Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23133 |
|---|---|
| ensemblid | ENSG00000172943.21 |
| hgncid | 20672 |
| symbol | PHF8 |
| name | PHD finger protein 8 |
| refseq_nuc | NM_015107.3 |
| refseq_prot | NP_055922.1 |
| ensembl_nuc | ENST00000338154.11 |
| ensembl_prot | ENSP00000338868.6 |
| mane_status | MANE Select |
| chr | chrX |
| start | 53936680 |
| end | 54044473 |
| strand | - |
| ver | v1.2 |
| region | chrX:53936680-54044473 |
| region5000 | chrX:53931680-54049473 |
| regionname0 | PHF8_chrX_53936680_54044473 |
| regionname5000 | PHF8_chrX_53931680_54049473 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1024 | 177 | 58 | 33 | 61 | 5 | 18 | 47 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0002 | 0/0 | 1023 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0003 | 0/0 | 23 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0004 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0005 | 0/0 | 191 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0006 | 0/0 | 101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0007 | 0/0 | 79 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3075 | 177 | 58 | 33 | 61 | 5 | 18 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0002 | 0/0 | 3072 | 3 | 3 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0003 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0004 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0005 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0006 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0007 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| c0008 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3283 | 131 | 23 | 25 | 63 | 5 | 14 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0002 | 0/1 | 3283 | 23 | 16 | 4 | 0 | 0 | 2 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0003 | 0/0 | 3283 | 19 | 15 | 4 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0004 | 0/0 | 3283 | 4 | 4 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0005 | 0/0 | 3283 | 2 | 2 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0006 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0007 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0008 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0009 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0010 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0011 | 0/0 | 3278 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| t0012 | 0/0 | 3283 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3075 | 177 | 58 | 33 | 61 | 5 | 18 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0002c0002 | 0/0 | 3072 | 3 | 3 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0002c0006 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0003c0003 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0004c0007 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0005c0008 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0006c0005 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0007c0004 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6357 | 127 | 23 | 25 | 59 | 5 | 14 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0002 | 0/1 | 6357 | 23 | 16 | 4 | 0 | 0 | 2 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0003 | 0/0 | 6357 | 19 | 15 | 4 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0005 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0006 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0007 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0008 | 0/0 | 6356 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0009 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0010 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0001c0001t0012 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0002c0002t0004 | 0/0 | 6354 | 3 | 3 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0002c0006t0004 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0003c0003t0011 | 0/0 | 6353 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0004c0007t0001 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0005c0008t0001 | 0/0 | 6359 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0006c0005t0001 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| a0007c0004t0001 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | copy fasta | chrX | 53931680 | 54049473 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0012g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0006t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0003c0003t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0004c0007t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0005c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0006c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0007c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02071 | hp1 | a0004 | c0007 | t0001 | g0022 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0146 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0123 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0147 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02809 | hp2 | a0002 | c0002 | t0004 | g0163 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0148 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0019 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0186 | SAS | BEB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18982 | hp1 | a0005 | c0008 | t0001 | g0087 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18984 | hp1 | a0006 | c0005 | t0001 | g0051 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19055 | hp1 | a0007 | c0004 | t0001 | g0058 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19086 | hp1 | a0003 | c0003 | t0011 | g0164 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | ASW | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ASW | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02559 | hp1 | a0002 | c0006 | t0004 | g0149 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0031 | REF | REF | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0064 | REF | REF | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:53940367
|
TGAG | T | 1 | a0002 | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.2796_2798delCTC | p.Ser933del | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 21/22 | 3602/6357 | 2796/3075 | 932/1024 | chrX | 53940367 | ||
| chrX:53993792
|
T | C | 1 | a0004 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1435A>G | p.Met479Val | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 13/22 | 2239/6357 | 1435/3075 | 479/1024 | chrX | 53993792 | ||
| chrX:54014491
|
T | TG | 1 | a0005 | 1 | NA18982.hp1 | frameshift_variant | HIGH | c.668_669insC | p.Glu223fs | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/22 | 1472/6357 | 668/3075 | 223/1024 | chrX | 54014491 | ||
| chrX:54016637
|
T | TC | 1 | a0005 | 1 | NA18982.hp1 | frameshift_variant | HIGH | c.553dupG | p.Glu185fs | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/22 | 1357/6357 | 553/3075 | 185/1024 | chrX | 54016637 | ||
| chrX:54022275
|
TC | T | 1 | a0006 | 1 | NA18984.hp1 | frameshift_variant | HIGH | c.276delG | p.Ser93fs | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/22 | 1080/6357 | 276/3075 | 92/1024 | chrX | 54022275 | ||
| chrX:54022338
|
GC | G | 1 | a0007 | 1 | NA19055.hp1 | frameshift_variant | HIGH | c.213delG | p.His72fs | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/22 | 1017/6357 | 213/3075 | 71/1024 | chrX | 54022338 | ||
| chrX:54042676
|
C | CG | 1 | a0003 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.52dupC | p.Arg18fs | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/22 | 856/6357 | 52/3075 | 18/1024 | chrX | 54042676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:53992762
|
T | G | 1 | a0002c0006 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1704A>C | p.Pro568Pro | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/22 | 2508/6357 | 1704/3075 | 568/1024 | chrX | 53992762 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:53936692
|
A | T | 1 | a0001c0001t0009 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2466T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 2466 | chrX | 53936692 | |||||
| chrX:53937191
|
T | C | 4 | a0001c0001t0002a0001c0001t0007a0002c0002t0004others(1): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1967A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 1967 | chrX | 53937191 | |||||
| chrX:53937789
|
G | A | 1 | a0001c0001t0005 | 2 | HG02723.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1369C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 1369 | chrX | 53937789 | |||||
| chrX:53937969
|
TG | T | 1 | a0001c0001t0008 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1188delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 1188 | chrX | 53937969 | |||||
| chrX:53938155
|
T | C | 1 | a0001c0001t0002 | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1003A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 1003 | chrX | 53938155 | |||||
| chrX:53938583
|
A | C | 1 | a0001c0001t0007 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 575 | chrX | 53938583 | |||||
| chrX:53938718
|
G | T | 1 | a0001c0001t0006 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*440C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 440 | chrX | 53938718 | |||||
| chrX:53939030
|
G | C | 1 | a0001c0001t0010 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 22/22 | 128 | chrX | 53939030 | |||||
| chrX:54042803
|
GT | G | 1 | a0003c0003t0011 | 1 | NA19086.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/22 | 76 | chrX | 54042803 | |||||
| chrX:54043877
|
CCACG | C | 1 | a0003c0003t0011 | 1 | NA19086.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212_-209delCGTG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/22 | 1150 | chrX | 54043877 | |||||
| chrX:54044390
|
G | A | 2 | a0001c0001t0003a0001c0001t0005 | 21 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-721C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/22 | 1662 | chrX | 54044390 | |||||
| chrX:54044424
|
T | C | 1 | a0001c0001t0012 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-755A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/22 | 1696 | chrX | 54044424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:53939449
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2987-203C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 21/21 | chrX | 53939449 | ||||||
| chrX:53939512
|
CCAAT | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0133a0001c0001t0002g0134others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2987-270_2987-267d others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 21/21 | chrX | 53939512 | ||||||
| chrX:53939555
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2987-309A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 21/21 | chrX | 53939555 | ||||||
| chrX:53939722
|
T | C | 31 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0061others(28): Show | 31 | HG01257.hp2 HG01258.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.2986+458A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 21/21 | chrX | 53939722 | ||||||
| chrX:53940551
|
G | C | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2650-35C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53940551 | ||||||
| chrX:53941015
|
A | T | 1 | a0001c0001t0003g0179 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2650-499T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53941015 | ||||||
| chrX:53941037
|
C | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2650-521G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53941037 | ||||||
| chrX:53941278
|
G | T | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2650-762C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53941278 | ||||||
| chrX:53941697
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2650-1181G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53941697 | ||||||
| chrX:53941725
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2650-1209T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53941725 | ||||||
| chrX:53941775
|
T | C | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2650-1259A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53941775 | ||||||
| chrX:53942087
|
C | G | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650-1571G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53942087 | ||||||
| chrX:53942164
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0063a0001c0001t0001g0117others(1): Show | 4 | NA18984.hp1 NA18994.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650-1648G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53942164 | ||||||
| chrX:53942324
|
C | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0061others(28): Show | 31 | HG01257.hp2 HG01258.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.2650-1808G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53942324 | ||||||
| chrX:53942463
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2649+1671G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53942463 | ||||||
| chrX:53942675
|
C | CGAGA | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2649+1458_2649+145 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53942675 | ||||||
| chrX:53942914
|
A | G | 24 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2649+1220T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53942914 | ||||||
| chrX:53943307
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2649+827A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53943307 | ||||||
| chrX:53943661
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0084 | 2 | NA18977.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2649+473G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53943661 | ||||||
| chrX:53943671
|
C | CA | 1 | a0001c0001t0001g0097 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2649+462dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53943671 | ||||||
| chrX:53943897
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2649+237A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53943897 | ||||||
| chrX:53944033
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2649+101A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53944033 | ||||||
| chrX:53944088
|
T | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2649+46A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 20/21 | chrX | 53944088 | ||||||
| chrX:53944373
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0012 | 2 | NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2540-130A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53944373 | ||||||
| chrX:53944590
|
T | C | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2540-347A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53944590 | ||||||
| chrX:53944699
|
C | T | 2 | a0001c0001t0003g0166a0001c0001t0003g0174 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2540-456G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53944699 | ||||||
| chrX:53944998
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2540-755T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53944998 | ||||||
| chrX:53945069
|
G | A | 7 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2540-826C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53945069 | ||||||
| chrX:53945117
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2540-874C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53945117 | ||||||
| chrX:53945344
|
C | CA | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2540-1102dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53945344 | ||||||
| chrX:53945461
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2540-1218C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53945461 | ||||||
| chrX:53945811
|
T | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2540-1568A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53945811 | ||||||
| chrX:53946121
|
G | A | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2540-1878C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53946121 | ||||||
| chrX:53946655
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2540-2412T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53946655 | ||||||
| chrX:53946868
|
GA | G | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2540-2626delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53946868 | ||||||
| chrX:53946916
|
A | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 58 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2540-2673T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53946916 | ||||||
| chrX:53947094
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2540-2851G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53947094 | ||||||
| chrX:53947361
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2540-3118A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53947361 | ||||||
| chrX:53947621
|
C | G | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2540-3378G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53947621 | ||||||
| chrX:53947699
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2540-3456C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53947699 | ||||||
| chrX:53948040
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0110 | 3 | HG02135.hp1 NA18974.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2540-3797A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53948040 | ||||||
| chrX:53948208
|
C | T | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2540-3965G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53948208 | ||||||
| chrX:53948326
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2540-4083C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53948326 | ||||||
| chrX:53949205
|
C | T | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2540-4962G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949205 | ||||||
| chrX:53949217
|
C | T | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2540-4974G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949217 | ||||||
| chrX:53949248
|
T | A | 1 | a0001c0001t0003g0170 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2540-5005A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949248 | ||||||
| chrX:53949508
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2540-5265C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949508 | ||||||
| chrX:53949594
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2540-5351C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949594 | ||||||
| chrX:53949609
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2540-5366T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949609 | ||||||
| chrX:53949615
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2540-5372T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949615 | ||||||
| chrX:53949656
|
C | T | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2540-5413G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949656 | ||||||
| chrX:53949811
|
C | CA | 12 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0082others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2540-5569dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949811 | ||||||
| chrX:53949811
|
C | CAA | 17 | a0001c0001t0001g0152a0001c0001t0002g0027a0001c0001t0002g0028others(14): Show | 17 | HG00733.hp1 HG01074.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2540-5570_2540-556 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949811 | ||||||
| chrX:53949811
|
C | CAAA | 5 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0137others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2540-5571_2540-556 others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949811 | ||||||
| chrX:53949811
|
CA | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0032others(31): Show | 34 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.2540-5569delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949811 | ||||||
| chrX:53949811
|
CAAAA | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0068a0001c0001t0001g0101 | 3 | HG02738.hp1 NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2540-5572_2540-556 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949811 | ||||||
| chrX:53949884
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(1): Show | 4 | NA18983.hp1 NA19000.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540-5641A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949884 | ||||||
| chrX:53949955
|
C | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(78): Show | 81 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.2540-5712G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949955 | ||||||
| chrX:53949983
|
C | CT | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2540-5741_2540-574 others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949983 | ||||||
| chrX:53949998
|
C | CA | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2540-5756dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949998 | ||||||
| chrX:53950003
|
A | G | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2540-5760T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53950003 | ||||||
| chrX:53950318
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2540-6075C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53950318 | ||||||
| chrX:53950341
|
A | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2540-6098T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53950341 | ||||||
| chrX:53951335
|
TAAC | T | 1 | a0001c0001t0003g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2540-7095_2540-709 others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951335 | ||||||
| chrX:53951456
|
A | AT | 2 | a0001c0001t0001g0103a0001c0001t0002g0045 | 2 | HG03831.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2540-7214dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951456 | ||||||
| chrX:53951456
|
AT | A | 1 | a0001c0001t0001g0081 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2540-7214delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951456 | ||||||
| chrX:53951599
|
C | T | 5 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2540-7356G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951599 | ||||||
| chrX:53951694
|
C | T | 3 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0183 | 3 | HG00735.hp1 HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2540-7451G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951694 | ||||||
| chrX:53951798
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | NA18948.hp1 NA18971.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540-7555G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951798 | ||||||
| chrX:53951867
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2540-7624G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53951867 | ||||||
| chrX:53952082
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2540-7839C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952082 | ||||||
| chrX:53952145
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2540-7902C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952145 | ||||||
| chrX:53952283
|
C | CA | 27 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0154others(24): Show | 27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2540-8041dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952283 | ||||||
| chrX:53952283
|
CA | C | 3 | a0001c0001t0001g0015a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG02109.hp2 HG03486.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2540-8041delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952283 | ||||||
| chrX:53952506
|
A | AAGATG | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0137others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540-8268_2540-826 others(9): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952506 | ||||||
| chrX:53952654
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2540-8411G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952654 | ||||||
| chrX:53952812
|
G | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2540-8569C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952812 | ||||||
| chrX:53952837
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2540-8594C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952837 | ||||||
| chrX:53952887
|
C | CA | 24 | a0001c0001t0001g0157a0001c0001t0002g0026a0001c0001t0002g0027others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2540-8645dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952887 | ||||||
| chrX:53952887
|
C | CAA | 1 | a0001c0001t0002g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2540-8646_2540-864 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952887 | ||||||
| chrX:53952887
|
CA | C | 1 | a0001c0001t0001g0060 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2540-8645delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952887 | ||||||
| chrX:53953180
|
G | A | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2540-8937C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953180 | ||||||
| chrX:53953273
|
C | CA | 3 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0001t0001g0101 | 3 | NA18986.hp1 NA19005.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2540-9031dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953273 | ||||||
| chrX:53953298
|
C | CA | 2 | a0001c0001t0001g0057a0001c0001t0001g0152 | 2 | NA18965.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2540-9056dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953298 | ||||||
| chrX:53953301
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2540-9058T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953301 | ||||||
| chrX:53953327
|
TA | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(180): Show |
intron_variant | MODIFIER | c.2540-9085delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953327 | ||||||
| chrX:53953328
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2540-9085T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953328 | ||||||
| chrX:53953334
|
A | G | 17 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(14): Show | 17 | HG02109.hp2 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.2540-9091T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953334 | ||||||
| chrX:53953643
|
C | CA | 3 | a0001c0001t0001g0086a0001c0001t0001g0105a0001c0001t0001g0113 | 3 | HG00733.hp2 HG01106.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.2539+9200dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953643 | ||||||
| chrX:53953643
|
CA | C | 2 | a0001c0001t0003g0178a0001c0001t0008g0019 | 2 | HG02622.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2539+9200delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953643 | ||||||
| chrX:53953656
|
A | AG | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2539+9187_2539+918 others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953656 | ||||||
| chrX:53953657
|
A | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2539+9187T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953657 | ||||||
| chrX:53953658
|
GC | G | 17 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2539+9185delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953658 | ||||||
| chrX:53953659
|
C | CG | 8 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 8 | HG01433.hp1 HG02074.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2539+9184dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953659 | ||||||
| chrX:53953659
|
C | CGG | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2539+9183_2539+918 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953659 | ||||||
| chrX:53953659
|
C | G | 5 | a0001c0001t0002g0131a0002c0002t0004g0147a0002c0002t0004g0148others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2539+9185G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953659 | ||||||
| chrX:53953868
|
A | AC | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2539+8975dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953868 | ||||||
| chrX:53954003
|
AAAG | A | 1 | a0001c0001t0002g0136 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2539+8838_2539+884 others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954003 | ||||||
| chrX:53954045
|
C | G | 22 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(19): Show | 22 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.2539+8799G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954045 | ||||||
| chrX:53954373
|
G | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2539+8471C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954373 | ||||||
| chrX:53954380
|
G | T | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2539+8464C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954380 | ||||||
| chrX:53954417
|
G | A | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2539+8427C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954417 | ||||||
| chrX:53954479
|
G | T | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2539+8365C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954479 | ||||||
| chrX:53954499
|
C | CA | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 56 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2539+8344dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954499 | ||||||
| chrX:53954499
|
C | CAA | 5 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0117others(2): Show | 5 | HG02723.hp1 NA18965.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.2539+8343_2539+834 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954499 | ||||||
| chrX:53954499
|
C | CAAA | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2539+8342_2539+834 others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954499 | ||||||
| chrX:53954499
|
CA | C | 27 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0108others(24): Show | 27 | HG00280.hp1 HG01167.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.2539+8344delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954499 | ||||||
| chrX:53954499
|
CAAAAAAA | C | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2539+8338_2539+834 others(11): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954499 | ||||||
| chrX:53954526
|
A | G | 2 | a0001c0001t0005g0172a0001c0001t0005g0173 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2539+8318T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954526 | ||||||
| chrX:53954642
|
GAT | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(167): Show |
intron_variant | MODIFIER | c.2539+8200_2539+820 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954642 | ||||||
| chrX:53954642
|
GATAT | G | 4 | a0001c0001t0001g0057a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539+8198_2539+820 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954642 | ||||||
| chrX:53954819
|
T | C | 1 | a0001c0001t0003g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2539+8025A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954819 | ||||||
| chrX:53955245
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2539+7599A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955245 | ||||||
| chrX:53955285
|
C | A | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2539+7559G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955285 | ||||||
| chrX:53955553
|
TTTTC | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2539+7287_2539+729 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955553 | ||||||
| chrX:53955557
|
C | CT | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(163): Show |
intron_variant | MODIFIER | c.2539+7286dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955557 | ||||||
| chrX:53955557
|
C | CTT | 8 | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0112others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2539+7285_2539+728 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955557 | ||||||
| chrX:53956301
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2539+6543A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956301 | ||||||
| chrX:53956317
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2539+6527C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956317 | ||||||
| chrX:53956675
|
C | CGT | 30 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(27): Show | 30 | HG00140.hp1 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2539+6167_2539+616 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956675 | ||||||
| chrX:53956675
|
C | CGTGT | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0062others(9): Show | 12 | HG01070.hp2 HG01074.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2539+6165_2539+616 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956675 | ||||||
| chrX:53956675
|
C | CGTGTGT | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2539+6163_2539+616 others(10): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956675 | ||||||
| chrX:53956675
|
CGT | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0035others(12): Show | 15 | HG00735.hp1 HG00735.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2539+6167_2539+616 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956675 | ||||||
| chrX:53956675
|
CGTGT | C | 1 | a0001c0001t0003g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2539+6165_2539+616 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956675 | ||||||
| chrX:53956675
|
CGTGTGT | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2539+6163_2539+616 others(10): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956675 | ||||||
| chrX:53956857
|
C | CA | 1 | a0001c0001t0001g0096 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2539+5986dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53956857 | ||||||
| chrX:53957174
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2539+5670C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957174 | ||||||
| chrX:53957181
|
C | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2539+5663G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957181 | ||||||
| chrX:53957190
|
CA | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(53): Show | 56 | HG00609.hp1 HG00621.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2539+5653delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957190 | ||||||
| chrX:53957190
|
CAA | C | 1 | a0001c0001t0003g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2539+5652_2539+565 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957190 | ||||||
| chrX:53957208
|
T | C | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2539+5636A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957208 | ||||||
| chrX:53957227
|
G | A | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2539+5617C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957227 | ||||||
| chrX:53957290
|
T | C | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2539+5554A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957290 | ||||||
| chrX:53957310
|
GC | G | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2539+5533delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957310 | ||||||
| chrX:53957504
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2539+5340C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957504 | ||||||
| chrX:53957550
|
C | CA | 2 | a0001c0001t0001g0113a0002c0002t0004g0148 | 2 | HG03516.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.2539+5293dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957550 | ||||||
| chrX:53957564
|
T | C | 1 | a0001c0001t0003g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2539+5280A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957564 | ||||||
| chrX:53957981
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2539+4863C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957981 | ||||||
| chrX:53958043
|
A | AT | 4 | a0001c0001t0001g0057a0001c0001t0001g0084a0001c0001t0001g0112others(1): Show | 4 | NA18940.hp1 NA18965.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539+4800dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958043 | ||||||
| chrX:53958043
|
AT | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(80): Show | 83 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.2539+4800delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958043 | ||||||
| chrX:53958147
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2539+4697A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958147 | ||||||
| chrX:53958230
|
C | CG | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2539+4613dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958230 | ||||||
| chrX:53958329
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0126 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2539+4515G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958329 | ||||||
| chrX:53958506
|
G | GC | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2539+4337dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958506 | ||||||
| chrX:53958553
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2539+4291C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958553 | ||||||
| chrX:53958566
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2539+4278C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958566 | ||||||
| chrX:53958732
|
C | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539+4112G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958732 | ||||||
| chrX:53958775
|
C | CA | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(50): Show | 53 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.2539+4068dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958775 | ||||||
| chrX:53958775
|
C | CAA | 13 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0152others(10): Show | 13 | HG01081.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2539+4067_2539+406 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958775 | ||||||
| chrX:53958775
|
C | CAAA | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2539+4066_2539+406 others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958775 | ||||||
| chrX:53958775
|
CA | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0112 | 2 | HG01256.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2539+4068delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958775 | ||||||
| chrX:53958985
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2539+3859T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958985 | ||||||
| chrX:53959009
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2539+3835T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959009 | ||||||
| chrX:53959235
|
A | T | 10 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 10 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2539+3609T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959235 | ||||||
| chrX:53959590
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2539+3254C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959590 | ||||||
| chrX:53959779
|
G | A | 1 | a0001c0001t0006g0107 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2539+3065C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959779 | ||||||
| chrX:53959820
|
C | T | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2539+3024G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959820 | ||||||
| chrX:53959863
|
C | CA | 30 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0052others(27): Show | 30 | HG01070.hp2 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2539+2980dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959863 | ||||||
| chrX:53959863
|
C | CAA | 7 | a0001c0001t0001g0057a0001c0001t0001g0122a0001c0001t0001g0126others(4): Show | 7 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2539+2979_2539+298 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959863 | ||||||
| chrX:53959863
|
CA | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0103others(1): Show | 4 | HG01943.hp1 HG02922.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539+2980delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959863 | ||||||
| chrX:53959990
|
T | C | 24 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2539+2854A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53959990 | ||||||
| chrX:53960082
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2539+2762C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960082 | ||||||
| chrX:53960233
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2539+2611C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960233 | ||||||
| chrX:53960297
|
G | C | 1 | a0001c0001t0003g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2539+2547C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960297 | ||||||
| chrX:53960354
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0098 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2539+2490G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960354 | ||||||
| chrX:53960475
|
C | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2539+2369G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960475 | ||||||
| chrX:53960686
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2539+2158A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960686 | ||||||
| chrX:53960756
|
TA | T | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2539+2087delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960756 | ||||||
| chrX:53960780
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2539+2064G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960780 | ||||||
| chrX:53960808
|
A | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0153a0001c0001t0001g0155others(4): Show | 7 | HG01099.hp1 HG01255.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2539+2036T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960808 | ||||||
| chrX:53960871
|
G | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0097 | 2 | HG01358.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2539+1973C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960871 | ||||||
| chrX:53960898
|
T | C | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2539+1946A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960898 | ||||||
| chrX:53961028
|
CT | C | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2539+1815delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961028 | ||||||
| chrX:53961327
|
A | AT | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2539+1516dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961327 | ||||||
| chrX:53961327
|
AT | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2539+1516delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961327 | ||||||
| chrX:53961701
|
A | AC | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2539+1142dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961701 | ||||||
| chrX:53961709
|
G | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539+1135C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961709 | ||||||
| chrX:53961743
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2539+1101G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961743 | ||||||
| chrX:53961773
|
T | TG | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2539+1070dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961773 | ||||||
| chrX:53962568
|
AG | A | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2539+275delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53962568 | ||||||
| chrX:53962713
|
A | G | 5 | a0001c0001t0003g0165a0001c0001t0003g0178a0001c0001t0003g0179others(2): Show | 5 | HG00738.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2539+131T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53962713 | ||||||
| chrX:53962726
|
T | C | 2 | a0001c0001t0003g0167a0001c0001t0003g0168 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2539+118A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53962726 | ||||||
| chrX:53962797
|
C | T | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2539+47G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53962797 | ||||||
| chrX:53963024
|
TC | T | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2444-86delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963024 | ||||||
| chrX:53963198
|
T | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-259A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963198 | ||||||
| chrX:53963236
|
T | G | 1 | a0001c0001t0002g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2444-297A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963236 | ||||||
| chrX:53963260
|
TC | T | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2444-322delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963260 | ||||||
| chrX:53963361
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444-422C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963361 | ||||||
| chrX:53963448
|
C | T | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444-509G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963448 | ||||||
| chrX:53963538
|
GA | G | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2444-600delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963538 | ||||||
| chrX:53963559
|
CA | C | 1 | a0001c0001t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2444-621delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963559 | ||||||
| chrX:53963586
|
A | G | 3 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0006t0004g0149 | 3 | HG02559.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2444-647T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963586 | ||||||
| chrX:53963591
|
TC | T | 1 | a0001c0001t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2444-653delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963591 | ||||||
| chrX:53963866
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2444-927G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963866 | ||||||
| chrX:53963912
|
T | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-973A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963912 | ||||||
| chrX:53964149
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-1210G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964149 | ||||||
| chrX:53964273
|
AC | A | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2444-1335delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964273 | ||||||
| chrX:53964352
|
T | C | 2 | a0001c0001t0005g0172a0001c0001t0005g0173 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2444-1413A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964352 | ||||||
| chrX:53964462
|
T | C | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444-1523A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964462 | ||||||
| chrX:53964623
|
TG | T | 1 | a0001c0001t0002g0026 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2444-1685delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964623 | ||||||
| chrX:53964771
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2444-1832C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964771 | ||||||
| chrX:53964868
|
C | CA | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(24): Show | 27 | HG00621.hp1 HG00733.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2444-1930dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964868 | ||||||
| chrX:53964868
|
CA | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0059others(5): Show | 8 | HG01109.hp1 HG02895.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.2444-1930delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964868 | ||||||
| chrX:53964876
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2444-1937T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964876 | ||||||
| chrX:53964945
|
AG | A | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2444-2007delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964945 | ||||||
| chrX:53964984
|
T | C | 24 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2444-2045A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964984 | ||||||
| chrX:53965162
|
T | C | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2444-2223A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965162 | ||||||
| chrX:53965554
|
G | C | 1 | a0001c0001t0002g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2444-2615C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965554 | ||||||
| chrX:53965563
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2444-2624G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965563 | ||||||
| chrX:53965564
|
G | T | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-2625C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965564 | ||||||
| chrX:53965712
|
CA | C | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-2774delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965712 | ||||||
| chrX:53965732
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-2793A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965732 | ||||||
| chrX:53965855
|
C | CA | 8 | a0001c0001t0001g0025a0001c0001t0001g0071a0001c0001t0001g0076others(5): Show | 8 | HG00280.hp1 HG00642.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2444-2917dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965855 | ||||||
| chrX:53965910
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0096a0001c0001t0001g0106others(6): Show | 9 | NA18747.hp1 NA18943.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.2444-2971T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965910 | ||||||
| chrX:53966001
|
CA | C | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2444-3063delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966001 | ||||||
| chrX:53966052
|
T | TA | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-3114dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966052 | ||||||
| chrX:53966064
|
C | A | 35 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0016others(32): Show | 35 | HG01257.hp2 HG01258.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.2444-3125G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966064 | ||||||
| chrX:53966492
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-3553G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966492 | ||||||
| chrX:53966674
|
C | T | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2444-3735G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966674 | ||||||
| chrX:53966716
|
C | CT | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-3778dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966716 | ||||||
| chrX:53966725
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-3787dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966725 | ||||||
| chrX:53966764
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2444-3825A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966764 | ||||||
| chrX:53966831
|
G | T | 22 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0137others(19): Show | 22 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.2444-3892C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966831 | ||||||
| chrX:53966845
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2444-3906C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966845 | ||||||
| chrX:53966850
|
T | TCGTCTGA others(187): Show |
1 | a0001c0001t0001g0039 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2444-4105_2444-391 others(198): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966850 | ||||||
| chrX:53966870
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-3932dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966870 | ||||||
| chrX:53966881
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-3943dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966881 | ||||||
| chrX:53966923
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2444-3984C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966923 | ||||||
| chrX:53966946
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2444-4007G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966946 | ||||||
| chrX:53966960
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0154a0001c0001t0001g0160others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-4021G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966960 | ||||||
| chrX:53966983
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2444-4045dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53966983 | ||||||
| chrX:53967001
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2444-4062C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967001 | ||||||
| chrX:53967023
|
A | AC | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2444-4085dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967023 | ||||||
| chrX:53967026
|
C | A | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2444-4087G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967026 | ||||||
| chrX:53967046
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2444-4107C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967046 | ||||||
| chrX:53967140
|
T | TGGGGGGG others(122): Show |
1 | a0001c0001t0001g0126 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2444-4202_2444-420 others(133): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967140 | ||||||
| chrX:53967140
|
T | TGGGGGGT others(120): Show |
5 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-4202_2444-420 others(131): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967140 | ||||||
| chrX:53967156
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(75): Show | 78 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2444-4217G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967156 | ||||||
| chrX:53967172
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0153a0001c0001t0001g0155others(3): Show | 6 | HG01255.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2444-4233G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967172 | ||||||
| chrX:53967174
|
G | A | 6 | a0001c0001t0001g0126a0001c0001t0001g0153a0001c0001t0001g0155others(3): Show | 6 | HG01255.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2444-4235C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967174 | ||||||
| chrX:53967174
|
G | GTCCGGGA others(121): Show |
1 | a0001c0001t0001g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2444-4236_2444-423 others(132): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967174 | ||||||
| chrX:53967174
|
G | GTCCGGGA others(120): Show |
46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(43): Show | 46 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2444-4236_2444-423 others(131): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967174 | ||||||
| chrX:53967174
|
G | GTCCGGGA others(120): Show |
1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-4236_2444-423 others(131): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967174 | ||||||
| chrX:53967191
|
C | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-4252G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967191 | ||||||
| chrX:53967205
|
CGCCCCTA others(217): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2444-4490_2444-426 others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967205 | ||||||
| chrX:53967232
|
TCTGCCCG others(42): Show |
T | 1 | a0001c0001t0001g0096 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2444-4342_2444-429 others(53): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967232 | ||||||
| chrX:53967234
|
TGCCCGGC others(91): Show |
T | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0097others(1): Show | 4 | HG00140.hp1 HG01358.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2444-4393_2444-429 others(102): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967234 | ||||||
| chrX:53967251
|
C | A | 1 | a0001c0001t0003g0178 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2444-4312G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967251 | ||||||
| chrX:53967255
|
C | CG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-4317dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967255 | ||||||
| chrX:53967266
|
T | TG | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2444-4328dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967266 | ||||||
| chrX:53967300
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2444-4361G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967300 | ||||||
| chrX:53967315
|
T | TG | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2444-4377dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967315 | ||||||
| chrX:53967315
|
TG | T | 1 | a0001c0001t0001g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2444-4377delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967315 | ||||||
| chrX:53967322
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2444-4383C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967322 | ||||||
| chrX:53967326
|
G | GC | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2444-4388dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967326 | ||||||
| chrX:53967345
|
G | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-4406C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967345 | ||||||
| chrX:53967364
|
T | TG | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2444-4426dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967364 | ||||||
| chrX:53967374
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-4436dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967374 | ||||||
| chrX:53967393
|
G | A | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2444-4454C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967393 | ||||||
| chrX:53967415
|
C | T | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2444-4476G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967415 | ||||||
| chrX:53967490
|
T | TG | 5 | a0001c0001t0001g0048a0001c0001t0001g0112a0002c0002t0004g0147others(2): Show | 5 | HG01261.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-4552dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967490 | ||||||
| chrX:53967490
|
T | TGG | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2444-4553_2444-455 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967490 | ||||||
| chrX:53967508
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-4569C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967508 | ||||||
| chrX:53967866
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2444-4927A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967866 | ||||||
| chrX:53967878
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2444-4939T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967878 | ||||||
| chrX:53967897
|
TA | T | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-4959delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967897 | ||||||
| chrX:53967906
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-4968dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967906 | ||||||
| chrX:53967918
|
C | CA | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-4980dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967918 | ||||||
| chrX:53967987
|
G | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(78): Show | 81 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.2444-5048C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967987 | ||||||
| chrX:53968125
|
T | TA | 2 | a0001c0001t0001g0099a0002c0002t0004g0148 | 2 | HG03516.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2444-5187dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968125 | ||||||
| chrX:53968125
|
TA | T | 13 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0056others(10): Show | 13 | HG01069.hp1 HG01167.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2444-5187delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968125 | ||||||
| chrX:53968357
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2444-5418A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968357 | ||||||
| chrX:53968362
|
TA | T | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-5424delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968362 | ||||||
| chrX:53968566
|
A | AG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-5628dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968566 | ||||||
| chrX:53968623
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-5685dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968623 | ||||||
| chrX:53968631
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2444-5692C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968631 | ||||||
| chrX:53968633
|
G | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-5694C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968633 | ||||||
| chrX:53968672
|
GC | G | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-5734delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968672 | ||||||
| chrX:53968794
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2444-5855G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968794 | ||||||
| chrX:53968806
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0010g0123 | 3 | HG02258.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2444-5867C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968806 | ||||||
| chrX:53968934
|
A | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444-5995T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968934 | ||||||
| chrX:53969080
|
C | CA | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-6142dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969080 | ||||||
| chrX:53969209
|
T | TG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-6271dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969209 | ||||||
| chrX:53969528
|
C | CT | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-6590dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969528 | ||||||
| chrX:53969581
|
C | CAGGT | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2444-6643_2444-664 others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969581 | ||||||
| chrX:53969583
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2444-6644T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969583 | ||||||
| chrX:53969587
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2444-6648T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969587 | ||||||
| chrX:53969589
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2444-6650G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969589 | ||||||
| chrX:53969591
|
ATGACATT others(2289): Show |
A | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2444-8948_2444-665 others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969591 | ||||||
| chrX:53969612
|
GA | G | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-6674delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969612 | ||||||
| chrX:53969674
|
G | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-6735C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969674 | ||||||
| chrX:53970629
|
CA | C | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-7691delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53970629 | ||||||
| chrX:53970734
|
C | CA | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-7796dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53970734 | ||||||
| chrX:53970734
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2444-7795G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53970734 | ||||||
| chrX:53970753
|
C | CA | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-7815dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53970753 | ||||||
| chrX:53971502
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2444-8563G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971502 | ||||||
| chrX:53971555
|
G | GA | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-8617dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971555 | ||||||
| chrX:53971811
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2444-8872T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971811 | ||||||
| chrX:53971828
|
A | AG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-8890dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971828 | ||||||
| chrX:53971980
|
T | G | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0141 | 3 | HG02970.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2444-9041A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971980 | ||||||
| chrX:53972186
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2444-9247T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972186 | ||||||
| chrX:53972321
|
C | CA | 28 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0073others(25): Show | 28 | HG00642.hp1 HG01074.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2444-9383dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972321 | ||||||
| chrX:53972321
|
C | CAA | 3 | a0001c0001t0001g0013a0001c0001t0002g0030a0001c0001t0002g0118 | 3 | HG00733.hp1 HG02572.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2444-9384_2444-938 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972321 | ||||||
| chrX:53972321
|
CA | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(24): Show | 27 | HG00609.hp1 HG00621.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.2444-9383delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972321 | ||||||
| chrX:53972321
|
CAA | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0119a0001c0001t0001g0159others(1): Show | 4 | HG01081.hp1 HG01081.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2444-9384_2444-938 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972321 | ||||||
| chrX:53972775
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0090a0001c0001t0001g0110 | 3 | HG02083.hp1 NA18974.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2444-9836A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972775 | ||||||
| chrX:53973330
|
A | C | 3 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0006t0004g0149 | 3 | HG02559.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2444-10391T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53973330 | ||||||
| chrX:53973383
|
A | AC | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2444-10445dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53973383 | ||||||
| chrX:53973707
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2444-10768C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53973707 | ||||||
| chrX:53973715
|
A | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2444-10776T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53973715 | ||||||
| chrX:53973954
|
A | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+10960T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53973954 | ||||||
| chrX:53973981
|
C | T | 13 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(10): Show | 13 | HG02109.hp2 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2443+10933G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53973981 | ||||||
| chrX:53974034
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2443+10880G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53974034 | ||||||
| chrX:53974282
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0035 | 2 | HG01934.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2443+10632T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53974282 | ||||||
| chrX:53974589
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2443+10325A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53974589 | ||||||
| chrX:53975008
|
A | AC | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+9905dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53975008 | ||||||
| chrX:53975068
|
GA | G | 3 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0006t0004g0149 | 3 | HG02559.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2443+9845delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53975068 | ||||||
| chrX:53975639
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2443+9275C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53975639 | ||||||
| chrX:53975729
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0084 | 2 | NA18977.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2443+9185G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53975729 | ||||||
| chrX:53975765
|
A | G | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+9149T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53975765 | ||||||
| chrX:53976209
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0098 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2443+8705C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976209 | ||||||
| chrX:53976213
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2443+8701C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976213 | ||||||
| chrX:53976248
|
C | T | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2443+8666G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976248 | ||||||
| chrX:53976304
|
C | CA | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+8609dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976304 | ||||||
| chrX:53976312
|
T | A | 21 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(18): Show | 21 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.2443+8602A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976312 | ||||||
| chrX:53976348
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2443+8566T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976348 | ||||||
| chrX:53976382
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+8532G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976382 | ||||||
| chrX:53976471
|
A | C | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2443+8443T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976471 | ||||||
| chrX:53976687
|
T | TA | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2443+8226dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976687 | ||||||
| chrX:53976687
|
T | TAA | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2443+8225_2443+822 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976687 | ||||||
| chrX:53976687
|
TA | T | 9 | a0001c0001t0001g0057a0001c0001t0001g0145a0001c0001t0001g0153others(6): Show | 9 | HG01243.hp1 HG01255.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2443+8226delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976687 | ||||||
| chrX:53976845
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+8069G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976845 | ||||||
| chrX:53977143
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2443+7771A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977143 | ||||||
| chrX:53977165
|
T | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+7749A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977165 | ||||||
| chrX:53977174
|
G | GA | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2443+7739dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977174 | ||||||
| chrX:53977174
|
GA | G | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01255.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2443+7739delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977174 | ||||||
| chrX:53977205
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0185 | 2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2443+7709G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977205 | ||||||
| chrX:53977289
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2443+7625G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977289 | ||||||
| chrX:53977340
|
CAAAGA | C | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01255.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2443+7569_2443+757 others(9): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977340 | ||||||
| chrX:53977648
|
C | CT | 2 | a0001c0001t0001g0017a0001c0001t0003g0178 | 2 | HG02622.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.2443+7265dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977648 | ||||||
| chrX:53977875
|
T | C | 1 | a0001c0001t0003g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2443+7039A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977875 | ||||||
| chrX:53977945
|
C | CT | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(14): Show | 17 | HG01257.hp2 HG01934.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.2443+6968dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977945 | ||||||
| chrX:53977982
|
T | TC | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+6931dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977982 | ||||||
| chrX:53978105
|
C | G | 15 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(12): Show | 15 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.2443+6809G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978105 | ||||||
| chrX:53978201
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+6713G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978201 | ||||||
| chrX:53978250
|
G | GT | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+6663dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978250 | ||||||
| chrX:53978726
|
A | AG | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+6187dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978726 | ||||||
| chrX:53978746
|
C | CA | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+6167dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978746 | ||||||
| chrX:53978773
|
A | AG | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+6140dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978773 | ||||||
| chrX:53978797
|
C | CA | 9 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0085others(6): Show | 9 | HG00735.hp1 HG00738.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2443+6116dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978797 | ||||||
| chrX:53978797
|
CA | C | 21 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(18): Show | 21 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.2443+6116delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978797 | ||||||
| chrX:53978914
|
A | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0103 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2443+6000T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978914 | ||||||
| chrX:53978915
|
G | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0103 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2443+5999C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978915 | ||||||
| chrX:53978916
|
A | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0103 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2443+5998T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978916 | ||||||
| chrX:53978962
|
A | AG | 2 | a0001c0001t0001g0032a0001c0001t0003g0165 | 2 | HG00621.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2443+5951dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978962 | ||||||
| chrX:53979011
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2443+5903A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53979011 | ||||||
| chrX:53979297
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0072 | 2 | NA18983.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2443+5617C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53979297 | ||||||
| chrX:53979381
|
CA | C | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+5532delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53979381 | ||||||
| chrX:53979468
|
C | G | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+5446G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53979468 | ||||||
| chrX:53979693
|
G | GA | 1 | a0001c0001t0001g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2443+5220dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53979693 | ||||||
| chrX:53980691
|
TG | T | 1 | a0001c0001t0001g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2443+4222delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53980691 | ||||||
| chrX:53980940
|
T | C | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2443+3974A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53980940 | ||||||
| chrX:53981083
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2443+3831C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981083 | ||||||
| chrX:53981138
|
A | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2443+3776T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981138 | ||||||
| chrX:53981140
|
G | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2443+3774C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981140 | ||||||
| chrX:53981456
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0095 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2443+3458T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981456 | ||||||
| chrX:53981511
|
G | GT | 2 | a0001c0001t0001g0145a0001c0001t0012g0186 | 2 | HG03831.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.2443+3402dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981511 | ||||||
| chrX:53981592
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0028 | 2 | HG01070.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2443+3322C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981592 | ||||||
| chrX:53981857
|
C | T | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2443+3057G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53981857 | ||||||
| chrX:53982143
|
CT | C | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2443+2770delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53982143 | ||||||
| chrX:53982565
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0137others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2443+2349C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53982565 | ||||||
| chrX:53982627
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0018 | 2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2443+2287T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53982627 | ||||||
| chrX:53982696
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2443+2218C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53982696 | ||||||
| chrX:53982931
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2443+1983G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53982931 | ||||||
| chrX:53983174
|
C | CA | 29 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(26): Show | 29 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.2443+1739dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983174 | ||||||
| chrX:53983174
|
CA | C | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2443+1739delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983174 | ||||||
| chrX:53983763
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2443+1151G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983763 | ||||||
| chrX:53983843
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2443+1071A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983843 | ||||||
| chrX:53983942
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2443+972T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983942 | ||||||
| chrX:53983990
|
CAA | C | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2443+922_2443+923d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983990 | ||||||
| chrX:53984099
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0185 | 2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2443+815G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53984099 | ||||||
| chrX:53984158
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0035 | 2 | HG01934.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2443+756C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53984158 | ||||||
| chrX:53984594
|
GAA | G | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2443+318_2443+319d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53984594 | ||||||
| chrX:53984638
|
T | C | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2443+276A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53984638 | ||||||
| chrX:53984760
|
T | C | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2443+154A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53984760 | ||||||
| chrX:53984842
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2443+72A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53984842 | ||||||
| chrX:53985312
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2130-85T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 17/21 | chrX | 53985312 | ||||||
| chrX:53985418
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2130-191G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 17/21 | chrX | 53985418 | ||||||
| chrX:53985419
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2130-192C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 17/21 | chrX | 53985419 | ||||||
| chrX:53985985
|
G | T | 1 | a0006c0005t0001g0051 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1996-36C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53985985 | ||||||
| chrX:53986051
|
CACCAAGT others(4): Show |
C | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1996-113_1996-103d others(13): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986051 | ||||||
| chrX:53986116
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1996-167A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986116 | ||||||
| chrX:53986231
|
A | G | 1 | a0002c0002t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1996-282T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986231 | ||||||
| chrX:53986239
|
C | T | 2 | a0001c0001t0005g0172a0001c0001t0005g0173 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1996-290G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986239 | ||||||
| chrX:53986311
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0006g0107 | 3 | NA18995.hp1 NA19004.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1996-362C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986311 | ||||||
| chrX:53986378
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1996-429T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986378 | ||||||
| chrX:53986410
|
T | A | 7 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(4): Show | 7 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1996-461A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986410 | ||||||
| chrX:53986424
|
A | G | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1996-475T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986424 | ||||||
| chrX:53986524
|
C | T | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1995+554G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986524 | ||||||
| chrX:53986529
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1995+549C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986529 | ||||||
| chrX:53986712
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1995+366G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986712 | ||||||
| chrX:53986754
|
G | A | 2 | a0001c0001t0001g0158a0002c0006t0004g0149 | 2 | HG01255.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1995+324C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986754 | ||||||
| chrX:53986798
|
T | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 14 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1995+280A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986798 | ||||||
| chrX:53986913
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995+165C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986913 | ||||||
| chrX:53987421
|
G | A | 26 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1910-258C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 15/21 | chrX | 53987421 | ||||||
| chrX:53987596
|
C | T | 3 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177 | 3 | HG02970.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1909+170G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 15/21 | chrX | 53987596 | ||||||
| chrX:53987677
|
C | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 10 | HG00609.hp1 HG00621.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+89G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 15/21 | chrX | 53987677 | ||||||
| chrX:53987966
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1731-22T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53987966 | ||||||
| chrX:53988620
|
A | AT | 6 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0076others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1731-677dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53988620 | ||||||
| chrX:53988620
|
AT | A | 1 | a0001c0001t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1731-677delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53988620 | ||||||
| chrX:53988754
|
C | CA | 3 | a0001c0001t0003g0171a0001c0001t0003g0178a0001c0001t0005g0173 | 3 | HG02145.hp1 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1731-811dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53988754 | ||||||
| chrX:53988754
|
CA | C | 14 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(11): Show | 14 | HG01167.hp1 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-811delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53988754 | ||||||
| chrX:53988960
|
C | CT | 3 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0120 | 3 | HG04115.hp1 NA18966.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1731-1017dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53988960 | ||||||
| chrX:53989509
|
G | GA | 6 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0076others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1731-1566dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53989509 | ||||||
| chrX:53989529
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1731-1585A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53989529 | ||||||
| chrX:53989707
|
A | C | 33 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(30): Show | 33 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1731-1763T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53989707 | ||||||
| chrX:53989788
|
T | C | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1731-1844A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53989788 | ||||||
| chrX:53990025
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1731-2081T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990025 | ||||||
| chrX:53990031
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1731-2087A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990031 | ||||||
| chrX:53990257
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0093 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1731-2313T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990257 | ||||||
| chrX:53990413
|
A | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1730+2323T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990413 | ||||||
| chrX:53990530
|
C | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1730+2206G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990530 | ||||||
| chrX:53990563
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0128 | 2 | HG02809.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1730+2173G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990563 | ||||||
| chrX:53990672
|
C | A | 1 | a0001c0001t0003g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1730+2064G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990672 | ||||||
| chrX:53990868
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1730+1868A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53990868 | ||||||
| chrX:53991179
|
AT | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0099 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1730+1556delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991179 | ||||||
| chrX:53991590
|
A | G | 22 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(19): Show | 22 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1730+1146T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991590 | ||||||
| chrX:53991600
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1730+1136A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991600 | ||||||
| chrX:53991661
|
C | CA | 38 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0020others(35): Show | 38 | HG00733.hp1 HG01109.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.1730+1074dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991661 | ||||||
| chrX:53991661
|
C | CAA | 7 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(4): Show | 7 | HG02572.hp1 HG02723.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+1073_1730+107 others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991661 | ||||||
| chrX:53991675
|
A | AC | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1730+1060_1730+106 others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991675 | ||||||
| chrX:53991686
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1730+1050G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991686 | ||||||
| chrX:53991714
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1730+1022A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991714 | ||||||
| chrX:53991837
|
AT | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1730+898delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991837 | ||||||
| chrX:53991933
|
C | T | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1730+803G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991933 | ||||||
| chrX:53991950
|
G | C | 1 | a0001c0001t0002g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1730+786C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991950 | ||||||
| chrX:53991951
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1730+785C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991951 | ||||||
| chrX:53991951
|
GAA | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+783_1730+784d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991951 | ||||||
| chrX:53992076
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1730+660G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53992076 | ||||||
| chrX:53992492
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1730+244A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53992492 | ||||||
| chrX:53992591
|
A | G | 22 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(19): Show | 22 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1730+145T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53992591 | ||||||
| chrX:53992694
|
C | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1730+42G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53992694 | ||||||
| chrX:53992862
|
C | T | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0121others(57): Show | 60 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.1627-23G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 13/21 | chrX | 53992862 | ||||||
| chrX:53993988
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-85C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53993988 | ||||||
| chrX:53993990
|
T | TACCA | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-88_1324-87ins others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53993990 | ||||||
| chrX:53993993
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-90A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53993993 | ||||||
| chrX:53993996
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-93A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53993996 | ||||||
| chrX:53993998
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-95G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53993998 | ||||||
| chrX:53994000
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-97T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994000 | ||||||
| chrX:53994001
|
TGGAA | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-102_1324-99de others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994001 | ||||||
| chrX:53994006
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-103C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994006 | ||||||
| chrX:53994009
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-106C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994009 | ||||||
| chrX:53994012
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-109A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994012 | ||||||
| chrX:53994013
|
A | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-110T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994013 | ||||||
| chrX:53994016
|
GA | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-114delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994016 | ||||||
| chrX:53994019
|
GC | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-117delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994019 | ||||||
| chrX:53994022
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-119G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994022 | ||||||
| chrX:53994023
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-120G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994023 | ||||||
| chrX:53994025
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-122G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994025 | ||||||
| chrX:53994027
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-124A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994027 | ||||||
| chrX:53994028
|
ATGCAC | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-130_1324-126d others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994028 | ||||||
| chrX:53994038
|
T | TTGAGTA | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-136_1324-135i others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994038 | ||||||
| chrX:53994039
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1324-136T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994039 | ||||||
| chrX:53994043
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-140A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994043 | ||||||
| chrX:53994045
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-142A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994045 | ||||||
| chrX:53994046
|
A | ACC | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-144_1324-143i others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994046 | ||||||
| chrX:53994048
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-145T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994048 | ||||||
| chrX:53994050
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-147T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994050 | ||||||
| chrX:53994052
|
TGA | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-151_1324-150d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994052 | ||||||
| chrX:53994057
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-154G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994057 | ||||||
| chrX:53994059
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-156A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994059 | ||||||
| chrX:53994060
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-157G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994060 | ||||||
| chrX:53994064
|
A | AC | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-162_1324-161i others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994064 | ||||||
| chrX:53995043
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1323+650A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53995043 | ||||||
| chrX:53995919
|
C | CA | 6 | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0095others(3): Show | 6 | HG01069.hp1 HG01952.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-138dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53995919 | ||||||
| chrX:53995919
|
C | CAA | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1234-139_1234-138d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53995919 | ||||||
| chrX:53996092
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1234-310A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996092 | ||||||
| chrX:53996120
|
C | CT | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1234-339dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996120 | ||||||
| chrX:53996120
|
CT | C | 1 | a0001c0001t0002g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1234-339delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996120 | ||||||
| chrX:53996430
|
A | AT | 1 | a0001c0001t0001g0105 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1234-649dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996430 | ||||||
| chrX:53996430
|
AT | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0157 | 2 | NA18906.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1234-649delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996430 | ||||||
| chrX:53996559
|
C | A | 2 | a0001c0001t0005g0172a0001c0001t0005g0173 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1234-777G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996559 | ||||||
| chrX:53996708
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-926C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996708 | ||||||
| chrX:53996713
|
A | G | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1234-931T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996713 | ||||||
| chrX:53996848
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(1): Show | 4 | NA18983.hp1 NA19000.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-1066C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996848 | ||||||
| chrX:53997019
|
G | C | 22 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(19): Show | 22 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1234-1237C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53997019 | ||||||
| chrX:53997576
|
AATC | A | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1234-1797_1234-179 others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53997576 | ||||||
| chrX:53998463
|
T | TAAATA | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+1402_1233+140 others(9): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53998463 | ||||||
| chrX:53998708
|
A | G | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1233+1162T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53998708 | ||||||
| chrX:53998750
|
AT | A | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1233+1119delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53998750 | ||||||
| chrX:53998843
|
A | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1027T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53998843 | ||||||
| chrX:53999191
|
C | T | 1 | a0006c0005t0001g0051 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1233+679G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53999191 | ||||||
| chrX:53999277
|
G | T | 1 | a0001c0001t0005g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1233+593C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53999277 | ||||||
| chrX:53999469
|
T | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1233+401A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53999469 | ||||||
| chrX:53999631
|
T | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+239A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53999631 | ||||||
| chrX:53999681
|
G | T | 17 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0167others(14): Show | 17 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1233+189C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53999681 | ||||||
| chrX:54000856
|
G | C | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1142-895C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54000856 | ||||||
| chrX:54000957
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1142-996G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54000957 | ||||||
| chrX:54001008
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1142-1047A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001008 | ||||||
| chrX:54001339
|
GA | G | 1 | a0001c0001t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1141+815delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001339 | ||||||
| chrX:54001490
|
A | AGAGT | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1141+661_1141+664d others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001490 | ||||||
| chrX:54001634
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1141+521A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001634 | ||||||
| chrX:54001837
|
GC | G | 1 | a0001c0001t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1141+317delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001837 | ||||||
| chrX:54001931
|
C | G | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1141+224G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001931 | ||||||
| chrX:54002053
|
A | C | 1 | a0001c0001t0003g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1141+102T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54002053 | ||||||
| chrX:54002406
|
T | C | 28 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1035-145A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 9/21 | chrX | 54002406 | ||||||
| chrX:54002558
|
A | C | 5 | a0001c0001t0003g0165a0001c0001t0003g0178a0001c0001t0003g0179others(2): Show | 5 | HG00738.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1034+37T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 9/21 | chrX | 54002558 | ||||||
| chrX:54002897
|
T | C | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.947-215A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54002897 | ||||||
| chrX:54003023
|
A | C | 1 | a0006c0005t0001g0051 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.947-341T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003023 | ||||||
| chrX:54003099
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.947-417C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003099 | ||||||
| chrX:54003400
|
T | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-718A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003400 | ||||||
| chrX:54003420
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.947-738C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003420 | ||||||
| chrX:54003611
|
C | T | 17 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(14): Show | 17 | HG02109.hp2 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.947-929G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003611 | ||||||
| chrX:54003636
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0117a0006c0005t0001g0051 | 3 | NA18984.hp1 NA18994.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.947-954C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003636 | ||||||
| chrX:54003821
|
G | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-1139C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003821 | ||||||
| chrX:54003885
|
T | C | 1 | a0001c0001t0012g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.947-1203A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54003885 | ||||||
| chrX:54004913
|
A | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-2231T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54004913 | ||||||
| chrX:54004923
|
C | CA | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.947-2242dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54004923 | ||||||
| chrX:54004923
|
CA | C | 65 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(62): Show | 65 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.947-2242delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54004923 | ||||||
| chrX:54004923
|
CAA | C | 1 | a0001c0001t0003g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.947-2243_947-2242d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54004923 | ||||||
| chrX:54005384
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.947-2702G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005384 | ||||||
| chrX:54005435
|
C | CA | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0097others(3): Show | 6 | HG00140.hp1 HG01358.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.947-2754dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005435 | ||||||
| chrX:54005435
|
CA | C | 1 | a0001c0001t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.947-2754delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005435 | ||||||
| chrX:54005465
|
G | GA | 2 | a0001c0001t0001g0016a0001c0001t0012g0186 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.947-2784dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005465 | ||||||
| chrX:54005622
|
T | TA | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0116others(7): Show | 10 | HG02559.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.947-2941dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005622 | ||||||
| chrX:54005622
|
TA | T | 20 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0079others(17): Show | 20 | HG00140.hp1 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.947-2941delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005622 | ||||||
| chrX:54005668
|
T | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.947-2986A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005668 | ||||||
| chrX:54005695
|
G | A | 1 | a0001c0001t0002g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.947-3013C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005695 | ||||||
| chrX:54005989
|
T | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0098 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.947-3307A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005989 | ||||||
| chrX:54006856
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.947-4174A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54006856 | ||||||
| chrX:54006939
|
C | CA | 7 | a0001c0001t0001g0020a0001c0001t0001g0081a0001c0001t0001g0113others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.946+4182dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54006939 | ||||||
| chrX:54006939
|
CA | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0056others(6): Show | 9 | HG01070.hp1 HG02132.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.946+4182delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54006939 | ||||||
| chrX:54007353
|
C | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0093 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.946+3769G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54007353 | ||||||
| chrX:54007397
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0018 | 2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.946+3725T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54007397 | ||||||
| chrX:54007609
|
C | CA | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.946+3512dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54007609 | ||||||
| chrX:54007670
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.946+3452G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54007670 | ||||||
| chrX:54007946
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+3176C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54007946 | ||||||
| chrX:54008151
|
G | A | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.946+2971C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008151 | ||||||
| chrX:54008321
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0185 | 2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.946+2801G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008321 | ||||||
| chrX:54008371
|
C | CA | 47 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 47 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.946+2750dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008371 | ||||||
| chrX:54008371
|
C | CAA | 3 | a0001c0001t0001g0018a0001c0001t0002g0138a0001c0001t0003g0180 | 3 | HG00738.hp1 HG01433.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.946+2749_946+2750d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008371 | ||||||
| chrX:54008371
|
CA | C | 3 | a0001c0001t0003g0174a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG01167.hp1 HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.946+2750delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008371 | ||||||
| chrX:54008390
|
AAAAAG | A | 2 | a0001c0001t0003g0169a0001c0001t0003g0171 | 2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.946+2727_946+2731d others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008390 | ||||||
| chrX:54008532
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0098 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.946+2590A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008532 | ||||||
| chrX:54008868
|
G | GT | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.946+2253dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008868 | ||||||
| chrX:54008899
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.946+2223C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008899 | ||||||
| chrX:54009165
|
G | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.946+1957C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009165 | ||||||
| chrX:54009825
|
AGAGT | A | 1 | a0001c0001t0003g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.946+1293_946+1296d others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009825 | ||||||
| chrX:54009844
|
G | GA | 57 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.946+1277dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAA | 15 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0032others(12): Show | 15 | HG00621.hp1 HG01952.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.946+1276_946+1277d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAAA | 2 | a0001c0001t0001g0023a0001c0001t0001g0121 | 2 | HG02135.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.946+1275_946+1277d others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAAAA | 2 | a0001c0001t0001g0004a0001c0001t0008g0019 | 2 | HG02922.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.946+1274_946+1277d others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAAAAA | 3 | a0001c0001t0001g0005a0001c0001t0003g0167a0001c0001t0003g0177 | 3 | HG03471.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.946+1273_946+1277d others(7): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAAAAAA | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.946+1272_946+1277d others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAAAAAAA others(1): Show |
2 | a0002c0002t0004g0147a0002c0002t0004g0148 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.946+1270_946+1277d others(10): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GAAAAAAA others(6): Show |
1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.946+1265_946+1277d others(15): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAA | 1 | a0001c0001t0002g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.946+1277_946+1278i others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAA | 2 | a0001c0001t0002g0132a0001c0001t0002g0137 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946+1277_946+1278i others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA | 2 | a0001c0001t0002g0131a0001c0001t0002g0141 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.946+1277_946+1278i others(9): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(5): Show |
1 | a0001c0001t0002g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.946+1277_946+1278i others(14): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(8): Show |
1 | a0001c0001t0002g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.946+1277_946+1278i others(17): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(10): Show |
1 | a0001c0001t0002g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.946+1277_946+1278i others(19): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(15): Show |
2 | a0001c0001t0002g0130a0001c0001t0002g0133 | 2 | HG02622.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.946+1277_946+1278i others(24): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(16): Show |
1 | a0001c0001t0002g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.946+1277_946+1278i others(25): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(19): Show |
1 | a0001c0001t0002g0136 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.946+1277_946+1278i others(28): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
G | GGAAAAAA others(22): Show |
1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.946+1277_946+1278i others(31): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
GAAAAAAA others(3): Show |
G | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.946+1268_946+1277d others(12): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
GAAAAAAA others(7): Show |
G | 5 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+1264_946+1277d others(16): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
GAAAAAAA others(8): Show |
G | 2 | a0001c0001t0001g0009a0001c0001t0001g0035 | 2 | HG01934.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.946+1263_946+1277d others(17): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.946+1261_946+1277d others(19): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
GAAAAAAA others(11): Show |
G | 14 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.946+1260_946+1277d others(20): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009844
|
GAAAAAAA others(12): Show |
G | 2 | a0001c0001t0001g0039a0001c0001t0003g0169 | 2 | HG02040.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.946+1259_946+1277d others(21): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009844 | ||||||
| chrX:54009845
|
A | G | 4 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(1): Show | 4 | HG02723.hp2 HG03831.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+1277T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009845 | ||||||
| chrX:54009898
|
A | G | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+1224T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009898 | ||||||
| chrX:54010040
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+1082C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54010040 | ||||||
| chrX:54010214
|
A | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+908T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54010214 | ||||||
| chrX:54010432
|
T | C | 1 | a0001c0001t0003g0178 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.946+690A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54010432 | ||||||
| chrX:54010847
|
C | T | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+275G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54010847 | ||||||
| chrX:54011383
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-99C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011383 | ||||||
| chrX:54011584
|
G | C | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.784-300C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011584 | ||||||
| chrX:54011853
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.784-569T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011853 | ||||||
| chrX:54011862
|
C | CA | 22 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0113others(19): Show | 22 | HG02559.hp1 HG02572.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.784-579dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011862 | ||||||
| chrX:54011862
|
C | CAA | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.784-580_784-579dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011862 | ||||||
| chrX:54011862
|
CA | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0047others(7): Show | 10 | HG01070.hp1 HG01515.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.784-579delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011862 | ||||||
| chrX:54011891
|
A | C | 24 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.784-607T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011891 | ||||||
| chrX:54011935
|
A | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.784-651T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54011935 | ||||||
| chrX:54012001
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0128 | 3 | HG02809.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.784-717G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012001 | ||||||
| chrX:54012177
|
T | C | 2 | a0001c0001t0003g0184a0001c0001t0003g0185 | 2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.784-893A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012177 | ||||||
| chrX:54012207
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.784-923A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012207 | ||||||
| chrX:54012641
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.784-1357T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012641 | ||||||
| chrX:54012693
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.784-1409A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012693 | ||||||
| chrX:54012697
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1413C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012697 | ||||||
| chrX:54012757
|
G | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1473C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012757 | ||||||
| chrX:54012939
|
C | CA | 4 | a0001c0001t0001g0090a0001c0001t0001g0114a0001c0001t0002g0131others(1): Show | 4 | HG02083.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+1437dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012939 | ||||||
| chrX:54012939
|
CA | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0081a0001c0001t0001g0152others(2): Show | 5 | HG01070.hp2 HG02622.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+1437delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012939 | ||||||
| chrX:54012957
|
AG | A | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+1419delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012957 | ||||||
| chrX:54012999
|
TC | T | 1 | a0001c0001t0003g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.783+1377delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54012999 | ||||||
| chrX:54013121
|
G | GA | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+1255dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013121 | ||||||
| chrX:54013272
|
G | GA | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+1104dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013272 | ||||||
| chrX:54013535
|
C | T | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.783+842G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013535 | ||||||
| chrX:54013610
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.783+767C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013610 | ||||||
| chrX:54013739
|
AC | A | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.783+637delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013739 | ||||||
| chrX:54013826
|
TC | T | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+550delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013826 | ||||||
| chrX:54013879
|
CA | C | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.783+497delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013879 | ||||||
| chrX:54013901
|
GA | G | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+475delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013901 | ||||||
| chrX:54013927
|
C | CA | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+449dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013927 | ||||||
| chrX:54013933
|
C | T | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+444G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013933 | ||||||
| chrX:54013934
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.783+443C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013934 | ||||||
| chrX:54013962
|
A | AT | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+414dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013962 | ||||||
| chrX:54013962
|
AT | A | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.783+414delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013962 | ||||||
| chrX:54014101
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.783+276C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014101 | ||||||
| chrX:54014235
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.783+142C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014235 | ||||||
| chrX:54014244
|
C | CT | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+132_783+133ins others(1): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014244 | ||||||
| chrX:54014250
|
C | CCG | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+126_783+127ins others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014250 | ||||||
| chrX:54014252
|
G | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+125C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014252 | ||||||
| chrX:54014326
|
T | TA | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+50dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014326 | ||||||
| chrX:54014636
|
C | CCA | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-74_597-73insTG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014636 | ||||||
| chrX:54014637
|
A | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-74T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014637 | ||||||
| chrX:54014691
|
C | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.597-128G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014691 | ||||||
| chrX:54014719
|
T | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0095 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.597-156A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014719 | ||||||
| chrX:54014763
|
TC | T | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.597-201delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014763 | ||||||
| chrX:54014766
|
CA | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-204delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014766 | ||||||
| chrX:54014773
|
A | C | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-210T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014773 | ||||||
| chrX:54014830
|
TC | T | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-268delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014830 | ||||||
| chrX:54014909
|
CT | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-347delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54014909 | ||||||
| chrX:54015162
|
CT | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(166): Show |
intron_variant | MODIFIER | c.597-600delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015162 | ||||||
| chrX:54015305
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.597-742C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015305 | ||||||
| chrX:54015433
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.597-870C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015433 | ||||||
| chrX:54015443
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.597-880C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015443 | ||||||
| chrX:54015469
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.597-906C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015469 | ||||||
| chrX:54015550
|
TG | T | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-988delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015550 | ||||||
| chrX:54015575
|
C | CA | 31 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0053others(28): Show | 31 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.597-1013dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015575 | ||||||
| chrX:54015575
|
C | CAA | 4 | a0001c0001t0002g0131a0001c0001t0003g0168a0001c0001t0003g0171others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-1014_597-1013d others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015575 | ||||||
| chrX:54015575
|
CA | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0082others(5): Show | 8 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-1013delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015575 | ||||||
| chrX:54015595
|
A | AC | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.596+999_596+1000in others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015595 | ||||||
| chrX:54015639
|
T | TA | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.596+955dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015639 | ||||||
| chrX:54015643
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.596+952A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015643 | ||||||
| chrX:54015692
|
CT | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.596+902delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015692 | ||||||
| chrX:54015768
|
CA | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.596+826delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015768 | ||||||
| chrX:54015804
|
AT | A | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.596+790delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015804 | ||||||
| chrX:54015918
|
T | TG | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.596+676dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015918 | ||||||
| chrX:54015948
|
GA | G | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.596+646delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015948 | ||||||
| chrX:54016035
|
CT | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.596+559delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54016035 | ||||||
| chrX:54016256
|
G | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+339C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54016256 | ||||||
| chrX:54016264
|
CG | C | 1 | a0005c0008t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.596+330delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54016264 | ||||||
| chrX:54016366
|
C | T | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.596+229G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54016366 | ||||||
| chrX:54016493
|
C | CA | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.596+101dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54016493 | ||||||
| chrX:54016493
|
CA | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0104a0001c0001t0001g0152others(2): Show | 5 | HG01167.hp1 HG01256.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+101delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54016493 | ||||||
| chrX:54016767
|
T | G | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.455-31A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54016767 | ||||||
| chrX:54016875
|
TTGGGGGG others(6): Show |
T | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.455-152_455-140del others(13): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54016875 | ||||||
| chrX:54017013
|
C | CT | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.455-278dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54017013 | ||||||
| chrX:54017118
|
T | TA | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.455-383dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54017118 | ||||||
| chrX:54017401
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.454+260A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54017401 | ||||||
| chrX:54017434
|
C | T | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.454+227G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54017434 | ||||||
| chrX:54017653
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | splice_region_variant&intron_variant | LOW | c.454+8A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 5/21 | chrX | 54017653 | ||||||
| chrX:54017997
|
C | T | 11 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 11 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.294-176G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54017997 | ||||||
| chrX:54018453
|
CT | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(61): Show | 64 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.294-633delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018453 | ||||||
| chrX:54018453
|
CTT | C | 4 | a0001c0001t0002g0044a0001c0001t0002g0135a0001c0001t0007g0146others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-634_294-633del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018453 | ||||||
| chrX:54018473
|
T | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.294-652A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018473 | ||||||
| chrX:54018510
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.294-689C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018510 | ||||||
| chrX:54018624
|
C | CT | 6 | a0001c0001t0002g0130a0001c0001t0002g0133a0001c0001t0002g0134others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-804dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018624 | ||||||
| chrX:54018669
|
G | A | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.294-848C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018669 | ||||||
| chrX:54018723
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(15): Show | 18 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.294-902G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018723 | ||||||
| chrX:54018850
|
C | A | 2 | a0002c0002t0004g0147a0002c0002t0004g0148 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.294-1029G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018850 | ||||||
| chrX:54018866
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.294-1045G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018866 | ||||||
| chrX:54018912
|
G | GC | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.294-1092dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018912 | ||||||
| chrX:54019278
|
C | CA | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.294-1458dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019278 | ||||||
| chrX:54019416
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294-1595A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019416 | ||||||
| chrX:54019665
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.294-1844G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019665 | ||||||
| chrX:54019710
|
C | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.294-1889G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019710 | ||||||
| chrX:54019723
|
G | GA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.294-1903_294-1902i others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019723 | ||||||
| chrX:54019782
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.294-1961G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019782 | ||||||
| chrX:54019787
|
C | CA | 10 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0116others(7): Show | 10 | HG00733.hp1 HG01175.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-1967dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019787 | ||||||
| chrX:54019787
|
CA | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0113others(3): Show | 6 | HG02572.hp1 HG02622.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-1967delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019787 | ||||||
| chrX:54019804
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.294-1983T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019804 | ||||||
| chrX:54020042
|
CG | C | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.293+2216delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020042 | ||||||
| chrX:54020083
|
T | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 185 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(182): Show |
intron_variant | MODIFIER | c.293+2176A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020083 | ||||||
| chrX:54020165
|
G | A | 1 | a0001c0001t0012g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.293+2094C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020165 | ||||||
| chrX:54020207
|
AT | A | 3 | a0001c0001t0003g0165a0001c0001t0003g0179a0001c0001t0003g0181 | 3 | HG02109.hp1 HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.293+2051delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020207 | ||||||
| chrX:54020209
|
A | C | 3 | a0001c0001t0003g0165a0001c0001t0003g0179a0001c0001t0003g0181 | 3 | HG02109.hp1 HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.293+2050T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020209 | ||||||
| chrX:54020514
|
A | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.293+1745T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020514 | ||||||
| chrX:54020768
|
GA | G | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.293+1490delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020768 | ||||||
| chrX:54020777
|
T | TA | 25 | a0001c0001t0001g0085a0001c0001t0001g0113a0001c0001t0001g0151others(22): Show | 25 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.293+1481dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020777 | ||||||
| chrX:54020841
|
TG | T | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.293+1417delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020841 | ||||||
| chrX:54020947
|
AC | A | 1 | a0001c0001t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.293+1311delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020947 | ||||||
| chrX:54021454
|
A | AT | 52 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(49): Show | 52 | HG00673.hp1 HG00738.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.293+804dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
A | ATT | 22 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(19): Show | 22 | HG00735.hp1 HG01192.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.293+803_293+804dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
A | ATTT | 6 | a0001c0001t0001g0041a0001c0001t0001g0055a0001c0001t0001g0098others(3): Show | 6 | HG01081.hp1 HG02602.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+802_293+804dup others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
A | ATTTT | 7 | a0001c0001t0001g0119a0001c0001t0002g0131a0001c0001t0002g0141others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.293+801_293+804dup others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
A | ATTTTTT | 1 | a0001c0001t0001g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293+799_293+804dup others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
AT | A | 24 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(21): Show | 24 | HG01070.hp1 HG01255.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.293+804delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
ATT | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0154others(14): Show | 17 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.293+803_293+804del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
ATTTT | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.293+801_293+804del others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
ATTTTTT | A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293+799_293+804del others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0127a0001c0001t0002g0042 | 2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.293+792_293+804del others(13): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021454
|
ATTTTTTT others(7): Show |
A | 4 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02809.hp1 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+791_293+804del others(14): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021454 | ||||||
| chrX:54021457
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0095 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.293+802A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021457 | ||||||
| chrX:54021471
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.293+788A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021471 | ||||||
| chrX:54021472
|
T | A | 1 | a0001c0001t0003g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.293+787A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021472 | ||||||
| chrX:54021558
|
T | TC | 1 | a0001c0001t0001g0081 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.293+700dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021558 | ||||||
| chrX:54021620
|
C | A | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.293+639G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021620 | ||||||
| chrX:54021817
|
AC | A | 1 | a0001c0001t0001g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.293+441delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54021817 | ||||||
| chrX:54022474
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.185-107C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 3/21 | chrX | 54022474 | ||||||
| chrX:54022688
|
TC | T | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.184+69delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 3/21 | chrX | 54022688 | ||||||
| chrX:54022846
|
GA | G | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | splice_region_variant&intron_variant | LOW | c.99-4delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54022846 | ||||||
| chrX:54022990
|
C | T | 1 | a0001c0001t0009g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.99-147G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54022990 | ||||||
| chrX:54023151
|
A | AT | 23 | a0001c0001t0001g0046a0001c0001t0002g0026a0001c0001t0002g0027others(20): Show | 23 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.99-309dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023151 | ||||||
| chrX:54023325
|
T | TA | 1 | a0001c0001t0001g0081 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.99-483dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023325 | ||||||
| chrX:54023325
|
TA | T | 1 | a0001c0001t0001g0084 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.99-483delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023325 | ||||||
| chrX:54023325
|
TAAAAA | T | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99-487_99-483delTT others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023325 | ||||||
| chrX:54023348
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99-505G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023348 | ||||||
| chrX:54023496
|
A | C | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-653T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023496 | ||||||
| chrX:54023516
|
TC | T | 1 | a0001c0001t0001g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.99-674delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023516 | ||||||
| chrX:54023521
|
CT | C | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.99-679delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023521 | ||||||
| chrX:54023662
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.99-819A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023662 | ||||||
| chrX:54023671
|
A | AG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-829dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023671 | ||||||
| chrX:54023691
|
AC | A | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.99-849delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023691 | ||||||
| chrX:54023706
|
AAAAC | A | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99-867_99-864delGT others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023706 | ||||||
| chrX:54023725
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.99-882T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023725 | ||||||
| chrX:54023780
|
A | AC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-938dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023780 | ||||||
| chrX:54023841
|
C | CA | 38 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0063others(35): Show | 38 | HG01243.hp1 HG01255.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.99-999dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023841 | ||||||
| chrX:54023841
|
C | CAA | 2 | a0001c0001t0001g0013a0001c0001t0003g0180 | 2 | HG00738.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.99-1000_99-999dupT others(1): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023841 | ||||||
| chrX:54023841
|
CA | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0097a0003c0003t0011g0164others(2): Show | 5 | HG02735.hp1 HG03492.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-999delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023841 | ||||||
| chrX:54023841
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0012g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99-1011_99-999delT others(12): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023841 | ||||||
| chrX:54023861
|
AAAAG | A | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.99-1022_99-1019del others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023861 | ||||||
| chrX:54023937
|
CA | C | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.99-1095delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023937 | ||||||
| chrX:54024212
|
CG | C | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-1370delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024212 | ||||||
| chrX:54024369
|
GC | G | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-1527delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024369 | ||||||
| chrX:54024495
|
A | T | 12 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(9): Show | 12 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.99-1652T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024495 | ||||||
| chrX:54024571
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.99-1728G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024571 | ||||||
| chrX:54024579
|
C | T | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99-1736G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024579 | ||||||
| chrX:54024617
|
C | A | 2 | a0001c0001t0003g0166a0001c0001t0003g0174 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.99-1774G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024617 | ||||||
| chrX:54024867
|
T | A | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-2024A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024867 | ||||||
| chrX:54024924
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99-2081A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024924 | ||||||
| chrX:54024978
|
GC | G | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2136delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024978 | ||||||
| chrX:54025038
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0105 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.99-2195T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025038 | ||||||
| chrX:54025171
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2328G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025171 | ||||||
| chrX:54025172
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2329C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025172 | ||||||
| chrX:54025203
|
C | CT | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2361dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025203 | ||||||
| chrX:54025341
|
A | AG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2499dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025341 | ||||||
| chrX:54025401
|
C | T | 1 | a0006c0005t0001g0051 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.99-2558G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025401 | ||||||
| chrX:54025540
|
TC | T | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2698delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025540 | ||||||
| chrX:54025988
|
A | AC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3146dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025988 | ||||||
| chrX:54026107
|
A | AT | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3265dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026107 | ||||||
| chrX:54026125
|
G | A | 2 | a0001c0001t0003g0167a0001c0001t0003g0168 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99-3282C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026125 | ||||||
| chrX:54026252
|
G | GC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3410dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026252 | ||||||
| chrX:54026296
|
G | GT | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3454dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026296 | ||||||
| chrX:54026315
|
C | CT | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3473dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026315 | ||||||
| chrX:54026346
|
T | TC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3504dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026346 | ||||||
| chrX:54026353
|
C | CA | 29 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0020others(26): Show | 29 | HG00733.hp1 HG00738.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.99-3511dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026353 | ||||||
| chrX:54026353
|
C | CAA | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99-3512_99-3511dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026353 | ||||||
| chrX:54026353
|
CA | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0060others(2): Show | 5 | HG02922.hp2 NA18944.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-3511delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026353 | ||||||
| chrX:54026530
|
TTTG | T | 1 | a0001c0001t0003g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99-3690_99-3688del others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026530 | ||||||
| chrX:54026553
|
TG | T | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99-3711delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026553 | ||||||
| chrX:54026554
|
G | GTTGTT | 27 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(24): Show | 27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.99-3712_99-3711ins others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026554 | ||||||
| chrX:54026623
|
T | TC | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-3781dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026623 | ||||||
| chrX:54027022
|
C | G | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-4179G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027022 | ||||||
| chrX:54027041
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0076 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.99-4198A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027041 | ||||||
| chrX:54027101
|
T | TG | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-4259dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027101 | ||||||
| chrX:54027130
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.99-4287G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027130 | ||||||
| chrX:54027131
|
A | ATTCCTT | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.99-4289_99-4288ins others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027131 | ||||||
| chrX:54027132
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.99-4289T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027132 | ||||||
| chrX:54027244
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-4401T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027244 | ||||||
| chrX:54027297
|
AC | A | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-4455delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027297 | ||||||
| chrX:54027332
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 13 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-4489G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027332 | ||||||
| chrX:54027432
|
C | T | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-4589G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027432 | ||||||
| chrX:54027462
|
C | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | NA18965.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.99-4619G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027462 | ||||||
| chrX:54027604
|
A | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99-4761T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027604 | ||||||
| chrX:54027704
|
C | T | 2 | a0002c0002t0004g0147a0002c0002t0004g0148 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99-4861G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027704 | ||||||
| chrX:54027806
|
C | CA | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99-4964dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027806 | ||||||
| chrX:54027922
|
GA | G | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.99-5080delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027922 | ||||||
| chrX:54027923
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.99-5080T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027923 | ||||||
| chrX:54027984
|
C | CCA | 11 | a0001c0001t0001g0018a0001c0001t0001g0096a0001c0001t0001g0109others(8): Show | 11 | HG01433.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-5143_99-5142dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027984
|
C | CCACA | 1 | a0001c0001t0001g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.99-5145_99-5142dup others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027984
|
C | CCACACA | 5 | a0001c0001t0002g0130a0001c0001t0002g0133a0001c0001t0002g0134others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-5147_99-5142dup others(6): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027984
|
C | CCACACAC others(1): Show |
11 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0029others(8): Show | 11 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-5149_99-5142dup others(8): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027984
|
C | CCACACAC others(3): Show |
3 | a0001c0001t0002g0027a0001c0001t0002g0045a0001c0001t0002g0140 | 3 | HG01257.hp1 HG02109.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.99-5151_99-5142dup others(10): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027984
|
CCA | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(42): Show | 45 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.99-5143_99-5142del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027984
|
CCACA | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0065 | 2 | HG01069.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.99-5145_99-5142del others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027984 | ||||||
| chrX:54027999
|
C | T | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99-5156G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027999 | ||||||
| chrX:54028022
|
T | TG | 1 | a0001c0001t0002g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.99-5180dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54028022 | ||||||
| chrX:54028725
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.99-5882A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54028725 | ||||||
| chrX:54028895
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99-6052A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54028895 | ||||||
| chrX:54029246
|
G | GC | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99-6404dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54029246 | ||||||
| chrX:54029489
|
TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.99-6647delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54029489 | ||||||
| chrX:54029927
|
A | C | 21 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(18): Show | 21 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.99-7084T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54029927 | ||||||
| chrX:54030270
|
T | C | 4 | a0002c0002t0004g0147a0002c0002t0004g0148a0002c0002t0004g0163others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-7427A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54030270 | ||||||
| chrX:54030330
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-7487G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54030330 | ||||||
| chrX:54030545
|
A | G | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.99-7702T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54030545 | ||||||
| chrX:54030593
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.99-7750T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54030593 | ||||||
| chrX:54031393
|
C | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-8550G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031393 | ||||||
| chrX:54031584
|
C | CA | 5 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0103others(2): Show | 5 | HG01099.hp1 HG01256.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-8742dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031584 | ||||||
| chrX:54031584
|
CA | C | 1 | a0001c0001t0001g0081 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.99-8742delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031584 | ||||||
| chrX:54031599
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 13 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-8756G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031599 | ||||||
| chrX:54031673
|
CA | C | 1 | a0001c0001t0001g0081 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.99-8831delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031673 | ||||||
| chrX:54031751
|
C | G | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0141 | 3 | HG02970.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.99-8908G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031751 | ||||||
| chrX:54031832
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.99-8989C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54031832 | ||||||
| chrX:54032016
|
G | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 185 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(182): Show |
intron_variant | MODIFIER | c.99-9173C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032016 | ||||||
| chrX:54032093
|
C | T | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99-9250G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032093 | ||||||
| chrX:54032226
|
TC | T | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.99-9384delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032226 | ||||||
| chrX:54032358
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99-9515A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032358 | ||||||
| chrX:54032529
|
G | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99-9686C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032529 | ||||||
| chrX:54032634
|
C | CA | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.99-9792dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032634 | ||||||
| chrX:54032647
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02723.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.99-9804A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032647 | ||||||
| chrX:54032767
|
CT | C | 1 | a0007c0004t0001g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.98+9863delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032767 | ||||||
| chrX:54033134
|
A | AC | 5 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0055others(2): Show | 5 | HG03139.hp1 NA18959.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+9496dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54033134 | ||||||
| chrX:54033542
|
A | G | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+9089T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54033542 | ||||||
| chrX:54033733
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.98+8898G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54033733 | ||||||
| chrX:54033927
|
T | TA | 1 | a0001c0001t0001g0003 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.98+8703dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54033927 | ||||||
| chrX:54034419
|
G | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0097 | 3 | HG00140.hp1 HG01358.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.98+8212C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034419 | ||||||
| chrX:54034588
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.98+8043G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034588 | ||||||
| chrX:54034756
|
G | A | 3 | a0001c0001t0003g0165a0001c0001t0003g0179a0001c0001t0003g0181 | 3 | HG02109.hp1 HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.98+7875C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034756 | ||||||
| chrX:54034810
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0063a0001c0001t0001g0117others(1): Show | 4 | NA18984.hp1 NA18994.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+7821G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034810 | ||||||
| chrX:54034823
|
C | CA | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(21): Show | 24 | HG01081.hp1 HG01109.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.98+7807dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034823 | ||||||
| chrX:54034823
|
C | CAA | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+7806_98+7807dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034823 | ||||||
| chrX:54034823
|
C | CAAAA | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.98+7804_98+7807dup others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034823 | ||||||
| chrX:54034823
|
CA | C | 23 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(20): Show | 23 | HG00738.hp1 HG01167.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+7807delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034823 | ||||||
| chrX:54034823
|
CAA | C | 1 | a0001c0001t0003g0178 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98+7806_98+7807del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54034823 | ||||||
| chrX:54035019
|
C | T | 3 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0177 | 3 | HG02970.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.98+7612G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035019 | ||||||
| chrX:54035356
|
C | CA | 23 | a0001c0001t0001g0054a0001c0001t0002g0026a0001c0001t0002g0027others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+7274dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035356 | ||||||
| chrX:54035356
|
C | CAA | 1 | a0001c0001t0002g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.98+7273_98+7274dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035356 | ||||||
| chrX:54035430
|
T | TTGACA | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+7200_98+7201ins others(5): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035430 | ||||||
| chrX:54035565
|
T | A | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+7066A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035565 | ||||||
| chrX:54035796
|
C | T | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+6835G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035796 | ||||||
| chrX:54035832
|
C | A | 1 | a0001c0001t0003g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.98+6799G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54035832 | ||||||
| chrX:54036102
|
C | CA | 3 | a0001c0001t0001g0151a0001c0001t0002g0045a0001c0001t0007g0146 | 3 | HG02027.hp1 HG02257.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.98+6528dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036102 | ||||||
| chrX:54036102
|
C | CAAA | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.98+6526_98+6528dup others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036102 | ||||||
| chrX:54036102
|
C | CAAAA | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 9 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.98+6525_98+6528dup others(4): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036102 | ||||||
| chrX:54036102
|
CA | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0152a0001c0001t0002g0130others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+6528delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036102 | ||||||
| chrX:54036274
|
C | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG00621.hp1 HG02040.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+6357G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036274 | ||||||
| chrX:54036309
|
A | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.98+6322T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036309 | ||||||
| chrX:54036350
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.98+6281G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036350 | ||||||
| chrX:54036375
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 5 | HG01081.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+6256G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036375 | ||||||
| chrX:54036418
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.98+6213T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036418 | ||||||
| chrX:54036571
|
C | CA | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.98+6059dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036571 | ||||||
| chrX:54036571
|
C | CAA | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+6058_98+6059dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036571 | ||||||
| chrX:54036571
|
CA | C | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+6059delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036571 | ||||||
| chrX:54036571
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98+6050_98+6059del others(10): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036571 | ||||||
| chrX:54036582
|
A | AAC | 1 | a0002c0006t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.98+6048_98+6049ins others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036582 | ||||||
| chrX:54036583
|
A | AAC | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+6047_98+6048ins others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036583 | ||||||
| chrX:54036592
|
A | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+6039T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036592 | ||||||
| chrX:54036594
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.98+6037T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036594 | ||||||
| chrX:54036598
|
A | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+6033T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036598 | ||||||
| chrX:54036599
|
AAC | A | 16 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(13): Show | 16 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.98+6030_98+6031del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036599 | ||||||
| chrX:54036600
|
AC | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0139others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+6030delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036600 | ||||||
| chrX:54036601
|
C | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0118a0001c0001t0003g0174others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+6030G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036601 | ||||||
| chrX:54036601
|
CT | C | 1 | a0001c0001t0009g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.98+6029delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54036601 | ||||||
| chrX:54037000
|
T | A | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+5631A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037000 | ||||||
| chrX:54037000
|
T | TA | 2 | a0001c0001t0002g0042a0004c0007t0001g0022 | 2 | HG02071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.98+5630dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037000 | ||||||
| chrX:54037000
|
T | TAA | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.98+5629_98+5630dup others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037000 | ||||||
| chrX:54037000
|
TA | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0060others(6): Show | 9 | HG01070.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+5630delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037000 | ||||||
| chrX:54037000
|
TAA | T | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.98+5629_98+5630del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037000 | ||||||
| chrX:54037007
|
A | T | 1 | a0001c0001t0003g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.98+5624T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037007 | ||||||
| chrX:54037008
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.98+5623T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037008 | ||||||
| chrX:54037186
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.98+5445A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037186 | ||||||
| chrX:54037239
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.98+5392A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037239 | ||||||
| chrX:54037359
|
C | CA | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.98+5271dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037359 | ||||||
| chrX:54037454
|
C | T | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+5177G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037454 | ||||||
| chrX:54037766
|
C | A | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+4865G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037766 | ||||||
| chrX:54037788
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.98+4843C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037788 | ||||||
| chrX:54037938
|
AC | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+4692delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037938 | ||||||
| chrX:54038054
|
A | AT | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+4576dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54038054 | ||||||
| chrX:54038102
|
T | C | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+4529A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54038102 | ||||||
| chrX:54038226
|
T | C | 1 | a0001c0001t0008g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.98+4405A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54038226 | ||||||
| chrX:54038353
|
C | T | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+4278G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54038353 | ||||||
| chrX:54039133
|
C | CA | 12 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0105others(9): Show | 12 | HG00733.hp2 HG01175.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.98+3497dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039133 | ||||||
| chrX:54039133
|
CA | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0053others(38): Show | 41 | HG00733.hp1 HG00738.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.98+3497delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039133 | ||||||
| chrX:54039133
|
CAA | C | 1 | a0001c0001t0002g0026 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.98+3496_98+3497del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039133 | ||||||
| chrX:54039382
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG01070.hp1 HG01261.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+3249G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039382 | ||||||
| chrX:54039490
|
G | GA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+3140dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039490 | ||||||
| chrX:54039514
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.98+3117A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039514 | ||||||
| chrX:54039686
|
C | CA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2944_98+2945ins others(1): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039686 | ||||||
| chrX:54039709
|
C | CA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2921dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039709 | ||||||
| chrX:54039836
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.98+2795T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039836 | ||||||
| chrX:54039907
|
TA | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2723delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039907 | ||||||
| chrX:54039912
|
CA | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2718delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039912 | ||||||
| chrX:54039979
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98+2652A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039979 | ||||||
| chrX:54039980
|
TA | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2650delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039980 | ||||||
| chrX:54040049
|
GT | G | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2581delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040049 | ||||||
| chrX:54040106
|
TA | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2524delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040106 | ||||||
| chrX:54040155
|
G | A | 22 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(19): Show | 22 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.98+2476C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040155 | ||||||
| chrX:54040172
|
TG | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2458delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040172 | ||||||
| chrX:54040266
|
AC | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2364delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040266 | ||||||
| chrX:54040365
|
TA | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2265delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040365 | ||||||
| chrX:54040424
|
GC | G | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2206delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040424 | ||||||
| chrX:54040446
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(78): Show | 81 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.98+2185G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040446 | ||||||
| chrX:54040489
|
T | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+2142A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040489 | ||||||
| chrX:54040576
|
A | AT | 2 | a0002c0002t0004g0147a0002c0002t0004g0148 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.98+2054_98+2055ins others(1): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040576 | ||||||
| chrX:54040667
|
CT | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1963delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040667 | ||||||
| chrX:54040693
|
G | C | 1 | a0001c0001t0007g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+1938C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040693 | ||||||
| chrX:54040716
|
T | TA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1914dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040716 | ||||||
| chrX:54040825
|
G | GC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1805dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040825 | ||||||
| chrX:54041240
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+1391G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041240 | ||||||
| chrX:54041253
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.98+1378C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041253 | ||||||
| chrX:54041269
|
A | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1362T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041269 | ||||||
| chrX:54041275
|
T | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1356A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041275 | ||||||
| chrX:54041305
|
AC | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1325delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041305 | ||||||
| chrX:54041320
|
G | GT | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1310dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041320 | ||||||
| chrX:54041388
|
T | TA | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.98+1242dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041388 | ||||||
| chrX:54041388
|
TA | T | 1 | a0001c0001t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.98+1242delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041388 | ||||||
| chrX:54041403
|
AAG | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1226_98+1227del others(2): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041403 | ||||||
| chrX:54041406
|
A | G | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1225T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041406 | ||||||
| chrX:54041458
|
GA | G | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1172delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041458 | ||||||
| chrX:54041831
|
A | AT | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+799dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041831 | ||||||
| chrX:54041894
|
C | CTG | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+735_98+736dupCA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041894 | ||||||
| chrX:54042021
|
G | GAC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+608_98+609dupGT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042021 | ||||||
| chrX:54042055
|
C | CA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+575dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042055 | ||||||
| chrX:54042062
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG02055.hp1 HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.98+569C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042062 | ||||||
| chrX:54042126
|
AAC | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.98+503_98+504delGT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042126 | ||||||
| chrX:54042192
|
CT | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+438delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042192 | ||||||
| chrX:54042272
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.98+359C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042272 | ||||||
| chrX:54042291
|
CT | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+339delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042291 | ||||||
| chrX:54042368
|
GA | G | 1 | a0001c0001t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.98+262delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042368 | ||||||
| chrX:54042372
|
A | AG | 17 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG01099.hp1 HG01175.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.98+258dupC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042372 | ||||||
| chrX:54042372
|
A | AGG | 3 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | NA18990.hp1 NA19000.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.98+257_98+258dupCC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042372 | ||||||
| chrX:54042372
|
AG | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0119others(35): Show | 38 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.98+258delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042372 | ||||||
| chrX:54042372
|
AGG | A | 13 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(10): Show | 13 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.98+257_98+258delCC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042372 | ||||||
| chrX:54042372
|
AGGG | A | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.98+256_98+258delCC others(1): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042372 | ||||||
| chrX:54042374
|
G | T | 1 | a0001c0001t0001g0006 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.98+257C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042374 | ||||||
| chrX:54042377
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.98+254C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042377 | ||||||
| chrX:54042389
|
TA | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+241delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042389 | ||||||
| chrX:54042395
|
T | TA | 1 | a0001c0001t0001g0003 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.98+235dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042395 | ||||||
| chrX:54042407
|
CA | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+223delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042407 | ||||||
| chrX:54042407
|
CAAAAG | C | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.98+219_98+223delCT others(3): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042407 | ||||||
| chrX:54042502
|
G | GA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+128dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042502 | ||||||
| chrX:54042532
|
T | TC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+98dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042532 | ||||||
| chrX:54042538
|
GC | G | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+92delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042538 | ||||||
| chrX:54042584
|
A | AC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+46dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042584 | ||||||
| chrX:54042837
|
CT | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-18delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54042837 | ||||||
| chrX:54042862
|
G | GC | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-92-43dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54042862 | ||||||
| chrX:54042869
|
A | AC | 1 | a0001c0001t0001g0003 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-92-50dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54042869 | ||||||
| chrX:54042883
|
A | AC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-64dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54042883 | ||||||
| chrX:54042914
|
CG | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-95delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54042914 | ||||||
| chrX:54043027
|
G | GC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-208dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043027 | ||||||
| chrX:54043081
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-92-261T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043081 | ||||||
| chrX:54043123
|
CG | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-304delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043123 | ||||||
| chrX:54043128
|
A | G | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-308T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043128 | ||||||
| chrX:54043129
|
G | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-309C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043129 | ||||||
| chrX:54043307
|
T | TC | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-93+454_-93+455ins others(1): Show |
PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043307 | ||||||
| chrX:54043349
|
AG | A | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-93+412delC | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043349 | ||||||
| chrX:54043353
|
G | GC | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-93+408dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043353 | ||||||
| chrX:54043427
|
TC | T | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-93+334delG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043427 | ||||||
| chrX:54043572
|
CA | C | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-93+189delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043572 | ||||||
| chrX:54043656
|
G | GC | 12 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(9): Show | 12 | HG01167.hp1 HG01255.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93+105dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043656 | ||||||
| chrX:54043661
|
C | G | 1 | a0001c0001t0009g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-93+101G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043661 | ||||||
| chrX:54043747
|
G | GC | 1 | a0002c0002t0004g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-93+14dupG | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043747 | ||||||
| chrX:54043752
|
C | CA | 1 | a0003c0003t0011g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-93+9dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043752 |