Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 181 | 58 | 33 | 65 | 5 | 18 | 51 | PHF8_chrX_53931680_54049473 | PHF8 | MASVP others(1019): Show |
chrX | 53931680 | 54049473 |
| a0002 | 0/0 | 1023 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | MASVP others(1018): Show |
chrX | 53931680 | 54049473 |
| a0003 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | MASVP others(1019): Show |
chrX | 53931680 | 54049473 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3072 | 181 | 58 | 33 | 65 | 5 | 18 | PHF8_chrX_53931680_54049473 | PHF8 | ATGGC others(3067): Show |
chrX | 53931680 | 54049473 | ||
| a0002c0002 | 0/0 | 3069 | 3 | 3 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | ATGGC others(3064): Show |
chrX | 53931680 | 54049473 | ||
| a0002c0003 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | ATGGC others(3064): Show |
chrX | 53931680 | 54049473 | ||
| a0003c0004 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | ATGGC others(3067): Show |
chrX | 53931680 | 54049473 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6357 | 132 | 23 | 25 | 63 | 5 | 15 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0002 | 0/1 | 6357 | 23 | 16 | 4 | 0 | 0 | 2 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0003 | 0/0 | 6357 | 19 | 15 | 4 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0005 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0006 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0007 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0008 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0009 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0001c0001t0010 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
chrX | 53931680 | 54049473 |
| a0002c0002t0004 | 0/0 | 6354 | 3 | 3 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6349): Show |
chrX | 53931680 | 54049473 |
| a0002c0003t0004 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6349): Show |
chrX | 53931680 | 54049473 |
| a0003c0004t0001 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | CTCGC others(6352): Show |
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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0045 | 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 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0087 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0123 | 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 |
| 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 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0026 | 0/1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0121 | 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 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0002g0144 | 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 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0002t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0002t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0002c0003t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| a0003c0004t0001g0019 | 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 | g0069 | EUR | FIN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0111 | 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 | g0097 | 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 | g0073 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0107 | 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 | g0020 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02071 | hp1 | a0003 | c0004 | t0001 | g0019 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0174 | 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 | g0150 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0126 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0139 | 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 | g0144 | 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 | g0151 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02809 | hp2 | a0002 | c0002 | t0004 | g0042 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0136 | 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 | g0142 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0161 | 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 | g0138 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0031 | 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 | g0141 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0152 | 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 | g0135 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0186 | SAS | BEB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | LWK | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0170 | 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 | g0143 | AFR | ASW | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0063 | 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 | g0134 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02559 | hp1 | a0002 | c0003 | t0004 | g0153 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0026 | REF | REF | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0070 | REF | REF | PHF8_chrX_53931680_54049473 | PHF8 | chrX | 53931680 | 54049473 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0003 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:53992762 | T | G | 1 | a0002c0003 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:53936692 | A | T | 1 | a0001c0001t0008 | 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 | a0001c0001t0002 a0001c0001t0007 a0002c0002t0004 others(1): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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:53938155 | T | C | 1 | a0001c0001t0002 | 22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0009 | 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:54044390 | G | A | 2 | a0001c0001t0003 a0001c0001t0005 |
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 | a0001c0001t0010 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-755A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/22 | 1696 | chrX | 54044424 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0002g0136 a0001c0001t0002g0139 a0001c0001t0002g0140 others(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 | a0001c0001t0002g0039 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0018 others(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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0063 | 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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0083 | 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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | 23 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(20): Show |
23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
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:53943897 | T | C | 1 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0068 | 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0096 |
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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0001c0001t0003g0166 a0001c0001t0003g0169 |
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 | a0001c0001t0001g0110 | 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 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(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 | a0001c0001t0001g0118 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2540-874C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53945117 | |||||||
| chrX:53945461 | G | C | 1 | a0001c0001t0001g0110 | 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 | a0001c0001t0007g0150 | 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 | a0002c0002t0004g0152 | 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 | a0001c0001t0002g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2540-2412T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53946655 | |||||||
| chrX:53946916 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): Show |
57 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(54): 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0117 |
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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0002c0003t0004g0153 | 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0003g0173 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0045 | 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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0009 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0002g0022 a0001c0001t0002g0023 others(13): Show |
16 | HG00733.hp1 HG01074.hp1 HG01257.hp1 others(13): 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 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0138 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0028 others(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:53949884 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0096 others(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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
80 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.2540-5712G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53949955 | |||||||
| chrX:53950003 | A | G | 1 | a0002c0002t0004g0042 | 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:53951599 | C | T | 5 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0183 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0021 | 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 | 26 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0156 others(23): Show |
26 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2540-8041dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952283 | |||||||
| chrX:53952506 | A | AAGATG | 4 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 others(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 | a0001c0001t0002g0039 | 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0051 | 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 | 23 | a0001c0001t0001g0159 a0001c0001t0002g0022 a0001c0001t0002g0023 others(20): Show |
23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2540-8645dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53952887 | |||||||
| chrX:53953180 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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:53953301 | A | C | 1 | a0001c0001t0001g0107 | 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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
182 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(179): Show |
intron_variant | MODIFIER | c.2540-9085delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53953327 | |||||||
| chrX:53953328 | A | T | 1 | a0001c0001t0001g0083 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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:53953657 | A | G | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | G | 5 | a0001c0001t0002g0137 a0002c0002t0004g0042 a0002c0002t0004g0151 others(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:53954045 | C | G | 22 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0154 | 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 | a0002c0002t0004g0152 | 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 | a0001c0001t0001g0017 | 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 | a0002c0002t0004g0042 | 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 | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
55 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2539+8344dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53954499 | |||||||
| chrX:53954499 | C | CAA | 5 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0120 others(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 | CA | C | 27 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0114 others(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:53954526 | A | G | 2 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
169 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(166): 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 | a0001c0001t0001g0055 a0001c0001t0002g0135 a0001c0001t0002g0137 others(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 | a0001c0001t0001g0130 | 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 | a0002c0003t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2539+7559G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955285 | |||||||
| chrX:53955557 | C | CT | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.2539+7286dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53955557 | |||||||
| chrX:53955557 | C | CTT | 8 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0016 | 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 | 29 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
29 | HG00140.hp1 HG00733.hp1 HG01257.hp1 others(26): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0048 others(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 | CGT | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0049 others(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:53957174 | G | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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:53957208 | T | C | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2539+5636A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957208 | |||||||
| chrX:53957227 | G | A | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2539+5617C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957227 | |||||||
| chrX:53957290 | T | C | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2539+5554A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957290 | |||||||
| chrX:53957504 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
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: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 | a0001c0001t0001g0060 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2539+4863C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53957981 | |||||||
| chrX:53958043 | AT | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
82 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2539+4800delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958043 | |||||||
| chrX:53958147 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2539+4697A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958147 | |||||||
| chrX:53958329 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0129 |
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:53958553 | G | A | 1 | a0001c0001t0002g0121 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(49): Show |
52 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.2539+4068dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53958775 | |||||||
| chrX:53958775 | C | CAA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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:53958985 | A | G | 1 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0021 | 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 | 9 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(6): Show |
9 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(6): 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0006g0113 | 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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0125 a0001c0001t0001g0129 others(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:53959990 | T | C | 23 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(20): Show |
23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0102 |
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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2539+2158A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960686 | |||||||
| chrX:53960780 | C | T | 1 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2539+1946A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53960898 | |||||||
| chrX:53961709 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0002g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2539+1101G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53961743 | |||||||
| chrX:53962713 | A | G | 5 | a0001c0001t0003g0165 a0001c0001t0003g0178 a0001c0001t0003g0179 others(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 | a0001c0001t0003g0170 a0001c0001t0003g0171 |
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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2539+47G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 19/21 | chrX | 53962797 | |||||||
| chrX:53963198 | T | C | 1 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-259A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53963198 | |||||||
| chrX:53963361 | G | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:53963586 | A | G | 3 | a0002c0002t0004g0151 a0002c0002t0004g0152 a0002c0003t0004g0153 |
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:53963866 | C | T | 1 | a0001c0001t0001g0097 | 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-1210G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964149 | |||||||
| chrX:53964352 | T | C | 2 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:53964771 | G | A | 1 | a0001c0001t0001g0046 | 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 | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(23): Show |
26 | HG00621.hp1 HG00733.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2444-1930dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964868 | |||||||
| chrX:53964868 | CA | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0049 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2444-1937T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964876 | |||||||
| chrX:53964984 | T | C | 23 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(20): Show |
23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2444-2045A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53964984 | |||||||
| chrX:53965162 | T | C | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2444-2223A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965162 | |||||||
| chrX:53965563 | C | T | 1 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2444-2625C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53965564 | |||||||
| chrX:53965732 | T | G | 1 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0100 others(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:53966064 | C | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 |
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:53966764 | T | C | 1 | a0001c0001t0001g0118 | 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 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 others(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 | a0001c0001t0001g0035 | 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:53966923 | G | A | 1 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0001g0162 others(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:53967001 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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:53967026 | C | A | 1 | a0002c0003t0004g0153 | 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 | a0001c0001t0002g0038 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
77 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(74): 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 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0036 | 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 |
45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(42): Show |
45 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(42): 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(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:53967300 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2444-4361G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967300 | |||||||
| chrX:53967322 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2444-4383C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967322 | |||||||
| chrX:53967345 | G | A | 1 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-4406C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967345 | |||||||
| chrX:53967393 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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:53967508 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0108 | 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:53967987 | G | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
80 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.2444-5048C>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53967987 | |||||||
| chrX:53968125 | TA | T | 13 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0105 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2444-5418A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968357 | |||||||
| chrX:53968631 | G | A | 1 | a0001c0001t0001g0098 | 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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-5694C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53968633 | |||||||
| 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 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0009g0126 |
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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:53969583 | A | C | 1 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0067 | 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:53969674 | G | A | 1 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2444-6735C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53969674 | |||||||
| chrX:53970734 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2444-7795G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53970734 | |||||||
| chrX:53971502 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2444-8563G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971502 | |||||||
| chrX:53971811 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2444-8872T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53971811 | |||||||
| chrX:53971980 | T | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 |
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 | a0001c0001t0001g0090 | 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 | 27 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0063 others(24): Show |
27 | HG00642.hp1 HG01074.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2444-9383dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53972321 | |||||||
| chrX:53972321 | CA | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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:53972775 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0001t0001g0117 |
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 | a0002c0002t0004g0151 a0002c0002t0004g0152 a0002c0003t0004g0153 |
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:53973707 | G | T | 1 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0007g0150 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2443+10325A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53974589 | |||||||
| chrX:53975639 | G | A | 1 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0102 |
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 | a0001c0001t0001g0105 | 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 | a0002c0003t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2443+8666G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976248 | |||||||
| chrX:53976312 | T | A | 21 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0017 | 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 | 21 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(18): Show |
21 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2443+8226dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53976687 | |||||||
| chrX:53976687 | TA | T | 9 | a0001c0001t0001g0055 a0001c0001t0001g0149 a0001c0001t0001g0155 others(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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+7749A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53977165 | |||||||
| chrX:53977174 | GA | G | 6 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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: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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0015 others(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:53978105 | C | G | 15 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+6713G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53978201 | |||||||
| chrX:53978797 | C | CA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0086 others(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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0109 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0109 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0109 |
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:53979011 | T | G | 1 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0099 |
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:53979468 | C | G | 1 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2443+5446G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53979468 | |||||||
| chrX:53980940 | T | C | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
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:53981592 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0027 |
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 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 |
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:53982565 | G | A | 4 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0003 | 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 | 28 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(25): Show |
28 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2443+1739dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983174 | |||||||
| chrX:53983763 | C | T | 1 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0069 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2443+972T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 18/21 | chrX | 53983942 | |||||||
| chrX:53984099 | C | T | 2 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0031 |
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:53984638 | T | C | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0002c0002t0004g0042 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0048 | 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 | a0002c0003t0004g0153 | 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 | a0001c0001t0001g0035 | 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 | a0002c0002t0004g0152 | 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 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0006g0113 |
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 | a0001c0001t0003g0174 | 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 | 6 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(3): Show |
6 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996-461A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 16/21 | chrX | 53986410 | |||||||
| chrX:53986424 | A | G | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0002g0121 | 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 | a0001c0001t0001g0160 a0002c0003t0004g0153 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0077 others(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:53988754 | CA | C | 14 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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:53989509 | G | GA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0034 | 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 | 32 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(29): Show |
32 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1731-1763T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53989707 | |||||||
| chrX:53989788 | T | C | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0095 |
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 | 24 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(21): 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 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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:53991590 | A | G | 22 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | 37 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(34): Show |
37 | HG00733.hp1 HG01109.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.1730+1074dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991661 | |||||||
| chrX:53991661 | C | CAA | 7 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1730+1022A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 14/21 | chrX | 53991714 | |||||||
| chrX:53991933 | C | T | 1 | a0002c0003t0004g0153 | 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 | a0001c0001t0002g0143 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-85C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53993988 | |||||||
| chrX:53993993 | T | A | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-97T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994000 | |||||||
| chrX:53994006 | G | C | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-110T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994013 | |||||||
| chrX:53994022 | C | T | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-124A>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994027 | |||||||
| chrX:53994039 | A | G | 1 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-142A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994045 | |||||||
| chrX:53994048 | A | C | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-147T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994050 | |||||||
| chrX:53994057 | C | T | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1324-157G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 12/21 | chrX | 53994060 | |||||||
| chrX:53995043 | T | C | 1 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0082 a0001c0001t0001g0098 others(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:53996092 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1234-310A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53996092 | |||||||
| chrX:53996559 | C | A | 2 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0096 others(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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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:53998463 | T | TAAATA | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1233+1162T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 11/21 | chrX | 53998708 | |||||||
| chrX:53998843 | A | G | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0005g0167 | 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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0169 others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0009 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1142-1047A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 10/21 | chrX | 54001008 | |||||||
| chrX:54001490 | A | AGAGT | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
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:54001931 | C | G | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(24): 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 | a0001c0001t0003g0165 a0001c0001t0003g0178 a0001c0001t0003g0179 others(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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0010g0186 | 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | CA | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0051 others(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:54005384 | C | T | 1 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(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:54005622 | T | TA | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(6): Show |
9 | HG02559.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.947-2941dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54005622 | |||||||
| chrX:54005622 | TA | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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:54005989 | T | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0102 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0095 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0016 |
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:54007670 | C | T | 1 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 |
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 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
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 | 46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(43): Show |
46 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.946+2750dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54008371 | |||||||
| chrX:54008532 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0102 |
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: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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.946+1957C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 8/21 | chrX | 54009165 | |||||||
| chrX:54009844 | G | GA | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0072 others(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 | GAAAAAAA others(6): Show |
1 | a0002c0003t0004g0153 | 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 | GGAAAAAA others(5): Show |
1 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0134 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0002g0136 a0001c0001t0002g0139 |
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 | a0001c0001t0002g0140 | 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 | a0001c0001t0002g0142 | 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 | a0001c0001t0002g0144 | 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 | a0002c0002t0004g0042 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0031 |
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 | a0001c0001t0003g0174 | 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 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0169 others(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 | a0001c0001t0001g0035 a0001c0001t0003g0172 |
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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0003g0169 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0099 others(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 | CA | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | 23 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(20): Show |
23 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(20): 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0131 |
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 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0156 | 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | CA | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0082 others(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:54013535 | C | T | 1 | a0002c0003t0004g0153 | 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 | a0001c0001t0001g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.783+767C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013610 | |||||||
| chrX:54013933 | C | T | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.783+443C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54013934 | |||||||
| chrX:54014101 | G | A | 1 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
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:54014252 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.783+125C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 7/21 | chrX | 54014252 | |||||||
| chrX:54014637 | A | C | 1 | a0001c0001t0001g0088 | 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 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
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:54014773 | A | C | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:54015162 | CT | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
168 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(165): Show |
intron_variant | MODIFIER | c.597-600delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015162 | |||||||
| chrX:54015305 | G | A | 1 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.597-906C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 6/21 | chrX | 54015469 | |||||||
| chrX:54015575 | C | CA | 31 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0055 others(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 | CA | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0083 others(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 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
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:54015643 | T | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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:54016256 | G | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:54016366 | C | T | 10 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | CA | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0008 | 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:54017401 | T | C | 1 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
63 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.294-633delA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018453 | |||||||
| chrX:54018473 | T | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0002g0136 a0001c0001t0002g0139 a0001c0001t0002g0140 others(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 | a0002c0003t0004g0153 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0002c0002t0004g0151 a0002c0002t0004g0152 |
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 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.294-1045G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54018866 | |||||||
| chrX:54019416 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 |
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 | a0001c0001t0002g0022 | 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 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.294-1889G>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019710 | |||||||
| chrX:54019782 | C | T | 1 | a0001c0001t0002g0039 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0084 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.294-1983T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54019804 | |||||||
| chrX:54020165 | G | A | 1 | a0001c0001t0010g0186 | 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 | a0001c0001t0003g0165 a0001c0001t0003g0179 a0001c0001t0003g0181 |
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 | a0001c0001t0003g0165 a0001c0001t0003g0179 a0001c0001t0003g0181 |
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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.293+1745T>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020514 | |||||||
| chrX:54020777 | T | TA | 24 | a0001c0001t0001g0086 a0001c0001t0001g0104 a0001c0001t0001g0119 others(21): Show |
24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.293+1481dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 4/21 | chrX | 54020777 | |||||||
| chrX:54021454 | A | AT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0135 a0001c0001t0002g0137 others(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 | AT | A | 24 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0156 others(13): Show |
16 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(13): 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 | ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0130 a0001c0001t0002g0038 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0107 | 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:54021620 | C | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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:54022474 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.185-107C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 3/21 | chrX | 54022474 | |||||||
| chrX:54022990 | C | T | 1 | a0001c0001t0008g0001 | 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 | 22 | a0001c0001t0001g0043 a0001c0001t0002g0022 a0001c0001t0002g0023 others(19): Show |
22 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.99-309dupA | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54023151 | |||||||
| 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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: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:54023725 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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:54023841 | C | CA | 38 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0062 others(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 | CA | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0088 others(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 | a0001c0001t0010g0186 | 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:54024495 | A | T | 12 | a0001c0001t0003g0166 a0001c0001t0003g0169 a0001c0001t0003g0170 others(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 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0017 | 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 | a0001c0001t0003g0166 a0001c0001t0003g0169 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0003g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99-2081A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54024924 | |||||||
| chrX:54025038 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0111 |
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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2329C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025172 | |||||||
| chrX:54025401 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.99-2558G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54025401 | |||||||
| chrX:54026125 | G | A | 2 | a0001c0001t0003g0170 a0001c0001t0003g0171 |
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:54026353 | C | CA | 28 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0080 others(25): Show |
28 | HG00733.hp1 HG00738.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.99-3511dupT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54026353 | |||||||
| chrX:54026353 | CA | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0058 others(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:54026554 | G | GTTGTT | 26 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(23): Show |
26 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(23): 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:54027022 | C | G | 4 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0077 |
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:54027130 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.99-4287G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027130 | |||||||
| chrX:54027132 | A | C | 1 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-4401T>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027244 | |||||||
| chrX:54027332 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0055 |
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 | a0001c0001t0007g0150 | 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 | a0002c0002t0004g0151 a0002c0002t0004g0152 |
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:54027923 | A | G | 1 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0115 others(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 | CCACACA | 5 | a0001c0001t0002g0136 a0001c0001t0002g0139 a0001c0001t0002g0140 others(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 |
10 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(7): Show |
10 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(7): 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 | a0001c0001t0002g0022 a0001c0001t0002g0039 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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:54027999 | C | T | 1 | a0002c0002t0004g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99-5156G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54027999 | |||||||
| chrX:54028725 | T | C | 1 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99-6052A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54028895 | |||||||
| chrX:54029927 | A | C | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(17): Show |
20 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(17): 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 | a0002c0002t0004g0042 a0002c0002t0004g0151 a0002c0002t0004g0152 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | 21 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(18): Show |
21 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(18): 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0109 others(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:54031599 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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:54031751 | C | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 |
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:54032093 | C | T | 1 | a0002c0002t0004g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99-9250G>A | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032093 | |||||||
| chrX:54032358 | T | C | 1 | a0001c0001t0001g0078 | 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 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99-9686C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54032529 | |||||||
| chrX:54032647 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0041 |
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:54033134 | A | AC | 5 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0052 others(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 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
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:54034419 | G | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0003g0165 a0001c0001t0003g0179 a0001c0001t0003g0181 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(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 | CA | C | 23 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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:54035019 | C | T | 3 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 |
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 | a0001c0001t0001g0051 a0001c0001t0002g0022 a0001c0001t0002g0023 others(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:54035430 | T | TTGACA | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | CAAAA | 9 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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:54036592 | A | C | 1 | a0001c0001t0007g0150 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | 15 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(12): Show |
15 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(12): 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 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0133 others(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 | a0001c0001t0002g0039 a0001c0001t0002g0121 a0001c0001t0003g0169 others(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:54037000 | T | A | 1 | a0001c0001t0007g0150 | 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 | TAA | 21 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(18): Show |
21 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(18): 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 | a0001c0001t0001g0043 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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: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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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:54037454 | C | T | 10 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.98+4843C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54037788 | |||||||
| chrX:54038102 | T | C | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0017 | 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 | 22 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(19): Show |
22 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0111 others(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 | 40 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0048 others(37): Show |
40 | HG00733.hp1 HG00738.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.98+3497delT | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039133 | |||||||
| chrX:54039382 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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:54039514 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.98+3117A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039514 | |||||||
| chrX:54039836 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
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:54039979 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98+2652A>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54039979 | |||||||
| chrX:54040155 | G | A | 22 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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:54040446 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
80 | HG00609.hp1 HG00621.hp1 HG00733.hp1 others(77): 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 | a0001c0001t0001g0154 | 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 | a0002c0002t0004g0151 a0002c0002t0004g0152 |
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:54040693 | G | C | 1 | a0001c0001t0007g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98+1938C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54040693 | |||||||
| chrX:54041240 | C | T | 1 | a0001c0001t0002g0121 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1356A>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041275 | |||||||
| chrX:54041406 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.98+1225T>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54041406 | |||||||
| chrX:54042062 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
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:54042272 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.98+359C>T | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 2/21 | chrX | 54042272 | |||||||
| chrX:54042372 | A | AG | 17 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | AG | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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:54042374 | G | T | 1 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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: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:54043128 | A | G | 1 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-309C>G | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043129 | |||||||
| chrX:54043656 | G | GC | 12 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0008g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-93+101G>C | PHF8 | ENSG00000172943.21 | transcript | ENST00000338154.11 | protein_coding | 1/21 | chrX | 54043661 |