Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5261 |
| ensemblid | ENSG00000156873.16 |
| hgncid | 8931 |
| symbol | PHKG2 |
| name | phosphorylase kinase catalytic subunit gamma 2 |
| refseq_nuc | NM_000294.3 |
| refseq_prot | NP_000285.1 |
| ensembl_nuc | ENST00000563588.6 |
| ensembl_prot | ENSP00000455607.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 30748425 |
| end | 30761176 |
| strand | + |
| ver | v1.2 |
| region | chr16:30748425-30761176 |
| region5000 | chr16:30743425-30766176 |
| regionname0 | PHKG2_chr16_30748425_30761176 |
| regionname5000 | PHKG2_chr16_30743425_30766176 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 406 | 260 | 81 | 62 | 70 | 11 | 34 | 43 | PHKG2_chr16_30743425_30766176 | PHKG2 | MTLDV others(401): Show |
chr16 | 30743425 | 30766176 |
| a0002 | 0/0 | 406 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | MTLDV others(401): Show |
chr16 | 30743425 | 30766176 |
| a0003 | 0/0 | 406 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | MTLDV others(401): Show |
chr16 | 30743425 | 30766176 |
| a0004 | 0/0 | 406 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | MTLDV others(401): Show |
chr16 | 30743425 | 30766176 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1218 | 258 | 81 | 62 | 68 | 11 | 34 | PHKG2_chr16_30743425_30766176 | PHKG2 | ATGAC others(1213): Show |
chr16 | 30743425 | 30766176 | ||
| a0001c0003 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | ATGAC others(1213): Show |
chr16 | 30743425 | 30766176 | ||
| a0001c0006 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | ATGAC others(1213): Show |
chr16 | 30743425 | 30766176 | ||
| a0002c0002 | 0/0 | 1218 | 2 | 1 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | ATGAC others(1213): Show |
chr16 | 30743425 | 30766176 | ||
| a0003c0005 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | ATGAC others(1213): Show |
chr16 | 30743425 | 30766176 | ||
| a0004c0004 | 0/0 | 1218 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | ATGAC others(1213): Show |
chr16 | 30743425 | 30766176 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5375 | 103 | 37 | 18 | 21 | 4 | 23 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0002 | 0/0 | 5377 | 83 | 8 | 25 | 44 | 2 | 4 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0003 | 0/1 | 5377 | 17 | 2 | 8 | 0 | 2 | 4 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0004 | 0/0 | 5375 | 9 | 9 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0005 | 1/0 | 5384 | 9 | 7 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5379): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0006 | 0/0 | 5374 | 5 | 4 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5369): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0007 | 0/0 | 5377 | 4 | 0 | 3 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0008 | 0/0 | 5384 | 3 | 3 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5379): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0009 | 0/0 | 5375 | 3 | 3 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0010 | 0/0 | 5375 | 2 | 2 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0011 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0012 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5369): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0013 | 0/0 | 5376 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5371): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0014 | 0/0 | 5376 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5371): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0015 | 0/0 | 5376 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5371): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0016 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0017 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0018 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0019 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0020 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0021 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0022 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0023 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0024 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0025 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0026 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0027 | 0/0 | 5375 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0028 | 0/0 | 5375 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5370): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0029 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0001t0030 | 0/0 | 5383 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5378): Show |
chr16 | 30743425 | 30766176 |
| a0001c0003t0002 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0001c0006t0002 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0002c0002t0002 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0002c0002t0008 | 0/0 | 5384 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5379): Show |
chr16 | 30743425 | 30766176 |
| a0003c0005t0002 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| a0004c0004t0002 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | GACTG others(5372): Show |
chr16 | 30743425 | 30766176 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 8 | 3 | 7 | 1 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0004 | 0/0 | 14 | 6 | 3 | 3 | 0 | 2 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 0 | 0 | 6 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0002 | 0/0 | 10 | 1 | 4 | 4 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0003 | 0/0 | 16 | 0 | 3 | 13 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0010 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0005g0006 | 1/0 | 7 | 5 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0007g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0010g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0013g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0014g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0015g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0017g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0018g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0020g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0022g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0023g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0024g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0025g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0026g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0027g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0028g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0029g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0001t0030g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0003t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0001c0006t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0002c0002t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0003c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| a0004c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0029 | g0002 | EUR | GBR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0065 | EUR | GBR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00639 | hp1 | a0001 | c0001 | t0016 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00741 | hp1 | a0001 | c0001 | t0023 | g0021 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0009 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0014 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01433 | hp1 | a0001 | c0001 | t0024 | g0002 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0093 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01975 | hp2 | a0001 | c0001 | t0018 | g0007 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02040 | hp2 | a0001 | c0001 | t0022 | g0045 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0020 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CDX | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0068 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02300 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02970 | hp2 | a0001 | c0001 | t0026 | g0030 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03486 | hp1 | a0002 | c0002 | t0008 | g0023 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03491 | hp2 | a0001 | c0001 | t0028 | g0079 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG04228 | hp2 | a0001 | c0001 | t0027 | g0001 | SAS | STU | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0016 | AFR | YRI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0033 | AFR | YRI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18962 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18980 | hp2 | a0001 | c0006 | t0002 | g0051 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18998 | hp1 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | LWK | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19063 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19240 | hp1 | a0001 | c0001 | t0030 | g0031 | AFR | YRI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | YRI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ASW | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20752 | hp1 | a0001 | c0001 | t0017 | g0010 | EUR | TSI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20805 | hp1 | a0004 | c0004 | t0002 | g0058 | EUR | TSI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | GIH | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0002 | AFR | USA | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0078 | AFR | USA | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | USA | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA21309 | hp1 | a0001 | c0001 | t0025 | g0001 | AFR | LWK | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0076 | REF | REF | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0006 | REF | REF | PHKG2_chr16_30743425_30766176 | PHKG2 | chr16 | 30743425 | 30766176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30751237 | G | A | 1 | a0004 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.227G>A | p.Arg76Gln | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 3/10 | 311/5384 | 227/1221 | 76/406 | chr16 | 30751237 | |||
| chr16:30756233 | T | C | 1 | a0003 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.608T>C | p.Met203Thr | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 7/10 | 692/5384 | 608/1221 | 203/406 | chr16 | 30756233 | |||
| chr16:30756666 | G | A | 1 | a0002 | 2 | HG00597.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.878G>A | p.Arg293His | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 9/10 | 962/5384 | 878/1221 | 293/406 | chr16 | 30756666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30748841 | G | A | 1 | a0001c0003 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.21G>A | p.Pro7Pro | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/10 | 105/5384 | 21/1221 | 7/406 | chr16 | 30748841 | |||
| chr16:30751184 | A | T | 1 | a0001c0006 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.174A>T | p.Thr58Thr | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 3/10 | 258/5384 | 174/1221 | 58/406 | chr16 | 30751184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30757171 | GCTCTGGC | G | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*85_*91delTGGCCTC | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 85 | INFO_REALIGN_3_PRIME | chr16 | 30757171 | |||||
| chr16:30757352 | C | T | 1 | a0001c0001t0029 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 255 | chr16 | 30757352 | ||||||
| chr16:30757636 | C | T | 1 | a0001c0001t0028 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 539 | chr16 | 30757636 | ||||||
| chr16:30757644 | G | A | 1 | a0001c0001t0011 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 547 | chr16 | 30757644 | ||||||
| chr16:30757659 | A | G | 1 | a0001c0001t0028 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*562A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 562 | chr16 | 30757659 | ||||||
| chr16:30757680 | G | A | 2 | a0001c0001t0004 a0001c0001t0012 |
10 | HG02109.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*583G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 583 | chr16 | 30757680 | ||||||
| chr16:30758072 | CT | C | 6 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 others(3): Show |
10 | HG01256.hp1 HG01256.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*992delT | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 992 | INFO_REALIGN_3_PRIME | chr16 | 30758072 | |||||
| chr16:30758094 | T | C | 1 | a0001c0001t0010 | 2 | HG01891.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*997T>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 997 | chr16 | 30758094 | ||||||
| chr16:30758247 | A | G | 1 | a0001c0001t0027 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1150A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1150 | chr16 | 30758247 | ||||||
| chr16:30758293 | G | T | 2 | a0001c0001t0009 a0001c0001t0026 |
4 | HG02055.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1196G>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1196 | chr16 | 30758293 | ||||||
| chr16:30758294 | A | T | 2 | a0001c0001t0009 a0001c0001t0026 |
4 | HG02055.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1197A>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1197 | chr16 | 30758294 | ||||||
| chr16:30758440 | A | G | 1 | a0001c0001t0025 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1343A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1343 | chr16 | 30758440 | ||||||
| chr16:30758753 | C | T | 5 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0023 others(2): Show |
8 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1656C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1656 | chr16 | 30758753 | ||||||
| chr16:30758804 | C | T | 1 | a0001c0001t0022 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1707C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1707 | chr16 | 30758804 | ||||||
| chr16:30758828 | T | G | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1731T>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1731 | chr16 | 30758828 | ||||||
| chr16:30758840 | C | T | 1 | a0001c0001t0021 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1743 | chr16 | 30758840 | ||||||
| chr16:30758946 | C | G | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1849C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1849 | chr16 | 30758946 | ||||||
| chr16:30759051 | C | G | 1 | a0001c0001t0026 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 1954 | chr16 | 30759051 | ||||||
| chr16:30759215 | C | T | 1 | a0001c0001t0020 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 2118 | chr16 | 30759215 | ||||||
| chr16:30759416 | G | A | 1 | a0001c0001t0016 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2319G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 2319 | chr16 | 30759416 | ||||||
| chr16:30759441 | G | A | 1 | a0001c0001t0023 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2344G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 2344 | chr16 | 30759441 | ||||||
| chr16:30759629 | T | C | 3 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0017 |
18 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2532T>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 2532 | chr16 | 30759629 | ||||||
| chr16:30760589 | C | T | 1 | a0001c0001t0019 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3492C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 3492 | chr16 | 30760589 | ||||||
| chr16:30760674 | A | C | 1 | a0001c0001t0024 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3577A>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 3577 | chr16 | 30760674 | ||||||
| chr16:30760683 | GAA | G | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(8): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*3590_*3591delAA | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 3590 | INFO_REALIGN_3_PRIME | chr16 | 30760683 | |||||
| chr16:30760719 | A | G | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(31): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*3622A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 3622 | chr16 | 30760719 | ||||||
| chr16:30760969 | A | G | 1 | a0001c0001t0017 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3872A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 3872 | chr16 | 30760969 | ||||||
| chr16:30761045 | G | T | 1 | a0001c0001t0018 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3948G>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 10/10 | 3948 | chr16 | 30761045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30748678 | A | AC | 12 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0112 others(9): Show |
14 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18-116dupC | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 30748678 | ||||||
| chr16:30748678 | AC | A | 29 | a0001c0001t0001g0007 a0001c0001t0002g0003 a0001c0001t0002g0005 others(26): Show |
60 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-18-116delC | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 30748678 | ||||||
| chr16:30748706 | G | C | 1 | a0001c0001t0002g0019 | 2 | HG01496.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-18-97G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 1/9 | chr16 | 30748706 | |||||||
| chr16:30748708 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-18-95C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 1/9 | chr16 | 30748708 | |||||||
| chr16:30748998 | CGGGTGGT others(4): Show |
C | 1 | a0001c0001t0001g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.95+85_95+95delGGTG others(7): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748998 | ||||||
| chr16:30748998 | CGGGTGGT others(21): Show |
C | 1 | a0001c0001t0004g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.95+86_95+113delGTG others(25): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748998 | ||||||
| chr16:30748999 | GGGT | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0002g0090 others(3): Show |
8 | HG01884.hp2 HG02040.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.95+173_95+175delGT others(1): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGT | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0027 others(4): Show |
10 | HG00099.hp2 HG00558.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.95+170_95+175delGT others(4): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(2): Show |
G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(5): Show |
13 | HG01071.hp1 HG01346.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.95+167_95+175delGT others(7): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(5): Show |
G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0017 others(13): Show |
21 | HG00408.hp2 HG00673.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.95+164_95+175delGT others(10): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(8): Show |
G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(9): Show |
21 | HG00140.hp1 HG01175.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.95+161_95+175delGT others(13): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(11): Show |
G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0036 others(8): Show |
15 | HG01496.hp2 HG01952.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.95+158_95+175delGT others(16): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(14): Show |
G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0005g0006 others(2): Show |
7 | HG01884.hp1 HG02735.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.95+155_95+175delGT others(19): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(17): Show |
G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0036 others(4): Show |
8 | HG01109.hp1 HG01516.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.95+152_95+175delGT others(22): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(20): Show |
G | 1 | a0001c0001t0003g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95+149_95+175delGT others(25): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(23): Show |
G | 3 | a0001c0001t0001g0091 a0001c0001t0002g0032 a0001c0001t0002g0086 |
3 | NA18985.hp1 NA18990.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.95+146_95+175delGT others(28): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(26): Show |
G | 7 | a0001c0001t0001g0001 a0001c0001t0002g0050 a0001c0001t0002g0095 others(4): Show |
9 | HG00609.hp1 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.95+143_95+175delGT others(31): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(29): Show |
G | 3 | a0001c0001t0003g0014 a0001c0001t0005g0031 a0001c0001t0013g0014 |
3 | HG01256.hp2 HG01258.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.95+140_95+175delGT others(34): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(32): Show |
G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0003g0014 |
3 | HG02647.hp2 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.95+137_95+175delGT others(37): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(35): Show |
G | 1 | a0001c0001t0003g0014 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95+134_95+175delGT others(40): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30748999 | GGGTGGTG others(41): Show |
G | 2 | a0001c0001t0002g0049 a0001c0001t0002g0108 |
2 | HG02129.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.95+128_95+175delGT others(46): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30748999 | ||||||
| chr16:30749004 | G | A | 1 | a0001c0001t0002g0003 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.95+89G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749004 | |||||||
| chr16:30749021 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.95+106G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749021 | |||||||
| chr16:30749031 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0109 |
3 | HG02109.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.95+116G>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749031 | |||||||
| chr16:30749034 | G | C | 1 | a0001c0001t0006g0054 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.95+119G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749034 | |||||||
| chr16:30749037 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0003g0056 a0001c0001t0006g0054 |
3 | HG01346.hp1 HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.95+122G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749037 | |||||||
| chr16:30749040 | G | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0002g0007 others(7): Show |
13 | HG00673.hp2 HG00741.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.95+125G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749040 | |||||||
| chr16:30749040 | GTGGTGGT others(44): Show |
G | 2 | a0001c0001t0002g0042 a0001c0001t0007g0065 |
2 | HG00140.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.95+128_95+178delGT others(49): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749040 | ||||||
| chr16:30749043 | G | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0055 others(40): Show |
85 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.95+128G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749043 | |||||||
| chr16:30749043 | GTGGTGGT others(44): Show |
G | 1 | a0001c0001t0008g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95+131_95+181delGT others(49): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749043 | ||||||
| chr16:30749046 | G | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0055 others(43): Show |
94 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.95+131G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749046 | |||||||
| chr16:30749046 | GTGGTGGT others(41): Show |
G | 2 | a0001c0001t0008g0023 a0002c0002t0008g0023 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.95+134_95+181delGT others(46): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749046 | ||||||
| chr16:30749049 | G | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0061 others(44): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.95+134G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749049 | |||||||
| chr16:30749049 | GTGGTGGT others(35): Show |
G | 1 | a0001c0001t0001g0069 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.95+137_95+178delGT others(40): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749049 | ||||||
| chr16:30749052 | G | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0055 others(43): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.95+137G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749052 | |||||||
| chr16:30749055 | G | C | 15 | a0001c0001t0001g0067 a0001c0001t0002g0009 a0001c0001t0002g0011 others(12): Show |
24 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.95+140G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749055 | |||||||
| chr16:30749055 | GTGGTGGT others(29): Show |
G | 1 | a0001c0001t0003g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95+143_95+178delGT others(34): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749055 | ||||||
| chr16:30749058 | G | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0025 others(33): Show |
78 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.95+143G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749058 | |||||||
| chr16:30749058 | GTGGTGGT others(26): Show |
G | 1 | a0001c0001t0003g0074 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.95+146_95+178delGT others(31): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749058 | ||||||
| chr16:30749061 | G | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0070 others(16): Show |
28 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.95+146G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749061 | |||||||
| chr16:30749064 | G | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0070 a0001c0001t0001g0072 others(10): Show |
15 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.95+149G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749064 | |||||||
| chr16:30749067 | G | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0025 others(45): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.95+152G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749067 | |||||||
| chr16:30749070 | G | C | 28 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0070 others(25): Show |
38 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.95+155G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749070 | |||||||
| chr16:30749070 | GTGGTGGT others(20): Show |
G | 1 | a0001c0001t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.95+158_95+184delGT others(25): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749070 | ||||||
| chr16:30749073 | G | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0025 others(53): Show |
99 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.95+158G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749073 | |||||||
| chr16:30749073 | GTGGTGGT others(44): Show |
G | 1 | a0001c0001t0006g0054 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.95+173_95+223delGT others(49): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749073 | ||||||
| chr16:30749076 | G | C | 29 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0072 others(26): Show |
39 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.95+161G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749076 | |||||||
| chr16:30749076 | GTGGTGGT others(41): Show |
G | 2 | a0001c0001t0001g0055 a0001c0001t0003g0056 |
2 | HG01346.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.95+179_95+226delCT others(46): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749076 | ||||||
| chr16:30749079 | G | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0025 others(24): Show |
48 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.95+164G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749079 | |||||||
| chr16:30749079 | GTGGTGGT others(5): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.95+167_95+178delGT others(10): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749079 | ||||||
| chr16:30749079 | GTGGTGGT others(38): Show |
G | 1 | a0001c0001t0002g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+176_95+220delCT others(43): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749079 | ||||||
| chr16:30749082 | G | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(24): Show |
48 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.95+167G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749082 | |||||||
| chr16:30749082 | GTGGTGGT others(35): Show |
G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0061 others(26): Show |
69 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.95+176_95+217delCT others(40): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749082 | ||||||
| chr16:30749085 | G | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(29): Show |
55 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.95+170G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749085 | |||||||
| chr16:30749085 | GTGGTGCT others(8): Show |
G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0070 a0001c0001t0001g0081 others(5): Show |
9 | HG00438.hp1 HG01070.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.95+173_95+187delGT others(13): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749085 | ||||||
| chr16:30749085 | GTGGTGCT others(14): Show |
G | 1 | a0001c0001t0022g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.95+173_95+193delGT others(19): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749085 | ||||||
| chr16:30749088 | G | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(39): Show |
74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.95+173G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749088 | |||||||
| chr16:30749088 | GTGCTGCT others(5): Show |
G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0075 others(4): Show |
8 | HG00280.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.95+185_95+196delCT others(10): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749088 | ||||||
| chr16:30749088 | GTGCTGCT others(29): Show |
G | 2 | a0001c0001t0002g0047 a0001c0001t0003g0024 |
3 | HG00280.hp1 HG01255.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.95+176_95+211delCT others(34): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749088 | ||||||
| chr16:30749091 | CTGCTGCT others(32): Show |
C | 11 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(8): Show |
19 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.95+179_95+217delCT others(37): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749091 | ||||||
| chr16:30749094 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.95+179C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749094 | |||||||
| chr16:30749097 | C | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(24): Show |
50 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.95+182C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749097 | |||||||
| chr16:30749100 | C | G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0089 others(3): Show |
6 | HG01099.hp1 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.95+185C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749100 | |||||||
| chr16:30749103 | C | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(38): Show |
71 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.95+188C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749103 | |||||||
| chr16:30749106 | C | CTGCTGCT others(8): Show |
1 | a0001c0001t0001g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.95+196_95+197insCT others(13): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGCTGCT others(5): Show |
1 | a0001c0001t0001g0001 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95+196_95+197insCT others(10): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGCTGCT others(2): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
6 | HG00673.hp1 HG01081.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+196_95+197insCT others(7): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGCTGG | 7 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0100 others(4): Show |
9 | HG02280.hp1 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.95+194_95+199dupCT others(4): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGCTGGT others(8): Show |
1 | a0001c0001t0026g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.95+199_95+200insCT others(13): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGG | 8 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
17 | HG00099.hp2 HG00558.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.95+193_95+194insGT others(1): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGGTGCT others(5): Show |
1 | a0001c0001t0009g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.95+193_95+194insGT others(10): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | CTGGTGCT others(5): Show |
1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.95+193_95+194insGT others(10): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749106 | ||||||
| chr16:30749106 | C | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(74): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.95+191C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749106 | |||||||
| chr16:30749109 | C | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0067 a0001c0001t0001g0080 others(4): Show |
8 | HG01891.hp1 HG01928.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.95+194C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749109 | |||||||
| chr16:30749112 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95+197G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749112 | |||||||
| chr16:30749112 | G | GTGC | 5 | a0001c0001t0001g0034 a0001c0001t0001g0067 a0001c0001t0004g0034 others(2): Show |
6 | HG01891.hp1 HG01928.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+199_95+200insCT others(1): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749112 | ||||||
| chr16:30749115 | G | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(35): Show |
67 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.95+200G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749115 | |||||||
| chr16:30749118 | C | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(51): Show |
84 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.95+203C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749118 | |||||||
| chr16:30749124 | C | G | 44 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(41): Show |
74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.95+209C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749124 | |||||||
| chr16:30749124 | CTGGTGG | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0070 others(14): Show |
19 | HG00280.hp2 HG00438.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.95+218_95+223delGT others(4): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749124 | ||||||
| chr16:30749130 | G | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.95+215G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749130 | |||||||
| chr16:30749130 | G | GTGC | 6 | a0001c0001t0001g0034 a0001c0001t0001g0067 a0001c0001t0001g0119 others(3): Show |
7 | HG01891.hp1 HG01928.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.95+217_95+218insCT others(1): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749130 | ||||||
| chr16:30749130 | G | GTGGTGGT others(2): Show |
25 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(22): Show |
50 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.95+221_95+229dupGT others(7): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749130 | ||||||
| chr16:30749133 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.95+218G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749133 | |||||||
| chr16:30749142 | GTGC | G | 5 | a0001c0001t0002g0090 a0001c0001t0002g0108 a0001c0001t0003g0071 others(2): Show |
5 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.95+230_95+232delCT others(1): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749142 | ||||||
| chr16:30749145 | C | G | 1 | a0001c0001t0022g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.95+230C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749145 | |||||||
| chr16:30749151 | G | C | 5 | a0001c0001t0002g0090 a0001c0001t0002g0108 a0001c0001t0003g0071 others(2): Show |
5 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.95+236G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749151 | |||||||
| chr16:30749154 | G | C | 1 | a0001c0001t0022g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.95+239G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749154 | |||||||
| chr16:30749157 | C | G | 1 | a0001c0001t0022g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.95+242C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749157 | |||||||
| chr16:30749166 | G | C | 2 | a0001c0001t0001g0099 a0001c0001t0022g0045 |
2 | HG02040.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.95+251G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749166 | |||||||
| chr16:30749169 | G | C | 4 | a0001c0001t0002g0090 a0001c0001t0003g0071 a0001c0001t0003g0074 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.95+254G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749169 | |||||||
| chr16:30749172 | C | G | 4 | a0001c0001t0002g0090 a0001c0001t0003g0071 a0001c0001t0003g0074 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.95+257C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749172 | |||||||
| chr16:30749196 | C | CTGG | 9 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0036 others(6): Show |
15 | HG02683.hp1 HG02735.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.95+290_95+292dupGT others(1): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749196 | ||||||
| chr16:30749204 | G | GGT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(121): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.95+308_95+309dupGT | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749204 | ||||||
| chr16:30749204 | G | GGTGT | 12 | a0001c0001t0001g0035 a0001c0001t0001g0109 a0001c0001t0002g0002 others(9): Show |
15 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.95+306_95+309dupGT others(2): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749204 | ||||||
| chr16:30749240 | GTGCTGGT others(2): Show |
G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0089 |
3 | HG02896.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.95+328_95+336delCT others(7): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749240 | ||||||
| chr16:30749264 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+349G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749264 | |||||||
| chr16:30749271 | T | TGCTGGTG others(6): Show |
1 | a0001c0001t0002g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+357_95+358insCT others(11): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749271 | ||||||
| chr16:30749280 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+365C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749280 | |||||||
| chr16:30749280 | CTG | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(141): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.95+381_95+382delGT | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749280 | ||||||
| chr16:30749280 | CTGTG | C | 4 | a0001c0001t0009g0030 a0001c0001t0009g0078 a0001c0001t0009g0083 others(1): Show |
4 | HG02055.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+379_95+382delGT others(2): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30749280 | ||||||
| chr16:30749282 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+367G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749282 | |||||||
| chr16:30749379 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.95+464G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749379 | |||||||
| chr16:30749410 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(140): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.95+495C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749410 | |||||||
| chr16:30749416 | C | T | 1 | a0004c0004t0002g0058 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.95+501C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749416 | |||||||
| chr16:30749636 | G | T | 1 | a0001c0001t0008g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.95+721G>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749636 | |||||||
| chr16:30749843 | G | A | 1 | a0001c0001t0022g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.95+928G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749843 | |||||||
| chr16:30749960 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.95+1045A>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749960 | |||||||
| chr16:30749964 | CA | C | 15 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0089 others(12): Show |
21 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.95+1050delA | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30749964 | |||||||
| chr16:30750089 | C | T | 3 | a0001c0001t0008g0023 a0001c0001t0008g0068 a0002c0002t0008g0023 |
3 | HG02280.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96-1017C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750089 | |||||||
| chr16:30750189 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.96-917T>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750189 | |||||||
| chr16:30750487 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.96-619C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750487 | |||||||
| chr16:30750678 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.96-428C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750678 | |||||||
| chr16:30750759 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0070 |
4 | HG00438.hp1 HG02132.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-347G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750759 | |||||||
| chr16:30750780 | ATCTT | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(140): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.96-319_96-316delTT others(2): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 30750780 | ||||||
| chr16:30750803 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0101 |
2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.96-303G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750803 | |||||||
| chr16:30750901 | C | T | 1 | a0001c0001t0008g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96-205C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 2/9 | chr16 | 30750901 | |||||||
| chr16:30751295 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.271+14C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 3/9 | chr16 | 30751295 | |||||||
| chr16:30751319 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(140): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.271+38C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 3/9 | chr16 | 30751319 | |||||||
| chr16:30751384 | C | G | 5 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0048 others(2): Show |
6 | HG01496.hp2 HG02145.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+103C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 3/9 | chr16 | 30751384 | |||||||
| chr16:30751417 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.272-132C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 3/9 | chr16 | 30751417 | |||||||
| chr16:30751862 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.326+259G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30751862 | |||||||
| chr16:30751903 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+300C>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30751903 | |||||||
| chr16:30751910 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(140): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.326+307A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30751910 | |||||||
| chr16:30752218 | C | CAAAACCC others(447): Show |
2 | a0001c0001t0002g0022 a0001c0001t0002g0086 |
3 | HG00609.hp2 HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.326+615_326+616ins others(454): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30752218 | |||||||
| chr16:30752218 | C | CGAAACCC others(447): Show |
1 | a0001c0001t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.326+636_326+637ins others(454): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 30752218 | ||||||
| chr16:30752218 | C | CGAAACCC others(447): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0091 others(4): Show |
13 | HG02683.hp1 HG02738.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.326+636_326+637ins others(454): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 30752218 | ||||||
| chr16:30752218 | C | CGAAACCC others(447): Show |
1 | a0001c0001t0002g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.326+636_326+637ins others(454): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 30752218 | ||||||
| chr16:30752218 | C | CGAAACCC others(447): Show |
4 | a0001c0001t0009g0030 a0001c0001t0009g0078 a0001c0001t0009g0083 others(1): Show |
4 | HG02055.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+636_326+637ins others(454): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 30752218 | ||||||
| chr16:30752218 | C | CGAAACCC others(447): Show |
1 | a0001c0006t0002g0051 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.326+636_326+637ins others(454): Show |
PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 30752218 | ||||||
| chr16:30752440 | A | G | 1 | a0001c0001t0008g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.327-792A>G | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30752440 | |||||||
| chr16:30752615 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.327-617G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30752615 | |||||||
| chr16:30752684 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0038 a0001c0001t0002g0047 others(1): Show |
11 | HG00558.hp2 HG01192.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.327-548G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | chr16 | 30752684 | |||||||
| chr16:30753040 | A | AT | 63 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0002g0002 others(60): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.327-191dupT | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 30753040 | ||||||
| chr16:30753594 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.556+37G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30753594 | |||||||
| chr16:30753698 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+141G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30753698 | |||||||
| chr16:30754170 | C | CT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0067 others(6): Show |
13 | HG01071.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+626dupT | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 30754170 | ||||||
| chr16:30754648 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.556+1091C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30754648 | |||||||
| chr16:30754890 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.557-1292G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30754890 | |||||||
| chr16:30754926 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(143): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.557-1256G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30754926 | |||||||
| chr16:30754933 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557-1249T>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30754933 | |||||||
| chr16:30754994 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.557-1188G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30754994 | |||||||
| chr16:30755152 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.557-1030G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755152 | |||||||
| chr16:30755393 | G | C | 2 | a0001c0001t0002g0040 a0001c0001t0002g0043 |
2 | NA18964.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.557-789G>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755393 | |||||||
| chr16:30755396 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.557-786C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755396 | |||||||
| chr16:30755397 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.557-785G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755397 | |||||||
| chr16:30755415 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0100 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.557-767C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755415 | |||||||
| chr16:30755493 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.557-689G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755493 | |||||||
| chr16:30755749 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.557-433A>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755749 | |||||||
| chr16:30755772 | AG | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0120 a0001c0001t0002g0062 |
5 | HG01175.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-408delG | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 30755772 | ||||||
| chr16:30755796 | C | T | 1 | a0001c0001t0008g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.557-386C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755796 | |||||||
| chr16:30755811 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.557-371G>A | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755811 | |||||||
| chr16:30755903 | G | T | 3 | a0001c0001t0008g0023 a0001c0001t0008g0068 a0002c0002t0008g0023 |
3 | HG02280.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.557-279G>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 6/9 | chr16 | 30755903 | |||||||
| chr16:30756296 | C | T | 1 | a0001c0001t0006g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.647+24C>T | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 7/9 | chr16 | 30756296 | |||||||
| chr16:30756766 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.928-38T>C | PHKG2 | ENSG00000156873.16 | transcript | ENST00000563588.6 | protein_coding | 9/9 | chr16 | 30756766 |