Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58986 |
| ensemblid | ENSG00000129925.11 |
| hgncid | 17205 |
| symbol | PGAP6 |
| name | post-GPI attachment to proteins 6 |
| refseq_nuc | NM_021259.3 |
| refseq_prot | NP_067082.2 |
| ensembl_nuc | ENST00000431232.7 |
| ensembl_prot | ENSP00000401338.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 370788 |
| end | 381978 |
| strand | - |
| ver | v1.2 |
| region | chr16:370788-381978 |
| region5000 | chr16:365788-386978 |
| regionname0 | PGAP6_chr16_370788_381978 |
| regionname5000 | PGAP6_chr16_365788_386978 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 771 | 176 | 42 | 36 | 78 | 4 | 14 | 53 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0002 | 0/0 | 771 | 122 | 36 | 27 | 36 | 6 | 17 | 25 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0003 | 0/0 | 771 | 52 | 7 | 7 | 18 | 4 | 16 | 11 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0004 | 0/0 | 771 | 9 | 5 | 2 | 1 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0005 | 0/0 | 771 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0006 | 0/0 | 771 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0007 | 0/0 | 771 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0008 | 0/0 | 771 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0009 | 0/0 | 771 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0010 | 0/0 | 771 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0011 | 0/0 | 129 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MAPGP others(124): Show |
chr16 | 365788 | 386978 |
| a0012 | 0/0 | 771 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0013 | 0/0 | 771 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0014 | 0/0 | 771 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0015 | 0/0 | 771 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0016 | 0/0 | 771 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0017 | 0/0 | 771 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0018 | 0/0 | 771 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0019 | 0/0 | 771 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0020 | 0/0 | 771 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| a0021 | 0/0 | 771 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | MGRAG others(766): Show |
chr16 | 365788 | 386978 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2313 | 149 | 20 | 36 | 75 | 4 | 12 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0001c0004 | 0/0 | 2313 | 13 | 13 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0001c0007 | 0/0 | 2313 | 9 | 9 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0001c0011 | 0/0 | 2313 | 2 | 0 | 0 | 0 | 0 | 2 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0001c0025 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0001c0029 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0001c0030 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0002c0002 | 0/0 | 2313 | 106 | 24 | 24 | 35 | 6 | 17 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0002c0005 | 0/0 | 2313 | 9 | 6 | 3 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0002c0009 | 0/0 | 2313 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0002c0010 | 0/0 | 2313 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0002c0021 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0003c0003 | 0/0 | 2313 | 46 | 2 | 6 | 18 | 4 | 16 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0003c0008 | 0/0 | 2313 | 6 | 5 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0004c0006 | 0/0 | 2313 | 9 | 5 | 2 | 1 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0005c0014 | 0/0 | 2313 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0006c0022 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0007c0026 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0008c0028 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0009c0032 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0010c0020 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0011c0012 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGC others(2298): Show |
chr16 | 365788 | 386978 | ||
| a0012c0027 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0013c0016 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0014c0015 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0015c0031 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0016c0018 | 0/0 | 2313 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0017c0019 | 0/0 | 2313 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0018c0013 | 0/0 | 2313 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0019c0024 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0020c0017 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 | ||
| a0021c0023 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | ATGGG others(2308): Show |
chr16 | 365788 | 386978 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3672 | 6 | 2 | 1 | 2 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0002 | 1/1 | 3672 | 131 | 13 | 33 | 69 | 4 | 10 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0004 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3666): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0005 | 0/0 | 3672 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0007 | 0/0 | 3674 | 3 | 0 | 0 | 3 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3669): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0008 | 0/0 | 3672 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0012 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0001t0019 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0004t0001 | 0/0 | 3672 | 6 | 6 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0004t0002 | 0/0 | 3672 | 5 | 5 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0004t0009 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3666): Show |
chr16 | 365788 | 386978 |
| a0001c0004t0013 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0007t0004 | 0/0 | 3671 | 9 | 9 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3666): Show |
chr16 | 365788 | 386978 |
| a0001c0011t0002 | 0/0 | 3672 | 2 | 0 | 0 | 0 | 0 | 2 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0025t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0029t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0001c0030t0003 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0001 | 0/0 | 3672 | 80 | 13 | 17 | 32 | 4 | 14 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0003 | 0/0 | 3672 | 17 | 7 | 6 | 0 | 1 | 3 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0006 | 0/0 | 3672 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0011 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0015 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0016 | 0/0 | 3672 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0002t0017 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3655): Show |
chr16 | 365788 | 386978 |
| a0002c0005t0001 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0005t0005 | 0/0 | 3672 | 5 | 4 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0005t0006 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0005t0010 | 0/0 | 3672 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0009t0001 | 0/0 | 3672 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0010t0001 | 0/0 | 3672 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0002c0021t0001 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0003c0003t0001 | 0/0 | 3672 | 45 | 2 | 6 | 17 | 4 | 16 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0003c0003t0014 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0003c0008t0004 | 0/0 | 3671 | 6 | 5 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3666): Show |
chr16 | 365788 | 386978 |
| a0004c0006t0001 | 0/0 | 3672 | 8 | 4 | 2 | 1 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0004c0006t0002 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0005c0014t0001 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0006c0022t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0007c0026t0002 | 0/0 | 3672 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0008c0028t0002 | 0/0 | 3672 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0009c0032t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0010c0020t0004 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3666): Show |
chr16 | 365788 | 386978 |
| a0011c0012t0018 | 0/0 | 3662 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3657): Show |
chr16 | 365788 | 386978 |
| a0012c0027t0001 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0013c0016t0001 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0014c0015t0005 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0015c0031t0009 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3666): Show |
chr16 | 365788 | 386978 |
| a0016c0018t0001 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0017c0019t0001 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0018c0013t0001 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0019c0024t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0020c0017t0001 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| a0021c0023t0002 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | AGTGC others(3667): Show |
chr16 | 365788 | 386978 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0001 | 1/0 | 93 | 4 | 27 | 53 | 4 | 4 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0007g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0008g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0001t0019g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0004t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0007t0004g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0007t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0007t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0007t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0007t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0011t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0025t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0029t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0001c0030t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0002 | 0/0 | 28 | 0 | 5 | 17 | 2 | 4 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0004 | 0/0 | 17 | 9 | 0 | 8 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0005 | 0/0 | 8 | 0 | 5 | 0 | 0 | 3 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0006 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0010 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0006g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0011g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0015g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0016g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0002t0017g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0005t0010g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0009t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0009t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0009t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0010t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0002c0021t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0003 | 0/0 | 21 | 1 | 4 | 10 | 2 | 4 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0008 | 0/0 | 6 | 0 | 0 | 0 | 0 | 6 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0003t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0003c0008t0004g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0004c0006t0001g0014 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0004c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0004c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0004c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0004c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0004c0006t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0005c0014t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0006c0022t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0007c0026t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0008c0028t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0009c0032t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0010c0020t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0011c0012t0018g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0012c0027t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0013c0016t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0014c0015t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0015c0031t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0016c0018t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0017c0019t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0018c0013t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0019c0024t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0020c0017t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| a0021c0023t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0003 | g0010 | EUR | GBR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0077 | EUR | GBR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0113 | EUR | GBR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | GBR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00280 | hp1 | a0005 | c0014 | t0001 | g0076 | EUR | FIN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00323 | hp2 | a0004 | c0006 | t0001 | g0098 | EUR | FIN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00408 | hp1 | a0002 | c0021 | t0001 | g0063 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00438 | hp1 | a0006 | c0022 | t0002 | g0121 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0107 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00642 | hp1 | a0004 | c0006 | t0001 | g0014 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | CHS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0093 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01069 | hp2 | a0002 | c0005 | t0010 | g0025 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01070 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01071 | hp2 | a0002 | c0005 | t0010 | g0025 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01106 | hp1 | a0002 | c0005 | t0005 | g0105 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0145 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01243 | hp1 | a0003 | c0008 | t0004 | g0007 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0034 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0091 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01346 | hp2 | a0002 | c0002 | t0016 | g0042 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0083 | EUR | IBS | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0011 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01891 | hp1 | a0002 | c0005 | t0006 | g0104 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01891 | hp2 | a0002 | c0002 | t0006 | g0012 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01934 | hp1 | a0007 | c0026 | t0002 | g0134 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01952 | hp1 | a0008 | c0028 | t0002 | g0137 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01981 | hp2 | a0004 | c0006 | t0001 | g0014 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02004 | hp2 | a0003 | c0003 | t0001 | g0085 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02015 | hp1 | a0009 | c0032 | t0002 | g0150 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02027 | hp1 | a0003 | c0003 | t0014 | g0090 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02055 | hp2 | a0002 | c0009 | t0001 | g0149 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02056 | hp1 | a0002 | c0002 | t0017 | g0151 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0084 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02080 | hp2 | a0004 | c0006 | t0001 | g0014 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02132 | hp1 | a0011 | c0012 | t0018 | g0152 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CDX | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02165 | hp2 | a0012 | c0027 | t0001 | g0136 | EAS | CDX | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0050 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0003 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02280 | hp2 | a0002 | c0005 | t0005 | g0026 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02451 | hp1 | a0001 | c0007 | t0004 | g0016 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02572 | hp1 | a0002 | c0010 | t0001 | g0035 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0009 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02615 | hp2 | a0001 | c0007 | t0004 | g0024 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02622 | hp1 | a0001 | c0007 | t0004 | g0125 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02647 | hp1 | a0013 | c0016 | t0001 | g0078 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02647 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02717 | hp1 | a0002 | c0002 | t0006 | g0012 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02723 | hp1 | a0003 | c0008 | t0004 | g0007 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02723 | hp2 | a0001 | c0007 | t0004 | g0028 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0106 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02818 | hp1 | a0001 | c0007 | t0004 | g0028 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02818 | hp2 | a0003 | c0008 | t0004 | g0007 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02886 | hp2 | a0002 | c0005 | t0005 | g0103 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02895 | hp1 | a0004 | c0006 | t0001 | g0097 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02896 | hp1 | a0002 | c0010 | t0001 | g0035 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02965 | hp1 | a0014 | c0015 | t0005 | g0087 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02970 | hp2 | a0015 | c0031 | t0009 | g0044 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0144 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0088 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0010 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03041 | hp2 | a0001 | c0007 | t0004 | g0016 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03098 | hp1 | a0004 | c0006 | t0001 | g0096 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03130 | hp1 | a0001 | c0004 | t0009 | g0045 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03195 | hp1 | a0001 | c0007 | t0004 | g0016 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03209 | hp2 | a0004 | c0006 | t0001 | g0100 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03225 | hp1 | a0002 | c0009 | t0001 | g0148 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03486 | hp1 | a0002 | c0005 | t0005 | g0102 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03486 | hp2 | a0004 | c0006 | t0001 | g0014 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0023 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03516 | hp1 | a0001 | c0007 | t0004 | g0024 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03540 | hp1 | a0002 | c0005 | t0005 | g0026 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03540 | hp2 | a0001 | c0004 | t0002 | g0048 | AFR | GWD | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03579 | hp1 | a0001 | c0004 | t0013 | g0049 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03579 | hp2 | a0001 | c0004 | t0002 | g0047 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0094 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0023 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03704 | hp2 | a0001 | c0001 | t0012 | g0130 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0008 | SAS | PJL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03831 | hp1 | a0016 | c0018 | t0001 | g0067 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0010 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03834 | hp2 | a0017 | c0019 | t0001 | g0086 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03927 | hp1 | a0001 | c0011 | t0002 | g0033 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0008 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | BEB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0066 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0008 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04204 | hp2 | a0018 | c0013 | t0001 | g0056 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0082 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | STU | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18522 | hp1 | a0003 | c0008 | t0004 | g0007 | AFR | YRI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | YRI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18906 | hp1 | a0001 | c0007 | t0004 | g0132 | AFR | YRI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0072 | AFR | YRI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18959 | hp2 | a0001 | c0030 | t0003 | g0043 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18979 | hp1 | a0019 | c0024 | t0002 | g0116 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18979 | hp2 | a0020 | c0017 | t0001 | g0080 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18982 | hp1 | a0021 | c0023 | t0002 | g0126 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18988 | hp1 | a0001 | c0001 | t0019 | g0153 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA18998 | hp2 | a0001 | c0029 | t0002 | g0139 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19011 | hp1 | a0001 | c0025 | t0002 | g0133 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0051 | AFR | LWK | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19030 | hp2 | a0002 | c0009 | t0001 | g0036 | AFR | LWK | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | LWK | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19054 | hp1 | a0002 | c0002 | t0015 | g0059 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0146 | AFR | YRI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | YRI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20129 | hp1 | a0001 | c0004 | t0002 | g0021 | AFR | ASW | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20129 | hp2 | a0003 | c0008 | t0004 | g0007 | AFR | ASW | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20752 | hp2 | a0002 | c0002 | t0011 | g0057 | EUR | TSI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0061 | EUR | TSI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | GIH | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20905 | hp2 | a0001 | c0011 | t0002 | g0033 | SAS | GIH | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0046 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02109 | hp2 | a0010 | c0020 | t0004 | g0092 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0101 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02486 | hp2 | a0002 | c0002 | t0006 | g0012 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03471 | hp1 | a0004 | c0006 | t0002 | g0099 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | MSL | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | USA | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| HG06807 | hp2 | a0003 | c0008 | t0004 | g0007 | AFR | USA | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA20300 | hp2 | a0002 | c0009 | t0001 | g0036 | AFR | USA | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| NA21309 | hp2 | a0002 | c0002 | t0006 | g0012 | AFR | LWK | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0114 | REF | REF | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | PGAP6_chr16_365788_386978 | PGAP6 | chr16 | 365788 | 386978 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:372168 | A | G | 1 | a0013 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2135T>C | p.Met712Thr | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 2292/3672 | 2135/2316 | 712/771 | chr16 | 372168 | |||
| chr16:372277 | G | A | 1 | a0007 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.2026C>T | p.Arg676Cys | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 2183/3672 | 2026/2316 | 676/771 | chr16 | 372277 | |||
| chr16:372676 | G | A | 1 | a0020 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1954C>T | p.Arg652Cys | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/13 | 2111/3672 | 1954/2316 | 652/771 | chr16 | 372676 | |||
| chr16:372693 | A | G | 1 | a0015 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1937T>C | p.Met646Thr | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/13 | 2094/3672 | 1937/2316 | 646/771 | chr16 | 372693 | |||
| chr16:374050 | C | A | 1 | a0012 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1857G>T | p.Trp619Cys | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/13 | 2014/3672 | 1857/2316 | 619/771 | chr16 | 374050 | |||
| chr16:374277 | G | A | 5 | a0003 a0010 a0014 others(2): Show |
56 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
missense_variant | MODERATE | c.1699C>T | p.Arg567Trp | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 10/13 | 1856/3672 | 1699/2316 | 567/771 | chr16 | 374277 | |||
| chr16:374288 | G | A | 1 | a0004 | 9 | HG00323.hp2 HG00642.hp1 HG01981.hp2 others(6): Show |
missense_variant | MODERATE | c.1688C>T | p.Ala563Val | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 10/13 | 1845/3672 | 1688/2316 | 563/771 | chr16 | 374288 | |||
| chr16:375194 | G | C | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1378C>G | p.Pro460Ala | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/13 | 1535/3672 | 1378/2316 | 460/771 | chr16 | 375194 | |||
| chr16:375203 | G | C | 1 | a0008 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1369C>G | p.Leu457Val | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/13 | 1526/3672 | 1369/2316 | 457/771 | chr16 | 375203 | |||
| chr16:375414 | C | T | 1 | a0021 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1246G>A | p.Val416Ile | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 7/13 | 1403/3672 | 1246/2316 | 416/771 | chr16 | 375414 | |||
| chr16:376288 | G | C | 1 | a0019 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.1072C>G | p.Arg358Gly | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/13 | 1229/3672 | 1072/2316 | 358/771 | chr16 | 376288 | |||
| chr16:376432 | T | C | 12 | a0002 a0003 a0004 others(9): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
missense_variant | MODERATE | c.928A>G | p.Ile310Val | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/13 | 1085/3672 | 928/2316 | 310/771 | chr16 | 376432 | |||
| chr16:376769 | G | A | 1 | a0017 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.679C>T | p.Arg227Trp | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 5/13 | 836/3672 | 679/2316 | 227/771 | chr16 | 376769 | |||
| chr16:377080 | C | T | 1 | a0014 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.592G>A | p.Val198Met | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/13 | 749/3672 | 592/2316 | 198/771 | chr16 | 377080 | |||
| chr16:377110 | C | T | 1 | a0005 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.562G>A | p.Val188Met | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/13 | 719/3672 | 562/2316 | 188/771 | chr16 | 377110 | |||
| chr16:377479 | T | C | 11 | a0002 a0003 a0004 others(8): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
missense_variant | MODERATE | c.406A>G | p.Thr136Ala | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/13 | 563/3672 | 406/2316 | 136/771 | chr16 | 377479 | |||
| chr16:377550 | G | A | 1 | a0010 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.335C>T | p.Pro112Leu | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/13 | 492/3672 | 335/2316 | 112/771 | chr16 | 377550 | |||
| chr16:377699 | C | G | 1 | a0018 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.271G>C | p.Ala91Pro | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/13 | 428/3672 | 271/2316 | 91/771 | chr16 | 377699 | |||
| chr16:377758 | C | T | 1 | a0021 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.212G>A | p.Arg71His | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/13 | 369/3672 | 212/2316 | 71/771 | chr16 | 377758 | |||
| chr16:377783 | C | T | 1 | a0006 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.187G>A | p.Gly63Ser | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/13 | 344/3672 | 187/2316 | 63/771 | chr16 | 377783 | |||
| chr16:381799 | G | A | 1 | a0009 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.23C>T | p.Thr8Ile | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 180/3672 | 23/2316 | 8/771 | chr16 | 381799 | |||
| chr16:381807 | GCCAGCCC others(3): Show |
G | 1 | a0011 | 1 | HG02132.hp1 | frameshift_variant | HIGH | c.5_14delGCCGGGCTGG | p.Gly2fs | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 171/3672 | 5/2316 | 2/771 | chr16 | 381807 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:372089 | C | T | 1 | a0002c0010 | 2 | HG02572.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.2214G>A | p.Pro738Pro | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 2371/3672 | 2214/2316 | 738/771 | chr16 | 372089 | |||
| chr16:372158 | G | A | 3 | a0001c0007 a0003c0008 a0010c0020 |
16 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(13): Show |
synonymous_variant | LOW | c.2145C>T | p.Ser715Ser | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 2302/3672 | 2145/2316 | 715/771 | chr16 | 372158 | |||
| chr16:372272 | G | A | 1 | a0001c0025 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.2031C>T | p.Cys677Cys | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 2188/3672 | 2031/2316 | 677/771 | chr16 | 372272 | |||
| chr16:376184 | G | A | 2 | a0002c0005 a0004c0006 |
18 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
synonymous_variant | LOW | c.1176C>T | p.Thr392Thr | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/13 | 1333/3672 | 1176/2316 | 392/771 | chr16 | 376184 | |||
| chr16:376289 | C | T | 1 | a0019c0024 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1071G>A | p.Thr357Thr | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/13 | 1228/3672 | 1071/2316 | 357/771 | chr16 | 376289 | |||
| chr16:376734 | G | A | 1 | a0001c0029 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.714C>T | p.Pro238Pro | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 5/13 | 871/3672 | 714/2316 | 238/771 | chr16 | 376734 | |||
| chr16:377435 | G | A | 1 | a0002c0009 | 4 | HG02055.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.450C>T | p.Pro150Pro | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/13 | 607/3672 | 450/2316 | 150/771 | chr16 | 377435 | |||
| chr16:377435 | G | T | 1 | a0001c0030 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.450C>A | p.Pro150Pro | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/13 | 607/3672 | 450/2316 | 150/771 | chr16 | 377435 | |||
| chr16:377498 | G | A | 1 | a0001c0011 | 2 | HG03927.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.387C>T | p.Val129Val | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/13 | 544/3672 | 387/2316 | 129/771 | chr16 | 377498 | |||
| chr16:377516 | T | C | 19 | a0001c0004 a0001c0030 a0002c0002 others(16): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
synonymous_variant | LOW | c.369A>G | p.Val123Val | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/13 | 526/3672 | 369/2316 | 123/771 | chr16 | 377516 | |||
| chr16:377769 | G | C | 1 | a0002c0021 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.201C>G | p.Leu67Leu | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/13 | 358/3672 | 201/2316 | 67/771 | chr16 | 377769 | |||
| chr16:377784 | G | A | 16 | a0002c0002 a0002c0005 a0002c0009 others(13): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
synonymous_variant | LOW | c.186C>T | p.Tyr62Tyr | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/13 | 343/3672 | 186/2316 | 62/771 | chr16 | 377784 | |||
| chr16:377820 | C | T | 15 | a0002c0002 a0002c0005 a0002c0010 others(12): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
synonymous_variant | LOW | c.150G>A | p.Ser50Ser | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/13 | 307/3672 | 150/2316 | 50/771 | chr16 | 377820 | |||
| chr16:381702 | G | A | 1 | a0002c0009 | 4 | HG02055.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.120C>T | p.Ser40Ser | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 277/3672 | 120/2316 | 40/771 | chr16 | 381702 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:370830 | AC | A | 6 | a0001c0001t0004 a0001c0004t0009 a0001c0007t0004 others(3): Show |
19 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1156delG | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 1156 | chr16 | 370830 | ||||||
| chr16:370848 | C | T | 1 | a0001c0004t0013 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1139G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 1139 | chr16 | 370848 | ||||||
| chr16:370886 | C | T | 1 | a0002c0005t0010 | 2 | HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1101G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 1101 | chr16 | 370886 | ||||||
| chr16:370899 | C | CAT | 1 | a0001c0001t0007 | 3 | HG00423.hp1 HG00609.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1086_*1087dupAT | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 1087 | chr16 | 370899 | ||||||
| chr16:370907 | T | C | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1080A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 1080 | chr16 | 370907 | ||||||
| chr16:370914 | C | T | 6 | a0001c0001t0004 a0001c0004t0009 a0001c0007t0004 others(3): Show |
19 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1073G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 1073 | chr16 | 370914 | ||||||
| chr16:370998 | G | C | 1 | a0002c0002t0016 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*989C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 989 | chr16 | 370998 | ||||||
| chr16:371032 | G | A | 1 | a0003c0003t0014 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*955C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 955 | chr16 | 371032 | ||||||
| chr16:371050 | G | A | 2 | a0002c0002t0006 a0002c0005t0006 |
5 | HG01891.hp1 HG01891.hp2 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 937 | chr16 | 371050 | ||||||
| chr16:371301 | G | A | 1 | a0002c0002t0015 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*686C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 686 | chr16 | 371301 | ||||||
| chr16:371387 | G | A | 4 | a0001c0001t0004 a0001c0007t0004 a0003c0008t0004 others(1): Show |
17 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*600C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 600 | chr16 | 371387 | ||||||
| chr16:371423 | C | A | 1 | a0001c0001t0019 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 564 | chr16 | 371423 | ||||||
| chr16:371424 | A | T | 1 | a0001c0001t0019 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*563T>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 563 | chr16 | 371424 | ||||||
| chr16:371524 | C | T | 4 | a0001c0001t0005 a0002c0005t0005 a0002c0005t0010 others(1): Show |
12 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*463G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 463 | chr16 | 371524 | ||||||
| chr16:371551 | C | T | 1 | a0001c0001t0012 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 436 | chr16 | 371551 | ||||||
| chr16:371723 | A | C | 2 | a0001c0001t0008 a0002c0002t0011 |
3 | HG01256.hp2 HG01258.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*264T>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 264 | chr16 | 371723 | ||||||
| chr16:371912 | G | A | 7 | a0001c0001t0005 a0001c0030t0003 a0002c0002t0003 others(4): Show |
31 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*75C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 13/13 | 75 | chr16 | 371912 | ||||||
| chr16:381825 | T | A | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 4 | chr16 | 381825 | ||||||
| chr16:381829 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 8 | chr16 | 381829 | ||||||
| chr16:381831 | C | A | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-10G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 10 | chr16 | 381831 | ||||||
| chr16:381832 | T | C | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 11 | chr16 | 381832 | ||||||
| chr16:381836 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 15 | chr16 | 381836 | ||||||
| chr16:381859 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 38 | chr16 | 381859 | ||||||
| chr16:381862 | C | T | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 41 | chr16 | 381862 | ||||||
| chr16:381863 | G | C | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 42 | chr16 | 381863 | ||||||
| chr16:381865 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 44 | chr16 | 381865 | ||||||
| chr16:381882 | G | T | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 61 | chr16 | 381882 | ||||||
| chr16:381883 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 62 | chr16 | 381883 | ||||||
| chr16:381884 | CCGGGCAG others(5): Show |
C | 1 | a0002c0002t0017 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-75_-64delAGAGGCTG others(4): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 64 | chr16 | 381884 | ||||||
| chr16:381886 | G | C | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-65C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 65 | chr16 | 381886 | ||||||
| chr16:381887 | G | T | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-66C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 66 | chr16 | 381887 | ||||||
| chr16:381890 | A | T | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69T>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 69 | chr16 | 381890 | ||||||
| chr16:381890 | AGCCTCTG others(8): Show |
A | 28 | a0001c0001t0002 a0001c0004t0001 a0001c0030t0003 others(25): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-70delGGAGGCGG others(7): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 70 | chr16 | 381890 | ||||||
| chr16:381901 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 80 | chr16 | 381901 | ||||||
| chr16:381902 | C | G | 1 | a0002c0002t0017 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 81 | chr16 | 381902 | ||||||
| chr16:381903 | T | C | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 82 | chr16 | 381903 | ||||||
| chr16:381903 | T | G | 1 | a0002c0002t0017 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 82 | chr16 | 381903 | ||||||
| chr16:381905 | C | A | 1 | a0002c0002t0017 | 1 | HG02056.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | chr16 | 381905 | |||||||
| chr16:381906 | G | C | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-85C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 85 | chr16 | 381906 | ||||||
| chr16:381908 | C | G | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 87 | chr16 | 381908 | ||||||
| chr16:381909 | T | C | 1 | a0011c0012t0018 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 88 | chr16 | 381909 | ||||||
| chr16:381958 | G | C | 1 | a0001c0001t0019 | 1 | NA18988.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/13 | 137 | chr16 | 381958 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:372326 | C | T | 1 | a0002c0005t0005g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2020-43G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/12 | chr16 | 372326 | |||||||
| chr16:372412 | G | A | 22 | a0001c0001t0001g0019 a0001c0004t0001g0015 a0001c0004t0001g0050 others(19): Show |
34 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.2020-129C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/12 | chr16 | 372412 | |||||||
| chr16:372435 | C | G | 1 | a0002c0002t0003g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2020-152G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/12 | chr16 | 372435 | |||||||
| chr16:372516 | T | G | 30 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0002c0002t0001g0064 others(27): Show |
61 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2019+95A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/12 | chr16 | 372516 | |||||||
| chr16:372544 | A | AG | 6 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(3): Show |
12 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2019+66dupC | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 12/12 | chr16 | 372544 | |||||||
| chr16:373203 | G | C | 1 | a0001c0001t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1903-476C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373203 | |||||||
| chr16:373394 | C | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0055 a0002c0002t0001g0060 others(11): Show |
41 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1902+611G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373394 | |||||||
| chr16:373405 | T | C | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1902+600A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373405 | |||||||
| chr16:373420 | C | T | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+585G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373420 | |||||||
| chr16:373423 | A | G | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+582T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373423 | |||||||
| chr16:373431 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1902+574C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373431 | |||||||
| chr16:373526 | T | A | 1 | a0001c0001t0002g0032 | 2 | NA18943.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1902+479A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373526 | |||||||
| chr16:373555 | G | A | 75 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(72): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1902+450C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373555 | |||||||
| chr16:373560 | T | A | 1 | a0002c0002t0003g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1902+445A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373560 | |||||||
| chr16:373619 | C | T | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+386G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373619 | |||||||
| chr16:373696 | C | T | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+309G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373696 | |||||||
| chr16:373741 | G | A | 1 | a0003c0003t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1902+264C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373741 | |||||||
| chr16:373750 | G | T | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+255C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373750 | |||||||
| chr16:373775 | T | C | 6 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(3): Show |
12 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1902+230A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373775 | |||||||
| chr16:373794 | CCACCATG others(29): Show |
C | 1 | a0001c0004t0002g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1902+175_1902+210d others(38): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373794 | |||||||
| chr16:373808 | C | A | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+197G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373808 | |||||||
| chr16:373809 | A | G | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+196T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373809 | |||||||
| chr16:373809 | AAGGCATT others(27): Show |
A | 8 | a0001c0004t0001g0015 a0001c0004t0001g0106 a0001c0004t0002g0021 others(5): Show |
11 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1902+162_1902+195d others(36): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373809 | |||||||
| chr16:373813 | C | G | 95 | a0001c0001t0001g0019 a0001c0001t0002g0017 a0001c0001t0002g0141 others(92): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1902+192G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373813 | |||||||
| chr16:373828 | CCA | C | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+175_1902+176d others(4): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373828 | |||||||
| chr16:373842 | C | A | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+163G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373842 | |||||||
| chr16:373843 | T | A | 1 | a0001c0004t0002g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1902+162A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373843 | |||||||
| chr16:373843 | T | G | 76 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1902+162A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373843 | |||||||
| chr16:373877 | G | A | 1 | a0003c0003t0001g0085 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1902+128C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 11/12 | chr16 | 373877 | |||||||
| chr16:374198 | C | A | 1 | a0001c0004t0002g0047 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1755+23G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 10/12 | chr16 | 374198 | |||||||
| chr16:374403 | C | T | 10 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0013 others(7): Show |
25 | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.1577-4G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 9/12 | chr16 | 374403 | |||||||
| chr16:374420 | C | G | 82 | a0001c0001t0005g0124 a0001c0030t0003g0043 a0002c0002t0001g0002 others(79): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1577-21G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 9/12 | chr16 | 374420 | |||||||
| chr16:374422 | C | T | 1 | a0003c0003t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1577-23G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 9/12 | chr16 | 374422 | |||||||
| chr16:374526 | G | A | 1 | a0002c0002t0001g0060 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1577-127C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 9/12 | chr16 | 374526 | |||||||
| chr16:374695 | A | G | 6 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(3): Show |
12 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1576+61T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 9/12 | chr16 | 374695 | |||||||
| chr16:374944 | TGCCACCA others(11): Show |
T | 1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1440-70_1440-53del others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/12 | chr16 | 374944 | |||||||
| chr16:374972 | G | A | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1440-80C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/12 | chr16 | 374972 | |||||||
| chr16:375046 | C | T | 1 | a0016c0018t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1439+87G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/12 | chr16 | 375046 | |||||||
| chr16:375068 | C | T | 1 | a0002c0005t0005g0103 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1439+65G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/12 | chr16 | 375068 | |||||||
| chr16:375069 | G | A | 1 | a0002c0005t0005g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1439+64C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 8/12 | chr16 | 375069 | |||||||
| chr16:375277 | C | T | 17 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(14): Show |
51 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1316-21G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 7/12 | chr16 | 375277 | |||||||
| chr16:375298 | G | T | 62 | a0001c0001t0005g0124 a0002c0002t0001g0002 a0002c0002t0001g0004 others(59): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1316-42C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 7/12 | chr16 | 375298 | |||||||
| chr16:375325 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1315+20C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 7/12 | chr16 | 375325 | |||||||
| chr16:375329 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1315+16G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 7/12 | chr16 | 375329 | |||||||
| chr16:375456 | G | A | 5 | a0001c0001t0001g0019 a0001c0004t0001g0015 a0001c0004t0001g0051 others(2): Show |
9 | HG00639.hp2 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1225-21C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375456 | |||||||
| chr16:375533 | C | CT | 6 | a0001c0001t0002g0030 a0001c0001t0002g0117 a0001c0001t0004g0120 others(3): Show |
7 | HG00323.hp2 HG00738.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225-99dupA | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375533 | |||||||
| chr16:375596 | G | A | 7 | a0001c0004t0002g0021 a0001c0004t0002g0046 a0001c0004t0002g0047 others(4): Show |
8 | HG02109.hp1 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225-161C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375596 | |||||||
| chr16:375605 | T | C | 79 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(76): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1225-170A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375605 | |||||||
| chr16:375611 | C | T | 1 | a0004c0006t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1225-176G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375611 | |||||||
| chr16:375766 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1225-331C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375766 | |||||||
| chr16:375782 | G | A | 1 | a0018c0013t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1225-347C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375782 | |||||||
| chr16:375785 | C | T | 74 | a0001c0030t0003g0043 a0002c0002t0001g0002 a0002c0002t0001g0004 others(71): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1225-350G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375785 | |||||||
| chr16:375826 | G | A | 3 | a0002c0009t0001g0036 a0002c0009t0001g0148 a0002c0009t0001g0149 |
4 | HG02055.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+310C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375826 | |||||||
| chr16:375891 | G | A | 5 | a0001c0001t0001g0019 a0001c0004t0001g0015 a0001c0004t0001g0050 others(2): Show |
9 | HG00639.hp2 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1224+245C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375891 | |||||||
| chr16:375937 | C | T | 13 | a0002c0005t0001g0101 a0002c0005t0005g0026 a0002c0005t0005g0102 others(10): Show |
18 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1224+199G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375937 | |||||||
| chr16:375942 | A | G | 6 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(3): Show |
12 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1224+194T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375942 | |||||||
| chr16:375947 | C | T | 2 | a0003c0003t0001g0082 a0003c0003t0001g0088 |
2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1224+189G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375947 | |||||||
| chr16:375962 | G | A | 2 | a0001c0004t0002g0021 a0001c0004t0002g0048 |
3 | HG02647.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1224+174C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375962 | |||||||
| chr16:375985 | A | C | 1 | a0001c0001t0002g0129 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1224+151T>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375985 | |||||||
| chr16:375990 | C | T | 1 | a0001c0001t0002g0020 | 3 | NA18971.hp2 NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1224+146G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 375990 | |||||||
| chr16:376004 | CCT | C | 60 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1224+130_1224+131d others(4): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376004 | |||||||
| chr16:376007 | G | A | 4 | a0002c0002t0001g0006 a0002c0002t0001g0013 a0002c0002t0001g0069 others(1): Show |
12 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1224+129C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376007 | |||||||
| chr16:376029 | G | A | 13 | a0002c0005t0001g0101 a0002c0005t0005g0026 a0002c0005t0005g0102 others(10): Show |
18 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1224+107C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376029 | |||||||
| chr16:376035 | G | C | 1 | a0001c0001t0002g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1224+101C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376035 | |||||||
| chr16:376067 | A | C | 1 | a0001c0001t0002g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1224+69T>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376067 | |||||||
| chr16:376087 | G | A | 1 | a0003c0003t0001g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1224+49C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376087 | |||||||
| chr16:376095 | G | A | 13 | a0002c0005t0001g0101 a0002c0005t0005g0026 a0002c0005t0005g0102 others(10): Show |
18 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1224+41C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376095 | |||||||
| chr16:376099 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1224+37C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 6/12 | chr16 | 376099 | |||||||
| chr16:376475 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.905-20A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 5/12 | chr16 | 376475 | |||||||
| chr16:376476 | T | C | 84 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(81): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.905-21A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 5/12 | chr16 | 376476 | |||||||
| chr16:376536 | C | T | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | splice_region_variant&intron_variant | LOW | c.904+8G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 5/12 | chr16 | 376536 | |||||||
| chr16:376874 | G | C | 7 | a0001c0004t0002g0021 a0001c0004t0002g0046 a0001c0004t0002g0047 others(4): Show |
8 | HG02109.hp1 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.636-62C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/12 | chr16 | 376874 | |||||||
| chr16:376967 | G | A | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.635+70C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/12 | chr16 | 376967 | |||||||
| chr16:377010 | C | T | 24 | a0002c0002t0003g0093 a0002c0010t0001g0035 a0003c0003t0001g0003 others(21): Show |
51 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.635+27G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/12 | chr16 | 377010 | |||||||
| chr16:377013 | G | C | 77 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(74): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.635+24C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/12 | chr16 | 377013 | |||||||
| chr16:377013 | G | T | 3 | a0001c0004t0009g0045 a0001c0004t0013g0049 a0015c0031t0009g0044 |
3 | HG02970.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.635+24C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 4/12 | chr16 | 377013 | |||||||
| chr16:377219 | G | T | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.508-55C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377219 | |||||||
| chr16:377241 | C | T | 3 | a0001c0001t0005g0124 a0002c0002t0001g0077 a0005c0014t0001g0076 |
3 | HG00099.hp2 HG00280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.508-77G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377241 | |||||||
| chr16:377303 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.507+75G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377303 | |||||||
| chr16:377309 | G | A | 83 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(80): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.507+69C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377309 | |||||||
| chr16:377332 | C | T | 2 | a0002c0009t0001g0036 a0002c0009t0001g0148 |
3 | HG03225.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.507+46G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377332 | |||||||
| chr16:377349 | C | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.507+29G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377349 | |||||||
| chr16:377373 | C | G | 1 | a0002c0002t0001g0075 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.507+5G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 3/12 | chr16 | 377373 | |||||||
| chr16:377594 | G | A | 1 | a0002c0021t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.300-9C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/12 | chr16 | 377594 | |||||||
| chr16:377657 | G | A | 81 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(78): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.299+14C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 2/12 | chr16 | 377657 | |||||||
| chr16:377860 | A | C | 4 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(1): Show |
6 | HG02257.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-12T>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 377860 | |||||||
| chr16:377866 | T | C | 84 | a0001c0030t0003g0043 a0002c0002t0001g0002 a0002c0002t0001g0004 others(81): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.122-18A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 377866 | |||||||
| chr16:377925 | T | C | 80 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(77): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.122-77A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 377925 | |||||||
| chr16:377999 | C | G | 106 | a0001c0001t0001g0019 a0001c0001t0002g0017 a0001c0001t0002g0140 others(103): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.122-151G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 377999 | |||||||
| chr16:378001 | A | C | 80 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(77): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.122-153T>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378001 | |||||||
| chr16:378095 | C | T | 25 | a0003c0003t0001g0003 a0003c0003t0001g0008 a0003c0003t0001g0023 others(22): Show |
56 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.122-247G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378095 | |||||||
| chr16:378122 | C | T | 4 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(1): Show |
6 | HG02257.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-274G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378122 | |||||||
| chr16:378138 | A | AGCCATCG others(209): Show |
2 | a0001c0001t0002g0029 a0001c0001t0002g0123 |
3 | HG02735.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.122-291_122-290ins others(216): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378138 | |||||||
| chr16:378166 | A | AC | 7 | a0001c0001t0002g0115 a0001c0001t0002g0122 a0001c0001t0004g0120 others(4): Show |
7 | HG00438.hp1 HG01978.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-319dupG | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378166 | |||||||
| chr16:378181 | C | CCCACCCG others(11): Show |
1 | a0003c0003t0001g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122-351_122-334dup others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378181 | |||||||
| chr16:378181 | C | CCCACCCG others(29): Show |
3 | a0002c0002t0003g0010 a0002c0002t0003g0145 a0002c0002t0016g0042 |
6 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-334_122-333ins others(36): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378181 | |||||||
| chr16:378181 | C | CCCACCCG others(281): Show |
1 | a0002c0002t0003g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122-334_122-333ins others(288): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378181 | |||||||
| chr16:378181 | C | CCCACCCG others(101): Show |
15 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(12): Show |
46 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.122-334_122-333ins others(108): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378181 | |||||||
| chr16:378181 | C | G | 1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-333G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378181 | |||||||
| chr16:378184 | A | ACCCGCAC others(102): Show |
2 | a0002c0002t0001g0073 a0002c0002t0001g0074 |
2 | HG02145.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.122-337_122-336ins others(109): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378184 | |||||||
| chr16:378189 | C | CACTGCCA others(83): Show |
1 | a0001c0007t0004g0016 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.122-342_122-341ins others(90): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378189 | |||||||
| chr16:378189 | C | CACTGCCA others(119): Show |
1 | a0002c0002t0001g0013 | 4 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-342_122-341ins others(126): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378189 | |||||||
| chr16:378189 | CACTGCCA others(11): Show |
C | 1 | a0009c0032t0002g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.122-359_122-342del others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378189 | |||||||
| chr16:378199 | G | C | 4 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0001c0030t0003g0043 others(1): Show |
7 | HG02451.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-351C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378199 | |||||||
| chr16:378204 | C | CCACACTG others(83): Show |
1 | a0001c0007t0004g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-357_122-356ins others(90): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378204 | C | CCCGCACT others(12): Show |
1 | a0004c0006t0001g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-357_122-356ins others(19): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378204 | C | CCGCACTG others(173): Show |
1 | a0002c0002t0003g0009 | 4 | HG01099.hp1 HG01192.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-357_122-356ins others(180): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378204 | C | CCGCACTG others(173): Show |
1 | a0002c0002t0003g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122-357_122-356ins others(180): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378204 | C | CCGCACTG others(11): Show |
28 | a0002c0002t0001g0002 a0002c0002t0001g0055 a0002c0002t0001g0060 others(25): Show |
60 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.122-357_122-356ins others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378204 | C | CCGCACTG others(101): Show |
1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-357_122-356ins others(108): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378204 | C | T | 3 | a0002c0009t0001g0036 a0002c0009t0001g0148 a0002c0009t0001g0149 |
4 | HG02055.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-356G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378204 | |||||||
| chr16:378206 | T | A | 2 | a0001c0007t0004g0016 a0001c0007t0004g0028 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.122-358A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378206 | |||||||
| chr16:378206 | T | C | 1 | a0003c0003t0001g0037 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.122-358A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378206 | |||||||
| chr16:378206 | T | G | 26 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0003g0011 others(23): Show |
62 | HG00140.hp2 HG00673.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.122-358A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378206 | |||||||
| chr16:378207 | G | C | 26 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0003g0011 others(23): Show |
64 | HG00140.hp2 HG00673.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.122-359C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378207 | |||||||
| chr16:378207 | G | GACTGCCA others(47): Show |
2 | a0002c0009t0001g0036 a0002c0009t0001g0148 |
3 | HG03225.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.122-360_122-359ins others(54): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378207 | |||||||
| chr16:378207 | G | GACTGCCA others(83): Show |
1 | a0001c0001t0002g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.122-360_122-359ins others(90): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378207 | |||||||
| chr16:378217 | G | C | 5 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(2): Show |
7 | HG02055.hp2 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-369C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378217 | |||||||
| chr16:378222 | C | T | 24 | a0002c0002t0003g0011 a0002c0010t0001g0035 a0003c0003t0001g0003 others(21): Show |
59 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.122-374G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378222 | |||||||
| chr16:378224 | T | A | 9 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(6): Show |
14 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-376A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378224 | |||||||
| chr16:378224 | T | G | 6 | a0001c0001t0002g0027 a0001c0007t0004g0016 a0001c0007t0004g0028 others(3): Show |
10 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-376A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378224 | |||||||
| chr16:378225 | G | C | 15 | a0001c0001t0002g0027 a0001c0004t0001g0015 a0001c0004t0001g0050 others(12): Show |
24 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-377C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378225 | |||||||
| chr16:378225 | G | GACTGCCA others(65): Show |
1 | a0002c0002t0003g0011 | 4 | HG01884.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-378_122-377ins others(72): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378225 | |||||||
| chr16:378235 | G | C | 4 | a0001c0001t0002g0027 a0001c0030t0003g0043 a0002c0002t0001g0013 others(1): Show |
8 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-387C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378235 | |||||||
| chr16:378240 | C | T | 1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-392G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378240 | |||||||
| chr16:378242 | G | T | 24 | a0002c0010t0001g0035 a0003c0003t0001g0003 a0003c0003t0001g0008 others(21): Show |
56 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.122-394C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378242 | |||||||
| chr16:378243 | C | CACTGCCA others(282): Show |
1 | a0001c0004t0001g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.122-396_122-395ins others(289): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378243 | |||||||
| chr16:378243 | C | CACTGCCA others(281): Show |
3 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 |
5 | HG02257.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-396_122-395ins others(288): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378243 | |||||||
| chr16:378243 | C | G | 24 | a0002c0010t0001g0035 a0003c0003t0001g0003 a0003c0003t0001g0008 others(21): Show |
56 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.122-395G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378243 | |||||||
| chr16:378253 | C | G | 36 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0001c0030t0003g0043 others(33): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.122-405G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378253 | |||||||
| chr16:378260 | G | A | 2 | a0001c0007t0004g0016 a0001c0007t0004g0028 |
3 | HG02818.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.122-412C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378260 | |||||||
| chr16:378260 | G | T | 1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-412C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378260 | |||||||
| chr16:378261 | C | CACTGCCA others(65): Show |
2 | a0001c0007t0004g0016 a0001c0007t0004g0028 |
3 | HG02818.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.122-414_122-413ins others(72): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378261 | |||||||
| chr16:378261 | C | CACTGCCA others(48): Show |
1 | a0002c0002t0003g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.122-414_122-413ins others(55): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378261 | |||||||
| chr16:378261 | C | CACTGCCA others(11): Show |
1 | a0002c0009t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.122-414_122-413ins others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378261 | |||||||
| chr16:378261 | C | CACTGCCA others(155): Show |
1 | a0001c0007t0004g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-414_122-413ins others(162): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378261 | |||||||
| chr16:378261 | C | CACTGCCA others(155): Show |
1 | a0001c0007t0004g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.122-414_122-413ins others(162): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378261 | |||||||
| chr16:378261 | C | G | 1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-413G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378261 | |||||||
| chr16:378271 | C | G | 30 | a0001c0030t0003g0043 a0002c0002t0003g0009 a0002c0002t0003g0144 others(27): Show |
65 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.122-423G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378271 | |||||||
| chr16:378276 | C | T | 2 | a0003c0003t0001g0083 a0003c0003t0001g0084 |
2 | HG01516.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.122-428G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378276 | |||||||
| chr16:378278 | A | G | 49 | a0001c0001t0002g0027 a0001c0001t0002g0119 a0001c0007t0004g0016 others(46): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.122-430T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378278 | |||||||
| chr16:378278 | A | T | 3 | a0003c0003t0001g0083 a0003c0003t0001g0084 a0004c0006t0001g0097 |
3 | HG01516.hp2 HG02071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.122-430T>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378278 | |||||||
| chr16:378278 | ACACTGCC others(11): Show |
A | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.122-448_122-431del others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378278 | |||||||
| chr16:378279 | C | CACTGCCA others(335): Show |
1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.122-432_122-431ins others(342): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378279 | |||||||
| chr16:378279 | C | CACTGCCA others(11): Show |
1 | a0004c0006t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.122-432_122-431ins others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378279 | |||||||
| chr16:378279 | C | G | 3 | a0003c0003t0001g0083 a0003c0003t0001g0084 a0004c0006t0001g0097 |
3 | HG01516.hp2 HG02071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.122-431G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378279 | |||||||
| chr16:378284 | C | A | 4 | a0002c0002t0003g0010 a0002c0002t0003g0145 a0002c0002t0003g0146 others(1): Show |
7 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-436G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378284 | |||||||
| chr16:378289 | G | C | 37 | a0001c0001t0002g0027 a0002c0002t0001g0002 a0002c0002t0001g0004 others(34): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.122-441C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378289 | |||||||
| chr16:378289 | G | GCCACCCT others(29): Show |
10 | a0002c0005t0001g0101 a0002c0005t0005g0026 a0002c0005t0005g0102 others(7): Show |
14 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-442_122-441ins others(36): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378289 | |||||||
| chr16:378294 | C | T | 4 | a0003c0003t0001g0083 a0003c0003t0001g0084 a0003c0003t0001g0085 others(1): Show |
4 | HG00140.hp1 HG01516.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-446G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378294 | |||||||
| chr16:378294 | CCGCA | C | 2 | a0002c0009t0001g0036 a0002c0009t0001g0148 |
3 | HG03225.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.122-450_122-447del others(4): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378294 | |||||||
| chr16:378296 | G | A | 1 | a0001c0001t0002g0027 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.122-448C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378296 | |||||||
| chr16:378296 | G | T | 5 | a0003c0003t0001g0083 a0003c0003t0001g0084 a0003c0003t0001g0085 others(2): Show |
5 | HG00140.hp1 HG01516.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-448C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378296 | |||||||
| chr16:378297 | C | G | 5 | a0003c0003t0001g0083 a0003c0003t0001g0084 a0003c0003t0001g0085 others(2): Show |
5 | HG00140.hp1 HG01516.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-449G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378297 | |||||||
| chr16:378299 | C | T | 20 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(17): Show |
57 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.122-451G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378299 | |||||||
| chr16:378302 | C | A | 43 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(40): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.122-454G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378302 | |||||||
| chr16:378302 | C | CCATCCCC others(11): Show |
1 | a0004c0006t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.122-455_122-454ins others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378302 | |||||||
| chr16:378302 | C | CCATCGCC others(47): Show |
1 | a0002c0005t0005g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122-455_122-454ins others(54): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378302 | |||||||
| chr16:378306 | CGCCACCC others(203): Show |
C | 1 | a0001c0001t0002g0027 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.122-668_122-459del | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378306 | |||||||
| chr16:378307 | G | C | 6 | a0001c0030t0003g0043 a0002c0009t0001g0149 a0003c0003t0001g0083 others(3): Show |
6 | HG01516.hp2 HG02004.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-459C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378307 | |||||||
| chr16:378307 | G | GCCACTCT others(29): Show |
21 | a0002c0010t0001g0035 a0003c0003t0001g0003 a0003c0003t0001g0008 others(18): Show |
53 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.122-460_122-459ins others(36): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378307 | |||||||
| chr16:378309 | C | T | 1 | a0002c0002t0003g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.122-461G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378309 | |||||||
| chr16:378312 | C | T | 1 | a0003c0003t0001g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122-464G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378312 | |||||||
| chr16:378314 | G | A | 24 | a0002c0010t0001g0035 a0003c0003t0001g0003 a0003c0003t0001g0008 others(21): Show |
56 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.122-466C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378314 | |||||||
| chr16:378314 | G | T | 3 | a0002c0002t0003g0009 a0002c0002t0003g0144 a0003c0003t0001g0113 |
6 | HG00140.hp1 HG01099.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-466C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378314 | |||||||
| chr16:378315 | C | G | 3 | a0002c0002t0003g0009 a0002c0002t0003g0144 a0003c0003t0001g0113 |
6 | HG00140.hp1 HG01099.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-467G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378315 | |||||||
| chr16:378320 | C | A | 1 | a0004c0006t0001g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.122-472G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378320 | |||||||
| chr16:378325 | G | C | 2 | a0003c0003t0001g0113 a0004c0006t0001g0096 |
2 | HG00140.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.122-477C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378325 | |||||||
| chr16:378327 | C | T | 45 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(42): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-479G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378327 | |||||||
| chr16:378330 | C | T | 1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-482G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378330 | |||||||
| chr16:378332 | G | A | 3 | a0002c0002t0003g0009 a0002c0002t0003g0144 a0003c0003t0001g0113 |
6 | HG00140.hp1 HG01099.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-484C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378332 | |||||||
| chr16:378332 | G | T | 3 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0017c0019t0001g0086 |
6 | HG02451.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-484C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378332 | |||||||
| chr16:378333 | C | CACTGACA others(48): Show |
1 | a0004c0006t0001g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-486_122-485ins others(55): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378333 | |||||||
| chr16:378333 | C | G | 3 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0017c0019t0001g0086 |
6 | HG02451.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-485G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378333 | |||||||
| chr16:378343 | G | C | 1 | a0004c0006t0001g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-495C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378343 | |||||||
| chr16:378343 | G | GCTACCCG others(29): Show |
1 | a0004c0006t0001g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.122-496_122-495ins others(36): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378343 | |||||||
| chr16:378348 | T | C | 35 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0003g0009 others(32): Show |
74 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.122-500A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378348 | |||||||
| chr16:378350 | T | A | 4 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0004c0006t0001g0096 others(1): Show |
7 | HG02451.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-502A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378350 | |||||||
| chr16:378350 | T | G | 27 | a0002c0002t0003g0009 a0002c0002t0003g0144 a0002c0010t0001g0035 others(24): Show |
62 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.122-502A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378350 | |||||||
| chr16:378351 | G | C | 31 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0003g0009 others(28): Show |
69 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.122-503C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378351 | |||||||
| chr16:378351 | G | GACTGCCA others(11): Show |
5 | a0002c0005t0005g0102 a0004c0006t0001g0014 a0004c0006t0001g0098 others(2): Show |
7 | HG00323.hp2 HG00642.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-504_122-503ins others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378351 | |||||||
| chr16:378351 | G | GACTGCCA others(499): Show |
1 | a0002c0002t0003g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.122-504_122-503ins others(506): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378351 | |||||||
| chr16:378353 | C | CTGCCATC others(425): Show |
2 | a0002c0002t0003g0010 a0002c0002t0016g0042 |
5 | HG00099.hp1 HG01070.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-506_122-505ins others(432): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378353 | |||||||
| chr16:378361 | C | G | 31 | a0002c0002t0003g0009 a0002c0002t0003g0093 a0002c0002t0003g0144 others(28): Show |
67 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.122-513G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378361 | |||||||
| chr16:378364 | A | ACCCACAC others(30): Show |
2 | a0002c0002t0001g0069 a0020c0017t0001g0080 |
2 | HG01978.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.122-517_122-516ins others(37): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378364 | |||||||
| chr16:378368 | G | A | 38 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(35): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.122-520C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378368 | |||||||
| chr16:378379 | G | C | 8 | a0002c0002t0003g0009 a0002c0002t0003g0093 a0002c0002t0003g0144 others(5): Show |
12 | HG00738.hp2 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.122-531C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378379 | |||||||
| chr16:378386 | T | A | 3 | a0001c0001t0002g0138 a0002c0002t0003g0010 a0002c0002t0016g0042 |
6 | HG00099.hp1 HG00558.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-538A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378386 | |||||||
| chr16:378386 | T | C | 4 | a0002c0002t0001g0002 a0002c0002t0017g0151 a0002c0005t0005g0026 others(1): Show |
4 | HG00733.hp2 HG01106.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-538A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378386 | |||||||
| chr16:378386 | T | G | 51 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(48): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.122-538A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378386 | |||||||
| chr16:378387 | G | C | 54 | a0001c0001t0002g0138 a0002c0002t0001g0002 a0002c0002t0001g0004 others(51): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.122-539C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378387 | |||||||
| chr16:378387 | G | GC | 4 | a0002c0002t0001g0002 a0002c0002t0017g0151 a0002c0005t0005g0026 others(1): Show |
4 | HG00733.hp2 HG01106.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-540_122-539ins others(1): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378387 | |||||||
| chr16:378389 | C | A | 2 | a0002c0002t0003g0010 a0002c0002t0016g0042 |
5 | HG00099.hp1 HG01070.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-541G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378389 | |||||||
| chr16:378392 | C | A | 2 | a0002c0002t0003g0009 a0002c0002t0003g0144 |
5 | HG01099.hp1 HG01192.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-544G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378392 | |||||||
| chr16:378397 | G | C | 3 | a0001c0001t0002g0138 a0002c0002t0003g0010 a0002c0002t0016g0042 |
6 | HG00099.hp1 HG00558.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-549C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378397 | |||||||
| chr16:378397 | G | GCCACCCA others(11): Show |
2 | a0001c0007t0004g0016 a0001c0007t0004g0028 |
3 | HG02818.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.122-550_122-549ins others(18): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378397 | |||||||
| chr16:378404 | G | A | 30 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0001g0069 others(27): Show |
62 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.122-556C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378404 | |||||||
| chr16:378404 | G | T | 4 | a0002c0002t0003g0093 a0002c0009t0001g0036 a0002c0009t0001g0148 others(1): Show |
5 | HG00738.hp2 HG02055.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-556C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378404 | |||||||
| chr16:378405 | C | CACTGCCA others(65): Show |
15 | a0002c0002t0001g0002 a0002c0002t0001g0060 a0002c0002t0001g0064 others(12): Show |
24 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-558_122-557ins others(72): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378405 | |||||||
| chr16:378405 | C | CACTGCCA others(63): Show |
1 | a0002c0005t0005g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122-558_122-557ins others(70): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378405 | |||||||
| chr16:378405 | C | G | 4 | a0002c0002t0003g0093 a0002c0009t0001g0036 a0002c0009t0001g0148 others(1): Show |
5 | HG00738.hp2 HG02055.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-557G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378405 | |||||||
| chr16:378407 | C | A | 3 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0003g0145 |
3 | HG01109.hp2 HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.122-559G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378407 | |||||||
| chr16:378415 | G | C | 31 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0001c0030t0003g0043 others(28): Show |
63 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.122-567C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378415 | |||||||
| chr16:378415 | G | GCCACCCT others(83): Show |
2 | a0002c0002t0003g0010 a0002c0002t0016g0042 |
5 | HG00099.hp1 HG01070.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-568_122-567ins others(90): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378415 | |||||||
| chr16:378422 | A | G | 50 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0001c0030t0003g0043 others(47): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.122-574T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378422 | |||||||
| chr16:378422 | A | T | 18 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(15): Show |
52 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.122-574T>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378422 | |||||||
| chr16:378423 | C | G | 18 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(15): Show |
52 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.122-575G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378423 | |||||||
| chr16:378425 | C | A | 20 | a0002c0002t0001g0002 a0002c0002t0001g0060 a0002c0002t0001g0064 others(17): Show |
30 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.122-577G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378425 | |||||||
| chr16:378428 | C | A | 2 | a0002c0002t0003g0009 a0002c0002t0003g0144 |
5 | HG01099.hp1 HG01192.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-580G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378428 | |||||||
| chr16:378430 | A | G | 3 | a0002c0009t0001g0036 a0002c0009t0001g0148 a0002c0009t0001g0149 |
4 | HG02055.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-582T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378430 | |||||||
| chr16:378433 | C | G | 68 | a0001c0001t0002g0138 a0001c0007t0004g0016 a0001c0007t0004g0028 others(65): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.122-585G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378433 | |||||||
| chr16:378440 | G | A | 18 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(15): Show |
52 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.122-592C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378440 | |||||||
| chr16:378440 | G | T | 41 | a0002c0002t0001g0002 a0002c0002t0001g0055 a0002c0002t0001g0061 others(38): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.122-592C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378440 | |||||||
| chr16:378441 | C | G | 41 | a0002c0002t0001g0002 a0002c0002t0001g0055 a0002c0002t0001g0061 others(38): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.122-593G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378441 | |||||||
| chr16:378450 | C | T | 1 | a0002c0002t0003g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.122-602G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378450 | |||||||
| chr16:378451 | G | C | 26 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0001g0004 others(23): Show |
64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122-603C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378451 | |||||||
| chr16:378451 | G | GCCACCCT others(227): Show |
1 | a0002c0002t0003g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122-604_122-603ins others(234): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378451 | |||||||
| chr16:378456 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.122-608G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378456 | |||||||
| chr16:378458 | A | G | 55 | a0001c0001t0002g0001 a0001c0004t0001g0015 a0001c0004t0001g0050 others(52): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.122-610T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378458 | |||||||
| chr16:378458 | A | T | 1 | a0001c0001t0002g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.122-610T>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378458 | |||||||
| chr16:378459 | C | G | 1 | a0001c0001t0002g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.122-611G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378459 | |||||||
| chr16:378461 | C | A | 27 | a0002c0002t0001g0069 a0002c0010t0001g0035 a0003c0003t0001g0003 others(24): Show |
59 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.122-613G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378461 | |||||||
| chr16:378466 | A | G | 3 | a0002c0002t0001g0002 a0002c0002t0001g0064 a0002c0002t0017g0151 |
5 | HG02056.hp1 HG02080.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-618T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378466 | |||||||
| chr16:378469 | G | C | 57 | a0001c0001t0002g0138 a0002c0002t0001g0002 a0002c0002t0001g0055 others(54): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.122-621C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378469 | |||||||
| chr16:378476 | G | T | 19 | a0001c0030t0003g0043 a0002c0002t0001g0004 a0002c0002t0001g0005 others(16): Show |
53 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.122-628C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378476 | |||||||
| chr16:378477 | C | G | 19 | a0001c0030t0003g0043 a0002c0002t0001g0004 a0002c0002t0001g0005 others(16): Show |
53 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.122-629G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378477 | |||||||
| chr16:378486 | C | T | 25 | a0002c0010t0001g0035 a0003c0003t0001g0003 a0003c0003t0001g0008 others(22): Show |
56 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.122-638G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378486 | |||||||
| chr16:378492 | T | C | 85 | a0001c0001t0002g0138 a0001c0007t0004g0016 a0001c0007t0004g0028 others(82): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.122-644A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378492 | |||||||
| chr16:378494 | T | A | 25 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0001c0030t0003g0043 others(22): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.122-646A>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378494 | |||||||
| chr16:378494 | T | C | 1 | a0004c0006t0001g0014 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.122-646A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378494 | |||||||
| chr16:378494 | T | G | 50 | a0001c0001t0002g0138 a0001c0007t0004g0016 a0001c0007t0004g0028 others(47): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.122-646A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378494 | |||||||
| chr16:378495 | G | C | 73 | a0001c0001t0002g0138 a0001c0007t0004g0016 a0001c0007t0004g0028 others(70): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.122-647C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378495 | |||||||
| chr16:378495 | G | GACTGCCA others(47): Show |
1 | a0004c0006t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.122-648_122-647ins others(54): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378495 | |||||||
| chr16:378497 | C | A | 18 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(15): Show |
52 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.122-649G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378497 | |||||||
| chr16:378504 | CCCCACCC others(5): Show |
C | 3 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0003g0093 |
4 | HG00738.hp2 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-668_122-657del others(12): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378504 | |||||||
| chr16:378505 | C | G | 35 | a0001c0001t0002g0138 a0001c0007t0004g0016 a0001c0007t0004g0028 others(32): Show |
72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.122-657G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378505 | |||||||
| chr16:378512 | G | A | 32 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0001g0002 others(29): Show |
69 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.122-664C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378512 | |||||||
| chr16:378515 | C | A | 13 | a0002c0002t0001g0002 a0002c0002t0001g0055 a0002c0002t0001g0061 others(10): Show |
37 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.122-667G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378515 | |||||||
| chr16:378516 | T | TGCCATC | 22 | a0001c0007t0004g0016 a0001c0007t0004g0028 a0002c0002t0001g0002 others(19): Show |
34 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(6): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCC others(71): Show |
2 | a0002c0002t0003g0011 a0002c0002t0003g0072 |
5 | HG01884.hp1 HG02258.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(78): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCC others(89): Show |
10 | a0002c0002t0001g0002 a0002c0002t0001g0055 a0002c0002t0001g0061 others(7): Show |
31 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(96): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCC others(359): Show |
1 | a0002c0002t0003g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(366): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCC others(377): Show |
1 | a0002c0002t0003g0009 | 4 | HG01099.hp1 HG01192.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(384): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCC others(71): Show |
1 | a0017c0019t0001g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-669_122-668ins others(78): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(17): Show |
26 | a0002c0010t0001g0035 a0003c0003t0001g0003 a0003c0003t0001g0008 others(23): Show |
58 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(24): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(54): Show |
1 | a0002c0002t0001g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.122-669_122-668ins others(61): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(73): Show |
1 | a0002c0005t0005g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(80): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(235): Show |
1 | a0001c0001t0002g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(242): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(53): Show |
14 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(11): Show |
48 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(60): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(35): Show |
1 | a0004c0006t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.122-669_122-668ins others(42): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(234): Show |
1 | a0001c0001t0002g0001 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(241): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(215): Show |
1 | a0001c0001t0002g0001 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(222): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(283): Show |
4 | a0001c0004t0002g0047 a0001c0004t0009g0045 a0001c0004t0013g0049 others(1): Show |
4 | HG02970.hp2 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(290): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(216): Show |
1 | a0001c0001t0002g0001 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(223): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(235): Show |
1 | a0001c0001t0004g0120 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122-669_122-668ins others(242): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(629): Show |
2 | a0001c0001t0002g0029 a0001c0001t0002g0123 |
2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.122-669_122-668ins others(636): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(234): Show |
1 | a0001c0001t0002g0001 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.122-669_122-668ins others(241): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(215): Show |
1 | a0001c0001t0002g0001 | 3 | HG00642.hp2 HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.122-669_122-668ins others(222): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(234): Show |
1 | a0001c0001t0007g0031 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(241): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(233): Show |
46 | a0001c0001t0001g0019 a0001c0001t0001g0108 a0001c0001t0001g0109 others(43): Show |
139 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(240): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(251): Show |
1 | a0001c0001t0002g0001 | 2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.122-669_122-668ins others(258): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(265): Show |
3 | a0001c0004t0002g0021 a0001c0004t0002g0046 a0001c0004t0002g0048 |
4 | HG02109.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(272): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(233): Show |
1 | a0001c0001t0002g0001 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.122-669_122-668ins others(240): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(215): Show |
2 | a0001c0001t0002g0001 a0001c0001t0019g0153 |
2 | NA18988.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.122-669_122-668ins others(222): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(125): Show |
3 | a0002c0009t0001g0036 a0002c0009t0001g0148 a0002c0009t0001g0149 |
4 | HG02055.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(132): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(197): Show |
2 | a0001c0001t0002g0138 a0001c0030t0003g0043 |
2 | HG00558.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.122-669_122-668ins others(204): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378516 | T | TGCCATCG others(251): Show |
3 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0106 |
5 | HG02257.hp2 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-669_122-668ins others(258): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378516 | |||||||
| chr16:378520 | A | ATCGCCAC others(18): Show |
1 | a0002c0002t0001g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-673_122-672ins others(25): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378520 | A | ATCGCCAC others(236): Show |
1 | a0001c0001t0002g0118 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.122-673_122-672ins others(243): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378520 | A | ATCGCCAC others(240): Show |
1 | a0001c0001t0002g0115 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.122-673_122-672ins others(247): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378520 | A | ATCGCCAC others(54): Show |
2 | a0002c0002t0001g0070 a0002c0002t0001g0071 |
2 | HG01993.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.122-673_122-672ins others(61): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378520 | A | ATCGCCAC others(237): Show |
1 | a0019c0024t0002g0116 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.122-673_122-672ins others(244): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378520 | A | ATCGCCAC others(236): Show |
1 | a0001c0001t0002g0117 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.122-673_122-672ins others(243): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378520 | A | ATCGCCAC others(252): Show |
1 | a0001c0004t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122-673_122-672ins others(259): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378520 | |||||||
| chr16:378524 | G | A | 1 | a0002c0002t0001g0064 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.122-676C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378524 | |||||||
| chr16:378573 | C | G | 1 | a0003c0003t0001g0082 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.122-725G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378573 | |||||||
| chr16:378648 | G | A | 1 | a0001c0004t0013g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122-800C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378648 | |||||||
| chr16:378735 | G | A | 1 | a0016c0018t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122-887C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378735 | |||||||
| chr16:378770 | G | C | 6 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(3): Show |
12 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-922C>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378770 | |||||||
| chr16:378852 | G | A | 1 | a0001c0001t0008g0034 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.122-1004C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378852 | |||||||
| chr16:378907 | A | G | 4 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(1): Show |
6 | HG02257.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-1059T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378907 | |||||||
| chr16:378916 | C | T | 1 | a0002c0002t0003g0011 | 4 | HG01884.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1068G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 378916 | |||||||
| chr16:379000 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.122-1152A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379000 | |||||||
| chr16:379059 | C | T | 64 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(61): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.122-1211G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379059 | |||||||
| chr16:379093 | G | A | 1 | a0003c0003t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.122-1245C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379093 | |||||||
| chr16:379106 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122-1258C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379106 | |||||||
| chr16:379129 | C | T | 60 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.122-1281G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379129 | |||||||
| chr16:379198 | C | T | 40 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(37): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.122-1350G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379198 | |||||||
| chr16:379207 | G | A | 7 | a0001c0004t0002g0021 a0001c0004t0002g0046 a0001c0004t0002g0047 others(4): Show |
8 | HG02109.hp1 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-1359C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379207 | |||||||
| chr16:379315 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.122-1467T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379315 | |||||||
| chr16:379419 | G | A | 1 | a0002c0002t0003g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122-1571C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379419 | |||||||
| chr16:379512 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.122-1664C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379512 | |||||||
| chr16:379552 | C | T | 1 | a0001c0001t0002g0111 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.122-1704G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379552 | |||||||
| chr16:379588 | G | A | 1 | a0002c0009t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.122-1740C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379588 | |||||||
| chr16:379691 | T | C | 8 | a0001c0001t0002g0053 a0001c0004t0002g0021 a0001c0004t0002g0046 others(5): Show |
9 | HG02109.hp1 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.122-1843A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379691 | |||||||
| chr16:379887 | C | T | 1 | a0002c0002t0001g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.121+1814G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379887 | |||||||
| chr16:379920 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.121+1781G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379920 | |||||||
| chr16:379926 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0052 |
3 | HG02055.hp1 HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.121+1775G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379926 | |||||||
| chr16:379934 | GGGCTGGG others(19): Show |
G | 1 | a0002c0002t0017g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121+1741_121+1766d others(28): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379934 | |||||||
| chr16:379951 | T | C | 87 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(84): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.121+1750A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 379951 | |||||||
| chr16:380011 | C | T | 17 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(14): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.121+1690G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380011 | |||||||
| chr16:380153 | C | T | 6 | a0004c0006t0001g0014 a0004c0006t0001g0096 a0004c0006t0001g0097 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+1548G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380153 | |||||||
| chr16:380215 | C | A | 6 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(3): Show |
12 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+1486G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380215 | |||||||
| chr16:380215 | C | T | 1 | a0001c0004t0001g0050 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.121+1486G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380215 | |||||||
| chr16:380248 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.121+1453G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380248 | |||||||
| chr16:380292 | C | G | 68 | a0001c0001t0002g0022 a0001c0030t0003g0043 a0002c0002t0001g0002 others(65): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.121+1409G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380292 | |||||||
| chr16:380304 | T | C | 68 | a0001c0001t0002g0022 a0001c0030t0003g0043 a0002c0002t0001g0002 others(65): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.121+1397A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380304 | |||||||
| chr16:380345 | A | G | 7 | a0002c0005t0001g0101 a0002c0005t0005g0026 a0002c0005t0005g0102 others(4): Show |
9 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+1356T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380345 | |||||||
| chr16:380362 | T | G | 6 | a0004c0006t0001g0014 a0004c0006t0001g0096 a0004c0006t0001g0097 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+1339A>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380362 | |||||||
| chr16:380366 | G | T | 6 | a0004c0006t0001g0014 a0004c0006t0001g0096 a0004c0006t0001g0097 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+1335C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380366 | |||||||
| chr16:380369 | T | C | 1 | a0002c0002t0017g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121+1332A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380369 | |||||||
| chr16:380369 | TTTC | T | 6 | a0004c0006t0001g0014 a0004c0006t0001g0096 a0004c0006t0001g0097 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+1329_121+1331d others(5): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380369 | |||||||
| chr16:380372 | C | CT | 11 | a0001c0001t0002g0017 a0001c0001t0002g0140 a0002c0005t0001g0101 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.121+1328dupA | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380372 | |||||||
| chr16:380372 | C | CTT | 6 | a0001c0004t0001g0015 a0001c0004t0001g0050 a0001c0004t0001g0051 others(3): Show |
8 | HG02257.hp2 HG02809.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.121+1327_121+1328d others(4): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380372 | |||||||
| chr16:380372 | C | T | 1 | a0002c0002t0017g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121+1329G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380372 | |||||||
| chr16:380372 | CT | C | 6 | a0001c0001t0002g0001 a0001c0001t0002g0054 a0002c0002t0001g0002 others(3): Show |
7 | HG02698.hp2 HG02976.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+1328delA | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380372 | |||||||
| chr16:380373 | T | C | 1 | a0002c0002t0017g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121+1328A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380373 | |||||||
| chr16:380397 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.121+1304G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380397 | |||||||
| chr16:380469 | C | G | 66 | a0001c0001t0002g0022 a0002c0002t0001g0002 a0002c0002t0001g0004 others(63): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.121+1232G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380469 | |||||||
| chr16:380538 | G | T | 1 | a0001c0001t0007g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.121+1163C>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380538 | |||||||
| chr16:380655 | G | A | 1 | a0002c0009t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121+1046C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380655 | |||||||
| chr16:380795 | CAGGGG | C | 9 | a0001c0004t0001g0015 a0001c0004t0001g0106 a0002c0005t0001g0101 others(6): Show |
13 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+901_121+905del others(5): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380795 | |||||||
| chr16:380842 | C | G | 91 | a0001c0001t0002g0022 a0001c0004t0001g0015 a0001c0004t0001g0106 others(88): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.121+859G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380842 | |||||||
| chr16:380851 | C | T | 1 | a0001c0007t0004g0024 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.121+850G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 380851 | |||||||
| chr16:381045 | C | G | 1 | a0015c0031t0009g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121+656G>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381045 | |||||||
| chr16:381058 | C | T | 1 | a0002c0002t0001g0055 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121+643G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381058 | |||||||
| chr16:381135 | G | A | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.121+566C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381135 | |||||||
| chr16:381148 | C | T | 3 | a0003c0003t0001g0023 a0003c0003t0001g0066 a0016c0018t0001g0067 |
4 | HG03490.hp1 HG03669.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+553G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381148 | |||||||
| chr16:381166 | C | A | 1 | a0002c0010t0001g0035 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.121+535G>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381166 | |||||||
| chr16:381209 | G | A | 11 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0144 others(8): Show |
17 | HG00099.hp1 HG00621.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.121+492C>T | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381209 | |||||||
| chr16:381303 | C | T | 14 | a0001c0001t0002g0022 a0002c0002t0001g0002 a0002c0002t0001g0055 others(11): Show |
42 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.121+398G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381303 | |||||||
| chr16:381313 | AGGCCGGA others(18): Show |
A | 1 | a0001c0001t0002g0147 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.121+363_121+387del others(25): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381313 | |||||||
| chr16:381366 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.121+335G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381366 | |||||||
| chr16:381399 | C | CGGCGCCG others(2): Show |
11 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0004t0001g0050 others(8): Show |
12 | HG02109.hp1 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+301_121+302ins others(9): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381399 | |||||||
| chr16:381400 | C | T | 11 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0004t0001g0050 others(8): Show |
12 | HG02109.hp1 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+301G>A | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381400 | |||||||
| chr16:381517 | T | C | 1 | a0002c0010t0001g0035 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.121+184A>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381517 | |||||||
| chr16:381540 | A | G | 1 | a0001c0030t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.121+161T>C | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381540 | |||||||
| chr16:381609 | A | C | 8 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0016g0042 others(5): Show |
14 | HG00099.hp1 HG00621.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+92T>G | PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 1/12 | chr16 | 381609 |