Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57649 |
| ensemblid | ENSG00000109118.14 |
| hgncid | 20816 |
| symbol | PHF12 |
| name | PHD finger protein 12 |
| refseq_nuc | NM_001033561.2 |
| refseq_prot | NP_001028733.1 |
| ensembl_nuc | ENST00000332830.9 |
| ensembl_prot | ENSP00000329933.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 28905250 |
| end | 28951518 |
| strand | - |
| ver | v1.2 |
| region | chr17:28905250-28951518 |
| region5000 | chr17:28900250-28956518 |
| regionname0 | PHF12_chr17_28905250_28951518 |
| regionname5000 | PHF12_chr17_28900250_28956518 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1004 | 226 | 75 | 43 | 70 | 8 | 28 | 54 | PHF12_chr17_28900250_28956518 | PHF12 | MWEKM others(999): Show |
chr17 | 28900250 | 28956518 |
| a0002 | 0/0 | 1004 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | MWEKM others(999): Show |
chr17 | 28900250 | 28956518 |
| a0003 | 0/0 | 1004 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | MWEKM others(999): Show |
chr17 | 28900250 | 28956518 |
| a0004 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | MWEKM others(999): Show |
chr17 | 28900250 | 28956518 |
| a0005 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | MWEKM others(999): Show |
chr17 | 28900250 | 28956518 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3012 | 218 | 73 | 42 | 69 | 8 | 24 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0001c0002 | 0/0 | 3012 | 4 | 0 | 0 | 0 | 0 | 4 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0001c0005 | 0/0 | 3012 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0001c0007 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0001c0009 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0002c0003 | 0/0 | 3012 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0003c0004 | 0/0 | 3012 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0004c0006 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 | ||
| a0005c0008 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | ATGTG others(3007): Show |
chr17 | 28900250 | 28956518 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4506 | 211 | 69 | 42 | 67 | 8 | 23 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0001t0002 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0001t0004 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0001t0005 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0001t0006 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0001t0007 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0001t0008 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0002t0001 | 0/0 | 4506 | 3 | 0 | 0 | 0 | 0 | 3 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0002t0003 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0005t0001 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0007t0001 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0001c0009t0001 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0002c0003t0001 | 0/0 | 4506 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0003c0004t0001 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0004c0006t0001 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| a0005c0008t0001 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | GGCGA others(4501): Show |
chr17 | 28900250 | 28956518 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0002 | 0/0 | 5 | 1 | 1 | 1 | 1 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0007t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0001c0009t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0003c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0003c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0004c0006t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| a0005c0008t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0165 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00673 | hp1 | a0001 | c0009 | t0001 | g0188 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01192 | hp2 | a0001 | c0007 | t0001 | g0042 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0102 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0080 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02273 | hp2 | a0004 | c0006 | t0001 | g0162 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0194 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02976 | hp2 | a0005 | c0008 | t0001 | g0033 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03130 | hp1 | a0003 | c0004 | t0001 | g0072 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0079 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0071 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0056 | REF | REF | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0116 | REF | REF | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28906897 | G | A | 1 | a0004 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.2639C>T | p.Thr880Ile | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 14/15 | 3197/4506 | 2639/3015 | 880/1004 | chr17 | 28906897 | |||
| chr17:28911117 | T | C | 1 | a0002 | 2 | HG00639.hp2 HG01261.hp1 |
missense_variant | MODERATE | c.2210A>G | p.Asn737Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/15 | 2768/4506 | 2210/3015 | 737/1004 | chr17 | 28911117 | |||
| chr17:28913986 | G | A | 1 | a0003 | 2 | HG03130.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1186C>T | p.Pro396Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/15 | 1744/4506 | 1186/3015 | 396/1004 | chr17 | 28913986 | |||
| chr17:28923938 | T | C | 1 | a0005 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.686A>G | p.Asn229Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/15 | 1244/4506 | 686/3015 | 229/1004 | chr17 | 28923938 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28912612 | C | T | 1 | a0001c0002 | 4 | HG02698.hp2 HG02738.hp2 HG03017.hp1 others(1): Show |
synonymous_variant | LOW | c.1959G>A | p.Pro653Pro | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/15 | 2517/4506 | 1959/3015 | 653/1004 | chr17 | 28912612 | |||
| chr17:28921696 | C | A | 1 | a0001c0007 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.828G>T | p.Thr276Thr | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/15 | 1386/4506 | 828/3015 | 276/1004 | chr17 | 28921696 | |||
| chr17:28924114 | G | A | 1 | a0001c0005 | 2 | HG01891.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.510C>T | p.Ser170Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/15 | 1068/4506 | 510/3015 | 170/1004 | chr17 | 28924114 | |||
| chr17:28950223 | G | A | 1 | a0001c0009 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.90C>T | p.Pro30Pro | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/15 | 648/4506 | 90/3015 | 30/1004 | chr17 | 28950223 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28905441 | T | C | 1 | a0001c0001t0006 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*742A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 15/15 | 742 | chr17 | 28905441 | ||||||
| chr17:28951029 | G | A | 1 | a0001c0001t0007 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 69 | chr17 | 28951029 | ||||||
| chr17:28951039 | C | G | 1 | a0001c0001t0002 | 2 | HG02630.hp1 HG02896.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 79 | chr17 | 28951039 | ||||||
| chr17:28951244 | C | T | 1 | a0001c0001t0005 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 284 | chr17 | 28951244 | ||||||
| chr17:28951267 | G | A | 1 | a0001c0001t0008 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-307C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 307 | chr17 | 28951267 | ||||||
| chr17:28951395 | G | T | 1 | a0001c0001t0004 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-435C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 435 | chr17 | 28951395 | ||||||
| chr17:28951474 | G | T | 1 | a0001c0002t0003 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-514C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 514 | chr17 | 28951474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28907285 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2542-291G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 13/14 | chr17 | 28907285 | |||||||
| chr17:28907489 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2541+101G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 13/14 | chr17 | 28907489 | |||||||
| chr17:28907813 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0164 |
3 | NA19056.hp1 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2459-141G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28907813 | |||||||
| chr17:28907972 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2459-300C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28907972 | |||||||
| chr17:28907974 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2459-302C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28907974 | |||||||
| chr17:28908123 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2459-451G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28908123 | |||||||
| chr17:28908181 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2459-509T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28908181 | |||||||
| chr17:28908232 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0062 |
3 | HG02559.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2458+551A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28908232 | |||||||
| chr17:28908962 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0062 |
3 | HG02559.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2360-81A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28908962 | |||||||
| chr17:28909358 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2360-477T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28909358 | |||||||
| chr17:28909417 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2360-536C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28909417 | |||||||
| chr17:28910119 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0085 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2359+107C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28910119 | |||||||
| chr17:28910567 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2216-198T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28910567 | |||||||
| chr17:28910633 | G | A | 2 | a0003c0004t0001g0071 a0003c0004t0001g0072 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2216-264C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28910633 | |||||||
| chr17:28910660 | CTGTGGGG others(11): Show |
C | 6 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG02280.hp1 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2216-309_2216-292d others(20): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28910660 | |||||||
| chr17:28911057 | G | A | 31 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0069 others(28): Show |
31 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2215+55C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28911057 | |||||||
| chr17:28911082 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2215+30G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28911082 | |||||||
| chr17:28911813 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2090-576C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/14 | chr17 | 28911813 | |||||||
| chr17:28911838 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2090-601G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/14 | chr17 | 28911838 | |||||||
| chr17:28912358 | G | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
54 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.2089+124C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/14 | chr17 | 28912358 | |||||||
| chr17:28913325 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294-48C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913325 | |||||||
| chr17:28913363 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294-86A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913363 | |||||||
| chr17:28913390 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0172 |
4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294-113A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913390 | |||||||
| chr17:28913556 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1294-279A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913556 | |||||||
| chr17:28913563 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294-286C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913563 | |||||||
| chr17:28913573 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1294-296C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913573 | |||||||
| chr17:28914064 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135-27C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914064 | |||||||
| chr17:28914438 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-401G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914438 | |||||||
| chr17:28914589 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-552T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914589 | |||||||
| chr17:28914671 | C | CA | 54 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
59 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1135-635dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAA | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0030 others(16): Show |
22 | HG00408.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1135-636_1135-635d others(4): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
12 | HG02055.hp1 HG02293.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1135-637_1135-635d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAAA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(14): Show |
26 | HG00544.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1135-638_1135-635d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAAAA | 11 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0053 others(8): Show |
15 | HG00408.hp1 HG01106.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1135-639_1135-635d others(7): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAAAAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
12 | HG00673.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135-640_1135-635d others(8): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0066 others(3): Show |
9 | HG01109.hp1 HG01891.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135-642_1135-635d others(10): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0052 others(2): Show |
6 | HG01346.hp1 HG02293.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-643_1135-635d others(11): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1135-644_1135-635d others(12): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914671 | CAAA | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0109 others(2): Show |
5 | HG02280.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-637_1135-635d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | |||||||
| chr17:28914703 | T | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0123 |
3 | HG00140.hp2 HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1135-666A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914703 | |||||||
| chr17:28914841 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1135-804T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914841 | |||||||
| chr17:28915071 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1135-1034A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915071 | |||||||
| chr17:28915071 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1135-1034A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915071 | |||||||
| chr17:28915224 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-1187A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915224 | |||||||
| chr17:28915302 | G | GA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-1266dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915302 | |||||||
| chr17:28915343 | G | A | 1 | a0004c0006t0001g0162 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1135-1306C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915343 | |||||||
| chr17:28915411 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00673.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1135-1374C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915411 | |||||||
| chr17:28915425 | TGGA | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
103 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1135-1391_1135-138 others(7): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915425 | |||||||
| chr17:28915497 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-1460A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915497 | |||||||
| chr17:28915682 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1134+1603G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915682 | |||||||
| chr17:28915687 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1134+1598G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915687 | |||||||
| chr17:28915721 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1134+1564T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915721 | |||||||
| chr17:28915987 | C | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0136 |
2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1134+1298G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915987 | |||||||
| chr17:28916175 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1134+1110C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916175 | |||||||
| chr17:28916398 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1134+887C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916398 | |||||||
| chr17:28916462 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(35): Show |
55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1134+823G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916462 | |||||||
| chr17:28916637 | G | C | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG02486.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+648C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916637 | |||||||
| chr17:28916719 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0133 |
2 | HG01361.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1134+566G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916719 | |||||||
| chr17:28916770 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1134+515G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916770 | |||||||
| chr17:28916803 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1134+482C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916803 | |||||||
| chr17:28917455 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
54 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(51): Show |
splice_region_variant&intron_variant | LOW | c.970-6C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28917455 | |||||||
| chr17:28917732 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.970-283C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28917732 | |||||||
| chr17:28917934 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.970-485C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28917934 | |||||||
| chr17:28918300 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.969+843A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918300 | |||||||
| chr17:28918301 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.969+842G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918301 | |||||||
| chr17:28918391 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.969+752T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918391 | |||||||
| chr17:28918604 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+539T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918604 | |||||||
| chr17:28918721 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0161 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.969+422A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918721 | |||||||
| chr17:28919350 | CCTCCCCT others(16): Show |
C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.837-98_837-76delAA others(21): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919350 | |||||||
| chr17:28919445 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.837-170A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919445 | |||||||
| chr17:28919524 | GGAGACT | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.837-255_837-250del others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919524 | |||||||
| chr17:28919624 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0169 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.837-349G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919624 | |||||||
| chr17:28919653 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.837-378A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919653 | |||||||
| chr17:28919664 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
166 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.837-389A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919664 | |||||||
| chr17:28919847 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.837-572G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919847 | |||||||
| chr17:28919917 | C | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | NA18960.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.837-642G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919917 | |||||||
| chr17:28920216 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.837-941T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920216 | |||||||
| chr17:28920665 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.836+1023A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920665 | |||||||
| chr17:28920674 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.836+1014A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920674 | |||||||
| chr17:28920936 | C | T | 1 | a0001c0001t0001g0005 | 3 | HG02886.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.836+752G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920936 | |||||||
| chr17:28921050 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.836+638C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921050 | |||||||
| chr17:28921175 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.836+513G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921175 | |||||||
| chr17:28921462 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0161 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.836+226G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921462 | |||||||
| chr17:28921665 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.836+23G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921665 | |||||||
| chr17:28921842 | T | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG02280.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.716-34A>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28921842 | |||||||
| chr17:28922118 | AATGTCCA others(4): Show |
A | 17 | a0001c0001t0001g0111 a0001c0001t0001g0134 a0001c0001t0001g0135 others(14): Show |
17 | HG00408.hp1 HG00673.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.716-321_716-311del others(11): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922118 | |||||||
| chr17:28922214 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.716-406A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922214 | |||||||
| chr17:28922420 | T | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG02280.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.716-612A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922420 | |||||||
| chr17:28922688 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01071.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.716-880G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922688 | |||||||
| chr17:28922807 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.716-999C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922807 | |||||||
| chr17:28922854 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0125 |
2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.716-1046C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922854 | |||||||
| chr17:28922937 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+972C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922937 | |||||||
| chr17:28922954 | A | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
105 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.715+955T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922954 | |||||||
| chr17:28923046 | C | CA | 30 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0069 others(27): Show |
30 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.715+862dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923046 | |||||||
| chr17:28923046 | CA | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
11 | HG01074.hp1 HG01109.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.715+862delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923046 | |||||||
| chr17:28923206 | GAGA | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(31): Show |
51 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.715+700_715+702del others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923206 | |||||||
| chr17:28923280 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.715+629C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923280 | |||||||
| chr17:28923349 | C | CT | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
226 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.715+559dupA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923349 | |||||||
| chr17:28923361 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.715+548T>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923361 | |||||||
| chr17:28923476 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+433C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923476 | |||||||
| chr17:28923651 | C | CAAAAAAA others(5): Show |
1 | a0003c0004t0001g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(12): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(8): Show |
2 | a0001c0005t0001g0079 a0001c0005t0001g0080 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.715+257_715+258ins others(15): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0076 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.715+257_715+258ins others(16): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(10): Show |
10 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0001g0078 others(7): Show |
10 | HG00408.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.715+257_715+258ins others(17): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(18): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0179 |
3 | HG01515.hp2 HG02572.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.715+257_715+258ins others(19): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG01069.hp1 HG01109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+257_715+258ins others(20): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(21): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0098 |
2 | HG02622.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.715+257_715+258ins others(24): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0083 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.715+257_715+258ins others(25): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923651 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(26): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | |||||||
| chr17:28923653 | C | A | 31 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0069 others(28): Show |
31 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.715+256G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CA | 13 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0103 others(10): Show |
14 | HG00621.hp1 HG01258.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.715+255dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(13): Show |
29 | HG00544.hp2 HG00642.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.715+254_715+255dup others(2): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0059 others(3): Show |
8 | HG01106.hp1 HG01952.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.715+253_715+255dup others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0111 others(7): Show |
12 | HG00673.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.715+251_715+255dup others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0176 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+246_715+255dup others(10): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0174 a0001c0002t0001g0142 a0001c0002t0001g0143 |
3 | HG02698.hp2 HG03139.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.715+245_715+255dup others(11): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(5): Show |
1 | a0001c0002t0003g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.715+244_715+255dup others(12): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.715+243_715+255dup others(13): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0185 others(1): Show |
4 | HG00621.hp2 HG01175.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+242_715+255dup others(14): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0145 |
3 | HG01258.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.715+240_715+255dup others(16): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0110 others(1): Show |
4 | HG00733.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+239_715+255dup others(17): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.715+238_715+255dup others(18): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0137 others(1): Show |
5 | HG02451.hp2 HG03225.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+237_715+255dup others(19): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715+236_715+255dup others(20): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(14): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0047 others(1): Show |
5 | HG01074.hp2 HG01168.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+235_715+255dup others(21): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.715+234_715+255dup others(22): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(23): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(24): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(19): Show |
5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0104 others(2): Show |
5 | HG01261.hp2 HG01433.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+255_715+256ins others(26): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(20): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0170 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.715+255_715+256ins others(27): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(21): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0171 |
2 | HG01515.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.715+255_715+256ins others(28): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(24): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0150 |
3 | HG02630.hp2 NA18955.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.715+255_715+256ins others(31): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00408.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.715+255_715+256ins others(32): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0002g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(33): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0153 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(34): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(33): Show |
1 | a0001c0001t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(40): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(34): Show |
1 | a0001c0001t0001g0154 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(41): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | C | CAAAAAAA others(35): Show |
1 | a0001c0001t0001g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.715+255_715+256ins others(42): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28923653 | CAAAAA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.715+251_715+255del others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | |||||||
| chr17:28924452 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.322-150C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924452 | |||||||
| chr17:28924950 | C | CA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG03195.hp1 NA19001.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-649dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924950 | |||||||
| chr17:28924950 | C | CAAA | 4 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
8 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.322-651_322-649dup others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924950 | |||||||
| chr17:28924950 | CA | C | 67 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0045 others(64): Show |
67 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.322-649delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924950 | |||||||
| chr17:28925399 | C | T | 7 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0081 others(4): Show |
7 | HG01069.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.322-1097G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925399 | |||||||
| chr17:28925694 | G | A | 2 | a0001c0001t0001g0040 a0001c0007t0001g0042 |
2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.321+1297C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925694 | |||||||
| chr17:28925759 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.321+1232C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925759 | |||||||
| chr17:28925941 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.321+1050G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925941 | |||||||
| chr17:28925971 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
56 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.321+1020G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925971 | |||||||
| chr17:28926343 | C | CA | 3 | a0001c0001t0001g0019 a0001c0001t0001g0114 a0001c0001t0001g0130 |
4 | HG00544.hp1 NA18952.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+647dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926343 | |||||||
| chr17:28926460 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.321+531G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926460 | |||||||
| chr17:28926502 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.321+489T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926502 | |||||||
| chr17:28926719 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.321+272G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926719 | |||||||
| chr17:28926952 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.321+39G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926952 | |||||||
| chr17:28927161 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
54 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.249-98G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927161 | |||||||
| chr17:28927323 | G | C | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0073 others(25): Show |
28 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.249-260C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927323 | |||||||
| chr17:28927649 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.249-586G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927649 | |||||||
| chr17:28927734 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.249-671A>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927734 | |||||||
| chr17:28927938 | C | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG03041.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-875G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927938 | |||||||
| chr17:28928009 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249-946C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928009 | |||||||
| chr17:28928173 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
57 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.249-1110A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928173 | |||||||
| chr17:28928599 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.249-1536G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928599 | |||||||
| chr17:28928714 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249-1651C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928714 | |||||||
| chr17:28928777 | A | AAAAC | 5 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
9 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.249-1718_249-1715d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928777 | |||||||
| chr17:28928845 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-1782G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928845 | |||||||
| chr17:28929075 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.249-2012C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929075 | |||||||
| chr17:28929103 | AAAC | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
54 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.249-2043_249-2041d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929103 | |||||||
| chr17:28929176 | C | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0130 |
2 | HG00544.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.249-2113G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929176 | |||||||
| chr17:28929189 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.249-2126C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929189 | |||||||
| chr17:28929228 | T | TA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(10): Show |
17 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.249-2166dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929228 | |||||||
| chr17:28930048 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-2985A>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930048 | |||||||
| chr17:28930345 | C | CA | 2 | a0001c0001t0001g0086 a0001c0001t0001g0091 |
2 | NA18986.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.249-3283dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930345 | |||||||
| chr17:28930460 | G | C | 31 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0069 others(28): Show |
31 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.249-3397C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930460 | |||||||
| chr17:28930667 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-3604T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930667 | |||||||
| chr17:28930699 | T | TA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-3637dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930699 | |||||||
| chr17:28930768 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0061 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.249-3705G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930768 | |||||||
| chr17:28930792 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.249-3729G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930792 | |||||||
| chr17:28930822 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.249-3759C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930822 | |||||||
| chr17:28930937 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0172 |
4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-3874G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930937 | |||||||
| chr17:28930943 | GAGCCTAT | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | NA18960.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.249-3887_249-3881d others(9): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930943 | |||||||
| chr17:28931104 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
98 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.249-4041G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931104 | |||||||
| chr17:28931128 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249-4065G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931128 | |||||||
| chr17:28931214 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249-4151G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931214 | |||||||
| chr17:28931256 | C | CT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-4194dupA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931256 | |||||||
| chr17:28931256 | CT | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
125 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.249-4194delA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931256 | |||||||
| chr17:28931288 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249-4225G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931288 | |||||||
| chr17:28931501 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.249-4438G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931501 | |||||||
| chr17:28931536 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-4473G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931536 | |||||||
| chr17:28931818 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-4755C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931818 | |||||||
| chr17:28931834 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.249-4771C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931834 | |||||||
| chr17:28932161 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-5098A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932161 | |||||||
| chr17:28932596 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249-5533G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932596 | |||||||
| chr17:28932763 | T | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-5700A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932763 | |||||||
| chr17:28932927 | C | CAGA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.249-5865_249-5864i others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932927 | |||||||
| chr17:28932964 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
152 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.249-5901A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932964 | |||||||
| chr17:28932999 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): Show |
64 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.249-5936G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932999 | |||||||
| chr17:28933127 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(31): Show |
51 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.249-6064G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933127 | |||||||
| chr17:28933638 | C | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
97 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.249-6575G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933638 | |||||||
| chr17:28933842 | G | A | 1 | a0001c0001t0008g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.249-6779C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933842 | |||||||
| chr17:28933917 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.249-6854A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933917 | |||||||
| chr17:28934005 | C | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-6942G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934005 | |||||||
| chr17:28934092 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.249-7029T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934092 | |||||||
| chr17:28934458 | T | C | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.249-7395A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934458 | |||||||
| chr17:28934609 | TA | T | 2 | a0001c0005t0001g0079 a0001c0005t0001g0080 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.249-7547delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934609 | |||||||
| chr17:28934610 | AT | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(9): Show |
13 | HG02559.hp1 HG02735.hp2 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.249-7548delA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934610 | |||||||
| chr17:28934610 | ATT | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
58 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.249-7549_249-7548d others(4): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934610 | |||||||
| chr17:28934773 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.249-7710C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934773 | |||||||
| chr17:28934951 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0007g0193 |
3 | HG02615.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.249-7888A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934951 | |||||||
| chr17:28934978 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0191 |
3 | NA19003.hp2 NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.249-7915G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934978 | |||||||
| chr17:28935122 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.249-8059T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935122 | |||||||
| chr17:28935134 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249-8071G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935134 | |||||||
| chr17:28935256 | CTATTT | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-8198_249-8194d others(7): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935256 | |||||||
| chr17:28935335 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
37 | HG00544.hp2 HG00642.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.249-8272C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935335 | |||||||
| chr17:28935364 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-8301G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935364 | |||||||
| chr17:28935365 | G | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01071.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.249-8302C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935365 | |||||||
| chr17:28935428 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.249-8365G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935428 | |||||||
| chr17:28935455 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02155.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.249-8392T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935455 | |||||||
| chr17:28935583 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.249-8520A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935583 | |||||||
| chr17:28935891 | A | G | 2 | a0003c0004t0001g0071 a0003c0004t0001g0072 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.249-8828T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935891 | |||||||
| chr17:28936044 | T | C | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.249-8981A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936044 | |||||||
| chr17:28936085 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9022A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936085 | |||||||
| chr17:28936101 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9038G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936101 | |||||||
| chr17:28936147 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.249-9084C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936147 | |||||||
| chr17:28936877 | TA | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9815delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936877 | |||||||
| chr17:28936923 | C | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9860G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936923 | |||||||
| chr17:28937075 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249-10012G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937075 | |||||||
| chr17:28937453 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.249-10390A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937453 | |||||||
| chr17:28937609 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.249-10546T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937609 | |||||||
| chr17:28937844 | T | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0163 a0001c0001t0001g0167 others(1): Show |
4 | HG02273.hp2 HG02300.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-10781A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937844 | |||||||
| chr17:28938048 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.249-10985A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28938048 | |||||||
| chr17:28938400 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.249-11337A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28938400 | |||||||
| chr17:28938952 | G | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+11113C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28938952 | |||||||
| chr17:28939125 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
54 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.248+10940C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939125 | |||||||
| chr17:28939314 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.248+10751G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939314 | |||||||
| chr17:28939422 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): Show |
64 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.248+10643G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939422 | |||||||
| chr17:28939716 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.248+10349C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939716 | |||||||
| chr17:28940067 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+9998A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940067 | |||||||
| chr17:28940157 | A | C | 1 | a0001c0001t0008g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248+9908T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940157 | |||||||
| chr17:28940314 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.248+9751G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940314 | |||||||
| chr17:28940490 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.248+9575T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940490 | |||||||
| chr17:28940855 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.248+9210G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940855 | |||||||
| chr17:28941039 | C | CT | 45 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00408.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.248+9025dupA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941039 | |||||||
| chr17:28941039 | CT | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(32): Show |
52 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.248+9025delA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941039 | |||||||
| chr17:28941319 | T | G | 1 | a0002c0003t0001g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.248+8746A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941319 | |||||||
| chr17:28941495 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0166 |
3 | HG00140.hp1 HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.248+8570C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941495 | |||||||
| chr17:28941580 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.248+8485A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941580 | |||||||
| chr17:28941779 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.248+8286C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941779 | |||||||
| chr17:28941859 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.248+8206C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941859 | |||||||
| chr17:28941919 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.248+8146G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941919 | |||||||
| chr17:28942546 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.248+7519C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942546 | |||||||
| chr17:28942577 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.248+7488G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942577 | |||||||
| chr17:28942703 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.248+7362G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942703 | |||||||
| chr17:28942752 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.248+7313C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942752 | |||||||
| chr17:28942864 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG02886.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.248+7201C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942864 | |||||||
| chr17:28943122 | G | A | 1 | a0005c0008t0001g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248+6943C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943122 | |||||||
| chr17:28943278 | C | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+6787G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943278 | |||||||
| chr17:28943503 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.248+6562T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943503 | |||||||
| chr17:28943612 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.248+6453C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943612 | |||||||
| chr17:28943636 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.248+6429A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943636 | |||||||
| chr17:28943636 | T | TAAAC | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): Show |
64 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.248+6425_248+6428d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943636 | |||||||
| chr17:28943636 | TAAAC | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG03130.hp1 HG03130.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+6425_248+6428d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943636 | |||||||
| chr17:28943699 | CACA | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0007t0001g0042 |
3 | HG01192.hp2 HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.248+6363_248+6365d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943699 | |||||||
| chr17:28943774 | T | TA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.248+6290_248+6291i others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943774 | |||||||
| chr17:28944203 | C | T | 1 | a0002c0003t0001g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.248+5862G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944203 | |||||||
| chr17:28944438 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.248+5627G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944438 | |||||||
| chr17:28944787 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0172 |
4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.248+5278C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944787 | |||||||
| chr17:28944830 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.248+5235A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944830 | |||||||
| chr17:28945088 | A | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+4977T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945088 | |||||||
| chr17:28945190 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0062 |
3 | HG02559.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.248+4875A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945190 | |||||||
| chr17:28945314 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.248+4751C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945314 | |||||||
| chr17:28945680 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.248+4385G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945680 | |||||||
| chr17:28945780 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248+4285C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945780 | |||||||
| chr17:28945857 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(35): Show |
55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.248+4208G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945857 | |||||||
| chr17:28946094 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+3971A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946094 | |||||||
| chr17:28946106 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.248+3959A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946106 | |||||||
| chr17:28946107 | C | T | 2 | a0001c0001t0001g0040 a0001c0007t0001g0042 |
2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.248+3958G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946107 | |||||||
| chr17:28946322 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.248+3743G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946322 | |||||||
| chr17:28946923 | AG | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0007g0193 |
3 | HG02615.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.248+3141delC | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946923 | |||||||
| chr17:28947210 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.248+2855A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947210 | |||||||
| chr17:28947294 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.248+2771C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947294 | |||||||
| chr17:28947475 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.248+2590C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947475 | |||||||
| chr17:28947492 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.248+2573G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947492 | |||||||
| chr17:28947611 | A | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.248+2454T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947611 | |||||||
| chr17:28947887 | C | CA | 25 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0065 others(22): Show |
25 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.248+2177dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947887 | |||||||
| chr17:28947887 | C | CAA | 6 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.248+2176_248+2177d others(4): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947887 | |||||||
| chr17:28947887 | CA | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
16 | HG01071.hp1 HG01109.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.248+2177delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947887 | |||||||
| chr17:28947967 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+2098A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947967 | |||||||
| chr17:28948102 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.248+1963A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948102 | |||||||
| chr17:28948213 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.248+1852A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948213 | |||||||
| chr17:28948291 | T | TA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+1773dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948291 | |||||||
| chr17:28948378 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01258.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.248+1687C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948378 | |||||||
| chr17:28948580 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.248+1485C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948580 | |||||||
| chr17:28948603 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.248+1462A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948603 | |||||||
| chr17:28948847 | CA | C | 33 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0069 others(30): Show |
33 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.248+1217delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948847 | |||||||
| chr17:28949105 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.248+960C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949105 | |||||||
| chr17:28949216 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.248+849T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949216 | |||||||
| chr17:28949286 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.248+779C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949286 | |||||||
| chr17:28949356 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
11 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.248+709C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949356 | |||||||
| chr17:28949403 | G | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): Show |
64 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.248+662C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949403 | |||||||
| chr17:28949593 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+472A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949593 | |||||||
| chr17:28949700 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+365T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949700 | |||||||
| chr17:28949707 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+358G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949707 | |||||||
| chr17:28950060 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | splice_region_variant&intron_variant | LOW | c.248+5G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28950060 | |||||||
| chr17:28950265 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
5 | NA18975.hp1 NA19003.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-19C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950265 | |||||||
| chr17:28950330 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0007g0193 |
3 | HG02615.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67-84G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950330 | |||||||
| chr17:28950732 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
8 | HG01934.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+163G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950732 | |||||||
| chr17:28950857 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.66+38G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950857 | |||||||
| chr17:28950886 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.66+9G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950886 |