718407 | |||||||
| chr12:132718410 | G | C | 1 | a0001c0001t0005g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.719+290G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718410 | |||||||
| chr12:132718422 | T | G | 1 | a0001c0001t0005g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.719+302T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718422 | |||||||
| chr12:132718436 | T | G | 1 | a0001c0001t0003g0196 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.719+316T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718436 | |||||||
| chr12:132718438 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(177): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.719+318T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718438 | |||||||
| chr12:132718438 | T | G | 1 | a0001c0004t0018g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.719+318T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718438 | |||||||
| chr12:132718438 | T | TCCTGGGT others(265): Show |
1 | a0001c0001t0003g0196 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.719+318_719+319ins others(272): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718438 | |||||||
| chr12:132718439 | G | A | 3 | a0001c0001t0003g0189 a0001c0001t0003g0192 a0001c0001t0008g0053 |
3 | HG00738.hp2 HG01243.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.719+319G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718439 | |||||||
| chr12:132718441 | G | C | 2 | a0001c0001t0003g0196 a0001c0004t0018g0164 |
2 | HG02145.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.719+321G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718441 | |||||||
| chr12:132718441 | G | GCTGGGTG others(7): Show |
70 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0013 others(67): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.719+332_719+345dup others(14): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718441 | ||||||
| chr12:132718441 | G | GCTGGTGG others(7): Show |
1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.719+325_719+326ins others(14): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718441 | ||||||
| chr12:132718447 | T | TGGGAGGT others(8): Show |
1 | a0001c0002t0004g0026 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.719+330_719+331ins others(15): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGAGGT others(190): Show |
1 | a0001c0002t0004g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.719+330_719+331ins others(197): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGGGGT others(8): Show |
5 | a0001c0001t0004g0019 a0001c0001t0004g0141 a0001c0002t0004g0019 others(2): Show |
7 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.719+331_719+345dup others(15): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGGGGT others(9): Show |
1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.719+330_719+345dup others(16): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGGGGT others(22): Show |
2 | a0001c0001t0039g0112 a0002c0003t0019g0153 |
2 | HG01433.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.719+345_719+346ins others(29): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGGGGT others(38): Show |
1 | a0001c0002t0004g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.719+345_719+346ins others(45): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGGGTG others(53): Show |
1 | a0001c0001t0008g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.719+332_719+333ins others(60): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718447 | T | TGGGGTGT others(193): Show |
1 | a0001c0002t0004g0142 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.719+331_719+332ins others(200): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718447 | ||||||
| chr12:132718452 | G | GGTCCTGG others(53): Show |
1 | a0001c0001t0021g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(60): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(22): Show |
1 | a0001c0001t0011g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.719+345_719+346ins others(29): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(552): Show |
1 | a0001c0001t0040g0179 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.719+345_719+346ins others(559): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(402): Show |
1 | a0001c0002t0004g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(409): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(326): Show |
1 | a0001c0001t0002g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(333): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(357): Show |
1 | a0001c0001t0003g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.719+345_719+346ins others(364): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(175): Show |
1 | a0001c0001t0005g0065 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(182): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(283): Show |
2 | a0001c0001t0005g0023 a0001c0001t0005g0098 |
4 | HG00099.hp2 HG01099.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.719+345_719+346ins others(290): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(8): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0128 a0001c0001t0006g0168 others(2): Show |
14 | HG00423.hp1 HG00558.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+345_719+346ins others(15): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(204): Show |
1 | a0002c0003t0006g0152 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.719+345_719+346ins others(211): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GGTCCTGG others(83): Show |
1 | a0001c0001t0039g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.719+393_719+394ins others(90): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718452 | G | GT | 7 | a0001c0001t0003g0189 a0001c0001t0003g0192 a0001c0001t0005g0069 others(4): Show |
7 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.719+332_719+333ins others(1): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718452 | |||||||
| chr12:132718452 | G | T | 3 | a0001c0001t0006g0157 a0001c0002t0004g0140 a0001c0002t0004g0142 |
3 | HG01243.hp2 HG03139.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.719+332G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718452 | |||||||
| chr12:132718452 | GGTCCTGG others(24): Show |
G | 3 | a0001c0001t0002g0061 a0001c0001t0002g0087 a0001c0001t0002g0108 |
3 | HG00673.hp2 HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.719+425_719+455del others(31): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718452 | ||||||
| chr12:132718455 | CCTGGGTG others(9): Show |
C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(47): Show |
109 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.719+346_719+361del others(16): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718455 | ||||||
| chr12:132718455 | CCTGGGTG others(40): Show |
C | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.719+346_719+392del others(47): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718455 | ||||||
| chr12:132718461 | T | TGGGGGGT others(8): Show |
1 | a0001c0002t0043g0216 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(15): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718461 | ||||||
| chr12:132718461 | TGGGGTGC others(10): Show |
T | 2 | a0001c0001t0015g0076 a0001c0001t0015g0114 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.719+348_719+364del others(17): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718461 | ||||||
| chr12:132718463 | G | GGGGGTCC others(67): Show |
5 | a0001c0001t0006g0154 a0002c0003t0006g0027 a0002c0003t0006g0149 others(2): Show |
7 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.719+345_719+346ins others(74): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718463 | ||||||
| chr12:132718463 | G | GGGGGTCC others(81): Show |
1 | a0001c0001t0038g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(88): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718463 | ||||||
| chr12:132718463 | G | GGGGTGTC others(22): Show |
1 | a0001c0001t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.719+345_719+346ins others(29): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718463 | ||||||
| chr12:132718464 | GGT | G | 4 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0013g0148 others(1): Show |
5 | HG02630.hp1 HG02717.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+346_719+347del others(2): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718464 | ||||||
| chr12:132718466 | T | G | 7 | a0001c0001t0001g0129 a0001c0001t0006g0154 a0001c0001t0038g0113 others(4): Show |
9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.719+346T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718466 | |||||||
| chr12:132718468 | C | G | 11 | a0001c0001t0001g0129 a0001c0001t0006g0154 a0001c0001t0008g0029 others(8): Show |
14 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+348C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718468 | |||||||
| chr12:132718469 | G | A | 5 | a0001c0001t0006g0157 a0001c0001t0006g0168 a0001c0001t0007g0010 others(2): Show |
10 | HG01106.hp2 HG01928.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.719+349G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718469 | |||||||
| chr12:132718471 | G | C | 11 | a0001c0001t0001g0129 a0001c0001t0006g0154 a0001c0001t0008g0029 others(8): Show |
14 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+351G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718471 | |||||||
| chr12:132718483 | T | G | 6 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0013g0148 others(3): Show |
7 | HG02630.hp1 HG02717.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.719+363T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718483 | |||||||
| chr12:132718483 | T | TGTCCTGG others(250): Show |
1 | a0001c0001t0008g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.719+393_719+394ins others(257): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718483 | ||||||
| chr12:132718500 | G | A | 74 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0013 others(71): Show |
106 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.719+380G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718500 | |||||||
| chr12:132718508 | T | TGGGGGGT others(39): Show |
1 | a0002c0003t0019g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.719+393_719+394ins others(46): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718508 | ||||||
| chr12:132718513 | GT | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0128 a0001c0001t0002g0099 others(9): Show |
16 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.719+394delT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718513 | |||||||
| chr12:132718514 | T | TGTCCTGG others(177): Show |
1 | a0001c0001t0002g0004 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.719+516_719+517ins others(184): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718514 | ||||||
| chr12:132718530 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.719+410C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718530 | |||||||
| chr12:132718531 | G | A | 8 | a0001c0001t0002g0099 a0001c0001t0003g0189 a0001c0001t0003g0192 others(5): Show |
8 | HG00738.hp2 HG01243.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.719+411G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718531 | |||||||
| chr12:132718531 | G | GTGCTGGG others(55): Show |
1 | a0001c0002t0041g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.719+438_719+439ins others(62): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718531 | ||||||
| chr12:132718531 | G | GTGCTGGG others(177): Show |
1 | a0001c0001t0005g0066 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.719+502_719+503ins others(184): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718531 | ||||||
| chr12:132718544 | GT | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(63): Show |
134 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.719+425delT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718544 | |||||||
| chr12:132718545 | T | G | 1 | a0001c0001t0001g0137 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.719+425T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718545 | |||||||
| chr12:132718545 | T | TGTCCTGG others(23): Show |
7 | a0001c0001t0005g0020 a0001c0001t0005g0032 a0001c0001t0005g0064 others(4): Show |
9 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.719+456_719+485dup others(30): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718545 | ||||||
| chr12:132718545 | T | TGTCCTGG others(99): Show |
1 | a0001c0001t0005g0020 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.719+468_719+469ins others(106): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718545 | ||||||
| chr12:132718545 | T | TGTCCTGG others(131): Show |
1 | a0001c0001t0002g0008 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.719+455_719+456ins others(138): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718545 | ||||||
| chr12:132718575 | G | GGTCCTGG others(8): Show |
3 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 |
4 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+468_719+469ins others(15): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(55): Show |
7 | a0001c0001t0004g0019 a0001c0001t0004g0141 a0001c0002t0004g0019 others(4): Show |
11 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.719+471_719+472ins others(62): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(39): Show |
1 | a0001c0001t0003g0196 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.719+471_719+472ins others(46): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(389): Show |
1 | a0001c0001t0012g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.719+485_719+486ins others(396): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(24): Show |
7 | a0001c0001t0006g0154 a0001c0001t0008g0055 a0001c0001t0038g0113 others(4): Show |
9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.719+486_719+516dup others(31): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(344): Show |
1 | a0001c0001t0003g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(351): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(388): Show |
1 | a0001c0002t0029g0063 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.719+499_719+500ins others(395): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(328): Show |
1 | a0001c0001t0003g0181 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(335): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(344): Show |
1 | a0001c0001t0017g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(351): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(538): Show |
1 | a0001c0001t0003g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(545): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(344): Show |
1 | a0001c0001t0003g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.719+499_719+500ins others(351): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(343): Show |
25 | a0001c0001t0003g0003 a0001c0001t0003g0045 a0001c0001t0003g0046 others(22): Show |
38 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.719+499_719+500ins others(350): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(327): Show |
2 | a0001c0001t0003g0174 a0001c0001t0012g0184 |
2 | NA19077.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.719+499_719+500ins others(334): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(357): Show |
1 | a0001c0001t0044g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(364): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(388): Show |
1 | a0001c0002t0004g0218 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.719+499_719+500ins others(395): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(388): Show |
1 | a0001c0001t0003g0185 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.719+499_719+500ins others(395): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(387): Show |
16 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0044 others(13): Show |
29 | HG00642.hp1 HG00735.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.719+499_719+500ins others(394): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(603): Show |
1 | a0001c0001t0003g0186 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(610): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(268): Show |
2 | a0001c0002t0004g0214 a0001c0002t0004g0215 |
2 | NA18990.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.719+499_719+500ins others(275): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GGTCCTGG others(55): Show |
1 | a0002c0003t0006g0149 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.719+516_719+517ins others(62): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718575 | ||||||
| chr12:132718575 | G | GT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.719+455_719+456ins others(1): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718575 | |||||||
| chr12:132718591 | C | CGTGCTGG others(948): Show |
1 | a0001c0002t0004g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.719+499_719+500ins others(955): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718591 | ||||||
| chr12:132718592 | G | A | 1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.719+472G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718592 | |||||||
| chr12:132718615 | T | TGGGGGGT others(399): Show |
1 | a0001c0002t0043g0216 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.719+499_719+500ins others(406): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718615 | ||||||
| chr12:132718618 | G | GGTGCGTG others(57): Show |
1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.719+508_719+509ins others(64): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132718618 | ||||||
| chr12:132718636 | G | GT | 17 | a0001c0001t0001g0160 a0001c0001t0002g0009 a0001c0001t0002g0015 others(14): Show |
31 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.719+516_719+517ins others(1): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718636 | |||||||
| chr12:132718641 | T | G | 2 | a0001c0001t0038g0113 a0001c0001t0039g0112 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.719+521T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718641 | |||||||
| chr12:132718653 | A | G | 1 | a0001c0001t0005g0065 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.719+533A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718653 | |||||||
| chr12:132718753 | C | T | 3 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG01934.hp1 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.719+633C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718753 | |||||||
| chr12:132718767 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(40): Show |
102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.719+647C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718767 | |||||||
| chr12:132718796 | C | G | 9 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(6): Show |
9 | HG01109.hp2 HG01243.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.719+676C>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718796 | |||||||
| chr12:132718837 | G | C | 1 | a0001c0001t0005g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.719+717G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718837 | |||||||
| chr12:132718915 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(67): Show |
139 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.719+795T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132718915 | |||||||
| chr12:132719002 | T | A | 2 | a0001c0001t0038g0113 a0001c0001t0039g0112 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.719+882T>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719002 | |||||||
| chr12:132719014 | T | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0090 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.719+894T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719014 | |||||||
| chr12:132719084 | G | C | 1 | a0001c0001t0003g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.719+964G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719084 | |||||||
| chr12:132719084 | G | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0011g0198 |
3 | HG01099.hp1 HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.719+964G>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719084 | |||||||
| chr12:132719118 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.719+998A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719118 | |||||||
| chr12:132719119 | A | C | 1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.719+999A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719119 | |||||||
| chr12:132719287 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.719+1167T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719287 | |||||||
| chr12:132719380 | C | T | 1 | a0001c0005t0009g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.719+1260C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719380 | |||||||
| chr12:132719491 | A | C | 1 | a0001c0004t0018g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720-1187A>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719491 | |||||||
| chr12:132719518 | C | T | 8 | a0001c0001t0006g0154 a0001c0004t0018g0164 a0002c0003t0006g0027 others(5): Show |
10 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.720-1160C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719518 | |||||||
| chr12:132719520 | C | T | 2 | a0001c0002t0004g0026 a0001c0002t0004g0140 |
4 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-1158C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719520 | |||||||
| chr12:132719579 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.720-1099T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719579 | |||||||
| chr12:132719685 | C | T | 3 | a0001c0004t0008g0057 a0001c0004t0008g0058 a0001c0004t0008g0059 |
3 | HG03139.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.720-993C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719685 | |||||||
| chr12:132719736 | C | T | 1 | a0001c0008t0006g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.720-942C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719736 | |||||||
| chr12:132719738 | G | A | 1 | a0001c0001t0003g0045 | 2 | NA18954.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.720-940G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719738 | |||||||
| chr12:132719771 | G | A | 1 | a0001c0001t0038g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.720-907G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719771 | |||||||
| chr12:132719901 | C | CTAT | 5 | a0001c0001t0002g0021 a0001c0001t0002g0077 a0001c0001t0002g0094 others(2): Show |
7 | HG01433.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.720-777_720-776ins others(3): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719901 | |||||||
| chr12:132719909 | G | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0093 |
5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.720-769G>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132719909 | |||||||
| chr12:132720023 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.720-655T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720023 | |||||||
| chr12:132720097 | A | G | 1 | a0001c0001t0005g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720-581A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720097 | |||||||
| chr12:132720098 | T | TGTCGATC others(15): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0130 |
2 | NA18979.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.720-572_720-571ins others(22): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132720098 | ||||||
| chr12:132720098 | T | TGTCGATC others(16): Show |
151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
253 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.720-568_720-546dup others(23): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132720098 | ||||||
| chr12:132720130 | C | CAGTCATC others(17): Show |
1 | a0001c0007t0004g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.720-546_720-545ins others(24): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132720130 | ||||||
| chr12:132720146 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.720-532G>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720146 | |||||||
| chr12:132720195 | C | A | 7 | a0001c0001t0005g0069 a0001c0001t0009g0031 a0001c0001t0009g0068 others(4): Show |
9 | HG02109.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.720-483C>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720195 | |||||||
| chr12:132720250 | CCCCCTGG others(34): Show |
C | 1 | a0001c0004t0018g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720-419_720-379del others(41): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132720250 | ||||||
| chr12:132720278 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.720-400T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720278 | |||||||
| chr12:132720313 | G | GT | 47 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0119 others(44): Show |
54 | HG00140.hp2 HG00597.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.720-352dupT | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132720313 | ||||||
| chr12:132720339 | GCT | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(51): Show |
117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.720-336_720-335del others(2): Show |
PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 132720339 | ||||||
| chr12:132720347 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(53): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.720-331A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720347 | |||||||
| chr12:132720393 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0166 a0001c0001t0024g0165 |
3 | HG01934.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.720-285C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720393 | |||||||
| chr12:132720433 | A | G | 1 | a0001c0001t0005g0065 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.720-245A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720433 | |||||||
| chr12:132720447 | A | G | 1 | a0001c0005t0009g0035 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.720-231A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720447 | |||||||
| chr12:132720452 | T | C | 11 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.720-226T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720452 | |||||||
| chr12:132720469 | A | G | 11 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.720-209A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720469 | |||||||
| chr12:132720497 | T | C | 7 | a0001c0001t0005g0069 a0001c0001t0009g0031 a0001c0001t0009g0068 others(4): Show |
9 | HG02109.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.720-181T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720497 | |||||||
| chr12:132720508 | C | T | 1 | a0001c0002t0004g0145 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.720-170C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720508 | |||||||
| chr12:132720517 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(166): Show |
274 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.720-161T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720517 | |||||||
| chr12:132720517 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.720-161T>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720517 | |||||||
| chr12:132720542 | T | A | 1 | a0001c0001t0021g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.720-136T>A | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720542 | |||||||
| chr12:132720585 | T | C | 11 | a0001c0001t0008g0029 a0001c0001t0008g0052 a0001c0001t0008g0053 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.720-93T>C | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720585 | |||||||
| chr12:132720596 | A | G | 116 | a0001c0001t0002g0022 a0001c0001t0002g0104 a0001c0001t0002g0105 others(113): Show |
158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.720-82A>G | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720596 | |||||||
| chr12:132720611 | C | T | 3 | a0001c0004t0008g0057 a0001c0004t0008g0058 a0001c0004t0008g0059 |
3 | HG03139.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.720-67C>T | PGAM5 | ENSG00000247077.8 | transcript | ENST00000498926.7 | protein_coding | 5/5 | chr12 | 132720611 |