Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5475 |
| ensemblid | ENSG00000086717.19 |
| hgncid | 9243 |
| symbol | PPEF1 |
| name | protein phosphatase with EF-hand domain 1 |
| refseq_nuc | NM_001377996.1 |
| refseq_prot | NP_001364925.1 |
| ensembl_nuc | ENST00000470157.2 |
| ensembl_prot | ENSP00000419273.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 18707645 |
| end | 18827917 |
| strand | + |
| ver | v1.2 |
| region | chrX:18707645-18827917 |
| region5000 | chrX:18702645-18832917 |
| regionname0 | PPEF1_chrX_18707645_18827917 |
| regionname5000 | PPEF1_chrX_18702645_18832917 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 653 | 217 | 57 | 37 | 96 | 6 | 19 | 74 | PPEF1_chrX_18702645_18832917 | PPEF1 | MGCSS others(648): Show |
chrX | 18702645 | 18832917 |
| a0002 | 0/0 | 653 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | MGCSS others(648): Show |
chrX | 18702645 | 18832917 |
| a0003 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | MGCSS others(648): Show |
chrX | 18702645 | 18832917 |
| a0004 | 0/0 | 653 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | MGCSS others(648): Show |
chrX | 18702645 | 18832917 |
| a0005 | 0/0 | 653 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | MGCSS others(648): Show |
chrX | 18702645 | 18832917 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1959 | 208 | 49 | 36 | 96 | 6 | 19 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0001c0003 | 0/0 | 1959 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0001c0004 | 0/0 | 1959 | 3 | 2 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0001c0005 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0001c0007 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0002c0002 | 0/0 | 1959 | 4 | 0 | 3 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0003c0006 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0004c0008 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 | ||
| a0005c0009 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | ATGGG others(1954): Show |
chrX | 18702645 | 18832917 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2528 | 204 | 49 | 36 | 93 | 5 | 19 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0001t0002 | 0/0 | 2528 | 2 | 0 | 0 | 2 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0001t0003 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0001t0004 | 0/0 | 2528 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0003t0001 | 0/0 | 2528 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0004t0001 | 0/0 | 2528 | 3 | 2 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0005t0001 | 0/0 | 2528 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0001c0007t0001 | 0/0 | 2528 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0002c0002t0001 | 0/0 | 2528 | 4 | 0 | 3 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0003c0006t0001 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0004c0008t0001 | 0/0 | 2528 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| a0005c0009t0001 | 0/0 | 2528 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | GTATT others(2523): Show |
chrX | 18702645 | 18832917 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0001g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0001c0007t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0003c0006t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0004c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| a0005c0009t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0073 | EUR | GBR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0118 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0090 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02015 | hp1 | a0003 | c0006 | t0001 | g0135 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0081 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02572 | hp1 | a0001 | c0007 | t0001 | g0082 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0185 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03516 | hp2 | a0004 | c0008 | t0001 | g0019 | AFR | ESN | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG04199 | hp1 | a0005 | c0009 | t0001 | g0214 | SAS | STU | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | LWK | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | ASW | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0005 | EUR | TSI | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0221 | REF | REF | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0060 | REF | REF | PPEF1_chrX_18702645_18832917 | PPEF1 | chrX | 18702645 | 18832917 |
| 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:18733793 | C | T | 1 | a0005 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.220C>T | p.His74Tyr | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/16 | 356/2528 | 220/1962 | 74/653 | chrX | 18733793 | |||
| chrX:18749827 | A | T | 1 | a0004 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.271A>T | p.Met91Leu | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/16 | 407/2528 | 271/1962 | 91/653 | chrX | 18749827 | |||
| chrX:18783953 | A | G | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.817A>G | p.Ile273Val | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/16 | 953/2528 | 817/1962 | 273/653 | chrX | 18783953 | |||
| chrX:18806478 | G | A | 1 | a0002 | 4 | HG00140.hp1 HG01074.hp1 HG01346.hp1 others(1): Show |
missense_variant | MODERATE | c.1327G>A | p.Gly443Ser | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/16 | 1463/2528 | 1327/1962 | 443/653 | chrX | 18806478 |
| 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:18749853 | C | T | 1 | a0001c0007 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.297C>T | p.Asp99Asp | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/16 | 433/2528 | 297/1962 | 99/653 | chrX | 18749853 | |||
| chrX:18779018 | C | T | 2 | a0001c0004 a0001c0007 |
4 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(1): Show |
synonymous_variant | LOW | c.567C>T | p.Leu189Leu | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/16 | 703/2528 | 567/1962 | 189/653 | chrX | 18779018 | |||
| chrX:18779087 | C | A | 1 | a0001c0005 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.636C>A | p.Ile212Ile | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/16 | 772/2528 | 636/1962 | 212/653 | chrX | 18779087 | |||
| chrX:18784036 | A | G | 1 | a0001c0003 | 4 | HG02451.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.900A>G | p.Val300Val | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/16 | 1036/2528 | 900/1962 | 300/653 | chrX | 18784036 |
| 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:18707679 | C | T | 1 | a0001c0001t0004 | 1 | NA20752.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-102C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/16 | chrX | 18707679 | |||||||
| chrX:18827620 | T | C | 1 | a0001c0001t0002 | 2 | HG00438.hp1 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*133T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 133 | chrX | 18827620 | ||||||
| chrX:18827871 | G | C | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 384 | chrX | 18827871 | ||||||
| chrX:18827872 | G | T | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 385 | chrX | 18827872 | ||||||
| chrX:18827877 | A | T | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 390 | chrX | 18827877 | ||||||
| chrX:18827878 | T | C | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 391 | chrX | 18827878 | ||||||
| chrX:18827879 | A | G | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 392 | chrX | 18827879 | ||||||
| chrX:18827881 | C | G | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 394 | chrX | 18827881 | ||||||
| chrX:18827882 | A | T | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 395 | chrX | 18827882 | ||||||
| chrX:18827884 | G | T | 1 | a0001c0001t0003 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*397G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 16/16 | 397 | chrX | 18827884 |
| 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:18708664 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0004g0005 |
2 | HG03490.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.46+838G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18708664 | |||||||
| chrX:18708789 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46+963T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18708789 | |||||||
| chrX:18708955 | T | A | 1 | a0001c0001t0001g0007 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.46+1129T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18708955 | |||||||
| chrX:18709115 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46+1289G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709115 | |||||||
| chrX:18709332 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.46+1506G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709332 | |||||||
| chrX:18709502 | G | GT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0078 others(118): Show |
122 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.46+1682dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18709502 | ||||||
| chrX:18709502 | G | GTT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0197 others(23): Show |
26 | HG00597.hp2 HG00741.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+1681_46+1682dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18709502 | ||||||
| chrX:18709509 | G | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
155 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.46+1683G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709509 | |||||||
| chrX:18709561 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.46+1735G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709561 | |||||||
| chrX:18709745 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.46+1919G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709745 | |||||||
| chrX:18709933 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.46+2107T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709933 | |||||||
| chrX:18709979 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02257.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.46+2153A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18709979 | |||||||
| chrX:18710485 | A | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.46+2659A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18710485 | |||||||
| chrX:18710547 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.46+2721T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18710547 | |||||||
| chrX:18710600 | G | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
35 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.46+2774G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18710600 | |||||||
| chrX:18710633 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0087 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.46+2807C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18710633 | |||||||
| chrX:18710892 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46+3066C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18710892 | |||||||
| chrX:18710915 | A | C | 16 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.46+3089A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18710915 | |||||||
| chrX:18710985 | A | AGT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(13): Show |
16 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.46+3172_46+3173dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18710985 | ||||||
| chrX:18711014 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.46+3188G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711014 | |||||||
| chrX:18711078 | ATG | A | 3 | a0001c0001t0001g0008 a0001c0004t0001g0081 a0001c0007t0001g0082 |
3 | HG02451.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.46+3266_46+3267del others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18711078 | ||||||
| chrX:18711090 | G | GTA | 107 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(104): Show |
108 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.46+3265_46+3266ins others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18711090 | ||||||
| chrX:18711090 | G | GTATA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0096 others(19): Show |
22 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.46+3265_46+3266ins others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18711090 | ||||||
| chrX:18711092 | G | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
148 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+3266G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711092 | |||||||
| chrX:18711092 | G | GTA | 2 | a0001c0001t0001g0017 a0001c0001t0001g0191 |
2 | HG00544.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.46+3280_46+3281dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18711092 | ||||||
| chrX:18711384 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00741.hp2 HG01081.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.46+3558A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711384 | |||||||
| chrX:18711400 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.46+3574G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711400 | |||||||
| chrX:18711490 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.46+3664G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711490 | |||||||
| chrX:18711586 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46+3760A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711586 | |||||||
| chrX:18711672 | A | ATGT | 155 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.46+3848_46+3850dup others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18711672 | ||||||
| chrX:18711754 | C | CT | 118 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(115): Show |
119 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.46+3945dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18711754 | ||||||
| chrX:18711878 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0076 others(16): Show |
19 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.46+4052C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711878 | |||||||
| chrX:18711995 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0087 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.46+4169G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711995 | |||||||
| chrX:18711999 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46+4173G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18711999 | |||||||
| chrX:18712216 | G | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0087 others(17): Show |
20 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.46+4390G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18712216 | |||||||
| chrX:18712733 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.46+4907T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18712733 | |||||||
| chrX:18712896 | T | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | NA18964.hp1 NA18969.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.46+5070T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18712896 | |||||||
| chrX:18713077 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.46+5251A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18713077 | |||||||
| chrX:18713165 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(18): Show |
21 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.46+5339C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18713165 | |||||||
| chrX:18713203 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.46+5377C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18713203 | |||||||
| chrX:18713334 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.46+5508T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18713334 | |||||||
| chrX:18713420 | C | CTTT | 6 | a0001c0001t0001g0102 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG00544.hp2 HG01109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+5610_46+5612dup others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713420 | C | CTTTT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(98): Show |
102 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.46+5609_46+5612dup others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713420 | C | CTTTTT | 5 | a0001c0001t0001g0008 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG01978.hp2 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+5608_46+5612dup others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713420 | C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0009 a0001c0001t0001g0188 a0001c0001t0001g0200 others(8): Show |
11 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.46+5603_46+5612dup others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713420 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(3): Show |
6 | HG02615.hp1 HG02886.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+5602_46+5612dup others(11): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713420 | C | CTTTTTTT others(7): Show |
1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.46+5599_46+5612dup others(14): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713420 | CTTTTTTT | C | 16 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.46+5606_46+5612del others(7): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18713420 | ||||||
| chrX:18713621 | A | G | 2 | a0001c0001t0001g0072 a0002c0002t0001g0073 |
2 | HG00140.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.46+5795A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18713621 | |||||||
| chrX:18713662 | T | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+5836T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18713662 | |||||||
| chrX:18714060 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.46+6234G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714060 | |||||||
| chrX:18714269 | G | GT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0078 others(82): Show |
86 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.46+6450dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18714269 | ||||||
| chrX:18714269 | G | GTT | 35 | a0001c0001t0001g0013 a0001c0001t0001g0080 a0001c0001t0001g0170 others(32): Show |
35 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.46+6449_46+6450dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18714269 | ||||||
| chrX:18714269 | G | GTTT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(6): Show |
9 | HG01081.hp1 HG01978.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.46+6448_46+6450dup others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18714269 | ||||||
| chrX:18714274 | TTTG | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02293.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+6451_46+6453del others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18714274 | ||||||
| chrX:18714277 | G | GT | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(41): Show |
45 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.46+6463dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18714277 | ||||||
| chrX:18714277 | G | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
132 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.46+6451G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714277 | |||||||
| chrX:18714298 | A | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
145 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.46+6472A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714298 | |||||||
| chrX:18714333 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
82 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.46+6507G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714333 | |||||||
| chrX:18714381 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.46+6555C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714381 | |||||||
| chrX:18714429 | G | A | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+6603G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714429 | |||||||
| chrX:18714514 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.46+6688G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714514 | |||||||
| chrX:18714634 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.46+6808T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714634 | |||||||
| chrX:18714643 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.46+6817A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714643 | |||||||
| chrX:18714657 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46+6831C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714657 | |||||||
| chrX:18714875 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.46+7049C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714875 | |||||||
| chrX:18714885 | C | G | 2 | a0001c0004t0001g0081 a0001c0007t0001g0082 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.46+7059C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18714885 | |||||||
| chrX:18715089 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.46+7263C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18715089 | |||||||
| chrX:18715138 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.46+7312G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18715138 | |||||||
| chrX:18715222 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.46+7396G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18715222 | |||||||
| chrX:18715397 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01496.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.46+7571C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18715397 | |||||||
| chrX:18715398 | G | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01496.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.46+7572G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18715398 | |||||||
| chrX:18715762 | T | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+7936T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18715762 | |||||||
| chrX:18716042 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46+8216G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716042 | |||||||
| chrX:18716259 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+8433G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716259 | |||||||
| chrX:18716303 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+8477C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716303 | |||||||
| chrX:18716511 | G | A | 1 | a0001c0004t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+8685G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716511 | |||||||
| chrX:18716531 | C | CA | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
10 | HG01515.hp1 HG01884.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+8728dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18716531 | ||||||
| chrX:18716531 | C | CAA | 17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(14): Show |
17 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.46+8727_46+8728dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18716531 | ||||||
| chrX:18716531 | CA | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(109): Show |
113 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.46+8728delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18716531 | ||||||
| chrX:18716531 | CAAAA | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+8725_46+8728del others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18716531 | ||||||
| chrX:18716558 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46+8732A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716558 | |||||||
| chrX:18716622 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02040.hp1 HG02129.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+8796C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716622 | |||||||
| chrX:18716668 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.46+8842C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716668 | |||||||
| chrX:18716856 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.46+9030G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18716856 | |||||||
| chrX:18717023 | G | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+9197G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717023 | |||||||
| chrX:18717067 | CT | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0087 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.46+9255delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18717067 | ||||||
| chrX:18717101 | A | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01070.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+9275A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717101 | |||||||
| chrX:18717103 | T | A | 1 | a0001c0004t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+9277T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717103 | |||||||
| chrX:18717144 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(13): Show |
16 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.46+9318C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717144 | |||||||
| chrX:18717253 | A | T | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+9427A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717253 | |||||||
| chrX:18717255 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+9429G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717255 | |||||||
| chrX:18717399 | C | G | 2 | a0001c0001t0001g0102 a0001c0007t0001g0082 |
2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.46+9573C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717399 | |||||||
| chrX:18717506 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.46+9680G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717506 | |||||||
| chrX:18717652 | C | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG01070.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+9826C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717652 | |||||||
| chrX:18717808 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.46+9982T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717808 | |||||||
| chrX:18717898 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46+10072A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717898 | |||||||
| chrX:18717902 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.46+10076C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717902 | |||||||
| chrX:18717933 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.46+10107C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18717933 | |||||||
| chrX:18718098 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.46+10272A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718098 | |||||||
| chrX:18718107 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.46+10281A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718107 | |||||||
| chrX:18718166 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.46+10340C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718166 | |||||||
| chrX:18718273 | C | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.46+10447C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718273 | |||||||
| chrX:18718319 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.46+10493C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718319 | |||||||
| chrX:18718342 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46+10516G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718342 | |||||||
| chrX:18718513 | C | A | 2 | a0001c0001t0001g0102 a0001c0007t0001g0082 |
2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.46+10687C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718513 | |||||||
| chrX:18718545 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.46+10719G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718545 | |||||||
| chrX:18718631 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.46+10805A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718631 | |||||||
| chrX:18718998 | G | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.46+11172G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18718998 | |||||||
| chrX:18719340 | CT | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(19): Show |
23 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.47-10824delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18719340 | ||||||
| chrX:18719372 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.47-10809G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18719372 | |||||||
| chrX:18719408 | G | A | 1 | a0002c0002t0001g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.47-10773G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18719408 | |||||||
| chrX:18719688 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.47-10493T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18719688 | |||||||
| chrX:18719937 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.47-10244G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18719937 | |||||||
| chrX:18720224 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.47-9957C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720224 | |||||||
| chrX:18720235 | GGA | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
93 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.47-9927_47-9926del others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18720235 | ||||||
| chrX:18720275 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
59 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.47-9906C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720275 | |||||||
| chrX:18720277 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47-9904A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720277 | |||||||
| chrX:18720324 | G | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.47-9857G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720324 | |||||||
| chrX:18720386 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.47-9795G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720386 | |||||||
| chrX:18720472 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
22 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.47-9709G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720472 | |||||||
| chrX:18720497 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 |
4 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-9684C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720497 | |||||||
| chrX:18720547 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-9634G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720547 | |||||||
| chrX:18720863 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
70 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.47-9318C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720863 | |||||||
| chrX:18720968 | G | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
69 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.47-9213G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18720968 | |||||||
| chrX:18721098 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.47-9083G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18721098 | |||||||
| chrX:18721229 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
69 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.47-8952C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18721229 | |||||||
| chrX:18721535 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.47-8646G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18721535 | |||||||
| chrX:18721565 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.47-8616G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18721565 | |||||||
| chrX:18721597 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.47-8584G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18721597 | |||||||
| chrX:18721939 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.47-8242C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18721939 | |||||||
| chrX:18722034 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.47-8147G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722034 | |||||||
| chrX:18722118 | C | T | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-8063C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722118 | |||||||
| chrX:18722205 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-7976A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722205 | |||||||
| chrX:18722333 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.47-7848C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722333 | |||||||
| chrX:18722355 | C | G | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-7826C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722355 | |||||||
| chrX:18722409 | G | C | 1 | a0001c0004t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.47-7772G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722409 | |||||||
| chrX:18722452 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.47-7729A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722452 | |||||||
| chrX:18722614 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47-7567T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722614 | |||||||
| chrX:18722690 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-7491A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722690 | |||||||
| chrX:18722715 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(78): Show |
83 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.47-7466G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722715 | |||||||
| chrX:18722824 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
82 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.47-7357A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722824 | |||||||
| chrX:18722842 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.47-7339G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722842 | |||||||
| chrX:18722907 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-7274G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18722907 | |||||||
| chrX:18722988 | A | AT | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
23 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.47-7179dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18722988 | ||||||
| chrX:18723023 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.47-7158C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723023 | |||||||
| chrX:18723071 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.47-7110G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723071 | |||||||
| chrX:18723164 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.47-7017T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723164 | |||||||
| chrX:18723230 | C | G | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-6951C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723230 | |||||||
| chrX:18723275 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.47-6906A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723275 | |||||||
| chrX:18723548 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-6633C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723548 | |||||||
| chrX:18723598 | A | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0123 |
3 | NA18984.hp1 NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.47-6583A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723598 | |||||||
| chrX:18723665 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.47-6516T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723665 | |||||||
| chrX:18723740 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.47-6441C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723740 | |||||||
| chrX:18723744 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.47-6437A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723744 | |||||||
| chrX:18723769 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.47-6412C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723769 | |||||||
| chrX:18723822 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
63 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.47-6359C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723822 | |||||||
| chrX:18723827 | T | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-6354T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723827 | |||||||
| chrX:18723872 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-6309C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723872 | |||||||
| chrX:18723880 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.47-6301A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723880 | |||||||
| chrX:18723916 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.47-6265A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723916 | |||||||
| chrX:18723984 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-6197C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18723984 | |||||||
| chrX:18724078 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG01070.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-6103G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724078 | |||||||
| chrX:18724220 | T | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.47-5961T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724220 | |||||||
| chrX:18724309 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.47-5872G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724309 | |||||||
| chrX:18724388 | G | T | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-5793G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724388 | |||||||
| chrX:18724389 | C | T | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-5792C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724389 | |||||||
| chrX:18724399 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.47-5782C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724399 | |||||||
| chrX:18724427 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-5754G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724427 | |||||||
| chrX:18724524 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-5657G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724524 | |||||||
| chrX:18724600 | C | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-5581C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724600 | |||||||
| chrX:18724635 | C | T | 2 | a0002c0002t0001g0039 a0002c0002t0001g0040 |
2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.47-5546C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724635 | |||||||
| chrX:18724636 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-5545G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724636 | |||||||
| chrX:18724777 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.47-5404G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724777 | |||||||
| chrX:18724778 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-5403G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724778 | |||||||
| chrX:18724815 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.47-5366T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724815 | |||||||
| chrX:18724902 | A | T | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-5279A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18724902 | |||||||
| chrX:18725169 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
92 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.47-5012T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18725169 | |||||||
| chrX:18725314 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-4867C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18725314 | |||||||
| chrX:18725315 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-4866G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18725315 | |||||||
| chrX:18725458 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.47-4723A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18725458 | |||||||
| chrX:18725597 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-4584G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18725597 | |||||||
| chrX:18726096 | C | T | 1 | a0005c0009t0001g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.47-4085C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18726096 | |||||||
| chrX:18726226 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.47-3955C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18726226 | |||||||
| chrX:18726351 | C | CAAAT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
53 | HG00544.hp1 HG00558.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-3789_47-3786dup others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18726351 | ||||||
| chrX:18726351 | C | CAAATAAA others(1): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0022 others(14): Show |
18 | HG01243.hp1 HG01346.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-3793_47-3786dup others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18726351 | ||||||
| chrX:18726351 | C | CAAATAAA others(5): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0200 a0001c0001t0001g0208 |
3 | HG01256.hp1 NA18612.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.47-3797_47-3786dup others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18726351 | ||||||
| chrX:18726351 | CAAAT | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0156 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-3789_47-3786del others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18726351 | ||||||
| chrX:18726351 | CAAATAAA others(1): Show |
C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0207 a0001c0001t0001g0209 |
3 | HG02738.hp1 HG04204.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.47-3793_47-3786del others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18726351 | ||||||
| chrX:18726568 | T | C | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.47-3613T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18726568 | |||||||
| chrX:18726662 | CT | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(74): Show |
78 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.47-3507delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18726662 | ||||||
| chrX:18726862 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.47-3319A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18726862 | |||||||
| chrX:18727014 | G | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG00558.hp1 HG03491.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.47-3167G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18727014 | |||||||
| chrX:18727029 | A | G | 2 | a0001c0004t0001g0081 a0001c0007t0001g0082 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.47-3152A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18727029 | |||||||
| chrX:18727246 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | NA18968.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.47-2935A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18727246 | |||||||
| chrX:18727479 | C | A | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.47-2702C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18727479 | |||||||
| chrX:18728015 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.47-2166C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728015 | |||||||
| chrX:18728124 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0188 a0001c0001t0001g0220 |
3 | NA18952.hp1 NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.47-2057A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728124 | |||||||
| chrX:18728143 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.47-2038C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728143 | |||||||
| chrX:18728156 | CCTCTCTC others(9): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.47-2010_47-1995del others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18728156 | ||||||
| chrX:18728184 | T | G | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.47-1997T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728184 | |||||||
| chrX:18728188 | GCT | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.47-1978_47-1977del others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18728188 | ||||||
| chrX:18728199 | C | CTA | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.47-1981_47-1980ins others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18728199 | ||||||
| chrX:18728201 | C | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
13 | HG01070.hp1 HG02257.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.47-1980C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728201 | |||||||
| chrX:18728203 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
87 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.47-1978C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728203 | |||||||
| chrX:18728203 | C | CTA | 2 | a0001c0001t0001g0210 a0001c0001t0001g0218 |
2 | HG00597.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.47-1968_47-1967dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chrX | 18728203 | ||||||
| chrX:18728205 | A | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0164 others(1): Show |
4 | HG02293.hp1 NA18956.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-1976A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728205 | |||||||
| chrX:18728256 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.47-1925C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728256 | |||||||
| chrX:18728595 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-1586C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728595 | |||||||
| chrX:18728706 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.47-1475G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728706 | |||||||
| chrX:18728842 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18959.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.47-1339A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728842 | |||||||
| chrX:18728845 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.47-1336G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18728845 | |||||||
| chrX:18729047 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.47-1134C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729047 | |||||||
| chrX:18729118 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-1063T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729118 | |||||||
| chrX:18729151 | C | CATACCAG | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
82 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.47-1030_47-1029ins others(7): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729151 | |||||||
| chrX:18729152 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
82 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.47-1029C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729152 | |||||||
| chrX:18729154 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(77): Show |
82 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.47-1027C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729154 | |||||||
| chrX:18729182 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.47-999A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729182 | |||||||
| chrX:18729268 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.47-913C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729268 | |||||||
| chrX:18729389 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.47-792G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729389 | |||||||
| chrX:18729603 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-578G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729603 | |||||||
| chrX:18729696 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.47-485A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729696 | |||||||
| chrX:18729893 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-288A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 1/15 | chrX | 18729893 | |||||||
| chrX:18730641 | A | G | 1 | a0001c0001t0003g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.174+333A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18730641 | |||||||
| chrX:18730673 | C | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG02055.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.174+365C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18730673 | |||||||
| chrX:18730727 | T | C | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+419T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18730727 | |||||||
| chrX:18730818 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.174+510G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18730818 | |||||||
| chrX:18730924 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.174+616A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18730924 | |||||||
| chrX:18731168 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.174+860T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18731168 | |||||||
| chrX:18731283 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.174+975G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18731283 | |||||||
| chrX:18731374 | T | TAAGAACA others(301): Show |
1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.174+1078_174+1079i others(310): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chrX | 18731374 | ||||||
| chrX:18731790 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.174+1482C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18731790 | |||||||
| chrX:18731956 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
97 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.174+1648A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18731956 | |||||||
| chrX:18731973 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.174+1665G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18731973 | |||||||
| chrX:18732110 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.175-1638C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18732110 | |||||||
| chrX:18732925 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.175-823C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18732925 | |||||||
| chrX:18733408 | A | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0209 |
2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.175-340A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18733408 | |||||||
| chrX:18733493 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175-255G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18733493 | |||||||
| chrX:18733497 | G | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0198 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-251G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18733497 | |||||||
| chrX:18733521 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG00597.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-227G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 2/15 | chrX | 18733521 | |||||||
| chrX:18734128 | T | TTTA | 3 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0197 |
3 | HG02886.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.235+337_235+339dup others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18734128 | ||||||
| chrX:18734128 | T | TTTATTA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
92 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.235+334_235+339dup others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18734128 | ||||||
| chrX:18734291 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+483A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734291 | |||||||
| chrX:18734424 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235+616C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734424 | |||||||
| chrX:18734531 | A | T | 3 | a0001c0001t0001g0102 a0001c0004t0001g0081 a0001c0007t0001g0082 |
3 | HG02451.hp2 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.235+723A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734531 | |||||||
| chrX:18734541 | G | C | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.235+733G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734541 | |||||||
| chrX:18734588 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.235+780T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734588 | |||||||
| chrX:18734590 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.235+782C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734590 | |||||||
| chrX:18734649 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.235+841C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734649 | |||||||
| chrX:18734723 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.235+915G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734723 | |||||||
| chrX:18734735 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+927A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734735 | |||||||
| chrX:18734756 | C | G | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.235+948C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734756 | |||||||
| chrX:18734761 | C | T | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+953C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734761 | |||||||
| chrX:18734906 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.235+1098G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18734906 | |||||||
| chrX:18735114 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0102 others(12): Show |
15 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+1306G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735114 | |||||||
| chrX:18735169 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.235+1361T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735169 | |||||||
| chrX:18735199 | G | T | 3 | a0001c0001t0001g0102 a0001c0004t0001g0081 a0001c0007t0001g0082 |
3 | HG02451.hp2 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.235+1391G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735199 | |||||||
| chrX:18735242 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+1434A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735242 | |||||||
| chrX:18735693 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+1885C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735693 | |||||||
| chrX:18735868 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02040.hp1 HG02129.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+2060G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735868 | |||||||
| chrX:18735941 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235+2133G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18735941 | |||||||
| chrX:18736037 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.235+2229A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736037 | |||||||
| chrX:18736066 | G | A | 1 | a0003c0006t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.235+2258G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736066 | |||||||
| chrX:18736087 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
92 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.235+2279G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736087 | |||||||
| chrX:18736090 | T | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
93 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.235+2282T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736090 | |||||||
| chrX:18736123 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0189 a0001c0005t0001g0185 |
3 | HG02647.hp1 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.235+2315T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736123 | |||||||
| chrX:18736580 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.235+2772C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736580 | |||||||
| chrX:18736779 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.235+2971G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736779 | |||||||
| chrX:18736927 | A | G | 8 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
8 | HG02071.hp1 NA18955.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+3119A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736927 | |||||||
| chrX:18736966 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.235+3158G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18736966 | |||||||
| chrX:18737122 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235+3314T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737122 | |||||||
| chrX:18737222 | G | A | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+3414G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737222 | |||||||
| chrX:18737491 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.235+3683G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737491 | |||||||
| chrX:18737570 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+3762T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737570 | |||||||
| chrX:18737663 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.235+3855G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737663 | |||||||
| chrX:18737775 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
94 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.235+3967A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737775 | |||||||
| chrX:18737778 | C | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
94 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.235+3970C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737778 | |||||||
| chrX:18737905 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0003g0219 |
2 | NA18962.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.235+4097C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737905 | |||||||
| chrX:18737976 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.235+4168G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18737976 | |||||||
| chrX:18738051 | A | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0198 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.235+4243A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738051 | |||||||
| chrX:18738116 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
94 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.235+4308T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738116 | |||||||
| chrX:18738151 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0159 a0001c0001t0001g0192 |
3 | HG02717.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.235+4343A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738151 | |||||||
| chrX:18738161 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.235+4353G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738161 | |||||||
| chrX:18738182 | T | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+4374T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738182 | |||||||
| chrX:18738191 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.235+4383C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738191 | |||||||
| chrX:18738192 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.235+4384G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738192 | |||||||
| chrX:18738220 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0077 |
3 | NA18941.hp2 NA18999.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.235+4412C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738220 | |||||||
| chrX:18738713 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.235+4905A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18738713 | |||||||
| chrX:18739087 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.235+5279C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739087 | |||||||
| chrX:18739176 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.235+5368G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739176 | |||||||
| chrX:18739202 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0198 a0001c0001t0001g0199 others(9): Show |
12 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+5394A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739202 | |||||||
| chrX:18739420 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+5612A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739420 | |||||||
| chrX:18739515 | C | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.235+5707C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739515 | |||||||
| chrX:18739517 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(8): Show |
12 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+5709T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739517 | |||||||
| chrX:18739537 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01070.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.235+5729C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739537 | |||||||
| chrX:18739574 | C | T | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+5766C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739574 | |||||||
| chrX:18739963 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.235+6155C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739963 | |||||||
| chrX:18739968 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.235+6160G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18739968 | |||||||
| chrX:18740068 | A | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.235+6260A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740068 | |||||||
| chrX:18740097 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.235+6289C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740097 | |||||||
| chrX:18740134 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(44): Show |
48 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.235+6326C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740134 | |||||||
| chrX:18740210 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.235+6402G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740210 | |||||||
| chrX:18740248 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.235+6440C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740248 | |||||||
| chrX:18740261 | A | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.235+6453A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740261 | |||||||
| chrX:18740381 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235+6573C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740381 | |||||||
| chrX:18740410 | TCTC | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(1): Show |
4 | HG02559.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+6603_235+6605d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740410 | |||||||
| chrX:18740413 | C | CT | 43 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
44 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.235+6619dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18740413 | ||||||
| chrX:18740440 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+6632C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740440 | |||||||
| chrX:18740441 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0176 |
2 | HG00609.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.235+6633G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740441 | |||||||
| chrX:18740444 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235+6636C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740444 | |||||||
| chrX:18740473 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+6665G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740473 | |||||||
| chrX:18740608 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.235+6800A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740608 | |||||||
| chrX:18740916 | A | AT | 11 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0102 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+7130dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18740916 | ||||||
| chrX:18740916 | AT | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0131 others(3): Show |
6 | HG00558.hp1 HG01943.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+7130delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18740916 | ||||||
| chrX:18740916 | ATT | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(9): Show |
13 | HG00741.hp1 HG01081.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+7129_235+7130d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18740916 | ||||||
| chrX:18740916 | ATTT | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(71): Show |
75 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.235+7128_235+7130d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18740916 | ||||||
| chrX:18740988 | G | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.235+7180G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18740988 | |||||||
| chrX:18741067 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.235+7259A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741067 | |||||||
| chrX:18741324 | C | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(14): Show |
17 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+7516C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741324 | |||||||
| chrX:18741365 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.235+7557A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741365 | |||||||
| chrX:18741424 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235+7616G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741424 | |||||||
| chrX:18741762 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+7954G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741762 | |||||||
| chrX:18741768 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
92 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.235+7960G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741768 | |||||||
| chrX:18741772 | C | CT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0054 others(5): Show |
8 | HG00544.hp1 HG00597.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+7988dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18741772 | ||||||
| chrX:18741772 | CT | C | 24 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0042 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.235+7988delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18741772 | ||||||
| chrX:18741852 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236-7940G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741852 | |||||||
| chrX:18741951 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236-7841G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18741951 | |||||||
| chrX:18742128 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
49 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.236-7664A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18742128 | |||||||
| chrX:18742351 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236-7441A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18742351 | |||||||
| chrX:18742708 | GTGTGTTG others(9): Show |
G | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236-7080_236-7065d others(18): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18742708 | ||||||
| chrX:18742814 | A | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(52): Show |
56 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.236-6978A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18742814 | |||||||
| chrX:18742850 | GA | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.236-6927delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18742850 | ||||||
| chrX:18742933 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.236-6859A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18742933 | |||||||
| chrX:18743446 | C | CT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
13 | HG01070.hp1 HG01106.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-6325dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18743446 | ||||||
| chrX:18743446 | C | CTTTTTTT others(8): Show |
1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236-6339_236-6325d others(17): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18743446 | ||||||
| chrX:18743446 | C | CTTTTTTT others(9): Show |
1 | a0001c0004t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236-6340_236-6325d others(18): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18743446 | ||||||
| chrX:18743446 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0025 |
3 | HG01243.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.236-6341_236-6325d others(19): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18743446 | ||||||
| chrX:18743446 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.236-6342_236-6325d others(20): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18743446 | ||||||
| chrX:18743446 | CT | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(50): Show |
54 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.236-6325delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18743446 | ||||||
| chrX:18743450 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.236-6342T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18743450 | |||||||
| chrX:18743452 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.236-6340T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18743452 | |||||||
| chrX:18743561 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.236-6231T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18743561 | |||||||
| chrX:18743568 | G | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG02293.hp1 NA18956.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-6224G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18743568 | |||||||
| chrX:18743645 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236-6147C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18743645 | |||||||
| chrX:18744000 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00558.hp2 HG00597.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-5792C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18744000 | |||||||
| chrX:18744138 | G | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
28 | HG00140.hp1 HG01070.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.236-5654G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18744138 | |||||||
| chrX:18744186 | C | T | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236-5606C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18744186 | |||||||
| chrX:18744438 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.236-5354T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18744438 | |||||||
| chrX:18744505 | A | G | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.236-5287A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18744505 | |||||||
| chrX:18744618 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236-5174T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18744618 | |||||||
| chrX:18744717 | GT | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0184 |
3 | HG00738.hp1 HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.236-5072delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18744717 | ||||||
| chrX:18744771 | GTAA | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0198 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-5012_236-5010d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18744771 | ||||||
| chrX:18745088 | A | AATATATA others(44): Show |
3 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG01109.hp1 HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.236-4684_236-4634d others(53): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18745088 | ||||||
| chrX:18745096 | T | TTATATAT others(15): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0044 |
2 | HG02132.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.236-4660_236-4639d others(24): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18745096 | ||||||
| chrX:18745118 | ATATATAT others(22): Show |
A | 1 | a0001c0004t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.236-4662_236-4634d others(31): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chrX | 18745118 | ||||||
| chrX:18745161 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236-4631A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18745161 | |||||||
| chrX:18745333 | G | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
61 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.236-4459G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18745333 | |||||||
| chrX:18745360 | C | T | 1 | a0002c0002t0001g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.236-4432C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18745360 | |||||||
| chrX:18745361 | G | A | 1 | a0001c0004t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236-4431G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18745361 | |||||||
| chrX:18745427 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.236-4365T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18745427 | |||||||
| chrX:18745994 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0206 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.236-3798T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18745994 | |||||||
| chrX:18746237 | A | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0138 a0001c0001t0001g0193 others(1): Show |
4 | HG02602.hp1 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-3555A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746237 | |||||||
| chrX:18746334 | A | C | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-3458A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746334 | |||||||
| chrX:18746438 | C | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.236-3354C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746438 | |||||||
| chrX:18746501 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.236-3291C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746501 | |||||||
| chrX:18746526 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.236-3266T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746526 | |||||||
| chrX:18746735 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.236-3057T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746735 | |||||||
| chrX:18746756 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(44): Show |
48 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.236-3036C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18746756 | |||||||
| chrX:18747191 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
63 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.236-2601G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18747191 | |||||||
| chrX:18747194 | A | T | 1 | a0001c0004t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236-2598A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18747194 | |||||||
| chrX:18747273 | A | T | 2 | a0001c0004t0001g0081 a0001c0007t0001g0082 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.236-2519A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18747273 | |||||||
| chrX:18747620 | C | T | 2 | a0001c0004t0001g0081 a0001c0007t0001g0082 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.236-2172C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18747620 | |||||||
| chrX:18748665 | T | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0198 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-1127T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18748665 | |||||||
| chrX:18748953 | A | C | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.236-839A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18748953 | |||||||
| chrX:18748954 | A | G | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-838A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18748954 | |||||||
| chrX:18749241 | C | G | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236-551C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18749241 | |||||||
| chrX:18749281 | A | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
67 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.236-511A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18749281 | |||||||
| chrX:18749301 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.236-491C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18749301 | |||||||
| chrX:18749682 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.236-110C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18749682 | |||||||
| chrX:18749759 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.236-33C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18749759 | |||||||
| chrX:18749763 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.236-29A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 3/15 | chrX | 18749763 | |||||||
| chrX:18750132 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.396+180T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18750132 | |||||||
| chrX:18750312 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.396+360G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18750312 | |||||||
| chrX:18750747 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.396+795A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18750747 | |||||||
| chrX:18750852 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.396+900T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18750852 | |||||||
| chrX:18750857 | T | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.396+905T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18750857 | |||||||
| chrX:18751490 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.396+1538A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18751490 | |||||||
| chrX:18751697 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.396+1745T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18751697 | |||||||
| chrX:18751721 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(53): Show |
57 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.396+1769A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18751721 | |||||||
| chrX:18751916 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.396+1964G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18751916 | |||||||
| chrX:18751965 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.396+2013A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18751965 | |||||||
| chrX:18752390 | C | T | 4 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.396+2438C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18752390 | |||||||
| chrX:18752447 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.396+2495T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18752447 | |||||||
| chrX:18752534 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.396+2582G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18752534 | |||||||
| chrX:18752567 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.396+2615G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18752567 | |||||||
| chrX:18752727 | C | CT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(60): Show |
64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.396+2789dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chrX | 18752727 | ||||||
| chrX:18752727 | C | CTT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
8 | HG01243.hp1 HG01981.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.396+2788_396+2789d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chrX | 18752727 | ||||||
| chrX:18752789 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.396+2837G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18752789 | |||||||
| chrX:18752931 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.396+2979A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18752931 | |||||||
| chrX:18753315 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
63 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.396+3363T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18753315 | |||||||
| chrX:18753432 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0098 a0001c0001t0001g0102 others(4): Show |
7 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.396+3480T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18753432 | |||||||
| chrX:18753471 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.396+3519A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18753471 | |||||||
| chrX:18753720 | A | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0198 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.396+3768A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18753720 | |||||||
| chrX:18753935 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
96 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.397-3692A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18753935 | |||||||
| chrX:18754052 | TA | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(55): Show |
59 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.397-3560delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chrX | 18754052 | ||||||
| chrX:18754578 | ATTGT | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(53): Show |
57 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.397-3043_397-3040d others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chrX | 18754578 | ||||||
| chrX:18754685 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.397-2942C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18754685 | |||||||
| chrX:18755028 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.397-2599C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755028 | |||||||
| chrX:18755182 | T | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-2445T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755182 | |||||||
| chrX:18755189 | T | TA | 7 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
8 | HG00544.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.397-2428dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chrX | 18755189 | ||||||
| chrX:18755304 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.397-2323C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755304 | |||||||
| chrX:18755332 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.397-2295C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755332 | |||||||
| chrX:18755572 | G | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.397-2055G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755572 | |||||||
| chrX:18755573 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
33 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.397-2054C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755573 | |||||||
| chrX:18755969 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(43): Show |
47 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.397-1658A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18755969 | |||||||
| chrX:18756075 | G | A | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.397-1552G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18756075 | |||||||
| chrX:18756241 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.397-1386G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18756241 | |||||||
| chrX:18756391 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.397-1236G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18756391 | |||||||
| chrX:18756431 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(45): Show |
49 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.397-1196C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18756431 | |||||||
| chrX:18757007 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.397-620C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18757007 | |||||||
| chrX:18757252 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.397-375C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18757252 | |||||||
| chrX:18757448 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.397-179T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18757448 | |||||||
| chrX:18757561 | T | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.397-66T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 4/15 | chrX | 18757561 | |||||||
| chrX:18758289 | GAAAC | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0193 others(1): Show |
4 | HG01496.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.511+550_511+553del others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chrX | 18758289 | ||||||
| chrX:18758511 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.511+770A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18758511 | |||||||
| chrX:18758560 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+819C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18758560 | |||||||
| chrX:18758816 | C | T | 2 | a0001c0004t0001g0081 a0001c0007t0001g0082 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.511+1075C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18758816 | |||||||
| chrX:18758931 | C | T | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.511+1190C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18758931 | |||||||
| chrX:18759089 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.511+1348T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759089 | |||||||
| chrX:18759319 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.511+1578G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759319 | |||||||
| chrX:18759353 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(56): Show |
60 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.511+1612C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759353 | |||||||
| chrX:18759383 | G | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+1642G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759383 | |||||||
| chrX:18759709 | G | C | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.512-1821G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759709 | |||||||
| chrX:18759719 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.512-1811T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759719 | |||||||
| chrX:18759766 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.512-1764T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759766 | |||||||
| chrX:18759846 | G | A | 2 | a0001c0004t0001g0081 a0001c0007t0001g0082 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.512-1684G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18759846 | |||||||
| chrX:18760026 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.512-1504C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18760026 | |||||||
| chrX:18760424 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(56): Show |
60 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.512-1106A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18760424 | |||||||
| chrX:18760760 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-770C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18760760 | |||||||
| chrX:18760777 | A | AT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(8): Show |
11 | HG00741.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.512-733dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chrX | 18760777 | ||||||
| chrX:18760777 | A | ATT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
54 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.512-734_512-733dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chrX | 18760777 | ||||||
| chrX:18760777 | A | ATTT | 5 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0049 others(2): Show |
5 | HG01106.hp1 HG03654.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-735_512-733dup others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chrX | 18760777 | ||||||
| chrX:18761020 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(44): Show |
48 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.512-510A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18761020 | |||||||
| chrX:18761229 | T | G | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.512-301T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18761229 | |||||||
| chrX:18761262 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-268C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18761262 | |||||||
| chrX:18761282 | C | A | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.512-248C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 5/15 | chrX | 18761282 | |||||||
| chrX:18761603 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.558+27A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18761603 | |||||||
| chrX:18761652 | T | C | 1 | a0001c0004t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.558+76T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18761652 | |||||||
| chrX:18761729 | C | CT | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(45): Show |
49 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.558+165dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18761729 | ||||||
| chrX:18761764 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
13 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+188A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18761764 | |||||||
| chrX:18761797 | A | G | 1 | a0001c0007t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.558+221A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18761797 | |||||||
| chrX:18761815 | A | G | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.558+239A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18761815 | |||||||
| chrX:18761821 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(44): Show |
48 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.558+245A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18761821 | |||||||
| chrX:18762062 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(99): Show |
104 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.558+486A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762062 | |||||||
| chrX:18762142 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.558+566A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762142 | |||||||
| chrX:18762282 | CA | C | 2 | a0001c0001t0001g0008 a0004c0008t0001g0019 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.558+707delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762282 | |||||||
| chrX:18762574 | CAT | C | 4 | a0001c0004t0001g0081 a0001c0004t0001g0090 a0001c0004t0001g0118 others(1): Show |
4 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+999_558+1000de others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762574 | |||||||
| chrX:18762645 | A | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+1069A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762645 | |||||||
| chrX:18762825 | G | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
49 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.558+1249G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762825 | |||||||
| chrX:18762868 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.558+1292C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762868 | |||||||
| chrX:18762910 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.558+1334C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18762910 | |||||||
| chrX:18763149 | C | T | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.558+1573C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18763149 | |||||||
| chrX:18763165 | A | G | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0057 others(12): Show |
15 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+1589A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18763165 | |||||||
| chrX:18763587 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(76): Show |
80 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.558+2011A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18763587 | |||||||
| chrX:18763632 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01070.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.558+2056A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18763632 | |||||||
| chrX:18763919 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(62): Show |
66 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.558+2343C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18763919 | |||||||
| chrX:18764103 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.558+2527G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764103 | |||||||
| chrX:18764248 | T | G | 4 | a0001c0001t0001g0210 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+2672T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764248 | |||||||
| chrX:18764625 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(62): Show |
66 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.558+3049T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764625 | |||||||
| chrX:18764662 | G | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+3086G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764662 | |||||||
| chrX:18764672 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+3096T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764672 | |||||||
| chrX:18764778 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
114 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.558+3202C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764778 | |||||||
| chrX:18764823 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.558+3247A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764823 | |||||||
| chrX:18764859 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
68 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.558+3283G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18764859 | |||||||
| chrX:18765023 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG01106.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.558+3447G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18765023 | |||||||
| chrX:18765177 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.558+3601G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18765177 | |||||||
| chrX:18765269 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
67 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.558+3693G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18765269 | |||||||
| chrX:18765481 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.558+3905G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18765481 | |||||||
| chrX:18765609 | AAAG | A | 4 | a0001c0004t0001g0081 a0001c0004t0001g0090 a0001c0004t0001g0118 others(1): Show |
4 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+4039_558+4041d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18765609 | ||||||
| chrX:18765965 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02257.hp1 HG02293.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.558+4389C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18765965 | |||||||
| chrX:18766064 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+4488T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18766064 | |||||||
| chrX:18766065 | CA | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG00621.hp1 HG01928.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+4508delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18766065 | ||||||
| chrX:18766065 | CAA | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(53): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.558+4507_558+4508d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18766065 | ||||||
| chrX:18766065 | CAAAAAAA | C | 6 | a0001c0001t0002g0173 a0001c0001t0002g0216 a0001c0004t0001g0081 others(3): Show |
6 | HG00438.hp1 HG01106.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+4502_558+4508d others(9): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18766065 | ||||||
| chrX:18766081 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.558+4505A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18766081 | |||||||
| chrX:18766268 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(48): Show |
52 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.558+4692C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18766268 | |||||||
| chrX:18766776 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.558+5200C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18766776 | |||||||
| chrX:18766786 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+5210C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18766786 | |||||||
| chrX:18766893 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.558+5326delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18766893 | ||||||
| chrX:18767083 | AAGAC | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0120 others(2): Show |
5 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+5511_558+5514d others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18767083 | ||||||
| chrX:18767481 | G | T | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.558+5905G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18767481 | |||||||
| chrX:18767500 | G | A | 1 | a0001c0004t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.558+5924G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18767500 | |||||||
| chrX:18767833 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0203 |
3 | HG02615.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.558+6257G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18767833 | |||||||
| chrX:18767907 | A | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
72 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.558+6331A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18767907 | |||||||
| chrX:18768089 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(48): Show |
52 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.558+6513A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18768089 | |||||||
| chrX:18768488 | G | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0203 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.558+6912G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18768488 | |||||||
| chrX:18768867 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+7291G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18768867 | |||||||
| chrX:18769636 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.558+8060A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18769636 | |||||||
| chrX:18769951 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0077 |
3 | NA18941.hp2 NA18999.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.558+8375T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18769951 | |||||||
| chrX:18769989 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.558+8413A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18769989 | |||||||
| chrX:18770072 | G | A | 4 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+8496G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18770072 | |||||||
| chrX:18770828 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0124 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-8182T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18770828 | |||||||
| chrX:18770901 | T | G | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-8109T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18770901 | |||||||
| chrX:18771288 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0203 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-7722A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771288 | |||||||
| chrX:18771320 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559-7690C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771320 | |||||||
| chrX:18771395 | T | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-7615T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771395 | |||||||
| chrX:18771515 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
78 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.559-7495T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771515 | |||||||
| chrX:18771659 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.559-7351A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771659 | |||||||
| chrX:18771704 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.559-7306A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771704 | |||||||
| chrX:18771723 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-7287C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771723 | |||||||
| chrX:18771912 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559-7098C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18771912 | |||||||
| chrX:18772035 | G | A | 1 | a0005c0009t0001g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.559-6975G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18772035 | |||||||
| chrX:18772225 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): Show |
108 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.559-6785T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18772225 | |||||||
| chrX:18772577 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.559-6433G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18772577 | |||||||
| chrX:18772800 | T | C | 5 | a0001c0001t0001g0072 a0002c0002t0001g0028 a0002c0002t0001g0039 others(2): Show |
5 | HG00140.hp1 HG01074.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-6210T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18772800 | |||||||
| chrX:18773638 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559-5372T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18773638 | |||||||
| chrX:18773931 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.559-5079C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18773931 | |||||||
| chrX:18774018 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(61): Show |
66 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.559-4992A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18774018 | |||||||
| chrX:18774088 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559-4922T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18774088 | |||||||
| chrX:18774723 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
78 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.559-4287A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18774723 | |||||||
| chrX:18774862 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.559-4148G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18774862 | |||||||
| chrX:18774956 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.559-4054C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18774956 | |||||||
| chrX:18775211 | C | CT | 40 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(37): Show |
40 | HG00673.hp1 HG00741.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.559-3775dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18775211 | ||||||
| chrX:18775211 | C | CTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
63 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.559-3776_559-3775d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18775211 | ||||||
| chrX:18775211 | C | CTTT | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(15): Show |
18 | HG01243.hp1 HG01496.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.559-3777_559-3775d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18775211 | ||||||
| chrX:18775211 | CT | C | 6 | a0001c0001t0001g0059 a0001c0001t0001g0070 a0001c0001t0001g0166 others(3): Show |
6 | HG02451.hp1 HG02976.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-3775delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18775211 | ||||||
| chrX:18775373 | GCCACCAC others(2514): Show |
G | 1 | a0001c0005t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.559-3614_559-1094d others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18775373 | ||||||
| chrX:18775813 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559-3197C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18775813 | |||||||
| chrX:18775969 | G | GCT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
78 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.559-3040_559-3039d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18775969 | ||||||
| chrX:18775978 | G | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-3032G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18775978 | |||||||
| chrX:18776209 | G | GTGGT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
63 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.559-2767_559-2764d others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18776209 | ||||||
| chrX:18776209 | G | GTGGTTGG others(1): Show |
14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0017 others(11): Show |
14 | HG00544.hp1 HG01515.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.559-2771_559-2764d others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18776209 | ||||||
| chrX:18776209 | GTGGT | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0154 a0001c0001t0001g0164 others(3): Show |
6 | HG01346.hp2 HG02293.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.559-2767_559-2764d others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chrX | 18776209 | ||||||
| chrX:18776227 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.559-2783G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18776227 | |||||||
| chrX:18776247 | T | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
78 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.559-2763T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18776247 | |||||||
| chrX:18776696 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.559-2314G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18776696 | |||||||
| chrX:18776719 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.559-2291A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18776719 | |||||||
| chrX:18776876 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.559-2134C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18776876 | |||||||
| chrX:18777529 | T | A | 5 | a0001c0001t0001g0197 a0001c0003t0001g0084 a0001c0003t0001g0085 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-1481T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18777529 | |||||||
| chrX:18777542 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559-1468C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18777542 | |||||||
| chrX:18777681 | G | A | 2 | a0001c0001t0001g0072 a0002c0002t0001g0073 |
2 | HG00140.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.559-1329G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18777681 | |||||||
| chrX:18777975 | A | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.559-1035A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18777975 | |||||||
| chrX:18778286 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.559-724C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18778286 | |||||||
| chrX:18778908 | C | G | 4 | a0001c0004t0001g0081 a0001c0004t0001g0090 a0001c0004t0001g0118 others(1): Show |
4 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-102C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18778908 | |||||||
| chrX:18778967 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559-43A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 6/15 | chrX | 18778967 | |||||||
| chrX:18779215 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.725+39G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18779215 | |||||||
| chrX:18779308 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.725+132A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18779308 | |||||||
| chrX:18779495 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.725+319G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18779495 | |||||||
| chrX:18779625 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.725+449C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18779625 | |||||||
| chrX:18780072 | T | C | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.725+896T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18780072 | |||||||
| chrX:18780102 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.725+926G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18780102 | |||||||
| chrX:18780139 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.725+963C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18780139 | |||||||
| chrX:18780605 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
68 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.725+1429G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18780605 | |||||||
| chrX:18780772 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01070.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.726-1594C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18780772 | |||||||
| chrX:18780913 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.726-1453G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18780913 | |||||||
| chrX:18781061 | C | CA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0004t0001g0081 others(3): Show |
6 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-1296dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chrX | 18781061 | ||||||
| chrX:18781071 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01070.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.726-1295G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781071 | |||||||
| chrX:18781131 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.726-1235C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781131 | |||||||
| chrX:18781255 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
85 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.726-1111A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781255 | |||||||
| chrX:18781387 | T | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.726-979T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781387 | |||||||
| chrX:18781431 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0208 |
2 | NA18612.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.726-935T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781431 | |||||||
| chrX:18781767 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
79 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.726-599G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781767 | |||||||
| chrX:18781791 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.726-575G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781791 | |||||||
| chrX:18781920 | GTTGTTCA others(9): Show |
G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.726-427_726-412del others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chrX | 18781920 | ||||||
| chrX:18781966 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.726-400T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18781966 | |||||||
| chrX:18782157 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.726-209C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18782157 | |||||||
| chrX:18782292 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.726-74G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 7/15 | chrX | 18782292 | |||||||
| chrX:18782413 | CT | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(65): Show |
69 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.762+27delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chrX | 18782413 | ||||||
| chrX:18782569 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.762+167G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18782569 | |||||||
| chrX:18782591 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.762+189T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18782591 | |||||||
| chrX:18782884 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
221 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.762+482C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18782884 | |||||||
| chrX:18782889 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.762+487G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18782889 | |||||||
| chrX:18782910 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.762+508C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18782910 | |||||||
| chrX:18782911 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+509G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18782911 | |||||||
| chrX:18783111 | C | CA | 10 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.762+727dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chrX | 18783111 | ||||||
| chrX:18783111 | CA | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
71 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.762+727delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chrX | 18783111 | ||||||
| chrX:18783185 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763-714C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18783185 | |||||||
| chrX:18783370 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-529G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | chrX | 18783370 | |||||||
| chrX:18783715 | C | CA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(64): Show |
69 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.763-174dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chrX | 18783715 | ||||||
| chrX:18784223 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.912+175T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18784223 | |||||||
| chrX:18784548 | C | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0190 |
3 | HG02630.hp2 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.912+500C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18784548 | |||||||
| chrX:18785274 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.912+1226G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18785274 | |||||||
| chrX:18785311 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.912+1263A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18785311 | |||||||
| chrX:18785569 | C | T | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0094 others(4): Show |
7 | HG02572.hp1 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.912+1521C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18785569 | |||||||
| chrX:18785991 | A | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.912+1943A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18785991 | |||||||
| chrX:18786061 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.912+2013G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786061 | |||||||
| chrX:18786075 | G | T | 1 | a0001c0004t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.912+2027G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786075 | |||||||
| chrX:18786282 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.912+2234A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786282 | |||||||
| chrX:18786438 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.912+2390A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786438 | |||||||
| chrX:18786655 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0004c0008t0001g0019 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.913-2466C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786655 | |||||||
| chrX:18786780 | C | CA | 8 | a0001c0001t0001g0078 a0001c0001t0001g0101 a0001c0001t0001g0133 others(5): Show |
8 | HG00738.hp1 HG01192.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-2321dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18786780 | ||||||
| chrX:18786795 | AAAAAAG | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
77 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.913-2321_913-2316d others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18786795 | ||||||
| chrX:18786939 | C | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(78): Show |
83 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.913-2182C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786939 | |||||||
| chrX:18786943 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
75 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.913-2178T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786943 | |||||||
| chrX:18786960 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.913-2161G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786960 | |||||||
| chrX:18786968 | C | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0189 others(2): Show |
5 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-2153C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18786968 | |||||||
| chrX:18787232 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.913-1889T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787232 | |||||||
| chrX:18787380 | G | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0062 others(59): Show |
62 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.913-1741G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787380 | |||||||
| chrX:18787483 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.913-1638A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787483 | |||||||
| chrX:18787594 | C | A | 1 | a0005c0009t0001g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.913-1527C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787594 | |||||||
| chrX:18787756 | C | CA | 65 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0059 others(62): Show |
65 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.913-1350dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18787756 | ||||||
| chrX:18787756 | C | CAA | 9 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0117 others(6): Show |
9 | HG02602.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1351_913-1350d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18787756 | ||||||
| chrX:18787768 | A | AG | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(68): Show |
72 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.913-1353_913-1352i others(3): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787768 | |||||||
| chrX:18787832 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(69): Show |
73 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.913-1289C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787832 | |||||||
| chrX:18787898 | A | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0059 others(60): Show |
63 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.913-1223A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18787898 | |||||||
| chrX:18788042 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0120 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.913-1079T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788042 | |||||||
| chrX:18788045 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0172 a0004c0008t0001g0019 |
3 | HG03516.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.913-1076A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788045 | |||||||
| chrX:18788052 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.913-1069C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788052 | |||||||
| chrX:18788054 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.913-1067C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788054 | |||||||
| chrX:18788062 | A | T | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.913-1059A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788062 | |||||||
| chrX:18788066 | G | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.913-1055G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788066 | |||||||
| chrX:18788066 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18945.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.913-1055G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788066 | |||||||
| chrX:18788098 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-1023C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788098 | |||||||
| chrX:18788133 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0037 others(5): Show |
8 | HG00741.hp2 HG01081.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.913-988G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788133 | |||||||
| chrX:18788138 | C | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(74): Show |
78 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.913-983C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788138 | |||||||
| chrX:18788150 | T | A | 3 | a0001c0001t0001g0011 a0001c0003t0001g0119 a0001c0004t0001g0081 |
3 | HG02451.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.913-971T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788150 | |||||||
| chrX:18788179 | T | C | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.913-942T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788179 | |||||||
| chrX:18788183 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.913-938G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788183 | |||||||
| chrX:18788185 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-936C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788185 | |||||||
| chrX:18788186 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.913-935G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788186 | |||||||
| chrX:18788259 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.913-862C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788259 | |||||||
| chrX:18788267 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.913-854T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788267 | |||||||
| chrX:18788273 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.913-848C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788273 | |||||||
| chrX:18788288 | G | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0117 a0001c0001t0001g0120 |
3 | HG02615.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.913-833G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788288 | |||||||
| chrX:18788304 | C | CA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.913-794dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18788304 | ||||||
| chrX:18788304 | C | CAA | 27 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0027 others(24): Show |
27 | HG00438.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.913-795_913-794dup others(2): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18788304 | ||||||
| chrX:18788333 | CT | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
82 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.913-786delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chrX | 18788333 | ||||||
| chrX:18788381 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.913-740C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788381 | |||||||
| chrX:18788570 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913-551G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 9/15 | chrX | 18788570 | |||||||
| chrX:18789880 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0117 a0001c0001t0001g0120 |
3 | HG02615.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1065+607T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18789880 | |||||||
| chrX:18790173 | G | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0142 a0001c0001t0001g0180 |
3 | NA18939.hp2 NA18964.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1065+900G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790173 | |||||||
| chrX:18790356 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1065+1083T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790356 | |||||||
| chrX:18790359 | C | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0092 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+1086C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790359 | |||||||
| chrX:18790498 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0003g0219 |
2 | NA18962.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1065+1225C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790498 | |||||||
| chrX:18790515 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1065+1242A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790515 | |||||||
| chrX:18790870 | C | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0107 a0001c0001t0001g0109 others(5): Show |
8 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065+1597C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790870 | |||||||
| chrX:18790886 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1065+1613G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790886 | |||||||
| chrX:18790950 | T | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
36 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1065+1677T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790950 | |||||||
| chrX:18790955 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1065+1682G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18790955 | |||||||
| chrX:18791606 | C | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(28): Show |
31 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1065+2333C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18791606 | |||||||
| chrX:18791963 | A | G | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1065+2690A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18791963 | |||||||
| chrX:18792052 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01070.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1065+2779C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792052 | |||||||
| chrX:18792263 | T | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(28): Show |
32 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1065+2990T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792263 | |||||||
| chrX:18792530 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00741.hp2 HG01070.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1065+3257C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792530 | |||||||
| chrX:18792556 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0117 a0001c0001t0001g0120 |
3 | HG02615.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1065+3283T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792556 | |||||||
| chrX:18792557 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0117 a0001c0001t0001g0120 |
3 | HG02615.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1065+3284T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792557 | |||||||
| chrX:18792565 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0117 a0001c0001t0001g0120 |
3 | HG02615.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1065+3292T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792565 | |||||||
| chrX:18792651 | C | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(32): Show |
36 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1065+3378C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792651 | |||||||
| chrX:18792748 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1065+3475C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792748 | |||||||
| chrX:18792913 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1065+3640A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18792913 | |||||||
| chrX:18793371 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(6): Show |
9 | HG01070.hp1 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065+4098C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18793371 | |||||||
| chrX:18793684 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1065+4411C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18793684 | |||||||
| chrX:18794317 | CA | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
221 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.1065+5046delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18794317 | ||||||
| chrX:18794581 | C | A | 1 | a0002c0002t0001g0040 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1065+5308C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18794581 | |||||||
| chrX:18794593 | G | C | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1065+5320G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18794593 | |||||||
| chrX:18794654 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1065+5381G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18794654 | |||||||
| chrX:18794859 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0026 |
3 | HG02109.hp1 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1065+5586A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18794859 | |||||||
| chrX:18794952 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1065+5679T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18794952 | |||||||
| chrX:18795170 | C | T | 4 | a0001c0001t0001g0196 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02293.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065+5897C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795170 | |||||||
| chrX:18795171 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0089 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065+5898G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795171 | |||||||
| chrX:18795192 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
221 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.1065+5919A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795192 | |||||||
| chrX:18795265 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1065+5992G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795265 | |||||||
| chrX:18795382 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0165 |
2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1065+6109A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795382 | |||||||
| chrX:18795630 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065+6357G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795630 | |||||||
| chrX:18795885 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(82): Show |
87 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1065+6612C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795885 | |||||||
| chrX:18795902 | G | T | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1065+6629G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795902 | |||||||
| chrX:18795925 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+6652T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18795925 | |||||||
| chrX:18796056 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
118 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1065+6783G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18796056 | |||||||
| chrX:18796240 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1065+6967G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18796240 | |||||||
| chrX:18796325 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1065+7052T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18796325 | |||||||
| chrX:18796792 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
101 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1066-7100C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18796792 | |||||||
| chrX:18797165 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-6727A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797165 | |||||||
| chrX:18797203 | C | T | 5 | a0001c0001t0001g0163 a0001c0001t0001g0196 a0001c0003t0001g0084 others(2): Show |
5 | HG01928.hp1 HG02293.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1066-6689C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797203 | |||||||
| chrX:18797502 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
101 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1066-6390C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797502 | |||||||
| chrX:18797518 | C | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-6374C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797518 | |||||||
| chrX:18797658 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1066-6234G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797658 | |||||||
| chrX:18797694 | TTC | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1066-6196_1066-619 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18797694 | ||||||
| chrX:18797811 | C | T | 22 | a0001c0001t0001g0044 a0001c0001t0001g0055 a0001c0001t0001g0059 others(19): Show |
22 | HG00741.hp2 HG01081.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1066-6081C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797811 | |||||||
| chrX:18797870 | A | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1066-6022A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797870 | |||||||
| chrX:18797892 | C | T | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-6000C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797892 | |||||||
| chrX:18797974 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-5918G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18797974 | |||||||
| chrX:18798077 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1066-5815A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798077 | |||||||
| chrX:18798078 | AT | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066-5802delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18798078 | ||||||
| chrX:18798087 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1066-5805T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798087 | |||||||
| chrX:18798133 | A | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(18): Show |
21 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1066-5759A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798133 | |||||||
| chrX:18798163 | A | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
13 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1066-5729A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798163 | |||||||
| chrX:18798279 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
114 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1066-5613C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798279 | |||||||
| chrX:18798325 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-5567G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798325 | |||||||
| chrX:18798342 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-5550A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798342 | |||||||
| chrX:18798386 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1066-5506G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798386 | |||||||
| chrX:18798571 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-5321G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798571 | |||||||
| chrX:18798756 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
13 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1066-5136T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798756 | |||||||
| chrX:18798780 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1066-5112C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798780 | |||||||
| chrX:18798798 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-5094A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798798 | |||||||
| chrX:18798822 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 |
3 | HG02622.hp2 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1066-5070C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18798822 | |||||||
| chrX:18799200 | TCCAG | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
13 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1066-4689_1066-468 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18799200 | ||||||
| chrX:18799211 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18945.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1066-4681C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799211 | |||||||
| chrX:18799232 | C | CA | 22 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
22 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1066-4645dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18799232 | ||||||
| chrX:18799249 | G | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1066-4643G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799249 | |||||||
| chrX:18799267 | G | A | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(4): Show |
7 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066-4625G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799267 | |||||||
| chrX:18799283 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-4609G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799283 | |||||||
| chrX:18799325 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1066-4567G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799325 | |||||||
| chrX:18799388 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-4504G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799388 | |||||||
| chrX:18799550 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-4342A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18799550 | |||||||
| chrX:18800045 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01070.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1066-3847C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800045 | |||||||
| chrX:18800097 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1066-3795T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800097 | |||||||
| chrX:18800116 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-3776G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800116 | |||||||
| chrX:18800458 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
6 | NA18939.hp1 NA18999.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066-3434G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800458 | |||||||
| chrX:18800489 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1066-3403A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800489 | |||||||
| chrX:18800583 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1066-3309T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800583 | |||||||
| chrX:18800696 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1066-3196G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800696 | |||||||
| chrX:18800801 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-3091G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18800801 | |||||||
| chrX:18801001 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1066-2891G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801001 | |||||||
| chrX:18801306 | C | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00741.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1066-2586C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801306 | |||||||
| chrX:18801444 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-2448G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801444 | |||||||
| chrX:18801534 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1066-2358G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801534 | |||||||
| chrX:18801566 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-2326G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801566 | |||||||
| chrX:18801640 | CAG | C | 4 | a0001c0001t0001g0196 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02293.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-2245_1066-224 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18801640 | ||||||
| chrX:18801738 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
119 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1066-2154C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801738 | |||||||
| chrX:18801760 | A | C | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(4): Show |
7 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066-2132A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801760 | |||||||
| chrX:18801800 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(5): Show |
8 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1066-2092C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801800 | |||||||
| chrX:18801923 | G | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0083 a0001c0001t0001g0091 others(1): Show |
4 | HG01243.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-1969G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18801923 | |||||||
| chrX:18801983 | C | CA | 17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
17 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1066-1895dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18801983 | ||||||
| chrX:18802379 | G | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
101 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1066-1513G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18802379 | |||||||
| chrX:18802589 | A | G | 22 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
22 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1066-1303A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18802589 | |||||||
| chrX:18802853 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
96 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1066-1029delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chrX | 18802853 | ||||||
| chrX:18802936 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
117 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.1066-956A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18802936 | |||||||
| chrX:18802973 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): Show |
108 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1066-919A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18802973 | |||||||
| chrX:18803083 | C | A | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-809C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18803083 | |||||||
| chrX:18803218 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1066-674T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18803218 | |||||||
| chrX:18803313 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
103 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1066-579A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18803313 | |||||||
| chrX:18803341 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1066-551G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18803341 | |||||||
| chrX:18803547 | C | T | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1066-345C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18803547 | |||||||
| chrX:18803570 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1066-322T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 10/15 | chrX | 18803570 | |||||||
| chrX:18804311 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1251+247delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chrX | 18804311 | ||||||
| chrX:18804327 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1251+250G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18804327 | |||||||
| chrX:18804358 | G | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(6): Show |
9 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251+281G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18804358 | |||||||
| chrX:18804559 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251+482G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18804559 | |||||||
| chrX:18804997 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1251+920T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18804997 | |||||||
| chrX:18805026 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1251+949G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805026 | |||||||
| chrX:18805028 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251+951C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805028 | |||||||
| chrX:18805044 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1251+967T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805044 | |||||||
| chrX:18805050 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
111 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1251+973A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805050 | |||||||
| chrX:18805055 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1251+978C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805055 | |||||||
| chrX:18805135 | C | T | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1251+1058C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805135 | |||||||
| chrX:18805143 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1251+1066C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805143 | |||||||
| chrX:18805302 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1252-1101A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805302 | |||||||
| chrX:18805512 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1252-891C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805512 | |||||||
| chrX:18805641 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1252-762G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805641 | |||||||
| chrX:18805666 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1252-737G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805666 | |||||||
| chrX:18805703 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1252-700C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805703 | |||||||
| chrX:18805712 | A | C | 1 | a0001c0001t0001g0199 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1252-691A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805712 | |||||||
| chrX:18805790 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
102 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1252-613G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805790 | |||||||
| chrX:18805835 | C | T | 1 | a0002c0002t0001g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1252-568C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805835 | |||||||
| chrX:18805837 | A | T | 1 | a0002c0002t0001g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1252-566A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805837 | |||||||
| chrX:18805841 | TA | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
112 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1252-543delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chrX | 18805841 | ||||||
| chrX:18805866 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0001t0001g0196 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1252-537C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805866 | |||||||
| chrX:18805959 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1252-444C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18805959 | |||||||
| chrX:18806085 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1252-318C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18806085 | |||||||
| chrX:18806112 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1252-291A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18806112 | |||||||
| chrX:18806156 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1252-247A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18806156 | |||||||
| chrX:18806166 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0001t0001g0196 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1252-237G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18806166 | |||||||
| chrX:18806331 | A | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0111 a0001c0001t0001g0168 others(2): Show |
5 | HG02040.hp1 HG02129.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-72A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18806331 | |||||||
| chrX:18806372 | C | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0127 a0001c0001t0001g0134 others(3): Show |
6 | HG00280.hp1 HG00609.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1252-31C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 11/15 | chrX | 18806372 | |||||||
| chrX:18806676 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1394+131T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18806676 | |||||||
| chrX:18806727 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
120 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1394+182A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18806727 | |||||||
| chrX:18806859 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1394+314A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18806859 | |||||||
| chrX:18806960 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1394+415C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18806960 | |||||||
| chrX:18807002 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1394+457T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807002 | |||||||
| chrX:18807003 | GGTT | G | 4 | a0001c0001t0001g0196 a0001c0003t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG02293.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394+459_1394+461d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807003 | |||||||
| chrX:18807004 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1394+459G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807004 | |||||||
| chrX:18807012 | TTTG | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
93 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1394+470_1394+472d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18807012 | ||||||
| chrX:18807014 | TG | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1394+470delG | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807014 | |||||||
| chrX:18807015 | G | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0080 a0001c0001t0001g0087 others(7): Show |
10 | HG02293.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+470G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807015 | |||||||
| chrX:18807019 | G | GT | 5 | a0001c0001t0001g0031 a0001c0001t0001g0070 a0001c0001t0001g0150 others(2): Show |
5 | HG02135.hp1 NA18942.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+482dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18807019 | ||||||
| chrX:18807019 | GT | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1394+482delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18807019 | ||||||
| chrX:18807029 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1394+484A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807029 | |||||||
| chrX:18807138 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1394+593T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807138 | |||||||
| chrX:18807662 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1394+1117C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807662 | |||||||
| chrX:18807941 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1394+1396T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807941 | |||||||
| chrX:18807964 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0208 |
2 | NA18612.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1394+1419C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807964 | |||||||
| chrX:18807965 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1394+1420G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18807965 | |||||||
| chrX:18807969 | A | AT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1394+1440dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18807969 | ||||||
| chrX:18807969 | A | ATT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(3): Show |
6 | HG02074.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+1439_1394+144 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18807969 | ||||||
| chrX:18807969 | AT | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
8 | HG03209.hp1 NA18939.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+1440delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18807969 | ||||||
| chrX:18808027 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(100): Show |
105 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1394+1482T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808027 | |||||||
| chrX:18808054 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1394+1509C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808054 | |||||||
| chrX:18808186 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(6): Show |
9 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1394+1641C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808186 | |||||||
| chrX:18808210 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
100 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1394+1665C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808210 | |||||||
| chrX:18808261 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1394+1716G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808261 | |||||||
| chrX:18808552 | CA | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(5): Show |
8 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+2020delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18808552 | ||||||
| chrX:18808552 | CAA | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
101 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1394+2019_1394+202 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18808552 | ||||||
| chrX:18808857 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1394+2312A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808857 | |||||||
| chrX:18808901 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
101 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1394+2356C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18808901 | |||||||
| chrX:18809091 | A | ATATC | 26 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0064 others(23): Show |
26 | HG00642.hp1 HG00738.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1394+2593_1394+259 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809091 | ||||||
| chrX:18809091 | A | ATATCTAT others(1): Show |
10 | a0001c0001t0001g0068 a0001c0001t0001g0106 a0001c0001t0001g0121 others(7): Show |
10 | HG00438.hp1 HG00558.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+2589_1394+259 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809091 | ||||||
| chrX:18809091 | A | ATATCTAT others(5): Show |
6 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0116 others(3): Show |
6 | HG02738.hp1 NA18939.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1394+2585_1394+259 others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809091 | ||||||
| chrX:18809091 | ATATC | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(48): Show |
53 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1394+2593_1394+259 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809091 | ||||||
| chrX:18809091 | ATATCTAT others(1): Show |
A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+2589_1394+259 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809091 | ||||||
| chrX:18809091 | ATATCTAT others(5): Show |
A | 1 | a0001c0001t0001g0167 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1394+2585_1394+259 others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809091 | ||||||
| chrX:18809093 | A | ATCTATCT others(5): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0139 a0001c0001t0001g0196 |
3 | HG01070.hp1 HG02293.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1394+2559_1394+256 others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809093 | ||||||
| chrX:18809093 | A | ATCTATCT others(9): Show |
1 | a0001c0001t0001g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1394+2559_1394+256 others(20): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809093 | ||||||
| chrX:18809097 | A | ATCTATCT others(1): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0089 others(4): Show |
7 | HG02451.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1394+2559_1394+256 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809097 | ||||||
| chrX:18809101 | A | ATCTG | 19 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(16): Show |
19 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1394+2559_1394+256 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809101 | ||||||
| chrX:18809101 | A | ATCTGTCT others(1): Show |
4 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0197 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394+2559_1394+256 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809101 | ||||||
| chrX:18809101 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1394+2556A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809101 | |||||||
| chrX:18809105 | A | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0044 others(29): Show |
32 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1394+2560A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809105 | |||||||
| chrX:18809109 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(40): Show |
45 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1394+2564A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809109 | |||||||
| chrX:18809113 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0079 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1394+2568A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809113 | |||||||
| chrX:18809309 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1394+2764A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809309 | |||||||
| chrX:18809336 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0195 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394+2791A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809336 | |||||||
| chrX:18809503 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(42): Show |
45 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.1394+2958C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809503 | |||||||
| chrX:18809504 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1394+2959G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809504 | |||||||
| chrX:18809632 | A | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0079 others(12): Show |
15 | HG01884.hp1 HG02145.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.1394+3087A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809632 | |||||||
| chrX:18809704 | C | CA | 14 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0077 others(11): Show |
14 | HG01496.hp2 HG02293.hp1 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.1394+3173dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809704 | ||||||
| chrX:18809704 | C | CAA | 8 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0083 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+3172_1394+317 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18809704 | ||||||
| chrX:18809721 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1394+3176C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809721 | |||||||
| chrX:18809910 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1394+3365A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809910 | |||||||
| chrX:18809951 | G | A | 1 | a0001c0004t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1394+3406G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18809951 | |||||||
| chrX:18810010 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
64 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1394+3465G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810010 | |||||||
| chrX:18810076 | C | CTG | 15 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(12): Show |
15 | HG00438.hp1 HG00738.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1394+3564_1394+356 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18810076 | ||||||
| chrX:18810076 | CTG | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0092 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1394+3564_1394+356 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18810076 | ||||||
| chrX:18810076 | CTGTG | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0034 others(34): Show |
37 | HG00597.hp1 HG00741.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1394+3562_1394+356 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18810076 | ||||||
| chrX:18810076 | CTGTGTG | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(60): Show |
65 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1394+3560_1394+356 others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18810076 | ||||||
| chrX:18810333 | G | GCA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0087 others(5): Show |
8 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+3809_1394+381 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18810333 | ||||||
| chrX:18810348 | CA | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1394+3804delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810348 | |||||||
| chrX:18810383 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1394+3838G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810383 | |||||||
| chrX:18810445 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
68 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1394+3900G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810445 | |||||||
| chrX:18810450 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
68 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1394+3905A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810450 | |||||||
| chrX:18810576 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1394+4031G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810576 | |||||||
| chrX:18810855 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0151 |
2 | NA18965.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1394+4310G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810855 | |||||||
| chrX:18810951 | AC | A | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1394+4407delC | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810951 | |||||||
| chrX:18810953 | T | A | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1394+4408T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18810953 | |||||||
| chrX:18811194 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1394+4649A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811194 | |||||||
| chrX:18811201 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1394+4656C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811201 | |||||||
| chrX:18811287 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0124 others(6): Show |
9 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1394+4742A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811287 | |||||||
| chrX:18811449 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
114 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1394+4904G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811449 | |||||||
| chrX:18811512 | T | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0087 others(4): Show |
7 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1394+4967T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811512 | |||||||
| chrX:18811575 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1394+5030A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811575 | |||||||
| chrX:18811587 | G | GTATA | 2 | a0001c0001t0001g0144 a0001c0001t0001g0169 |
2 | NA18986.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1394+5068_1394+507 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811587 | ||||||
| chrX:18811587 | GTA | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
76 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1394+5070_1394+507 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811587 | ||||||
| chrX:18811587 | GTATATAT others(1): Show |
G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+5064_1394+507 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811587 | ||||||
| chrX:18811599 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1394+5056_1394+507 others(23): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811599 | ||||||
| chrX:18811601 | ATATATAT others(11): Show |
A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0122 |
3 | HG02970.hp2 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1394+5058_1394+507 others(22): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811601 | ||||||
| chrX:18811601 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0004c0008t0001g0019 |
3 | HG01070.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1394+5058_1394+507 others(23): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811601 | ||||||
| chrX:18811601 | ATATATAT others(13): Show |
A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
61 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1394+5058_1394+507 others(24): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811601 | ||||||
| chrX:18811601 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1394+5058_1394+507 others(25): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811601 | ||||||
| chrX:18811603 | ATATATAT others(12): Show |
A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0092 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1394+5060_1394+507 others(23): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811603 | ||||||
| chrX:18811605 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1394+5060A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811605 | |||||||
| chrX:18811609 | ATATATAT others(1): Show |
A | 20 | a0001c0001t0001g0044 a0001c0001t0001g0055 a0001c0001t0001g0059 others(17): Show |
20 | HG00741.hp2 HG01192.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1394+5066_1394+507 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811609 | ||||||
| chrX:18811612 | TATA | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0203 |
3 | HG02056.hp1 NA18522.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1394+5068_1394+507 others(7): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811612 | |||||||
| chrX:18811614 | TA | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0198 |
2 | HG01175.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1394+5070delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811614 | |||||||
| chrX:18811615 | A | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0042 others(9): Show |
12 | HG00438.hp2 HG01106.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1394+5070A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811615 | |||||||
| chrX:18811615 | ATT | A | 5 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0137 others(2): Show |
5 | HG00597.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+5089_1394+509 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18811615 | ||||||
| chrX:18811619 | T | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0004t0001g0081 |
3 | HG02451.hp2 HG02809.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1394+5074T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811619 | |||||||
| chrX:18811621 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1394+5076T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811621 | |||||||
| chrX:18811639 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0068 others(4): Show |
7 | HG00558.hp1 HG03491.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1394+5094A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811639 | |||||||
| chrX:18811694 | G | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0124 others(6): Show |
9 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1394+5149G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811694 | |||||||
| chrX:18811886 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1394+5341C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811886 | |||||||
| chrX:18811937 | T | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+5392T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18811937 | |||||||
| chrX:18812358 | G | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
120 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1395-5681G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18812358 | |||||||
| chrX:18812631 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1395-5408A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18812631 | |||||||
| chrX:18812850 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0122 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-5189C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18812850 | |||||||
| chrX:18812859 | C | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1395-5180C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18812859 | |||||||
| chrX:18813064 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-4975T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813064 | |||||||
| chrX:18813100 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395-4939G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813100 | |||||||
| chrX:18813128 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1395-4911C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813128 | |||||||
| chrX:18813251 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(54): Show |
59 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1395-4788C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813251 | |||||||
| chrX:18813252 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1395-4787G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813252 | |||||||
| chrX:18813304 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1395-4735G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813304 | |||||||
| chrX:18813378 | C | CA | 22 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(19): Show |
22 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1395-4641dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18813378 | ||||||
| chrX:18813378 | CA | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0099 others(2): Show |
5 | HG03579.hp1 NA18955.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395-4641delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18813378 | ||||||
| chrX:18813399 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1395-4640C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813399 | |||||||
| chrX:18813542 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395-4497C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813542 | |||||||
| chrX:18813649 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0122 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-4390A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813649 | |||||||
| chrX:18813695 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1395-4344T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813695 | |||||||
| chrX:18813938 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1395-4101C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18813938 | |||||||
| chrX:18814005 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
120 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1395-4034A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814005 | |||||||
| chrX:18814026 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1395-4013A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814026 | |||||||
| chrX:18814305 | C | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0007t0001g0082 |
3 | HG02145.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1395-3734C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814305 | |||||||
| chrX:18814411 | T | C | 1 | a0001c0003t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1395-3628T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814411 | |||||||
| chrX:18814587 | G | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
221 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.1395-3452G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814587 | |||||||
| chrX:18814604 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0122 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-3435C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814604 | |||||||
| chrX:18814996 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1395-3043C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18814996 | |||||||
| chrX:18815060 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
96 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1395-2979G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815060 | |||||||
| chrX:18815269 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1395-2770A>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815269 | |||||||
| chrX:18815315 | A | ATCTT | 8 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(5): Show |
8 | HG01106.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-2722_1395-271 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18815315 | ||||||
| chrX:18815716 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1395-2323T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815716 | |||||||
| chrX:18815799 | AT | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
42 | HG00741.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1395-2238delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18815799 | ||||||
| chrX:18815903 | ATT | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0095 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-2123_1395-212 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18815903 | ||||||
| chrX:18815907 | T | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
118 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1395-2132T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815907 | |||||||
| chrX:18815911 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1395-2128T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815911 | |||||||
| chrX:18815922 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1395-2117T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815922 | |||||||
| chrX:18815982 | C | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1395-2057C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18815982 | |||||||
| chrX:18816050 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1395-1989G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816050 | |||||||
| chrX:18816074 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1395-1965A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816074 | |||||||
| chrX:18816100 | C | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-1939C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816100 | |||||||
| chrX:18816115 | T | C | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1395-1924T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816115 | |||||||
| chrX:18816323 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1395-1716T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816323 | |||||||
| chrX:18816369 | CAATA | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395-1666_1395-166 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18816369 | ||||||
| chrX:18816455 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1395-1584C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816455 | |||||||
| chrX:18816597 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1395-1442C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816597 | |||||||
| chrX:18816631 | T | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0007t0001g0082 |
3 | HG02572.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1395-1408T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816631 | |||||||
| chrX:18816639 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1395-1400T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816639 | |||||||
| chrX:18816721 | T | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0161 |
2 | HG01255.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1395-1318T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18816721 | |||||||
| chrX:18817067 | C | CGT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG02055.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395-972_1395-971i others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817067 | |||||||
| chrX:18817067 | C | CGTGT | 2 | a0001c0001t0001g0012 a0001c0001t0001g0095 |
2 | HG01070.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1395-972_1395-971i others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817067 | |||||||
| chrX:18817067 | C | CGTGTGTG others(1): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1395-972_1395-971i others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817067 | |||||||
| chrX:18817067 | CAT | C | 6 | a0001c0001t0001g0184 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
6 | HG01496.hp2 HG02293.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-971_1395-970d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817067 | |||||||
| chrX:18817067 | CATGTGTG others(19): Show |
C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-971_1395-946d others(28): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817067 | |||||||
| chrX:18817068 | A | ATATG | 4 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0117 others(1): Show |
4 | HG00597.hp1 HG02647.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-970_1395-969i others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | ATATGTG | 3 | a0001c0001t0001g0032 a0001c0001t0001g0091 a0001c0001t0001g0120 |
3 | HG01175.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1395-970_1395-969i others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | ATATGTGT others(1): Show |
36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(33): Show |
38 | HG00140.hp1 HG00558.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1395-970_1395-969i others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | ATATGTGT others(3): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0111 others(3): Show |
6 | HG00544.hp1 HG01981.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-970_1395-969i others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | ATATGTGT others(5): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0094 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1395-970_1395-969i others(14): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | ATATGTGT others(7): Show |
2 | a0002c0002t0001g0039 a0002c0002t0001g0040 |
2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1395-970_1395-969i others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | ATG | 4 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0137 others(1): Show |
4 | HG02071.hp1 NA18974.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-935_1395-934d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(16): Show |
19 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1395-971A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817068 | |||||||
| chrX:18817068 | ATGTGTGT others(1): Show |
A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00741.hp2 HG01081.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1395-941_1395-934d others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817068 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0068 a0001c0005t0001g0185 |
2 | HG00558.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1395-943_1395-934d others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817068 | ||||||
| chrX:18817078 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00741.hp2 HG01081.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1395-961G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817078 | |||||||
| chrX:18817080 | G | A | 1 | a0001c0005t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1395-959G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817080 | |||||||
| chrX:18817127 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0195 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-912A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817127 | |||||||
| chrX:18817293 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1395-746G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817293 | |||||||
| chrX:18817350 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1395-689T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817350 | |||||||
| chrX:18817365 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1395-674A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817365 | |||||||
| chrX:18817526 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1395-513G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817526 | |||||||
| chrX:18817674 | G | GT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
91 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1395-364dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chrX | 18817674 | ||||||
| chrX:18817697 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1395-342C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817697 | |||||||
| chrX:18817886 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1395-153T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 12/15 | chrX | 18817886 | |||||||
| chrX:18818370 | CT | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
109 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1501+243delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18818370 | ||||||
| chrX:18818527 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1501+382C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18818527 | |||||||
| chrX:18818660 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1501+515G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18818660 | |||||||
| chrX:18818699 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0195 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+554G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18818699 | |||||||
| chrX:18818717 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
92 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1501+572A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18818717 | |||||||
| chrX:18818990 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1501+845C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18818990 | |||||||
| chrX:18819010 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1501+865T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18819010 | |||||||
| chrX:18819192 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1501+1047A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18819192 | |||||||
| chrX:18819454 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1501+1309G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18819454 | |||||||
| chrX:18819528 | C | CA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0088 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1501+1392dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18819528 | ||||||
| chrX:18819560 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1501+1415G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18819560 | |||||||
| chrX:18819693 | TCAAA | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501+1557_1501+156 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18819693 | ||||||
| chrX:18820006 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1501+1861G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18820006 | |||||||
| chrX:18820388 | CT | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
97 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1501+2258delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18820388 | ||||||
| chrX:18820394 | T | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1501+2249T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18820394 | |||||||
| chrX:18820408 | TG | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+2265delG | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18820408 | ||||||
| chrX:18820598 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0196 a0001c0003t0001g0084 others(2): Show |
5 | HG02293.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1501+2453A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18820598 | |||||||
| chrX:18820662 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501+2517A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18820662 | |||||||
| chrX:18820674 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1501+2529C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18820674 | |||||||
| chrX:18820691 | CT | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(2): Show |
5 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1501+2552delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18820691 | ||||||
| chrX:18820932 | C | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0021 others(48): Show |
51 | HG00741.hp2 HG01081.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.1501+2787C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18820932 | |||||||
| chrX:18821065 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1502-2858T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821065 | |||||||
| chrX:18821095 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1502-2828C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821095 | |||||||
| chrX:18821137 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1502-2786G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821137 | |||||||
| chrX:18821177 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1502-2746T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821177 | |||||||
| chrX:18821178 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1502-2745G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821178 | |||||||
| chrX:18821180 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG01081.hp1 HG01099.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1502-2743G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821180 | |||||||
| chrX:18821222 | C | CA | 8 | a0001c0001t0001g0056 a0001c0001t0001g0115 a0001c0001t0001g0128 others(5): Show |
8 | HG01884.hp2 HG03927.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-2683dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821222 | ||||||
| chrX:18821222 | CA | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(53): Show |
58 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1502-2683delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821222 | ||||||
| chrX:18821566 | G | A | 2 | a0001c0004t0001g0118 a0001c0005t0001g0185 |
2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1502-2357G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821566 | |||||||
| chrX:18821668 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
107 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1502-2255C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821668 | |||||||
| chrX:18821758 | C | CGA | 13 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0066 others(10): Show |
13 | HG00558.hp1 HG01346.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1502-2120_1502-211 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | C | CGAGA | 3 | a0001c0001t0001g0098 a0001c0001t0001g0142 a0001c0001t0001g0175 |
3 | HG02083.hp1 NA18939.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1502-2122_1502-211 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | C | CGAGAGA | 6 | a0001c0001t0001g0027 a0001c0001t0001g0100 a0001c0001t0001g0103 others(3): Show |
6 | HG01081.hp1 NA18522.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1502-2124_1502-211 others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | C | CGAGAGAG others(1): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0205 |
2 | HG01099.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1502-2126_1502-211 others(12): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | C | CGAGAGAG others(5): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1502-2130_1502-211 others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | C | CGAGAGAG others(15): Show |
1 | a0001c0001t0001g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1502-2140_1502-211 others(26): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGA | C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0121 a0001c0001t0001g0150 others(4): Show |
7 | HG01978.hp2 HG02886.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-2120_1502-211 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGAGA | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0087 others(2): Show |
5 | HG00673.hp1 HG01496.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1502-2122_1502-211 others(8): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGAGAGA | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(26): Show |
30 | HG00438.hp2 HG00621.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.1502-2124_1502-211 others(10): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGAGAGAG others(3): Show |
C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0094 others(7): Show |
10 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1502-2128_1502-211 others(14): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGAGAGAG others(5): Show |
C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
92 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1502-2130_1502-211 others(16): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGAGAGAG others(7): Show |
C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0080 others(17): Show |
20 | HG00280.hp1 HG00609.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1502-2132_1502-211 others(18): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821758 | CGAGAGAG others(15): Show |
C | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1502-2140_1502-211 others(26): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18821758 | ||||||
| chrX:18821799 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
56 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1502-2124G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821799 | |||||||
| chrX:18821801 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
101 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1502-2122G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821801 | |||||||
| chrX:18821803 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
110 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1502-2120G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821803 | |||||||
| chrX:18821804 | A | AG | 5 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0108 others(2): Show |
5 | HG00544.hp2 HG02056.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1502-2119_1502-211 others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821804 | |||||||
| chrX:18821804 | A | AGAGAGAG others(20): Show |
1 | a0001c0001t0001g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1502-2119_1502-211 others(31): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821804 | |||||||
| chrX:18821805 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1502-2118A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821805 | |||||||
| chrX:18821806 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1502-2117A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821806 | |||||||
| chrX:18821807 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1502-2116A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821807 | |||||||
| chrX:18821888 | G | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(16): Show |
19 | HG01070.hp1 HG01884.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1502-2035G>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18821888 | |||||||
| chrX:18822082 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1502-1841G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18822082 | |||||||
| chrX:18822353 | C | CA | 10 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(7): Show |
10 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1502-1556dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18822353 | ||||||
| chrX:18822353 | CAA | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0139 others(4): Show |
7 | HG02451.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-1557_1502-155 others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18822353 | ||||||
| chrX:18822593 | C | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(18): Show |
21 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1502-1330C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18822593 | |||||||
| chrX:18822733 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1502-1190A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18822733 | |||||||
| chrX:18822979 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0189 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-944A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18822979 | |||||||
| chrX:18823153 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
85 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1502-770C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18823153 | |||||||
| chrX:18823347 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0139 others(4): Show |
7 | HG02451.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-576G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18823347 | |||||||
| chrX:18823524 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0122 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1502-399G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18823524 | |||||||
| chrX:18823600 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1502-323C>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18823600 | |||||||
| chrX:18823635 | AAAAT | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(8): Show |
11 | HG01070.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1502-273_1502-270d others(6): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chrX | 18823635 | ||||||
| chrX:18823639 | T | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-284T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18823639 | |||||||
| chrX:18823889 | C | T | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1502-34C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 13/15 | chrX | 18823889 | |||||||
| chrX:18824296 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1665+210C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824296 | |||||||
| chrX:18824306 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1665+220C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824306 | |||||||
| chrX:18824666 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
85 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1665+580T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824666 | |||||||
| chrX:18824720 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1665+634G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824720 | |||||||
| chrX:18824733 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0122 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+647G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824733 | |||||||
| chrX:18824774 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1665+688C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824774 | |||||||
| chrX:18824799 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1665+713G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824799 | |||||||
| chrX:18824808 | C | T | 1 | a0004c0008t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1665+722C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824808 | |||||||
| chrX:18824822 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1665+736C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824822 | |||||||
| chrX:18824985 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1666-766A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18824985 | |||||||
| chrX:18825026 | G | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(8): Show |
11 | HG01070.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1666-725G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825026 | |||||||
| chrX:18825083 | GA | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
122 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1666-665delA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chrX | 18825083 | ||||||
| chrX:18825234 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0122 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1666-517C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825234 | |||||||
| chrX:18825306 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1666-445G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825306 | |||||||
| chrX:18825327 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1666-424C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825327 | |||||||
| chrX:18825424 | G | A | 4 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 others(1): Show |
4 | HG02451.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1666-327G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825424 | |||||||
| chrX:18825431 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1666-320A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825431 | |||||||
| chrX:18825738 | A | C | 1 | a0001c0001t0003g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1666-13A>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825738 | |||||||
| chrX:18825739 | T | A | 1 | a0001c0001t0003g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1666-12T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825739 | |||||||
| chrX:18825742 | T | A | 1 | a0001c0001t0003g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1666-9T>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825742 | |||||||
| chrX:18825743 | T | G | 1 | a0001c0001t0003g0219 | 1 | NA18967.hp1 | splice_region_variant&intron_variant | LOW | c.1666-8T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825743 | |||||||
| chrX:18825746 | T | G | 1 | a0001c0001t0003g0219 | 1 | NA18967.hp1 | splice_region_variant&intron_variant | LOW | c.1666-5T>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 14/15 | chrX | 18825746 | |||||||
| chrX:18825871 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1750+36G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18825871 | |||||||
| chrX:18825894 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
100 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1750+59G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18825894 | |||||||
| chrX:18826053 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1750+218C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826053 | |||||||
| chrX:18826061 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1750+226C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826061 | |||||||
| chrX:18826250 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1750+415C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826250 | |||||||
| chrX:18826417 | C | CT | 32 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0033 others(29): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1750+610dupT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chrX | 18826417 | ||||||
| chrX:18826417 | C | CTT | 10 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0087 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1750+609_1750+610d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chrX | 18826417 | ||||||
| chrX:18826417 | C | CTTT | 8 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
8 | HG01070.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1750+608_1750+610d others(5): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chrX | 18826417 | ||||||
| chrX:18826417 | CT | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0032 others(18): Show |
21 | HG00558.hp2 HG00741.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1750+610delT | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chrX | 18826417 | ||||||
| chrX:18826417 | CTT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
75 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1750+609_1750+610d others(4): Show |
PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chrX | 18826417 | ||||||
| chrX:18826522 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
85 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1750+687G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826522 | |||||||
| chrX:18826562 | G | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(18): Show |
21 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1751-714G>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826562 | |||||||
| chrX:18826717 | C | T | 2 | a0001c0001t0001g0033 a0003c0006t0001g0135 |
2 | HG02015.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1751-559C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826717 | |||||||
| chrX:18826718 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0114 a0001c0001t0001g0138 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1751-558G>A | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826718 | |||||||
| chrX:18826778 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1751-498C>T | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826778 | |||||||
| chrX:18826779 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0113 |
2 | NA18990.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1751-497A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826779 | |||||||
| chrX:18826816 | G | GA | 5 | a0001c0001t0001g0094 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02738.hp1 HG02922.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751-446dupA | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chrX | 18826816 | ||||||
| chrX:18826848 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1751-428A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826848 | |||||||
| chrX:18826912 | C | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
28 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1751-364C>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826912 | |||||||
| chrX:18826930 | T | C | 3 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0086 |
3 | HG02451.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1751-346T>C | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18826930 | |||||||
| chrX:18827254 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0122 others(3): Show |
6 | HG02451.hp1 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1751-22A>G | PPEF1 | ENSG00000086717.19 | transcript | ENST00000470157.2 | protein_coding | 15/15 | chrX | 18827254 |