Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7512 |
|---|---|
| ensemblid | ENSG00000122121.12 |
| hgncid | 12823 |
| symbol | XPNPEP2 |
| name | X-prolyl aminopeptidase 2 |
| refseq_nuc | NM_003399.6 |
| refseq_prot | NP_003390.4 |
| ensembl_nuc | ENST00000371106.4 |
| ensembl_prot | ENSP00000360147.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 129738979 |
| end | 129769536 |
| strand | + |
| ver | v1.2 |
| region | chrX:129738979-129769536 |
| region5000 | chrX:129733979-129774536 |
| regionname0 | XPNPEP2_chrX_129738979_129769536 |
| regionname5000 | XPNPEP2_chrX_129733979_129774536 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 674 | 278 | 74 | 49 | 116 | 9 | 28 | 88 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0002 | 0/0 | 674 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0003 | 0/0 | 674 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0004 | 0/0 | 674 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0005 | 0/0 | 26 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0006 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0007 | 0/0 | 242 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0008 | 0/0 | 242 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0009 | 0/0 | 242 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0010 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0011 | 0/0 | 309 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0012 | 0/0 | 674 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0013 | 0/0 | 319 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0014 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0015 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0016 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0017 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0018 | 0/0 | 487 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0019 | 0/0 | 487 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0020 | 0/0 | 533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0021 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0022 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0023 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0024 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0025 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0026 | 0/0 | 187 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0027 | 0/0 | 156 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0028 | 0/0 | 121 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2025 | 189 | 68 | 17 | 89 | 2 | 13 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0002 | 1/1 | 2025 | 85 | 5 | 31 | 27 | 6 | 14 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0003 | 0/0 | 2025 | 3 | 2 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0004 | 0/0 | 2025 | 3 | 0 | 0 | 2 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0005 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0006 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 1 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0007 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0008 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0009 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0010 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0011 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0012 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0013 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0014 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0015 | 0/0 | 2026 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0016 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0017 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0018 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0019 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0020 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0021 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0022 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0023 | 0/0 | 1993 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0024 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0025 | 0/0 | 2024 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0026 | 0/0 | 2026 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0027 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0028 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0029 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0030 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0031 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| c0032 | 0/0 | 2029 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1287 | 124 | 5 | 37 | 50 | 8 | 22 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0002 | 0/0 | 1287 | 57 | 25 | 9 | 17 | 0 | 6 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0003 | 0/0 | 1287 | 44 | 8 | 0 | 34 | 0 | 2 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0004 | 0/0 | 1287 | 23 | 3 | 1 | 19 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0005 | 0/0 | 1287 | 15 | 15 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0006 | 0/0 | 1287 | 8 | 3 | 1 | 3 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0007 | 0/0 | 1287 | 7 | 7 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0008 | 0/0 | 1287 | 6 | 4 | 2 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0009 | 0/0 | 1287 | 4 | 4 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0010 | 0/0 | 1287 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0011 | 0/0 | 1287 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0012 | 0/0 | 1287 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0013 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0014 | 0/0 | 1283 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0015 | 0/0 | 1286 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0016 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0017 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0018 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0019 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0020 | 0/0 | 1291 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0021 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0022 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0023 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0024 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| t0025 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2025 | 189 | 68 | 17 | 89 | 2 | 13 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0002 | 1/1 | 2025 | 85 | 5 | 31 | 27 | 6 | 14 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0006 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 1 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0010 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0020 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0002c0003 | 0/0 | 2025 | 3 | 2 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0003c0004 | 0/0 | 2025 | 3 | 0 | 0 | 2 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0004c0005 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0005c0032 | 0/0 | 2029 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0006c0031 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0007c0022 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0008c0008 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0009c0009 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0010c0021 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0011c0019 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0012c0024 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0013c0025 | 0/0 | 2024 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0014c0018 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0015c0012 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0016c0027 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0017c0013 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0018c0029 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0019c0015 | 0/0 | 2026 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0020c0014 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0021c0028 | 0/0 | 2024 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0022c0016 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0023c0017 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0024c0026 | 0/0 | 2026 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0025c0011 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0026c0023 | 0/0 | 1993 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0027c0007 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0028c0030 | 0/0 | 2026 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3311 | 35 | 2 | 6 | 20 | 1 | 6 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0002 | 0/0 | 3311 | 49 | 21 | 7 | 16 | 0 | 5 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0003 | 0/0 | 3311 | 39 | 8 | 0 | 29 | 0 | 2 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0004 | 0/0 | 3311 | 19 | 3 | 1 | 15 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0005 | 0/0 | 3311 | 13 | 13 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0006 | 0/0 | 3311 | 4 | 2 | 1 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0007 | 0/0 | 3311 | 5 | 5 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0008 | 0/0 | 3311 | 6 | 4 | 2 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0009 | 0/0 | 3311 | 4 | 4 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0010 | 0/0 | 3311 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0011 | 0/0 | 3311 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0012 | 0/0 | 3311 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0015 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0017 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0018 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0022 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0023 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0001t0024 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0002t0001 | 1/1 | 3311 | 78 | 2 | 31 | 24 | 6 | 13 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0002t0002 | 0/0 | 3311 | 4 | 3 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0002t0013 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0002t0019 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0002t0021 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0006t0001 | 0/0 | 3311 | 2 | 0 | 0 | 0 | 1 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0010t0002 | 0/0 | 3311 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0001c0020t0005 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0002c0003t0002 | 0/0 | 3311 | 2 | 1 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0002c0003t0005 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0003c0004t0006 | 0/0 | 3311 | 3 | 0 | 0 | 2 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0004c0005t0007 | 0/0 | 3311 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0005c0032t0025 | 0/0 | 3320 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0006c0031t0016 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0007c0022t0003 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0008c0008t0003 | 0/0 | 3313 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0009c0009t0003 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0010c0021t0004 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0011c0019t0001 | 0/0 | 3313 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0012c0024t0001 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0013c0025t0001 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0014c0018t0004 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0015c0012t0004 | 0/0 | 3313 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0016c0027t0001 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0017c0013t0003 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0018c0029t0001 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0019c0015t0002 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0020c0014t0004 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0021c0028t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0022c0016t0001 | 0/0 | 3313 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0023c0017t0006 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0024c0026t0001 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0025c0011t0014 | 0/0 | 3304 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0026c0023t0003 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0027c0007t0020 | 0/0 | 3316 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| a0028c0030t0001 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | copy fasta | chrX | 129733979 | 129774536 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0012g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0012g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0017g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0018g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0022g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0023g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0013g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0019g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0021g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0006t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0010t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0020t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0002c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0002c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0002c0003t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0003c0004t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0003c0004t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0003c0004t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0004c0005t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0004c0005t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0005c0032t0025g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0006c0031t0016g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0007c0022t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0008c0008t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0009c0009t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0010c0021t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0011c0019t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0012c0024t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0013c0025t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0014c0018t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0015c0012t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0016c0027t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0017c0013t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0018c0029t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0019c0015t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0020c0014t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0021c0028t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0022c0016t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0023c0017t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0024c0026t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0025c0011t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0026c0023t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0027c0007t0020g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0028c0030t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0229 | EUR | GBR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | GBR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0264 | EUR | GBR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0228 | EUR | FIN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00323 | hp1 | a0001 | c0006 | t0001 | g0110 | EUR | FIN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0262 | EUR | FIN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01081 | hp1 | a0001 | c0010 | t0002 | g0009 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0196 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0210 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01243 | hp1 | a0002 | c0003 | t0002 | g0295 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0270 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0198 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02080 | hp1 | a0007 | c0022 | t0003 | g0181 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | CDX | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CDX | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02258 | hp1 | a0004 | c0005 | t0007 | g0289 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02280 | hp1 | a0001 | c0020 | t0005 | g0209 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0193 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02523 | hp1 | a0020 | c0014 | t0004 | g0030 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0207 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0285 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0286 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02738 | hp1 | a0019 | c0015 | t0002 | g0016 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02896 | hp2 | a0001 | c0001 | t0017 | g0212 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0247 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02965 | hp1 | a0001 | c0001 | t0022 | g0291 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0213 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0288 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0238 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0296 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03490 | hp1 | a0013 | c0025 | t0001 | g0274 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03516 | hp2 | a0004 | c0005 | t0007 | g0287 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03669 | hp1 | a0001 | c0006 | t0001 | g0092 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03669 | hp2 | a0001 | c0002 | t0019 | g0244 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04184 | hp2 | a0003 | c0004 | t0006 | g0280 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04199 | hp1 | a0012 | c0024 | t0001 | g0249 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0216 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18947 | hp1 | a0001 | c0001 | t0012 | g0167 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18959 | hp1 | a0016 | c0027 | t0001 | g0182 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18964 | hp1 | a0014 | c0018 | t0004 | g0066 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18967 | hp1 | a0008 | c0008 | t0003 | g0085 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18972 | hp1 | a0001 | c0002 | t0013 | g0281 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18972 | hp2 | a0011 | c0019 | t0001 | g0089 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18975 | hp1 | a0003 | c0004 | t0006 | g0130 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18987 | hp1 | a0027 | c0007 | t0020 | g0015 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18987 | hp2 | a0001 | c0001 | t0015 | g0150 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18994 | hp1 | a0015 | c0012 | t0004 | g0079 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18997 | hp2 | a0001 | c0001 | t0010 | g0163 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18998 | hp1 | a0009 | c0009 | t0003 | g0041 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0162 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19010 | hp1 | a0018 | c0029 | t0001 | g0251 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0307 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0293 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19056 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19057 | hp1 | a0006 | c0031 | t0016 | g0179 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19059 | hp1 | a0005 | c0032 | t0025 | g0002 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19059 | hp2 | a0025 | c0011 | t0014 | g0008 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19063 | hp1 | a0001 | c0002 | t0021 | g0091 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19067 | hp1 | a0028 | c0030 | t0001 | g0178 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19072 | hp1 | a0003 | c0004 | t0006 | g0088 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19074 | hp2 | a0001 | c0001 | t0024 | g0283 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19075 | hp1 | a0026 | c0023 | t0003 | g0001 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0241 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19082 | hp1 | a0022 | c0016 | t0001 | g0117 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19083 | hp1 | a0021 | c0028 | t0001 | g0049 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19086 | hp1 | a0010 | c0021 | t0004 | g0140 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0142 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19091 | hp1 | a0017 | c0013 | t0003 | g0069 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0308 | AFR | ASW | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ASW | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0231 | EUR | TSI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20805 | hp1 | a0001 | c0001 | t0018 | g0219 | EUR | TSI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0189 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02486 | hp1 | a0001 | c0001 | t0023 | g0205 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0294 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02559 | hp2 | a0024 | c0026 | t0001 | g0301 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03471 | hp1 | a0002 | c0003 | t0002 | g0292 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0310 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA21309 | hp1 | a0023 | c0017 | t0006 | g0183 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0235 | REF | REF | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0234 | REF | REF | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| 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:129739217
|
GC | G | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.7delC | p.Arg3fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 242/3311 | 7/2025 | 3/674 | INFO_REALIGN_3_PRIME | chrX | 129739217 | |
| chrX:129742128
|
A | AAG | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.71_72dupAG | p.Pro25fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/21 | 308/3311 | 73/2025 | 25/674 | INFO_REALIGN_3_PRIME | chrX | 129742128 | |
| chrX:129744028
|
A | G | 1 | a0003 | 3 | HG04184.hp2 NA18975.hp1 NA19072.hp1 |
missense_variant | MODERATE | c.191A>G | p.Gln64Arg | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/21 | 426/3311 | 191/2025 | 64/674 | chrX | 129744028 | ||
| chrX:129744049
|
TC | T | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.215delC | p.Pro72fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/21 | 450/3311 | 215/2025 | 72/674 | INFO_REALIGN_3_PRIME | chrX | 129744049 | |
| chrX:129745211
|
C | CA | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.244dupA | p.Ile82fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/21 | 480/3311 | 245/2025 | 82/674 | INFO_REALIGN_3_PRIME | chrX | 129745211 | |
| chrX:129745233
|
C | T | 1 | a0006 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.265C>T | p.Arg89Cys | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/21 | 500/3311 | 265/2025 | 89/674 | chrX | 129745233 | ||
| chrX:129745254
|
A | AC | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.287dupC | p.Gly97fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/21 | 523/3311 | 288/2025 | 96/674 | INFO_REALIGN_3_PRIME | chrX | 129745254 | |
| chrX:129746296
|
A | AG | 1 | a0028 | 1 | NA19067.hp1 | frameshift_variant | HIGH | c.361dupG | p.Ala121fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/21 | 597/3311 | 362/2025 | 121/674 | INFO_REALIGN_3_PRIME | chrX | 129746296 | |
| chrX:129746304
|
C | CG | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.369dupG | p.Gln124fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/21 | 605/3311 | 370/2025 | 124/674 | INFO_REALIGN_3_PRIME | chrX | 129746304 | |
| chrX:129746331
|
C | CA | 1 | a0005 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.395dupA | p.His132fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/21 | 631/3311 | 396/2025 | 132/674 | INFO_REALIGN_3_PRIME | chrX | 129746331 | |
| chrX:129746598
|
G | GCAC | 1 | a0027 | 1 | NA18987.hp1 | disruptive_inframe_insertion | MODERATE | c.411_413dupCAC | p.Thr138dup | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/21 | 649/3311 | 414/2025 | 138/674 | INFO_REALIGN_3_PRIME | chrX | 129746598 | |
| chrX:129746618
|
TG | T | 1 | a0027 | 1 | NA18987.hp1 | frameshift_variant | HIGH | c.429delG | p.Trp143fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/21 | 664/3311 | 429/2025 | 143/674 | INFO_REALIGN_3_PRIME | chrX | 129746618 | |
| chrX:129746637
|
CT | C | 1 | a0027 | 1 | NA18987.hp1 | frameshift_variant | HIGH | c.447delT | p.Ala150fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/21 | 682/3311 | 447/2025 | 149/674 | chrX | 129746637 | ||
| chrX:129746652
|
TG | T | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.464delG | p.Gly155fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/21 | 699/3311 | 464/2025 | 155/674 | INFO_REALIGN_3_PRIME | chrX | 129746652 | |
| chrX:129747679
|
TG | T | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.565delG | p.Asp189fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/21 | 800/3311 | 565/2025 | 189/674 | INFO_REALIGN_3_PRIME | chrX | 129747679 | |
| chrX:129750476
|
T | TG | 1 | a0007 | 1 | HG02080.hp1 | frameshift_variant | HIGH | c.648dupG | p.Gln217fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/21 | 884/3311 | 649/2025 | 217/674 | INFO_REALIGN_3_PRIME | chrX | 129750476 | |
| chrX:129750501
|
G | GA | 1 | a0008 | 1 | NA18967.hp1 | frameshift_variant | HIGH | c.673dupA | p.Ser225fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/21 | 909/3311 | 674/2025 | 225/674 | INFO_REALIGN_3_PRIME | chrX | 129750501 | |
| chrX:129750514
|
G | GA | 1 | a0009 | 1 | NA18998.hp1 | frameshift_variant | HIGH | c.686dupA | p.His230fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/21 | 922/3311 | 687/2025 | 229/674 | INFO_REALIGN_3_PRIME | chrX | 129750514 | |
| chrX:129750558
|
A | AG | 1 | a0008 | 1 | NA18967.hp1 | frameshift_variant | HIGH | c.730dupG | p.Glu244fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/21 | 966/3311 | 731/2025 | 244/674 | INFO_REALIGN_3_PRIME | chrX | 129750558 | |
| chrX:129751743
|
A | AG | 1 | a0010 | 1 | NA19086.hp1 | frameshift_variant&splice_region_variant | HIGH | c.741dupG | p.Leu248fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/21 | 977/3311 | 742/2025 | 248/674 | INFO_REALIGN_3_PRIME | chrX | 129751743 | |
| chrX:129751759
|
C | G | 1 | a0004 | 2 | HG02258.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.754C>G | p.Arg252Gly | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/21 | 989/3311 | 754/2025 | 252/674 | chrX | 129751759 | ||
| chrX:129751769
|
A | AC | 1 | a0010 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.765dupC | p.Ile256fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/21 | 1001/3311 | 766/2025 | 256/674 | INFO_REALIGN_3_PRIME | chrX | 129751769 | |
| chrX:129752222
|
G | GT | 1 | a0010 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.895dupT | p.Cys299fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1131/3311 | 896/2025 | 299/674 | INFO_REALIGN_3_PRIME | chrX | 129752222 | |
| chrX:129752227
|
T | TG | 1 | a0011 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.900dupG | p.Gln301fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1136/3311 | 901/2025 | 301/674 | INFO_REALIGN_3_PRIME | chrX | 129752227 | |
| chrX:129752254
|
G | A | 1 | a0012 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.926G>A | p.Arg309His | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1161/3311 | 926/2025 | 309/674 | chrX | 129752254 | ||
| chrX:129752278
|
TG | T | 1 | a0013 | 1 | HG03490.hp1 | frameshift_variant | HIGH | c.953delG | p.Gly318fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1188/3311 | 953/2025 | 318/674 | INFO_REALIGN_3_PRIME | chrX | 129752278 | |
| chrX:129752300
|
T | TG | 1 | a0010 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.975dupG | p.Thr326fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1211/3311 | 976/2025 | 326/674 | INFO_REALIGN_3_PRIME | chrX | 129752300 | |
| chrX:129752321
|
TG | T | 1 | a0009 | 1 | NA18998.hp1 | frameshift_variant | HIGH | c.996delG | p.Ile333fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1231/3311 | 996/2025 | 332/674 | INFO_REALIGN_3_PRIME | chrX | 129752321 | |
| chrX:129753183
|
TC | T | 1 | a0025 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.1046delC | p.Pro349fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/21 | 1281/3311 | 1046/2025 | 349/674 | INFO_REALIGN_3_PRIME | chrX | 129753183 | |
| chrX:129753208
|
T | TG | 1 | a0014 | 1 | NA18964.hp1 | frameshift_variant | HIGH | c.1068dupG | p.Lys357fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/21 | 1304/3311 | 1069/2025 | 357/674 | INFO_REALIGN_3_PRIME | chrX | 129753208 | |
| chrX:129753228
|
G | GC | 1 | a0024 | 1 | HG02559.hp2 | frameshift_variant | HIGH | c.1090dupC | p.Leu364fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/21 | 1326/3311 | 1091/2025 | 364/674 | INFO_REALIGN_3_PRIME | chrX | 129753228 | |
| chrX:129754475
|
C | CG | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1114dupG | p.Asp372fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1350/3311 | 1115/2025 | 372/674 | INFO_REALIGN_3_PRIME | chrX | 129754475 | |
| chrX:129754481
|
G | GC | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1118dupC | p.Val374fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1354/3311 | 1119/2025 | 373/674 | INFO_REALIGN_3_PRIME | chrX | 129754481 | |
| chrX:129754487
|
G | GC | 1 | a0015 | 1 | NA18994.hp1 | frameshift_variant | HIGH | c.1124dupC | p.Val376fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1360/3311 | 1125/2025 | 375/674 | INFO_REALIGN_3_PRIME | chrX | 129754487 | |
| chrX:129754496
|
C | CG | 1 | a0011 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.1134dupG | p.Tyr379fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1370/3311 | 1135/2025 | 379/674 | INFO_REALIGN_3_PRIME | chrX | 129754496 | |
| chrX:129754496
|
C | CT | 1 | a0015 | 1 | NA18994.hp1 | frameshift_variant | HIGH | c.1132_1133insT | p.Arg378fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1368/3311 | 1133/2025 | 378/674 | chrX | 129754496 | ||
| chrX:129754518
|
A | G | 1 | a0023 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1154A>G | p.Lys385Arg | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1389/3311 | 1154/2025 | 385/674 | chrX | 129754518 | ||
| chrX:129754551
|
C | T | 1 | a0002 | 3 | HG01243.hp1 HG02976.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1187C>T | p.Ser396Leu | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1422/3311 | 1187/2025 | 396/674 | chrX | 129754551 | ||
| chrX:129755310
|
TC | T | 1 | a0025 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.1236delC | p.Gly413fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/21 | 1471/3311 | 1236/2025 | 412/674 | INFO_REALIGN_3_PRIME | chrX | 129755310 | |
| chrX:129756483
|
G | GC | 2 | a0016a0017 | 2 | NA18959.hp1 NA19091.hp1 |
frameshift_variant | HIGH | c.1298dupC | p.Thr434fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1534/3311 | 1299/2025 | 433/674 | INFO_REALIGN_3_PRIME | chrX | 129756483 | |
| chrX:129756490
|
CA | C | 1 | a0016 | 1 | NA18959.hp1 | frameshift_variant | HIGH | c.1304delA | p.Lys435fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1539/3311 | 1304/2025 | 435/674 | INFO_REALIGN_3_PRIME | chrX | 129756490 | |
| chrX:129756499
|
G | GA | 1 | a0016 | 1 | NA18959.hp1 | frameshift_variant | HIGH | c.1313dupA | p.Asn438fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1549/3311 | 1314/2025 | 438/674 | INFO_REALIGN_3_PRIME | chrX | 129756499 | |
| chrX:129756526
|
G | GTA | 1 | a0022 | 1 | NA19082.hp1 | frameshift_variant | HIGH | c.1339_1340dupTA | p.Leu448fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1576/3311 | 1341/2025 | 447/674 | INFO_REALIGN_3_PRIME | chrX | 129756526 | |
| chrX:129756541
|
T | TG | 1 | a0018 | 1 | NA19010.hp1 | frameshift_variant | HIGH | c.1359dupG | p.Gln454fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1595/3311 | 1360/2025 | 454/674 | INFO_REALIGN_3_PRIME | chrX | 129756541 | |
| chrX:129756541
|
TG | T | 1 | a0021 | 1 | NA19083.hp1 | frameshift_variant | HIGH | c.1359delG | p.Gln454fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1594/3311 | 1359/2025 | 453/674 | INFO_REALIGN_3_PRIME | chrX | 129756541 | |
| chrX:129756546
|
G | A | 1 | a0016 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1358G>A | p.Gly453Glu | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1593/3311 | 1358/2025 | 453/674 | chrX | 129756546 | ||
| chrX:129759178
|
AG | A | 1 | a0017 | 1 | NA19091.hp1 | frameshift_variant&splice_region_variant | HIGH | c.1369delG | p.Asp457fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/21 | 1604/3311 | 1369/2025 | 457/674 | INFO_REALIGN_3_PRIME | chrX | 129759178 | |
| chrX:129759214
|
T | TG | 1 | a0019 | 1 | HG02738.hp1 | frameshift_variant | HIGH | c.1406dupG | p.Thr470fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/21 | 1642/3311 | 1407/2025 | 469/674 | INFO_REALIGN_3_PRIME | chrX | 129759214 | |
| chrX:129760498
|
CCTCTCCC others(39): Show |
C | 1 | a0026 | 1 | NA19075.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1429-13_1461delCTC others(43): Show |
p.Glu477_Asp488del | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/21 | 1429/2025 | 477/674 | chrX | 129760498 | |||
| chrX:129760546
|
A | AC | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1465dupC | p.Leu489fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/21 | 1701/3311 | 1466/2025 | 489/674 | INFO_REALIGN_3_PRIME | chrX | 129760546 | |
| chrX:129760563
|
T | C | 1 | a0026 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.1480T>C | p.Phe494Leu | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/21 | 1715/3311 | 1480/2025 | 494/674 | chrX | 129760563 | ||
| chrX:129761211
|
A | AC | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1538_1539insC | p.Ala514fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/21 | 1774/3311 | 1539/2025 | 513/674 | chrX | 129761211 | ||
| chrX:129761227
|
TG | T | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1556delG | p.Gly519fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/21 | 1791/3311 | 1556/2025 | 519/674 | INFO_REALIGN_3_PRIME | chrX | 129761227 | |
| chrX:129761236
|
G | GA | 1 | a0020 | 1 | HG02523.hp1 | frameshift_variant | HIGH | c.1564dupA | p.Thr522fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/21 | 1800/3311 | 1565/2025 | 522/674 | INFO_REALIGN_3_PRIME | chrX | 129761236 | |
| chrX:129762725
|
G | GAT | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1696_1697dupAT | p.Arg567fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/21 | 1933/3311 | 1698/2025 | 566/674 | INFO_REALIGN_3_PRIME | chrX | 129762725 | |
| chrX:129762735
|
GA | G | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1707delA | p.Asp570fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/21 | 1942/3311 | 1707/2025 | 569/674 | INFO_REALIGN_3_PRIME | chrX | 129762735 | |
| chrX:129762760
|
CA | C | 1 | a0026 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1733delA | p.Lys578fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/21 | 1968/3311 | 1733/2025 | 578/674 | INFO_REALIGN_3_PRIME | chrX | 129762760 | |
| chrX:129768432
|
TG | T | 1 | a0025 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.1975delG | p.Ala659fs | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 2210/3311 | 1975/2025 | 659/674 | INFO_REALIGN_3_PRIME | chrX | 129768432 | |
| chrX:129769534
|
A | G | 1 | a0001 | 3 | NA18997.hp2 NA19056.hp1 NA19090.hp1 |
splice_region_variant | LOW | c.*1049A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | chrX | 129769534 |
| 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:129742136
|
G | T | 1 | a0005c0032 | 1 | NA19059.hp1 | synonymous_variant | LOW | c.78G>T | p.Val26Val | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/21 | 313/3311 | 78/2025 | 26/674 | chrX | 129742136 | ||
| chrX:129746638
|
T | C | 23 | a0001c0001a0001c0010a0001c0020others(20): Show | 216 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(213): Show |
synonymous_variant | LOW | c.447T>C | p.Pro149Pro | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/21 | 682/3311 | 447/2025 | 149/674 | chrX | 129746638 | ||
| chrX:129752174
|
T | C | 1 | a0001c0010 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.846T>C | p.Phe282Phe | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1081/3311 | 846/2025 | 282/674 | chrX | 129752174 | ||
| chrX:129752201
|
C | T | 1 | a0001c0020 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.873C>T | p.Asn291Asn | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1108/3311 | 873/2025 | 291/674 | chrX | 129752201 | ||
| chrX:129762728
|
C | A | 1 | a0026c0023 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.1698C>A | p.Ile566Ile | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/21 | 1933/3311 | 1698/2025 | 566/674 | chrX | 129762728 | ||
| chrX:129767686
|
C | G | 1 | a0001c0006 | 2 | HG00323.hp1 HG03669.hp1 |
synonymous_variant | LOW | c.1824C>G | p.Pro608Pro | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/21 | 2059/3311 | 1824/2025 | 608/674 | chrX | 129767686 |
| 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:129738999
|
CA | C | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 212 | INFO_REALIGN_3_PRIME | chrX | 129738999 | ||||
| chrX:129739065
|
A | AC | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 145 | INFO_REALIGN_3_PRIME | chrX | 129739065 | ||||
| chrX:129739079
|
C | T | 1 | a0001c0001t0024 | 1 | NA19074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-135C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | chrX | 129739079 | ||||||
| chrX:129739104
|
A | G | 1 | a0001c0001t0023 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 110 | chrX | 129739104 | |||||
| chrX:129739109
|
C | CT | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-104dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 103 | INFO_REALIGN_3_PRIME | chrX | 129739109 | ||||
| chrX:129739124
|
C | T | 3 | a0001c0001t0007a0001c0001t0022a0004c0005t0007 | 8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-90C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 90 | chrX | 129739124 | |||||
| chrX:129739138
|
A | AG | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 73 | INFO_REALIGN_3_PRIME | chrX | 129739138 | ||||
| chrX:129739148
|
C | CG | 1 | a0001c0002t0021 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 61 | INFO_REALIGN_3_PRIME | chrX | 129739148 | ||||
| chrX:129739162
|
T | TC | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 48 | INFO_REALIGN_3_PRIME | chrX | 129739162 | ||||
| chrX:129739180
|
C | CAT | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34_-33insAT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 33 | chrX | 129739180 | |||||
| chrX:129739181
|
T | C | 1 | a0005c0032t0025 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 33 | chrX | 129739181 | |||||
| chrX:129768507
|
A | AC | 1 | a0001c0002t0013 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 26 | INFO_REALIGN_3_PRIME | chrX | 129768507 | ||||
| chrX:129768632
|
TG | T | 1 | a0025c0011t0014 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 149 | INFO_REALIGN_3_PRIME | chrX | 129768632 | ||||
| chrX:129768648
|
C | A | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(16): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*163C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 163 | chrX | 129768648 | |||||
| chrX:129768656
|
A | G | 1 | a0006c0031t0016 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 171 | chrX | 129768656 | |||||
| chrX:129768671
|
GC | G | 2 | a0001c0001t0015a0025c0011t0014 | 2 | NA18987.hp2 NA19059.hp2 |
3_prime_UTR_variant | MODIFIER | c.*190delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 190 | INFO_REALIGN_3_PRIME | chrX | 129768671 | ||||
| chrX:129768716
|
C | G | 1 | a0001c0001t0008 | 6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*231C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 231 | chrX | 129768716 | |||||
| chrX:129768817
|
G | A | 3 | a0001c0001t0007a0001c0001t0009a0004c0005t0007 | 11 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 332 | chrX | 129768817 | |||||
| chrX:129768887
|
G | A | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*402G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 402 | chrX | 129768887 | |||||
| chrX:129768919
|
C | T | 13 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(10): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 434 | chrX | 129768919 | |||||
| chrX:129768922
|
A | G | 1 | a0001c0001t0011 | 3 | HG06807.hp2 NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 437 | chrX | 129768922 | |||||
| chrX:129768962
|
AC | A | 1 | a0025c0011t0014 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 483 | INFO_REALIGN_3_PRIME | chrX | 129768962 | ||||
| chrX:129769123
|
C | A | 1 | a0001c0001t0018 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 638 | chrX | 129769123 | |||||
| chrX:129769128
|
G | A | 1 | a0001c0001t0012 | 3 | NA18947.hp1 NA18999.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*643G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 643 | chrX | 129769128 | |||||
| chrX:129769155
|
T | TGGG | 1 | a0027c0007t0020 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672_*673insGGG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 673 | INFO_REALIGN_3_PRIME | chrX | 129769155 | ||||
| chrX:129769163
|
G | GA | 1 | a0027c0007t0020 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 680 | INFO_REALIGN_3_PRIME | chrX | 129769163 | ||||
| chrX:129769218
|
TC | T | 1 | a0025c0011t0014 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 736 | INFO_REALIGN_3_PRIME | chrX | 129769218 | ||||
| chrX:129769275
|
T | C | 1 | a0001c0002t0019 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*790T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 790 | chrX | 129769275 | |||||
| chrX:129769302
|
AG | A | 1 | a0001c0001t0017 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 822 | INFO_REALIGN_3_PRIME | chrX | 129769302 | ||||
| chrX:129769496
|
G | T | 7 | a0001c0001t0004a0005c0032t0025a0006c0031t0016others(4): Show | 25 | HG01106.hp1 HG02083.hp1 HG02155.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1011G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 1011 | chrX | 129769496 | |||||
| chrX:129769518
|
TA | T | 1 | a0001c0002t0013 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 1037 | INFO_REALIGN_3_PRIME | chrX | 129769518 |
| 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:129739267
|
GTGCATCC others(6): Show |
G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.49+6_49+18delTGCAT others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739267 | ||||||
| chrX:129739305
|
T | TC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+47dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739305 | |||||
| chrX:129739348
|
G | C | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.49+86G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739348 | ||||||
| chrX:129739410
|
TG | T | 1 | a0001c0001t0003g0004 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.49+153delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739410 | |||||
| chrX:129739453
|
C | G | 7 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0003g0304others(4): Show | 7 | HG02647.hp1 HG03098.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+191C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739453 | ||||||
| chrX:129739470
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+216dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739470 | |||||
| chrX:129739470
|
GA | G | 1 | a0001c0001t0002g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.49+216delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739470 | |||||
| chrX:129739471
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.49+209A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739471 | ||||||
| chrX:129739484
|
T | TA | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+222_49+223insA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739484 | ||||||
| chrX:129739491
|
C | T | 1 | a0024c0026t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.49+229C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739491 | ||||||
| chrX:129739610
|
A | AG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+353dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739610 | |||||
| chrX:129739751
|
C | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+489C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739751 | ||||||
| chrX:129739835
|
TG | T | 2 | a0005c0032t0025g0002a0025c0011t0014g0008 | 2 | NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.49+578delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739835 | |||||
| chrX:129739949
|
C | G | 1 | a0001c0001t0004g0300 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.49+687C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739949 | ||||||
| chrX:129739982
|
A | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.49+720A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739982 | ||||||
| chrX:129739994
|
TC | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+734delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129739994 | |||||
| chrX:129740004
|
G | A | 2 | a0001c0001t0005g0010a0001c0010t0002g0009 | 2 | HG01081.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.49+742G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740004 | ||||||
| chrX:129740083
|
C | G | 1 | a0001c0002t0001g0297 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.49+821C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740083 | ||||||
| chrX:129740244
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+984dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740244 | |||||
| chrX:129740344
|
T | TG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+1084dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740344 | |||||
| chrX:129740353
|
G | A | 90 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0002g0012others(87): Show | 90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.49+1091G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740353 | ||||||
| chrX:129740373
|
TC | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+1114delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740373 | |||||
| chrX:129740390
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+1130delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740390 | |||||
| chrX:129740402
|
G | C | 7 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0003g0304others(4): Show | 7 | HG02647.hp1 HG03098.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+1140G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740402 | ||||||
| chrX:129740417
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+1157delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740417 | |||||
| chrX:129740432
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.49+1172delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740432 | |||||
| chrX:129740438
|
C | A | 102 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0095others(99): Show | 102 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.49+1176C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740438 | ||||||
| chrX:129740462
|
A | G | 106 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0095others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.49+1200A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740462 | ||||||
| chrX:129740471
|
A | G | 6 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0004g0305others(3): Show | 6 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+1209A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740471 | ||||||
| chrX:129740484
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+1224delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740484 | |||||
| chrX:129740500
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.49+1238G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740500 | ||||||
| chrX:129740522
|
G | C | 1 | a0023c0017t0006g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+1260G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740522 | ||||||
| chrX:129740523
|
G | C | 106 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0095others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.49+1261G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740523 | ||||||
| chrX:129740526
|
G | C | 1 | a0001c0002t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+1264G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740526 | ||||||
| chrX:129740553
|
C | G | 8 | a0001c0001t0007g0284a0001c0001t0007g0285a0001c0001t0007g0286others(5): Show | 8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+1291C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740553 | ||||||
| chrX:129740607
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+1349dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740607 | |||||
| chrX:129740622
|
C | CG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+1360_49+1361ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740622 | ||||||
| chrX:129740628
|
C | CA | 42 | a0001c0001t0001g0087a0001c0001t0001g0208a0001c0001t0002g0188others(39): Show | 42 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.49+1380dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740628 | |||||
| chrX:129740628
|
C | CAA | 1 | a0001c0001t0006g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.49+1379_49+1380dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740628 | |||||
| chrX:129740628
|
CA | C | 3 | a0001c0001t0003g0084a0001c0001t0024g0283a0016c0027t0001g0182 | 3 | HG02723.hp2 NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.49+1380delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740628 | |||||
| chrX:129740643
|
T | TGCTGG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.49+1383_49+1384ins others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740643 | |||||
| chrX:129740645
|
C | CG | 2 | a0005c0032t0025g0002a0007c0022t0003g0181 | 2 | HG02080.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.49+1386dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740645 | |||||
| chrX:129740651
|
C | CG | 3 | a0001c0001t0001g0180a0001c0002t0001g0282a0025c0011t0014g0008 | 3 | HG01192.hp1 NA18990.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.49+1395dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740651 | |||||
| chrX:129740734
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-1372dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740734 | |||||
| chrX:129740739
|
A | AG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1368dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740739 | |||||
| chrX:129740778
|
T | TA | 2 | a0005c0032t0025g0002a0026c0023t0003g0001 | 2 | NA19059.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.50-1325dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740778 | |||||
| chrX:129740878
|
GT | G | 1 | a0001c0002t0001g0214 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.50-1228delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740878 | |||||
| chrX:129740892
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-1215dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740892 | |||||
| chrX:129740901
|
C | CCA | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1207_50-1206ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740901 | ||||||
| chrX:129740902
|
A | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1206A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740902 | ||||||
| chrX:129740908
|
C | CCT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1200_50-1199ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740908 | ||||||
| chrX:129740909
|
T | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1199T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740909 | ||||||
| chrX:129740939
|
C | CA | 6 | a0001c0001t0001g0087a0001c0001t0002g0012a0001c0001t0003g0090others(3): Show | 6 | HG04228.hp1 NA18939.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-1155dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740939 | |||||
| chrX:129740939
|
CA | C | 2 | a0005c0032t0025g0002a0006c0031t0016g0179 | 2 | NA19057.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.50-1155delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740939 | |||||
| chrX:129740956
|
A | AG | 136 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0143others(133): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.50-1145dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740956 | |||||
| chrX:129740956
|
A | AGG | 10 | a0001c0001t0002g0176a0001c0001t0003g0082a0001c0001t0004g0080others(7): Show | 10 | HG00597.hp2 HG02074.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-1146_50-1145dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740956 | |||||
| chrX:129740956
|
A | AGGG | 1 | a0001c0002t0001g0214 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.50-1147_50-1145dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740956 | |||||
| chrX:129740964
|
C | G | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.50-1144C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740964 | ||||||
| chrX:129740965
|
G | GGC | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.50-1142_50-1141ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740965 | |||||
| chrX:129740988
|
A | C | 1 | a0001c0002t0001g0246 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.50-1120A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740988 | ||||||
| chrX:129740995
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1109delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740995 | |||||
| chrX:129741010
|
AG | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1095delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741010 | |||||
| chrX:129741033
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-1069delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741033 | |||||
| chrX:129741083
|
C | A | 1 | a0001c0001t0008g0294 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.50-1025C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741083 | ||||||
| chrX:129741088
|
CT | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1017delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741088 | |||||
| chrX:129741096
|
AG | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1010delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741096 | |||||
| chrX:129741172
|
T | TG | 60 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0002g0065others(57): Show | 60 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.50-927dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | |||||
| chrX:129741172
|
T | TGG | 122 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(119): Show | 122 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.50-928_50-927dupGG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | |||||
| chrX:129741172
|
T | TGGG | 15 | a0001c0001t0001g0180a0001c0001t0002g0014a0001c0001t0002g0052others(12): Show | 15 | HG00544.hp1 HG01243.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-929_50-927dupGG others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | |||||
| chrX:129741172
|
T | TGGGG | 1 | a0002c0003t0002g0292 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-930_50-927dupGG others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | |||||
| chrX:129741172
|
TG | T | 30 | a0001c0001t0001g0208a0001c0001t0002g0188a0001c0001t0002g0191others(27): Show | 30 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.50-927delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | |||||
| chrX:129741174
|
G | T | 1 | a0001c0002t0001g0245 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.50-934G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741174 | ||||||
| chrX:129741240
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.50-868A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741240 | ||||||
| chrX:129741242
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-864dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741242 | |||||
| chrX:129741245
|
C | T | 1 | a0001c0002t0013g0281 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.50-863C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741245 | ||||||
| chrX:129741266
|
CT | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-837delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741266 | |||||
| chrX:129741350
|
CA | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-755delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741350 | |||||
| chrX:129741363
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-744dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741363 | |||||
| chrX:129741364
|
AC | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-742delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741364 | |||||
| chrX:129741376
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-730delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741376 | |||||
| chrX:129741378
|
G | GT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-729dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741378 | |||||
| chrX:129741384
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-722dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741384 | |||||
| chrX:129741505
|
T | A | 1 | a0001c0002t0001g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.50-603T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741505 | ||||||
| chrX:129741600
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-504dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741600 | |||||
| chrX:129741608
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-498delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741608 | |||||
| chrX:129741641
|
G | GA | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-464dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741641 | |||||
| chrX:129741657
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-449delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741657 | |||||
| chrX:129741664
|
AT | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-442delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741664 | |||||
| chrX:129741673
|
AAC | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-434_50-433delAC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741673 | ||||||
| chrX:129741692
|
T | A | 1 | a0001c0001t0002g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50-416T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741692 | ||||||
| chrX:129741737
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.50-371G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741737 | ||||||
| chrX:129741760
|
GA | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-344delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741760 | |||||
| chrX:129741773
|
CA | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-330delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741773 | |||||
| chrX:129741783
|
AT | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-322delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741783 | |||||
| chrX:129741794
|
A | G | 20 | a0001c0001t0002g0192a0001c0001t0002g0194a0001c0001t0002g0199others(17): Show | 20 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.50-314A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741794 | ||||||
| chrX:129741812
|
AC | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-293delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741812 | |||||
| chrX:129741825
|
C | T | 83 | a0001c0001t0001g0062a0001c0001t0001g0174a0001c0001t0002g0012others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.50-283C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741825 | ||||||
| chrX:129741871
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-237_50-236insA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741871 | ||||||
| chrX:129741900
|
A | AC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-207dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741900 | |||||
| chrX:129741932
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-174delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741932 | |||||
| chrX:129741962
|
G | T | 3 | a0001c0001t0002g0199a0001c0001t0017g0212a0002c0003t0005g0213 | 3 | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-146G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741962 | ||||||
| chrX:129742002
|
G | A | 126 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0002g0012others(123): Show | 126 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.50-106G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742002 | ||||||
| chrX:129742020
|
C | CG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-88_50-87insG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742020 | ||||||
| chrX:129742027
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-81_50-80insA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742027 | ||||||
| chrX:129742050
|
C | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0137a0001c0001t0009g0198 | 3 | HG01891.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.50-58C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742050 | ||||||
| chrX:129742060
|
GA | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-46delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129742060 | |||||
| chrX:129742081
|
A | AC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-24dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129742081 | |||||
| chrX:129742085
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.50-21delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129742085 | |||||
| chrX:129742098
|
C | T | 1 | a0001c0001t0006g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.50-10C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742098 | ||||||
| chrX:129742188
|
G | GC | 1 | a0001c0001t0001g0144 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.123+12dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742188 | |||||
| chrX:129742195
|
G | GC | 3 | a0001c0002t0001g0013a0019c0015t0002g0016a0026c0023t0003g0001 | 3 | HG00544.hp1 HG02738.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.123+20dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742195 | |||||
| chrX:129742195
|
G | GCC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+19_123+20dupCC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742195 | |||||
| chrX:129742209
|
G | GC | 5 | a0001c0001t0001g0087a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG02080.hp1 NA18939.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+34dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742209 | |||||
| chrX:129742210
|
C | G | 1 | a0019c0015t0002g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123+29C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742210 | ||||||
| chrX:129742227
|
A | AC | 14 | a0001c0001t0001g0136a0001c0001t0001g0172a0001c0001t0001g0279others(11): Show | 14 | HG00544.hp2 HG00597.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.123+53dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742227 | |||||
| chrX:129742227
|
AC | A | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.123+53delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742227 | |||||
| chrX:129742228
|
C | CT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+47_123+48insT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742228 | ||||||
| chrX:129742235
|
A | AC | 1 | a0001c0002t0021g0091 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+58dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742235 | |||||
| chrX:129742246
|
A | G | 2 | a0001c0001t0003g0084a0001c0001t0006g0189 | 2 | HG01123.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.123+65A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742246 | ||||||
| chrX:129742266
|
A | AC | 7 | a0001c0001t0002g0099a0001c0001t0003g0090a0001c0002t0001g0248others(4): Show | 7 | HG01192.hp1 HG01243.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+90dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742266 | |||||
| chrX:129742269
|
CCCGCCCT others(64): Show |
C | 3 | a0001c0001t0002g0093a0001c0001t0002g0134a0001c0001t0002g0135 | 3 | HG02523.hp2 NA18999.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.123+91_123+161delG others(70): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742269 | |||||
| chrX:129742272
|
G | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+91G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742272 | ||||||
| chrX:129742273
|
C | CCG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+93_123+94insGC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742273 | |||||
| chrX:129742333
|
G | GGC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+153_123+154dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742333 | |||||
| chrX:129742362
|
C | G | 1 | a0001c0002t0001g0133 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.123+181C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742362 | ||||||
| chrX:129742373
|
T | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+192T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742373 | ||||||
| chrX:129742374
|
C | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+193C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742374 | ||||||
| chrX:129742421
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+245delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742421 | |||||
| chrX:129742454
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+276delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742454 | |||||
| chrX:129742506
|
T | TG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+327dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742506 | |||||
| chrX:129742561
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+385delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742561 | |||||
| chrX:129742580
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.123+399G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742580 | ||||||
| chrX:129742585
|
G | A | 14 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(11): Show | 14 | HG00673.hp1 HG01496.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.123+404G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742585 | ||||||
| chrX:129742619
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+440delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742619 | |||||
| chrX:129742624
|
G | A | 55 | a0001c0001t0001g0174a0001c0001t0002g0042a0001c0001t0002g0302others(52): Show | 55 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.123+443G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742624 | ||||||
| chrX:129742673
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+494dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742673 | |||||
| chrX:129742700
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.123+519G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742700 | ||||||
| chrX:129742719
|
TG | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+540delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742719 | |||||
| chrX:129742723
|
G | GA | 2 | a0026c0023t0003g0001a0028c0030t0001g0178 | 2 | NA19067.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.123+545dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742723 | |||||
| chrX:129742739
|
TA | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+563delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742739 | |||||
| chrX:129742760
|
G | A | 101 | a0001c0001t0001g0174a0001c0001t0002g0014a0001c0001t0002g0018others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.123+579G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742760 | ||||||
| chrX:129742761
|
G | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+580G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742761 | ||||||
| chrX:129742762
|
C | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+581C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742762 | ||||||
| chrX:129742763
|
A | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+582A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742763 | ||||||
| chrX:129742783
|
TC | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+606delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742783 | |||||
| chrX:129742794
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0194 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123+613C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742794 | ||||||
| chrX:129742805
|
G | A | 5 | a0001c0001t0004g0305a0001c0001t0008g0195a0001c0001t0008g0196others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+624G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742805 | ||||||
| chrX:129742821
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.123+640G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742821 | ||||||
| chrX:129742841
|
G | GT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+660_123+661ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742841 | ||||||
| chrX:129742874
|
T | TCTGGGCG others(56): Show |
1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+694_123+756dup others(63): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742874 | |||||
| chrX:129742917
|
C | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+736C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742917 | ||||||
| chrX:129742918
|
A | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+737A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742918 | ||||||
| chrX:129742961
|
A | AG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+782dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742961 | |||||
| chrX:129743088
|
A | G | 1 | a0001c0020t0005g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124-873A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743088 | ||||||
| chrX:129743203
|
G | A | 5 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0011g0307others(2): Show | 5 | HG02647.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-758G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743203 | ||||||
| chrX:129743239
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.124-722G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743239 | ||||||
| chrX:129743248
|
CT | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-709delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743248 | |||||
| chrX:129743284
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.124-677T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743284 | ||||||
| chrX:129743309
|
T | TC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-652_124-651ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743309 | ||||||
| chrX:129743347
|
A | G | 83 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0087others(80): Show | 83 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.124-614A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743347 | ||||||
| chrX:129743348
|
C | CT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-612dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743348 | |||||
| chrX:129743367
|
A | AC | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-592dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743367 | |||||
| chrX:129743372
|
T | TG | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-586dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743372 | |||||
| chrX:129743381
|
AC | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-578delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743381 | |||||
| chrX:129743429
|
A | AC | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-529dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743429 | |||||
| chrX:129743445
|
AT | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-512delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743445 | |||||
| chrX:129743463
|
GA | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-496delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743463 | |||||
| chrX:129743481
|
C | T | 5 | a0001c0001t0004g0305a0001c0001t0008g0195a0001c0001t0008g0196others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-480C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743481 | ||||||
| chrX:129743514
|
C | T | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-447C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743514 | ||||||
| chrX:129743517
|
T | TA | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-440dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743517 | |||||
| chrX:129743600
|
A | ACC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-357_124-356dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743600 | |||||
| chrX:129743600
|
AC | A | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-356delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743600 | |||||
| chrX:129743629
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.124-332G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743629 | ||||||
| chrX:129743630
|
C | A | 48 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0095others(45): Show | 48 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.124-331C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743630 | ||||||
| chrX:129743664
|
G | GC | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-296dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743664 | |||||
| chrX:129743673
|
A | AC | 1 | a0001c0001t0004g0045 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.124-285dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743673 | |||||
| chrX:129743673
|
A | ACACC | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-287_124-286ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743673 | |||||
| chrX:129743675
|
C | A | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-286C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743675 | ||||||
| chrX:129743683
|
A | ATAT | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-277_124-275dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743683 | |||||
| chrX:129743723
|
CT | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-235delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743723 | |||||
| chrX:129743801
|
A | AC | 2 | a0001c0001t0003g0090a0008c0008t0003g0085 | 2 | NA18967.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.124-156dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743801 | |||||
| chrX:129743835
|
T | TCC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-122_124-121dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743835 | |||||
| chrX:129743835
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-121delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743835 | |||||
| chrX:129743862
|
T | TG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-94dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743862 | |||||
| chrX:129743900
|
T | TCC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-61_124-60insCC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743900 | ||||||
| chrX:129743923
|
G | GT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.124-35dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129743923 | |||||
| chrX:129744080
|
C | CG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+9_234+10insG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744080 | ||||||
| chrX:129744081
|
A | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+10A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744081 | ||||||
| chrX:129744220
|
AG | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.234+152delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744220 | |||||
| chrX:129744283
|
TC | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+213delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744283 | ||||||
| chrX:129744295
|
A | C | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+224A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744295 | ||||||
| chrX:129744296
|
C | T | 2 | a0002c0003t0002g0292a0002c0003t0002g0295 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.234+225C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744296 | ||||||
| chrX:129744370
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234+302dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744370 | |||||
| chrX:129744401
|
TG | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.234+333delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744401 | |||||
| chrX:129744435
|
AG | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+366delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744435 | |||||
| chrX:129744442
|
C | T | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.234+371C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744442 | ||||||
| chrX:129744456
|
A | C | 85 | a0001c0001t0001g0174a0001c0001t0002g0014a0001c0001t0002g0018others(82): Show | 85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.234+385A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744456 | ||||||
| chrX:129744497
|
C | T | 1 | a0001c0001t0003g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+426C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744497 | ||||||
| chrX:129744499
|
C | CA | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+428_234+429ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744499 | ||||||
| chrX:129744518
|
G | A | 1 | a0001c0001t0006g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.234+447G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744518 | ||||||
| chrX:129744531
|
A | ACC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+461_234+462dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744531 | |||||
| chrX:129744584
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+516delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744584 | |||||
| chrX:129744635
|
A | AT | 1 | a0001c0001t0004g0043 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.235-564dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744635 | |||||
| chrX:129744744
|
TC | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.235-457delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744744 | |||||
| chrX:129744861
|
C | T | 3 | a0001c0001t0002g0199a0001c0001t0017g0212a0002c0003t0005g0213 | 3 | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235-342C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744861 | ||||||
| chrX:129744862
|
CA | C | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.235-338delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744862 | |||||
| chrX:129744897
|
GA | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.235-304delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744897 | |||||
| chrX:129744905
|
A | AG | 1 | a0001c0001t0003g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.235-295dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744905 | |||||
| chrX:129744940
|
C | T | 81 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0087others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.235-263C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744940 | ||||||
| chrX:129744977
|
CG | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.235-221delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129744977 | |||||
| chrX:129745052
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.235-151G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745052 | ||||||
| chrX:129745072
|
G | A | 2 | a0001c0001t0004g0050a0001c0001t0004g0051 | 2 | HG01106.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.235-131G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745072 | ||||||
| chrX:129745118
|
GA | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.235-82delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 129745118 | |||||
| chrX:129745168
|
G | A | 9 | a0001c0001t0002g0223a0001c0002t0001g0106a0001c0002t0001g0215others(6): Show | 9 | HG01975.hp1 HG02015.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-35G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745168 | ||||||
| chrX:129745198
|
C | CT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | splice_region_variant&intron_variant | LOW | c.235-5_235-4insT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745198 | ||||||
| chrX:129745279
|
AC | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.298+16delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745279 | |||||
| chrX:129745284
|
G | GC | 1 | a0001c0002t0021g0091 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.298+22dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745284 | |||||
| chrX:129745284
|
GC | G | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.298+22delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745284 | |||||
| chrX:129745300
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.298+36delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745300 | |||||
| chrX:129745388
|
C | CT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.298+123dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745388 | |||||
| chrX:129745390
|
A | G | 1 | a0001c0020t0005g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.298+124A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745390 | ||||||
| chrX:129745402
|
TC | T | 2 | a0005c0032t0025g0002a0026c0023t0003g0001 | 2 | NA19059.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.298+139delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745402 | |||||
| chrX:129745411
|
C | T | 1 | a0001c0001t0004g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+145C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745411 | ||||||
| chrX:129745412
|
A | AC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.298+150dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745412 | |||||
| chrX:129745412
|
AC | A | 3 | a0025c0011t0014g0008a0026c0023t0003g0001a0028c0030t0001g0178 | 3 | NA19059.hp2 NA19067.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.298+150delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745412 | |||||
| chrX:129745492
|
G | GT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.298+226_298+227ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745492 | ||||||
| chrX:129745516
|
C | T | 6 | a0001c0001t0004g0305a0001c0001t0008g0195a0001c0001t0008g0196others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+250C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745516 | ||||||
| chrX:129745551
|
G | A | 1 | a0001c0020t0005g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.298+285G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745551 | ||||||
| chrX:129745594
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.298+328C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745594 | ||||||
| chrX:129745613
|
AG | A | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.298+350delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745613 | |||||
| chrX:129745679
|
C | T | 75 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(72): Show | 75 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.298+413C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745679 | ||||||
| chrX:129745680
|
A | G | 220 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(217): Show | 220 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.298+414A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745680 | ||||||
| chrX:129745727
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.298+465dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745727 | |||||
| chrX:129745727
|
AG | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.298+465delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745727 | |||||
| chrX:129745740
|
C | G | 69 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(66): Show | 69 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.298+474C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745740 | ||||||
| chrX:129745812
|
AC | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.299-423delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745812 | ||||||
| chrX:129745933
|
C | A | 1 | a0001c0001t0022g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-303C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745933 | ||||||
| chrX:129745939
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.299-293delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745939 | |||||
| chrX:129745959
|
G | A | 2 | a0001c0001t0018g0219a0001c0002t0001g0097 | 2 | NA19074.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.299-277G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745959 | ||||||
| chrX:129746132
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0002g0065 | 2 | NA19003.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.299-104C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129746132 | ||||||
| chrX:129746184
|
GC | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.299-50delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129746184 | |||||
| chrX:129746189
|
GT | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.299-45delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129746189 | |||||
| chrX:129746194
|
TC | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.299-38delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129746194 | |||||
| chrX:129746229
|
G | GC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.299-3dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129746229 | |||||
| chrX:129746230
|
C | T | 1 | a0001c0010t0002g0009 | 1 | HG01081.hp1 | splice_region_variant&intron_variant | LOW | c.299-6C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129746230 | ||||||
| chrX:129746375
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.403+38delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 129746375 | |||||
| chrX:129746414
|
G | A | 64 | a0001c0001t0001g0174a0001c0001t0003g0003a0001c0001t0003g0004others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.403+74G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | chrX | 129746414 | ||||||
| chrX:129746432
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.403+95dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 129746432 | |||||
| chrX:129746439
|
C | CT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.403+100dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 129746439 | |||||
| chrX:129746442
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.403+106delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 129746442 | |||||
| chrX:129746544
|
TG | T | 2 | a0005c0032t0025g0002a0025c0011t0014g0008 | 2 | NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.404-47delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 129746544 | |||||
| chrX:129746691
|
TC | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.490+12delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746691 | |||||
| chrX:129746737
|
TC | T | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.490+59delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746737 | |||||
| chrX:129746748
|
TA | T | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.490+70delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746748 | |||||
| chrX:129746770
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.490+91delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746770 | |||||
| chrX:129746771
|
G | GA | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+90_490+91insA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129746771 | ||||||
| chrX:129746847
|
TG | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+168delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746847 | |||||
| chrX:129746869
|
T | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+188T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129746869 | ||||||
| chrX:129746924
|
GA | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.490+245delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746924 | |||||
| chrX:129746953
|
TG | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+274delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746953 | |||||
| chrX:129746999
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.490+321delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129746999 | |||||
| chrX:129747005
|
GA | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+326delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747005 | |||||
| chrX:129747016
|
A | G | 1 | a0001c0001t0004g0032 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.490+335A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747016 | ||||||
| chrX:129747066
|
A | AGGGTCAA others(9): Show |
1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.490+387_490+402dup others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747066 | |||||
| chrX:129747071
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.490+394delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747071 | |||||
| chrX:129747098
|
T | TA | 1 | a0001c0002t0001g0214 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.490+427dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747098 | |||||
| chrX:129747128
|
T | TC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+450dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747128 | |||||
| chrX:129747161
|
G | GC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.491-443dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747161 | |||||
| chrX:129747209
|
GTGCTTTA others(13): Show |
G | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.491-394_491-375del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747209 | |||||
| chrX:129747265
|
CT | C | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.491-338delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747265 | |||||
| chrX:129747403
|
TG | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.491-202delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747403 | |||||
| chrX:129747424
|
GA | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.491-180delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747424 | |||||
| chrX:129747451
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.491-154delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747451 | |||||
| chrX:129747453
|
C | CG | 1 | a0001c0001t0003g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.491-149dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747453 | |||||
| chrX:129747459
|
T | TG | 2 | a0001c0001t0012g0167a0027c0007t0020g0015 | 2 | NA18947.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.491-142dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747459 | |||||
| chrX:129747466
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.491-138delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747466 | |||||
| chrX:129747490
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0276 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.491-117C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747490 | ||||||
| chrX:129747493
|
G | GC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.491-113dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747493 | |||||
| chrX:129747518
|
A | G | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.491-89A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747518 | ||||||
| chrX:129747538
|
G | A | 10 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0022others(7): Show | 10 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-69G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747538 | ||||||
| chrX:129747550
|
A | AT | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.491-51dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747550 | |||||
| chrX:129747550
|
AT | A | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.491-51delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747550 | |||||
| chrX:129747766
|
GC | G | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.637+16delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129747766 | |||||
| chrX:129747774
|
T | TC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.637+23dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129747774 | |||||
| chrX:129747800
|
T | TC | 1 | a0001c0001t0003g0138 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.637+50dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129747800 | |||||
| chrX:129747878
|
C | G | 1 | a0001c0001t0009g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.637+125C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129747878 | ||||||
| chrX:129747898
|
GTT | G | 1 | a0001c0001t0002g0012 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.637+147_637+148del others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129747898 | |||||
| chrX:129747907
|
G | GC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.637+155dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129747907 | |||||
| chrX:129747919
|
G | GC | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.637+171dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129747919 | |||||
| chrX:129747993
|
A | T | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.637+240A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129747993 | ||||||
| chrX:129748031
|
AG | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.637+281delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748031 | |||||
| chrX:129748064
|
AC | A | 3 | a0001c0001t0003g0072a0001c0001t0003g0082a0001c0001t0024g0283 | 3 | HG00597.hp2 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.637+315delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748064 | |||||
| chrX:129748318
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.637+565_637+566ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748318 | ||||||
| chrX:129748331
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.637+578G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748331 | ||||||
| chrX:129748348
|
C | A | 80 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(77): Show | 80 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.637+595C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748348 | ||||||
| chrX:129748431
|
C | T | 1 | a0001c0010t0002g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.637+678C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748431 | ||||||
| chrX:129748530
|
T | TCCGCATG others(31): Show |
1 | a0001c0001t0003g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.637+778_637+815dup others(38): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748530 | |||||
| chrX:129748620
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.637+871dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748620 | |||||
| chrX:129748681
|
A | AT | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.637+929dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748681 | |||||
| chrX:129748692
|
AT | A | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637+944delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748692 | |||||
| chrX:129748786
|
A | AG | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637+1036dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748786 | |||||
| chrX:129748796
|
G | GA | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637+1048dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748796 | |||||
| chrX:129748832
|
T | TTTCTTCC others(1): Show |
1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637+1079_637+1080i others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748832 | ||||||
| chrX:129748861
|
AC | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.637+1111delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748861 | |||||
| chrX:129748865
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.637+1112G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748865 | ||||||
| chrX:129748877
|
CA | C | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637+1126delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748877 | |||||
| chrX:129748900
|
G | A | 1 | a0001c0001t0018g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.637+1147G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748900 | ||||||
| chrX:129748929
|
CT | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.637+1178delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748929 | |||||
| chrX:129748976
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.637+1227dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748976 | |||||
| chrX:129749033
|
C | T | 36 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(33): Show | 36 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.637+1280C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749033 | ||||||
| chrX:129749046
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.637+1293A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749046 | ||||||
| chrX:129749078
|
TC | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.637+1326delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749078 | ||||||
| chrX:129749192
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-1273delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749192 | |||||
| chrX:129749223
|
AT | A | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1242delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749223 | |||||
| chrX:129749224
|
T | C | 3 | a0001c0001t0002g0111a0001c0001t0002g0191a0001c0001t0002g0211 | 3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-1244T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749224 | ||||||
| chrX:129749229
|
TG | T | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1235delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749229 | |||||
| chrX:129749263
|
CT | C | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1203delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749263 | |||||
| chrX:129749272
|
T | C | 1 | a0001c0010t0002g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.638-1196T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749272 | ||||||
| chrX:129749279
|
T | A | 1 | a0001c0001t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.638-1189T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749279 | ||||||
| chrX:129749302
|
G | A | 8 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0197others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-1166G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749302 | ||||||
| chrX:129749322
|
C | T | 3 | a0001c0001t0002g0131a0001c0001t0002g0170a0001c0001t0002g0302 | 3 | HG02735.hp1 HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.638-1146C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749322 | ||||||
| chrX:129749327
|
G | GT | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1139dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749327 | |||||
| chrX:129749333
|
CA | C | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1133delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749333 | |||||
| chrX:129749374
|
TA | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-1089delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749374 | |||||
| chrX:129749378
|
A | G | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1090A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749378 | ||||||
| chrX:129749379
|
AG | A | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1088delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749379 | ||||||
| chrX:129749387
|
A | T | 1 | a0001c0001t0002g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.638-1081A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749387 | ||||||
| chrX:129749394
|
G | GT | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.638-1070dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749394 | |||||
| chrX:129749478
|
CA | C | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-987delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749478 | |||||
| chrX:129749502
|
G | GT | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-962dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749502 | |||||
| chrX:129749502
|
G | T | 5 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0011g0307others(2): Show | 5 | HG02647.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-966G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749502 | ||||||
| chrX:129749524
|
AT | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-939delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749524 | |||||
| chrX:129749576
|
CT | C | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.638-890delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749576 | |||||
| chrX:129749620
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-844dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749620 | |||||
| chrX:129749620
|
AG | A | 2 | a0008c0008t0003g0085a0013c0025t0001g0274 | 2 | HG03490.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.638-844delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749620 | |||||
| chrX:129749688
|
AGATATAA others(13): Show |
A | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.638-777_638-758del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749688 | |||||
| chrX:129749728
|
G | GT | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.638-737dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749728 | |||||
| chrX:129749753
|
G | C | 137 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(134): Show | 137 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.638-715G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749753 | ||||||
| chrX:129749762
|
CA | C | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.638-704delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749762 | |||||
| chrX:129749786
|
ATTAAG | A | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.638-681_638-677del others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749786 | ||||||
| chrX:129749822
|
G | GT | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.638-644dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749822 | |||||
| chrX:129749829
|
TC | T | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.638-636delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749829 | |||||
| chrX:129749883
|
T | TG | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-584dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749883 | |||||
| chrX:129749911
|
T | TG | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.638-554dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749911 | |||||
| chrX:129749916
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-549delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749916 | |||||
| chrX:129749945
|
G | A | 6 | a0001c0001t0004g0305a0001c0001t0008g0195a0001c0001t0008g0196others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-523G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749945 | ||||||
| chrX:129749964
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-502delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749964 | |||||
| chrX:129749979
|
TG | T | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-485delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749979 | |||||
| chrX:129750012
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-455dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750012 | |||||
| chrX:129750017
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.638-451C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750017 | ||||||
| chrX:129750069
|
T | TA | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-399_638-398ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750069 | ||||||
| chrX:129750114
|
A | AC | 1 | a0001c0002t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.638-352dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750114 | |||||
| chrX:129750117
|
AT | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-349delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750117 | |||||
| chrX:129750122
|
G | T | 1 | a0001c0001t0009g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.638-346G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750122 | ||||||
| chrX:129750137
|
AT | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.638-329delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750137 | |||||
| chrX:129750147
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-319dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750147 | |||||
| chrX:129750171
|
A | AG | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-295dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750171 | |||||
| chrX:129750178
|
T | C | 11 | a0001c0001t0004g0305a0001c0001t0005g0005a0001c0001t0005g0006others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-290T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750178 | ||||||
| chrX:129750179
|
G | A | 81 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.638-289G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750179 | ||||||
| chrX:129750213
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-251delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750213 | |||||
| chrX:129750228
|
A | AG | 2 | a0001c0001t0003g0024a0001c0002t0001g0224 | 2 | HG01255.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.638-236dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750228 | |||||
| chrX:129750267
|
TG | T | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-199delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750267 | |||||
| chrX:129750284
|
G | C | 8 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0197others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-184G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750284 | ||||||
| chrX:129750291
|
A | AT | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-176dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750291 | |||||
| chrX:129750313
|
A | C | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.638-155A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750313 | ||||||
| chrX:129750339
|
G | GT | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-126dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750339 | |||||
| chrX:129750344
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-122delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750344 | |||||
| chrX:129750356
|
C | T | 55 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(52): Show | 55 | HG00673.hp1 HG01123.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.638-112C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750356 | ||||||
| chrX:129750361
|
CT | C | 2 | a0025c0011t0014g0008a0026c0023t0003g0001 | 2 | NA19059.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.638-102delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750361 | |||||
| chrX:129750411
|
C | T | 3 | a0001c0002t0001g0273a0001c0002t0002g0217a0001c0002t0002g0238 | 3 | HG00639.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.638-57C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750411 | ||||||
| chrX:129750433
|
T | TC | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.638-34dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750433 | |||||
| chrX:129750448
|
TG | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.638-16delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129750448 | |||||
| chrX:129750591
|
T | TG | 1 | a0018c0029t0001g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.739+25dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750591 | |||||
| chrX:129750603
|
T | TG | 1 | a0001c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.739+37dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750603 | |||||
| chrX:129750603
|
TG | T | 2 | a0008c0008t0003g0085a0026c0023t0003g0001 | 2 | NA18967.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.739+37delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750603 | |||||
| chrX:129750609
|
TC | T | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.739+44delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750609 | |||||
| chrX:129750631
|
G | A | 3 | a0001c0001t0009g0293a0002c0003t0002g0292a0002c0003t0002g0295 | 3 | HG01243.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.739+62G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750631 | ||||||
| chrX:129750674
|
G | GC | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.739+108dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750674 | |||||
| chrX:129750682
|
AT | A | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.739+115delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750682 | |||||
| chrX:129750703
|
A | AC | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.739+135dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750703 | |||||
| chrX:129750718
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.739+151delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750718 | |||||
| chrX:129750729
|
A | AG | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+165dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750729 | |||||
| chrX:129750729
|
AG | A | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.739+165delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750729 | |||||
| chrX:129750737
|
G | T | 1 | a0001c0010t0002g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.739+168G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750737 | ||||||
| chrX:129750739
|
A | C | 5 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.739+170A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750739 | ||||||
| chrX:129750754
|
A | AAAAAGGA others(1): Show |
1 | a0006c0031t0016g0179 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.739+192_739+199dup others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750754 | |||||
| chrX:129750791
|
A | AGCCCACA others(1): Show |
1 | a0001c0002t0001g0237 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.739+226_739+233dup others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750791 | |||||
| chrX:129750838
|
T | C | 1 | a0001c0001t0003g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.739+269T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750838 | ||||||
| chrX:129750888
|
GC | G | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.739+321delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750888 | |||||
| chrX:129750894
|
A | AC | 2 | a0001c0002t0001g0220a0008c0008t0003g0085 | 2 | NA18964.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.739+329dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750894 | |||||
| chrX:129750931
|
T | TG | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+365dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750931 | |||||
| chrX:129750975
|
T | TC | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.739+409dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750975 | |||||
| chrX:129750983
|
G | GC | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.739+415dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129750983 | |||||
| chrX:129751002
|
A | AG | 2 | a0001c0002t0001g0075a0009c0009t0003g0041 | 2 | NA18949.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.739+436dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751002 | |||||
| chrX:129751043
|
A | AT | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.739+479dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751043 | |||||
| chrX:129751050
|
T | TG | 1 | a0001c0002t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.739+487dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751050 | |||||
| chrX:129751050
|
TG | T | 3 | a0001c0001t0007g0288a0001c0002t0001g0106a0013c0025t0001g0274 | 3 | HG02976.hp2 HG03490.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.739+487delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751050 | |||||
| chrX:129751091
|
C | CG | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+523dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751091 | |||||
| chrX:129751096
|
A | AC | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+528dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751096 | |||||
| chrX:129751097
|
C | CT | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.739+529dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751097 | |||||
| chrX:129751098
|
T | TC | 4 | a0001c0001t0002g0058a0001c0001t0005g0247a0001c0002t0001g0272others(1): Show | 4 | HG02004.hp1 HG02280.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+534dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751098 | |||||
| chrX:129751099
|
C | T | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.739+530C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751099 | ||||||
| chrX:129751102
|
C | CA | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.739+533_739+534ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751102 | ||||||
| chrX:129751102
|
CCA | C | 1 | a0001c0002t0001g0246 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.739+535_739+536del others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751102 | |||||
| chrX:129751103
|
C | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.739+534C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751103 | ||||||
| chrX:129751103
|
CA | C | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.739+535delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751103 | ||||||
| chrX:129751104
|
A | AC | 27 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0191others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.739+547dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751104
|
A | ACC | 6 | a0001c0001t0002g0211a0001c0001t0005g0247a0001c0002t0001g0225others(3): Show | 6 | HG01109.hp1 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+546_739+547dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751104
|
A | ACCC | 5 | a0001c0001t0005g0187a0001c0001t0005g0204a0001c0001t0005g0218others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.739+545_739+547dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751104
|
A | ACCCC | 3 | a0001c0001t0005g0186a0001c0001t0005g0202a0001c0001t0005g0203 | 3 | HG02109.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.739+544_739+547dup others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751104
|
A | C | 3 | a0004c0005t0007g0287a0009c0009t0003g0041a0025c0011t0014g0008 | 3 | HG03516.hp2 NA18998.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.739+535A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751104 | ||||||
| chrX:129751104
|
AC | A | 84 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0095others(81): Show | 84 | HG00323.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.739+547delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751104
|
ACC | A | 44 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0122others(41): Show | 44 | HG00544.hp2 HG00639.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.739+546_739+547del others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751104
|
ACCC | A | 1 | a0028c0030t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.739+545_739+547del others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | |||||
| chrX:129751105
|
C | A | 2 | a0001c0002t0001g0246a0004c0005t0007g0287 | 2 | HG03516.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.739+536C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751105 | ||||||
| chrX:129751106
|
C | A | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.739+537C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751106 | ||||||
| chrX:129751107
|
C | CCCA | 1 | a0001c0001t0005g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.739+540_739+541ins others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751107 | |||||
| chrX:129751109
|
C | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0194 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.739+540C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751109 | ||||||
| chrX:129751110
|
C | A | 8 | a0001c0001t0002g0046a0001c0001t0007g0284a0001c0001t0007g0285others(5): Show | 8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.739+541C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751110 | ||||||
| chrX:129751112
|
C | CG | 1 | a0001c0001t0017g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.739+543_739+544ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751112 | ||||||
| chrX:129751112
|
C | G | 4 | a0001c0001t0002g0199a0001c0001t0009g0193a0001c0002t0002g0217others(1): Show | 4 | HG02451.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+543C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751112 | ||||||
| chrX:129751113
|
C | A | 42 | a0001c0001t0001g0174a0001c0001t0003g0003a0001c0001t0003g0011others(39): Show | 42 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.739+544C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751113 | ||||||
| chrX:129751113
|
C | CA | 21 | a0001c0001t0003g0004a0001c0001t0003g0038a0001c0001t0003g0039others(18): Show | 21 | HG00423.hp1 HG00423.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+544_739+545ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751113 | ||||||
| chrX:129751113
|
C | CCA | 2 | a0001c0001t0003g0082a0026c0023t0003g0001 | 2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.739+545_739+546ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751113 | |||||
| chrX:129751113
|
C | G | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.739+544C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751113 | ||||||
| chrX:129751114
|
CCCG | C | 1 | a0001c0010t0002g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.739+546_739+548del others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751114 | ||||||
| chrX:129751116
|
C | CCCG | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.739+547_739+548ins others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751116 | ||||||
| chrX:129751119
|
CA | C | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.739+555delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751119 | |||||
| chrX:129751132
|
T | TA | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+565dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751132 | |||||
| chrX:129751153
|
A | G | 140 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(137): Show | 140 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.739+584A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751153 | ||||||
| chrX:129751179
|
A | G | 217 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0086others(214): Show | 217 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.740-566A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751179 | ||||||
| chrX:129751215
|
T | TG | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-529dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751215 | |||||
| chrX:129751227
|
G | GC | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.740-516dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751227 | |||||
| chrX:129751227
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.740-516delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751227 | |||||
| chrX:129751229
|
C | CG | 4 | a0001c0001t0002g0099a0001c0001t0004g0100a0001c0002t0001g0233others(1): Show | 4 | HG01978.hp2 HG02080.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-513dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751229 | |||||
| chrX:129751229
|
C | T | 1 | a0001c0001t0023g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.740-516C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751229 | ||||||
| chrX:129751254
|
TC | T | 1 | a0001c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.740-488delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751254 | |||||
| chrX:129751278
|
T | TG | 1 | a0019c0015t0002g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.740-464dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751278 | |||||
| chrX:129751284
|
G | GA | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-460dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751284 | |||||
| chrX:129751290
|
C | CT | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-454dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751290 | |||||
| chrX:129751295
|
G | T | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-450G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751295 | ||||||
| chrX:129751309
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.740-436A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751309 | ||||||
| chrX:129751313
|
G | GC | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.740-430dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751313 | |||||
| chrX:129751353
|
C | CA | 1 | a0001c0001t0003g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.740-387dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751353 | |||||
| chrX:129751353
|
CA | C | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-387delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751353 | |||||
| chrX:129751353
|
CAAAA | C | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.740-390_740-387del others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751353 | |||||
| chrX:129751386
|
CA | C | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-356delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751386 | |||||
| chrX:129751389
|
AC | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.740-353delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751389 | |||||
| chrX:129751400
|
TG | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.740-342delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751400 | |||||
| chrX:129751430
|
C | A | 3 | a0001c0001t0009g0293a0002c0003t0002g0292a0002c0003t0002g0295 | 3 | HG01243.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.740-315C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751430 | ||||||
| chrX:129751441
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.740-304G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751441 | ||||||
| chrX:129751444
|
A | C | 1 | a0001c0010t0002g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.740-301A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751444 | ||||||
| chrX:129751446
|
T | TG | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-298dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751446 | |||||
| chrX:129751452
|
G | GGT | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-293_740-292ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751452 | ||||||
| chrX:129751453
|
A | G | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-292A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751453 | ||||||
| chrX:129751454
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-291G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751454 | ||||||
| chrX:129751466
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.740-278dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751466 | |||||
| chrX:129751469
|
CT | C | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-275delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751469 | ||||||
| chrX:129751477
|
TG | T | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-265delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751477 | |||||
| chrX:129751487
|
A | AG | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.740-257dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751487 | |||||
| chrX:129751500
|
C | CA | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.740-239dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751500 | |||||
| chrX:129751500
|
CA | C | 2 | a0010c0021t0004g0140a0026c0023t0003g0001 | 2 | NA19075.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.740-239delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751500 | |||||
| chrX:129751511
|
G | A | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-234G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751511 | ||||||
| chrX:129751512
|
A | G | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-233A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751512 | ||||||
| chrX:129751520
|
G | GAAGA | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-223_740-222ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751520 | |||||
| chrX:129751523
|
A | AAAAGAAA others(6): Show |
1 | a0001c0002t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.740-220_740-219ins others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751523 | |||||
| chrX:129751523
|
A | AAAG | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.740-219_740-217dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751523 | |||||
| chrX:129751523
|
A | AG | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.740-222_740-221ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751523 | ||||||
| chrX:129751523
|
A | G | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-222A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751523 | ||||||
| chrX:129751527
|
AAAGAAAG others(1): Show |
A | 1 | a0006c0031t0016g0179 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.740-210_740-203del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751527 | |||||
| chrX:129751531
|
A | AAAG | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.740-213_740-211dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751531 | |||||
| chrX:129751533
|
AG | A | 2 | a0008c0008t0003g0085a0016c0027t0001g0182 | 2 | NA18959.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.740-210delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751533 | |||||
| chrX:129751534
|
G | GA | 1 | a0001c0002t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.740-211_740-210ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751534 | ||||||
| chrX:129751534
|
G | GAA | 1 | a0001c0002t0001g0255 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.740-211_740-210ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751534 | ||||||
| chrX:129751535
|
G | A | 4 | a0001c0002t0001g0242a0001c0002t0001g0273a0007c0022t0003g0181others(1): Show | 4 | HG00639.hp2 HG02080.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-210G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751535 | ||||||
| chrX:129751535
|
G | GA | 1 | a0001c0001t0001g0277 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.740-208dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
G | GAAGA | 4 | a0001c0001t0003g0113a0001c0002t0001g0222a0001c0002t0001g0256others(1): Show | 4 | HG01346.hp2 HG03195.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-150_740-147dup others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
G | GAAGAAAG others(1): Show |
2 | a0001c0001t0003g0190a0001c0002t0001g0229 | 2 | HG00099.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.740-154_740-147dup others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
G | GAAGAAAG others(5): Show |
1 | a0001c0002t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.740-158_740-147dup others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
G | GAAGAAAG others(9): Show |
1 | a0001c0001t0002g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.740-162_740-147dup others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GA | G | 1 | a0001c0001t0003g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.740-208delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGA | G | 20 | a0001c0001t0002g0211a0001c0001t0003g0037a0001c0001t0003g0040others(17): Show | 20 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.740-150_740-147del others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGAAAG others(1): Show |
G | 21 | a0001c0001t0003g0011a0001c0001t0008g0296a0001c0001t0018g0219others(18): Show | 21 | HG00140.hp1 HG01071.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-154_740-147del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGAAAG others(5): Show |
G | 11 | a0001c0001t0003g0072a0001c0001t0003g0151a0001c0001t0006g0206others(8): Show | 11 | HG00099.hp2 HG00558.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.740-158_740-147del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGAAAG others(9): Show |
G | 6 | a0001c0001t0003g0068a0001c0002t0001g0200a0001c0002t0001g0243others(3): Show | 6 | HG00741.hp2 HG01975.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.740-162_740-147del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGAAAG others(13): Show |
G | 2 | a0001c0001t0002g0191a0001c0001t0004g0076 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.740-166_740-147del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGAAAG others(17): Show |
G | 4 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0004g0305others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-170_740-147del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751535
|
GAAGAAAG others(25): Show |
G | 1 | a0001c0001t0005g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.740-178_740-147del others(32): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | |||||
| chrX:129751537
|
A | AG | 1 | a0018c0029t0001g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.740-207dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751537 | |||||
| chrX:129751537
|
A | G | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-208A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751537 | ||||||
| chrX:129751538
|
G | A | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-207G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751538 | ||||||
| chrX:129751538
|
GA | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0171a0001c0001t0002g0094 | 3 | HG03688.hp1 NA19004.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.740-204delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751538 | |||||
| chrX:129751538
|
GAAA | G | 1 | a0001c0001t0002g0099 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.740-206_740-204del others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751538 | ||||||
| chrX:129751539
|
A | AAG | 1 | a0001c0002t0001g0242 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.740-205_740-204ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751539 | |||||
| chrX:129751539
|
A | G | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-206A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751539 | ||||||
| chrX:129751542
|
GA | G | 1 | a0001c0002t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.740-200delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751542 | |||||
| chrX:129751546
|
G | GA | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-196dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751546 | |||||
| chrX:129751547
|
A | AG | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.740-198_740-197ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751547 | ||||||
| chrX:129751558
|
G | GA | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-184dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751558 | |||||
| chrX:129751558
|
G | GAAAT | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.740-184_740-183ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751558 | |||||
| chrX:129751559
|
AAAGAAAG others(33): Show |
A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.740-182_740-143del others(40): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751559 | |||||
| chrX:129751562
|
G | GA | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.740-180dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751562 | |||||
| chrX:129751562
|
GAA | G | 1 | a0001c0001t0011g0307 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.740-181_740-180del others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751562 | |||||
| chrX:129751563
|
A | AAAGAAG | 1 | a0001c0002t0001g0133 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.740-177_740-176ins others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751563 | |||||
| chrX:129751563
|
AAAGAAAG others(37): Show |
A | 1 | a0001c0001t0005g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.740-178_740-135del others(44): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751563 | |||||
| chrX:129751570
|
G | GA | 2 | a0009c0009t0003g0041a0021c0028t0001g0049 | 2 | NA18998.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.740-172dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751570 | |||||
| chrX:129751570
|
G | GAAAGAAA others(2): Show |
1 | a0001c0001t0002g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.740-172_740-164dup others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751570 | |||||
| chrX:129751574
|
GA | G | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.740-168delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751574 | |||||
| chrX:129751575
|
AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0004g0051a0001c0001t0005g0186 | 2 | HG01106.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.740-166_740-143del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751575 | |||||
| chrX:129751579
|
AAAGAAAG others(13): Show |
A | 4 | a0001c0001t0005g0187a0001c0001t0007g0286a0001c0002t0001g0270others(1): Show | 4 | HG01258.hp1 HG01884.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-162_740-143del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751579 | |||||
| chrX:129751579
|
AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0005g0197a0001c0001t0005g0203 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.740-162_740-139del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751579 | |||||
| chrX:129751581
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.740-163dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751581 | |||||
| chrX:129751581
|
AGAAAGAA others(10): Show |
A | 1 | a0001c0001t0004g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.740-160_740-144del others(17): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751581 | |||||
| chrX:129751582
|
GA | G | 2 | a0001c0001t0003g0024a0009c0009t0003g0041 | 2 | NA18998.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.740-160delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751582 | |||||
| chrX:129751583
|
A | AAAGG | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.740-159_740-158ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | |||||
| chrX:129751583
|
A | AAAGGAAG others(1): Show |
1 | a0001c0001t0004g0300 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.740-159_740-158ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | |||||
| chrX:129751583
|
A | G | 2 | a0001c0001t0004g0173a0006c0031t0016g0179 | 2 | HG02155.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.740-162A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751583 | ||||||
| chrX:129751583
|
AAAGAAAG others(9): Show |
A | 4 | a0001c0001t0002g0199a0001c0001t0007g0285a0001c0001t0017g0212others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-158_740-143del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | |||||
| chrX:129751583
|
AAAGAAAG others(13): Show |
A | 4 | a0001c0001t0005g0204a0001c0001t0005g0218a0001c0001t0005g0247others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-158_740-139del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | |||||
| chrX:129751583
|
AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0008g0196a0001c0001t0008g0210 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.740-158_740-135del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | |||||
| chrX:129751583
|
AAAGAAAG others(21): Show |
A | 1 | a0001c0001t0002g0165 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.740-158_740-131del others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | |||||
| chrX:129751586
|
GA | G | 2 | a0001c0001t0001g0143a0001c0002t0001g0272 | 2 | HG02004.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.740-156delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751586 | |||||
| chrX:129751587
|
A | AAAGG | 2 | a0001c0001t0004g0035a0015c0012t0004g0079 | 2 | NA18986.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.740-155_740-154ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
A | AAAGGAAA others(6): Show |
1 | a0001c0001t0004g0045 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.740-155_740-154ins others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
A | AAAGGAAG others(1): Show |
1 | a0001c0001t0004g0043 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.740-155_740-154ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
A | AAG | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.740-157_740-156ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
A | AAGGAAGG others(4): Show |
1 | a0001c0001t0004g0032 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.740-157_740-156ins others(11): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
A | G | 12 | a0001c0001t0001g0174a0001c0001t0002g0191a0001c0001t0003g0039others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.740-158A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751587 | ||||||
| chrX:129751587
|
AAAGAAAG others(5): Show |
A | 2 | a0001c0001t0007g0288a0001c0002t0001g0226 | 2 | HG01175.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.740-154_740-143del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
AAAGAAAG others(13): Show |
A | 4 | a0001c0001t0002g0058a0001c0001t0002g0166a0001c0001t0002g0303others(1): Show | 4 | HG01346.hp1 HG02280.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-154_740-135del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751587
|
AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0002g0019a0001c0001t0003g0112 | 2 | HG00673.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.740-154_740-131del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | |||||
| chrX:129751588
|
AAGAAAGA others(11): Show |
A | 1 | a0001c0001t0005g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.740-156_740-139del others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751588 | ||||||
| chrX:129751591
|
A | AAAGG | 4 | a0001c0001t0004g0148a0001c0002t0001g0013a0001c0002t0001g0047others(1): Show | 4 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-151_740-150ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
A | AAAGGAAG others(1): Show |
2 | a0001c0001t0004g0100a0016c0027t0001g0182 | 2 | NA18949.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.740-151_740-150ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
A | AAAGGAAG others(5): Show |
1 | a0001c0001t0004g0034 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.740-151_740-150ins others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
A | AAG | 1 | a0001c0001t0003g0070 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.740-153_740-152ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
A | AAGG | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-153_740-152ins others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
A | G | 43 | a0001c0001t0001g0174a0001c0001t0002g0111a0001c0001t0002g0191others(40): Show | 43 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.740-154A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751591 | ||||||
| chrX:129751591
|
AAAGAAAG others(1): Show |
A | 7 | a0001c0001t0008g0294a0001c0002t0001g0225a0001c0002t0001g0282others(4): Show | 7 | HG01169.hp2 HG01192.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.740-150_740-143del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
AAAGAAAG others(5): Show |
A | 2 | a0001c0002t0001g0227a0002c0003t0005g0213 | 2 | HG01943.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.740-150_740-139del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
AAAGAAAG others(9): Show |
A | 3 | a0001c0001t0002g0014a0001c0001t0002g0028a0001c0001t0002g0056 | 3 | HG01496.hp1 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.740-150_740-135del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
AAAGAAAG others(13): Show |
A | 3 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0002g0052 | 3 | HG01934.hp1 NA18953.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.740-150_740-131del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751591
|
AAAGAAAG others(21): Show |
A | 3 | a0001c0001t0001g0062a0001c0001t0002g0012a0003c0004t0006g0088 | 3 | NA18940.hp1 NA19072.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.740-150_740-123del others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | |||||
| chrX:129751593
|
A | AG | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.740-151dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751593 | |||||
| chrX:129751595
|
A | AAAGAAAG others(13): Show |
1 | a0001c0006t0001g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(7): Show |
1 | a0001c0002t0001g0097 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(9): Show |
1 | a0024c0026t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.740-147_740-146ins others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(13): Show |
1 | a0001c0001t0004g0101 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(7): Show |
1 | a0001c0001t0003g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(23): Show |
1 | a0001c0001t0003g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(16): Show |
1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(23): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(1): Show |
3 | a0001c0002t0001g0031a0001c0002t0001g0074a0001c0002t0001g0216 | 3 | HG00642.hp1 HG01358.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.740-147_740-146ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAAG others(5): Show |
4 | a0001c0001t0003g0147a0001c0001t0003g0159a0001c0001t0008g0195others(1): Show | 4 | HG00621.hp1 HG02970.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-147_740-146ins others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAGA others(15): Show |
1 | a0018c0029t0001g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGAAGG others(8): Show |
1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(15): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGG | 3 | a0001c0002t0001g0237a0001c0002t0019g0244a0001c0006t0001g0092 | 3 | HG01256.hp1 HG03669.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.740-105_740-102dup others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGGAAG others(1): Show |
1 | a0001c0002t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.740-109_740-102dup others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAAGGAAG others(5): Show |
1 | a0001c0001t0004g0102 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.740-113_740-102dup others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAG | 2 | a0001c0002t0001g0255a0007c0022t0003g0181 | 2 | HG00735.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.740-149_740-148ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAGG | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-149_740-148ins others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AAGGAAGG | 1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.740-149_740-148ins others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
A | AGAAGG | 1 | a0001c0002t0002g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.740-150_740-149ins others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751595 | ||||||
| chrX:129751595
|
A | G | 82 | a0001c0001t0001g0174a0001c0001t0002g0046a0001c0001t0002g0111others(79): Show | 82 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.740-150A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751595 | ||||||
| chrX:129751595
|
AAAGG | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0006g0185others(4): Show | 7 | HG01255.hp1 HG02040.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.740-105_740-102del others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
AAAGGAAG others(1): Show |
A | 7 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0180others(4): Show | 7 | HG02723.hp2 HG03239.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.740-109_740-102del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
AAAGGAAG others(5): Show |
A | 18 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0115others(15): Show | 18 | HG00639.hp1 HG01243.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.740-113_740-102del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
AAAGGAAG others(9): Show |
A | 16 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0118others(13): Show | 16 | HG01069.hp1 HG01175.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.740-117_740-102del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
AAAGGAAG others(13): Show |
A | 15 | a0001c0001t0001g0053a0001c0001t0001g0096a0001c0001t0001g0119others(12): Show | 15 | HG00408.hp2 HG00544.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.740-121_740-102del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751595
|
AAAGGAAG others(17): Show |
A | 13 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0146others(10): Show | 13 | HG01496.hp2 HG02809.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-125_740-102del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | |||||
| chrX:129751597
|
AGGAAGGA others(2): Show |
A | 1 | a0001c0001t0002g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.740-146_740-138del others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751597 | |||||
| chrX:129751597
|
AGGAAGGA others(6): Show |
A | 2 | a0001c0001t0002g0065a0001c0001t0002g0170 | 2 | HG02735.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.740-146_740-134del others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751597 | |||||
| chrX:129751597
|
AGGAAGGA others(10): Show |
A | 2 | a0001c0001t0001g0143a0001c0001t0009g0198 | 2 | HG01891.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.740-146_740-130del others(17): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751597 | |||||
| chrX:129751598
|
G | GAAAGAAA | 1 | a0001c0001t0006g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751598 | ||||||
| chrX:129751599
|
G | A | 15 | a0001c0001t0001g0144a0001c0001t0001g0208a0001c0001t0002g0026others(12): Show | 15 | HG01081.hp1 HG01884.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-146G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751599 | ||||||
| chrX:129751602
|
G | A | 1 | a0001c0001t0006g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.740-143G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751602 | ||||||
| chrX:129751602
|
G | GGAA | 1 | a0001c0002t0001g0242 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.740-141_740-139dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751602 | |||||
| chrX:129751603
|
G | A | 13 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0144others(10): Show | 13 | HG01978.hp2 HG02040.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-142G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751603 | ||||||
| chrX:129751605
|
A | AG | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-138dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751605 | |||||
| chrX:129751606
|
G | A | 1 | a0001c0001t0006g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.740-139G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751606 | ||||||
| chrX:129751606
|
GGAAGGAA others(7): Show |
G | 1 | a0001c0001t0001g0208 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.740-138_740-125del others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751606 | ||||||
| chrX:129751607
|
G | A | 16 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0144others(13): Show | 16 | HG01978.hp2 HG02040.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.740-138G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751607 | ||||||
| chrX:129751608
|
AAGGAAGG others(4): Show |
A | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.740-135_740-125del others(11): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751608 | |||||
| chrX:129751610
|
GGAAGGAA others(3): Show |
G | 1 | a0001c0001t0001g0144 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.740-134_740-125del others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751610 | ||||||
| chrX:129751611
|
G | A | 23 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0115others(20): Show | 23 | HG00639.hp1 HG01978.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.740-134G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751611 | ||||||
| chrX:129751614
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0170 | 2 | HG02735.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.740-131G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751614 | ||||||
| chrX:129751615
|
G | A | 36 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0095others(33): Show | 36 | HG00639.hp1 HG01069.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.740-130G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751615 | ||||||
| chrX:129751618
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0002g0065a0001c0001t0002g0170others(1): Show | 4 | HG01891.hp2 HG02735.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-127G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751618 | ||||||
| chrX:129751619
|
G | A | 48 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0095others(45): Show | 48 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.740-126G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751619 | ||||||
| chrX:129751622
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0208a0001c0001t0009g0198 | 3 | HG01891.hp2 HG02148.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.740-123G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751622 | ||||||
| chrX:129751622
|
GGAA | G | 1 | a0001c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.740-121_740-119del others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751622 | |||||
| chrX:129751623
|
G | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0137 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.740-122G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751623 | ||||||
| chrX:129751626
|
G | GGAA | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.740-117_740-115dup others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751626 | |||||
| chrX:129751629
|
AG | A | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.740-114delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751629 | |||||
| chrX:129751634
|
GGAA | G | 1 | a0006c0031t0016g0179 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.740-109_740-107del others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751634 | |||||
| chrX:129751637
|
A | AG | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-106dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751637 | |||||
| chrX:129751640
|
A | AAGGAAGG others(9): Show |
1 | a0001c0001t0003g0103 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.740-102_740-101ins others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | |||||
| chrX:129751640
|
A | AAGGAAGG others(5): Show |
1 | a0001c0001t0003g0105 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.740-102_740-101ins others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | |||||
| chrX:129751640
|
A | AAGGAAGG others(1): Show |
5 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0044others(2): Show | 5 | HG00408.hp1 HG02027.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.740-102_740-101ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | |||||
| chrX:129751640
|
A | AAGGG | 6 | a0001c0001t0003g0023a0001c0001t0003g0082a0001c0001t0003g0138others(3): Show | 6 | HG00423.hp2 HG00597.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-101_740-98dupG others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | |||||
| chrX:129751640
|
A | AGG | 1 | a0008c0008t0003g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.740-105_740-104ins others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751640 | ||||||
| chrX:129751640
|
A | G | 28 | a0001c0001t0003g0011a0001c0001t0003g0021a0001c0001t0003g0024others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.740-105A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751640 | ||||||
| chrX:129751640
|
AAG | A | 1 | a0001c0002t0001g0154 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.740-104_740-103del others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751640 | ||||||
| chrX:129751641
|
A | G | 1 | a0006c0031t0016g0179 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.740-104A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751641 | ||||||
| chrX:129751641
|
AG | A | 2 | a0001c0001t0002g0027a0013c0025t0001g0274 | 2 | HG02896.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.740-101delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751641 | |||||
| chrX:129751642
|
G | GGAA | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.740-102_740-101ins others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751642 | |||||
| chrX:129751642
|
G | GGAGAGGG others(1): Show |
1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.740-102_740-101ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751642 | |||||
| chrX:129751643
|
G | GA | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-102_740-101ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751643 | ||||||
| chrX:129751644
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-101G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751644 | ||||||
| chrX:129751645
|
AG | A | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.740-98delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751645 | |||||
| chrX:129751654
|
A | G | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-91A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751654 | ||||||
| chrX:129751656
|
A | AAG | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-88_740-87dupAG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751656 | |||||
| chrX:129751672
|
GAA | G | 1 | a0001c0002t0001g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-67_740-66delAA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751672 | |||||
| chrX:129751714
|
A | G | 8 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0197others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.740-31A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751714 | ||||||
| chrX:129751730
|
CA | C | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.740-13delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751730 | |||||
| chrX:129751833
|
C | CT | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.821+11dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129751833 | |||||
| chrX:129751840
|
T | TAGCTTG | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+14_821+15insAG others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751840 | ||||||
| chrX:129751841
|
T | C | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+15T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751841 | ||||||
| chrX:129751842
|
A | T | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+16A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751842 | ||||||
| chrX:129751884
|
G | GC | 2 | a0001c0002t0001g0224a0026c0023t0003g0001 | 2 | HG01255.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.821+62dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129751884 | |||||
| chrX:129751897
|
TC | T | 1 | a0001c0001t0003g0024 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.821+74delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129751897 | |||||
| chrX:129751914
|
G | GC | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.821+91dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129751914 | |||||
| chrX:129751951
|
CA | C | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.821+126delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751951 | ||||||
| chrX:129751974
|
G | A | 2 | a0001c0001t0003g0113a0001c0001t0003g0157 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.821+148G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751974 | ||||||
| chrX:129751994
|
T | TA | 1 | a0001c0002t0001g0141 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.822-153dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129751994 | |||||
| chrX:129752009
|
A | G | 49 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(46): Show | 49 | HG00673.hp1 HG01081.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.822-141A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129752009 | ||||||
| chrX:129752047
|
T | TC | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.822-103_822-102ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129752047 | ||||||
| chrX:129752073
|
A | AG | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.822-74dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129752073 | |||||
| chrX:129752099
|
T | TG | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.822-50dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129752099 | |||||
| chrX:129752135
|
T | TC | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.822-12dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129752135 | |||||
| chrX:129752139
|
A | AC | 2 | a0009c0009t0003g0041a0010c0021t0004g0140 | 2 | NA18998.hp1 NA19086.hp1 |
splice_region_variant&intron_variant | LOW | c.822-7dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 129752139 | |||||
| chrX:129752350
|
G | GT | 1 | a0009c0009t0003g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1017+8dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752350 | |||||
| chrX:129752365
|
G | GC | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1017+23dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752365 | |||||
| chrX:129752378
|
A | AC | 1 | a0010c0021t0004g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017+35dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752378 | |||||
| chrX:129752427
|
G | GC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1017+86dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752427 | |||||
| chrX:129752476
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1017+134dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752476 | |||||
| chrX:129752493
|
TG | T | 2 | a0001c0001t0005g0247a0026c0023t0003g0001 | 2 | HG02897.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1017+151delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752493 | |||||
| chrX:129752511
|
G | GA | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1017+169dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752511 | |||||
| chrX:129752568
|
C | T | 8 | a0001c0001t0007g0284a0001c0001t0007g0285a0001c0001t0007g0286others(5): Show | 8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+223C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752568 | ||||||
| chrX:129752667
|
GC | G | 1 | a0001c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1017+324delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752667 | |||||
| chrX:129752756
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0194 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1018-403T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752756 | ||||||
| chrX:129752779
|
T | C | 1 | a0001c0001t0004g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1018-380T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752779 | ||||||
| chrX:129752814
|
G | GA | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1018-342dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752814 | |||||
| chrX:129752838
|
T | TG | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1018-320dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129752838 | |||||
| chrX:129752968
|
A | C | 51 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(48): Show | 51 | HG00673.hp1 HG01081.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1018-191A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752968 | ||||||
| chrX:129753026
|
T | C | 51 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(48): Show | 51 | HG00673.hp1 HG01081.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1018-133T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753026 | ||||||
| chrX:129753064
|
T | TC | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1018-93dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129753064 | |||||
| chrX:129753076
|
A | G | 2 | a0001c0001t0004g0050a0001c0001t0004g0051 | 2 | HG01106.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1018-83A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753076 | ||||||
| chrX:129753076
|
AC | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1018-79delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129753076 | |||||
| chrX:129753105
|
G | T | 1 | a0001c0001t0003g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1018-54G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753105 | ||||||
| chrX:129753111
|
C | CA | 1 | a0024c0026t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1018-48_1018-47ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753111 | ||||||
| chrX:129753148
|
G | GC | 1 | a0018c0029t0001g0251 | 1 | NA19010.hp1 | splice_region_variant&intron_variant | LOW | c.1018-6dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129753148 | |||||
| chrX:129753148
|
GC | G | 1 | a0001c0002t0001g0237 | 1 | HG01256.hp1 | splice_region_variant&intron_variant | LOW | c.1018-6delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 129753148 | |||||
| chrX:129753254
|
TC | T | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.1107+8delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753254 | |||||
| chrX:129753272
|
TG | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1107+26delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753272 | |||||
| chrX:129753274
|
G | GC | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1107+28dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753274 | |||||
| chrX:129753292
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1107+46dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753292 | |||||
| chrX:129753364
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1107+119dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753364 | |||||
| chrX:129753368
|
C | T | 12 | a0001c0002t0001g0184a0001c0002t0001g0214a0001c0002t0001g0224others(9): Show | 12 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.1107+120C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129753368 | ||||||
| chrX:129753381
|
G | A | 2 | a0002c0003t0002g0292a0002c0003t0002g0295 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1107+133G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129753381 | ||||||
| chrX:129753488
|
CA | C | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1107+245delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753488 | |||||
| chrX:129753500
|
AG | A | 1 | a0024c0026t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1107+254delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753500 | |||||
| chrX:129753541
|
G | GC | 1 | a0001c0001t0004g0080 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1107+294dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753541 | |||||
| chrX:129753614
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1107+368delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753614 | |||||
| chrX:129753632
|
C | CA | 3 | a0017c0013t0003g0069a0018c0029t0001g0251a0021c0028t0001g0049 | 3 | NA19010.hp1 NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1107+393dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753632 | |||||
| chrX:129753632
|
CA | C | 4 | a0016c0027t0001g0182a0024c0026t0001g0301a0026c0023t0003g0001others(1): Show | 4 | HG02559.hp2 NA18959.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1107+393delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753632 | |||||
| chrX:129753650
|
GA | G | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1107+405delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753650 | |||||
| chrX:129753663
|
A | AT | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1107+416dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753663 | |||||
| chrX:129753675
|
A | AC | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1107+428dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753675 | |||||
| chrX:129753687
|
TC | T | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1107+441delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753687 | |||||
| chrX:129753695
|
G | A | 65 | a0001c0001t0001g0174a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1107+447G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129753695 | ||||||
| chrX:129753718
|
G | GC | 2 | a0017c0013t0003g0069a0021c0028t0001g0049 | 2 | NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1107+475dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753718 | |||||
| chrX:129753730
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1107+483dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753730 | |||||
| chrX:129753777
|
CA | C | 1 | a0024c0026t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1107+532delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753777 | |||||
| chrX:129753788
|
TC | T | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1107+542delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753788 | |||||
| chrX:129753817
|
AC | A | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1107+571delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753817 | |||||
| chrX:129753849
|
A | AC | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1107+605dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129753849 | |||||
| chrX:129754012
|
AT | A | 1 | a0024c0026t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1108-455delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754012 | |||||
| chrX:129754017
|
TA | T | 3 | a0001c0001t0001g0174a0001c0001t0012g0241a0027c0007t0020g0015 | 3 | HG00558.hp2 NA18987.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1108-449delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754017 | |||||
| chrX:129754059
|
TA | T | 2 | a0024c0026t0001g0301a0027c0007t0020g0015 | 2 | HG02559.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1108-405delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754059 | |||||
| chrX:129754076
|
C | T | 33 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(30): Show | 33 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.1108-396C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754076 | ||||||
| chrX:129754168
|
G | GC | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1108-302dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754168 | |||||
| chrX:129754179
|
C | CT | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1108-291dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754179 | |||||
| chrX:129754215
|
A | AC | 3 | a0001c0001t0003g0103a0001c0002t0001g0078a0001c0002t0001g0184 | 3 | HG00741.hp1 NA18981.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1108-252dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754215 | |||||
| chrX:129754215
|
A | ACC | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1108-253_1108-252d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754215 | |||||
| chrX:129754235
|
CT | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1108-233delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754235 | |||||
| chrX:129754274
|
G | A | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1108-198G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754274 | ||||||
| chrX:129754292
|
CA | C | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1108-175delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754292 | |||||
| chrX:129754365
|
C | CA | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1108-104dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754365 | |||||
| chrX:129754418
|
G | GTCT | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1108-54_1108-53ins others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754418 | ||||||
| chrX:129754425
|
A | AC | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1108-45dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754425 | |||||
| chrX:129754434
|
C | T | 9 | a0001c0001t0002g0046a0001c0001t0004g0305a0001c0001t0008g0195others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108-38C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754434 | ||||||
| chrX:129754449
|
T | C | 1 | a0001c0002t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1108-23T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754449 | ||||||
| chrX:129754459
|
T | TC | 1 | a0018c0029t0001g0251 | 1 | NA19010.hp1 | splice_region_variant&intron_variant | LOW | c.1108-9dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754459 | |||||
| chrX:129754629
|
C | CG | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1217+48_1217+49ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754629 | ||||||
| chrX:129754632
|
T | TG | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1217+56dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754632 | |||||
| chrX:129754643
|
A | AG | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1217+67dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754643 | |||||
| chrX:129754644
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1217+63_1217+64ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754644 | ||||||
| chrX:129754684
|
C | T | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+103C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754684 | ||||||
| chrX:129754724
|
A | AG | 1 | a0011c0019t0001g0089 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1217+145dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754724 | |||||
| chrX:129754749
|
G | A | 1 | a0001c0001t0009g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1217+168G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754749 | ||||||
| chrX:129754761
|
A | AG | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1217+185dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754761 | |||||
| chrX:129754767
|
C | T | 33 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(30): Show | 33 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.1217+186C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754767 | ||||||
| chrX:129754772
|
G | C | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+191G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754772 | ||||||
| chrX:129754794
|
A | G | 1 | a0001c0002t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1217+213A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754794 | ||||||
| chrX:129754840
|
G | T | 34 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0171others(31): Show | 34 | HG00408.hp2 HG01891.hp2 HG02004.hp2 others(31): Show |
intron_variant | MODIFIER | c.1217+259G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754840 | ||||||
| chrX:129754854
|
C | CGGT | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1217+274_1217+276d others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754854 | |||||
| chrX:129754898
|
G | GC | 1 | a0018c0029t0001g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1217+321dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754898 | |||||
| chrX:129754906
|
AC | A | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1217+327delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754906 | |||||
| chrX:129754926
|
A | AG | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1217+348dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754926 | |||||
| chrX:129754964
|
AG | A | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1218-327delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129754964 | |||||
| chrX:129755008
|
TG | T | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1218-281delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129755008 | |||||
| chrX:129755052
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1218-240delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129755052 | |||||
| chrX:129755116
|
TA | T | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1218-175delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129755116 | |||||
| chrX:129755185
|
GT | G | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1218-107delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129755185 | |||||
| chrX:129755215
|
T | C | 1 | a0001c0001t0010g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1218-79T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129755215 | ||||||
| chrX:129755219
|
A | AT | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1218-72dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129755219 | |||||
| chrX:129755232
|
T | TC | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1218-59dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 129755232 | |||||
| chrX:129755235
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1218-59C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129755235 | ||||||
| chrX:129755381
|
G | GA | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1295+15dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755381 | |||||
| chrX:129755381
|
GA | G | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1295+15delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755381 | |||||
| chrX:129755406
|
TG | T | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1295+39delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755406 | |||||
| chrX:129755410
|
G | A | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1295+39G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129755410 | ||||||
| chrX:129755447
|
A | AG | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1295+81dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755447 | |||||
| chrX:129755459
|
TG | T | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1295+91delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755459 | |||||
| chrX:129755488
|
G | A | 40 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0095others(37): Show | 40 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1295+117G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129755488 | ||||||
| chrX:129755502
|
T | TG | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1295+136dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755502 | |||||
| chrX:129755518
|
A | AG | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1295+148dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755518 | |||||
| chrX:129755533
|
A | AG | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1295+165dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755533 | |||||
| chrX:129755574
|
T | TG | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1295+208dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755574 | |||||
| chrX:129755574
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1295+208delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755574 | |||||
| chrX:129755595
|
A | AC | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1295+226dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755595 | |||||
| chrX:129755612
|
C | CT | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1295+245dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755612 | |||||
| chrX:129755706
|
GC | G | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1295+337delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755706 | |||||
| chrX:129755745
|
GC | G | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1295+377delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755745 | |||||
| chrX:129755782
|
GA | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1295+415delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755782 | |||||
| chrX:129755807
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1295+438dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755807 | |||||
| chrX:129755844
|
AG | A | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1295+476delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755844 | |||||
| chrX:129755860
|
GTCCC | G | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1295+490_1295+493d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129755860 | ||||||
| chrX:129755884
|
T | TC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1295+517dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755884 | |||||
| chrX:129755889
|
T | TG | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1295+520dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755889 | |||||
| chrX:129755896
|
T | TC | 1 | a0001c0002t0001g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1295+528dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755896 | |||||
| chrX:129755896
|
TC | T | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1295+528delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755896 | |||||
| chrX:129755923
|
G | GC | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1295+556dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755923 | |||||
| chrX:129755939
|
CG | C | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-542delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129755939 | |||||
| chrX:129756013
|
T | TC | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1296-468dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756013 | |||||
| chrX:129756021
|
T | C | 1 | a0001c0002t0001g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1296-463T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756021 | ||||||
| chrX:129756042
|
GC | G | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1296-439delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756042 | |||||
| chrX:129756057
|
A | AG | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1296-425dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756057 | |||||
| chrX:129756060
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1296-423dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756060 | |||||
| chrX:129756080
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1296-401delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756080 | |||||
| chrX:129756101
|
G | A | 4 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(1): Show | 4 | HG02257.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296-383G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756101 | ||||||
| chrX:129756107
|
G | GC | 1 | a0001c0002t0001g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1296-374dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756107 | |||||
| chrX:129756132
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1296-352G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756132 | ||||||
| chrX:129756200
|
TG | T | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-278delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756200 | |||||
| chrX:129756207
|
T | TC | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1296-276dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756207 | |||||
| chrX:129756211
|
T | TA | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-272dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756211 | |||||
| chrX:129756224
|
G | A | 3 | a0001c0001t0002g0111a0001c0001t0002g0191a0001c0001t0002g0211 | 3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1296-260G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756224 | ||||||
| chrX:129756246
|
CCT | C | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-230_1296-229d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756246 | |||||
| chrX:129756265
|
G | A | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-219G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756265 | ||||||
| chrX:129756266
|
A | C | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-218A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756266 | ||||||
| chrX:129756268
|
CAG | C | 1 | a0022c0016t0001g0117 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1296-215_1296-214d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756268 | ||||||
| chrX:129756272
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1296-212G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756272 | ||||||
| chrX:129756410
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1296-74C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756410 | ||||||
| chrX:129756417
|
C | T | 1 | a0001c0020t0005g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1296-67C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756417 | ||||||
| chrX:129756434
|
A | AC | 1 | a0001c0002t0001g0075 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1296-47dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756434 | |||||
| chrX:129756441
|
G | A | 9 | a0001c0001t0002g0046a0001c0001t0004g0305a0001c0001t0008g0195others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1296-43G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756441 | ||||||
| chrX:129756454
|
GC | G | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-27delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 129756454 | |||||
| chrX:129756562
|
A | AC | 2 | a0001c0002t0001g0275a0007c0022t0003g0181 | 2 | HG02080.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1367+11dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756562 | |||||
| chrX:129756614
|
CA | C | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1367+61delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756614 | |||||
| chrX:129756641
|
TG | T | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1367+89delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756641 | |||||
| chrX:129756644
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+91delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756644 | |||||
| chrX:129756646
|
C | CA | 1 | a0001c0001t0003g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1367+92dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756646 | |||||
| chrX:129756662
|
GA | G | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1367+112delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756662 | |||||
| chrX:129756695
|
T | TC | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1367+142dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756695 | |||||
| chrX:129756714
|
T | TG | 4 | a0001c0001t0003g0038a0001c0002t0001g0075a0001c0002t0001g0269others(1): Show | 4 | HG02602.hp1 HG03516.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+164dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756714 | |||||
| chrX:129756714
|
TG | T | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1367+164delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756714 | |||||
| chrX:129756720
|
T | TC | 1 | a0001c0001t0003g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1367+168dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756720 | |||||
| chrX:129756757
|
TG | T | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1367+204delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756757 | |||||
| chrX:129756768
|
AG | A | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1367+215delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756768 | |||||
| chrX:129756819
|
G | GT | 3 | a0001c0001t0002g0188a0001c0001t0002g0194a0017c0013t0003g0069 | 3 | HG02109.hp1 NA19091.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1367+270dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756819 | |||||
| chrX:129756830
|
G | GTTGT | 9 | a0001c0001t0002g0046a0001c0001t0004g0305a0001c0001t0008g0195others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367+290_1367+293d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756830 | |||||
| chrX:129756928
|
GT | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+375delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756928 | |||||
| chrX:129756996
|
C | CTA | 27 | a0001c0001t0001g0239a0001c0001t0002g0093a0001c0001t0002g0111others(24): Show | 27 | HG00597.hp1 HG00741.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1367+468_1367+469d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATA | 7 | a0001c0001t0001g0146a0001c0001t0002g0191a0001c0001t0006g0125others(4): Show | 7 | HG02280.hp1 HG02886.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+466_1367+469d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(5): Show |
5 | a0001c0001t0003g0004a0001c0001t0003g0038a0001c0001t0003g0044others(2): Show | 5 | HG02027.hp1 NA18906.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1367+458_1367+469d others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(7): Show |
16 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0021others(13): Show | 16 | HG00423.hp1 HG00423.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+456_1367+469d others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(9): Show |
6 | a0001c0001t0003g0073a0001c0001t0003g0077a0001c0001t0003g0090others(3): Show | 6 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+454_1367+469d others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(11): Show |
8 | a0001c0001t0003g0039a0001c0001t0003g0072a0001c0001t0003g0082others(5): Show | 8 | HG00597.hp2 HG02523.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+452_1367+469d others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(13): Show |
2 | a0001c0001t0003g0132a0001c0001t0004g0032 | 2 | NA18943.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1367+450_1367+469d others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0003g0175 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1367+444_1367+469d others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
C | CTATATAT others(21): Show |
1 | a0001c0001t0003g0036 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1367+442_1367+469d others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
CTA | C | 23 | a0001c0001t0002g0056a0001c0001t0004g0305a0001c0001t0005g0186others(20): Show | 23 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1367+468_1367+469d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
CTATA | C | 5 | a0001c0001t0002g0046a0001c0001t0002g0306a0001c0001t0002g0309others(2): Show | 5 | HG01081.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+466_1367+469d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129756996
|
CTATATA | C | 13 | a0001c0001t0003g0084a0001c0001t0003g0112a0001c0001t0003g0114others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+464_1367+469d others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | |||||
| chrX:129757019
|
T | C | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1367+464T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757019 | ||||||
| chrX:129757019
|
TATATAC | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0094a0001c0001t0007g0286 | 3 | HG02280.hp2 HG02723.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1367+466_1367+471d others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757019 | |||||
| chrX:129757021
|
T | C | 29 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(26): Show | 29 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1367+466T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757021 | ||||||
| chrX:129757021
|
TATAC | T | 1 | a0001c0001t0003g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1367+468_1367+471d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757021 | |||||
| chrX:129757023
|
T | C | 39 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(36): Show | 39 | HG00673.hp1 HG01346.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1367+468T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757023 | ||||||
| chrX:129757023
|
T | TAC | 2 | a0001c0001t0001g0143a0001c0002t0001g0242 | 2 | NA18944.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1367+482_1367+483d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(5): Show |
1 | a0005c0032t0025g0002 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1367+469_1367+470i others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(7): Show |
7 | a0001c0001t0001g0174a0001c0001t0004g0034a0001c0001t0004g0035others(4): Show | 7 | HG00558.hp2 HG03516.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+469_1367+470i others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(9): Show |
1 | a0001c0001t0004g0101 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1367+469_1367+470i others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(9): Show |
4 | a0001c0001t0004g0100a0001c0001t0004g0102a0001c0001t0004g0148others(1): Show | 4 | HG02083.hp1 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+469_1367+470i others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(11): Show |
5 | a0001c0001t0003g0071a0001c0001t0004g0050a0001c0001t0004g0051others(2): Show | 5 | HG01106.hp1 HG02080.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+469_1367+470i others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(13): Show |
3 | a0001c0001t0004g0080a0001c0001t0004g0173a0010c0021t0004g0140 | 3 | HG02155.hp1 NA18939.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1367+469_1367+470i others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(15): Show |
3 | a0001c0001t0003g0067a0001c0001t0003g0104a0001c0001t0003g0138 | 3 | HG02132.hp1 NA18948.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1367+469_1367+470i others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757023
|
T | TATATATA others(21): Show |
1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1367+469_1367+470i others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | |||||
| chrX:129757025
|
C | T | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1367+470C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757025 | ||||||
| chrX:129757029
|
C | CATATATA others(1): Show |
1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1367+475_1367+476i others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757029 | |||||
| chrX:129757031
|
C | CATATATA others(3): Show |
28 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(25): Show | 28 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.1367+477_1367+478i others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757031 | |||||
| chrX:129757031
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1367+476C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757031 | ||||||
| chrX:129757037
|
C | T | 2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1367+482C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757037 | ||||||
| chrX:129757039
|
T | C | 69 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1367+484T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757039 | ||||||
| chrX:129757047
|
T | C | 4 | a0001c0001t0003g0038a0001c0001t0003g0104a0001c0001t0003g0138others(1): Show | 4 | HG02080.hp1 HG02132.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+492T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757047 | ||||||
| chrX:129757047
|
T | TAC | 5 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0102others(2): Show | 5 | NA18949.hp1 NA18952.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+500_1367+501d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757047 | |||||
| chrX:129757055
|
C | T | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1367+500C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757055 | ||||||
| chrX:129757059
|
T | C | 29 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(26): Show | 29 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1367+504T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757059 | ||||||
| chrX:129757061
|
T | C | 29 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(26): Show | 29 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1367+506T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757061 | ||||||
| chrX:129757061
|
T | TAC | 2 | a0001c0001t0004g0050a0001c0001t0004g0051 | 2 | HG01106.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1367+507_1367+508i others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757061 | |||||
| chrX:129757063
|
T | C | 37 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(34): Show | 37 | HG00673.hp1 HG01106.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1367+508T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757063 | ||||||
| chrX:129757063
|
T | TAC | 51 | a0001c0001t0001g0174a0001c0001t0003g0003a0001c0001t0003g0004others(48): Show | 51 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1367+516_1367+517d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757063 | |||||
| chrX:129757063
|
T | TACAC | 3 | a0001c0001t0004g0032a0001c0001t0004g0173a0020c0014t0004g0030 | 3 | HG02155.hp1 HG02523.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1367+514_1367+517d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757063 | |||||
| chrX:129757071
|
CAT | C | 1 | a0006c0031t0016g0179 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1367+518_1367+519d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757071 | |||||
| chrX:129757073
|
T | C | 92 | a0001c0001t0001g0174a0001c0001t0002g0014a0001c0001t0002g0018others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1367+518T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757073 | ||||||
| chrX:129757073
|
T | TACACACA others(7): Show |
2 | a0001c0001t0002g0058a0001c0001t0007g0286 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1367+524_1367+537d others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | |||||
| chrX:129757073
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1367+522_1367+537d others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | |||||
| chrX:129757073
|
T | TACACACA others(11): Show |
7 | a0001c0001t0002g0094a0001c0001t0003g0304a0001c0001t0005g0005others(4): Show | 7 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367+520_1367+537d others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | |||||
| chrX:129757073
|
T | TACACACA others(15): Show |
1 | a0001c0001t0009g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1367+537_1367+538i others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | |||||
| chrX:129757073
|
TAC | T | 8 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0197others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367+536_1367+537d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | |||||
| chrX:129757088
|
A | AC | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1367+534dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757088 | |||||
| chrX:129757090
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1367+535A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757090 | ||||||
| chrX:129757093
|
T | C | 1 | a0001c0002t0001g0215 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1367+538T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757093 | ||||||
| chrX:129757093
|
TA | T | 1 | a0016c0027t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1367+539delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757093 | ||||||
| chrX:129757135
|
G | GT | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+582dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757135 | |||||
| chrX:129757196
|
G | A | 74 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(71): Show | 74 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1367+641G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757196 | ||||||
| chrX:129757200
|
T | TG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+648dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757200 | |||||
| chrX:129757264
|
A | AT | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+711dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757264 | |||||
| chrX:129757314
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+759C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757314 | ||||||
| chrX:129757346
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1367+791A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757346 | ||||||
| chrX:129757389
|
G | GCCCCC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+835_1367+839d others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757389 | |||||
| chrX:129757402
|
C | CA | 1 | a0001c0001t0004g0032 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1367+848dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757402 | |||||
| chrX:129757424
|
G | T | 1 | a0001c0001t0005g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1367+869G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757424 | ||||||
| chrX:129757464
|
CT | C | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+912delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757464 | |||||
| chrX:129757508
|
CAG | C | 1 | a0001c0002t0001g0097 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1367+955_1367+956d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757508 | |||||
| chrX:129757516
|
A | G | 131 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(128): Show | 131 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.1367+961A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757516 | ||||||
| chrX:129757537
|
G | A | 9 | a0001c0001t0002g0046a0001c0001t0004g0305a0001c0001t0008g0195others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367+982G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757537 | ||||||
| chrX:129757563
|
T | TG | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1367+1011dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757563 | |||||
| chrX:129757563
|
TG | T | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1011delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757563 | |||||
| chrX:129757596
|
AG | A | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1043delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757596 | |||||
| chrX:129757627
|
G | GA | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1075dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757627 | |||||
| chrX:129757651
|
CA | C | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1101delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757651 | |||||
| chrX:129757668
|
T | TGGTG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1115_1367+111 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757668 | |||||
| chrX:129757671
|
T | TG | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1367+1118dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757671 | |||||
| chrX:129757682
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+1130delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757682 | |||||
| chrX:129757687
|
AG | A | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1135delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757687 | |||||
| chrX:129757727
|
G | A | 41 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(38): Show | 41 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1367+1172G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757727 | ||||||
| chrX:129757741
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+1188delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757741 | |||||
| chrX:129757790
|
T | TA | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1367+1239dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757790 | |||||
| chrX:129757796
|
G | GA | 1 | a0001c0001t0010g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1367+1243dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGA | 28 | a0001c0001t0001g0062a0001c0001t0001g0239a0001c0001t0002g0098others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1367+1302_1367+130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAA | 1 | a0001c0001t0002g0099 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1367+1242_1367+124 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAAG others(1): Show |
6 | a0001c0001t0002g0169a0001c0001t0003g0070a0001c0001t0003g0151others(3): Show | 6 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+1298_1367+130 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAAG others(3): Show |
1 | a0001c0002t0021g0091 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1367+1242_1367+125 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAAG others(5): Show |
11 | a0001c0001t0001g0279a0001c0001t0002g0052a0001c0001t0002g0158others(8): Show | 11 | HG01496.hp2 HG01934.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+1294_1367+130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAAG others(13): Show |
1 | a0001c0001t0004g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1367+1286_1367+130 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAAG others(17): Show |
2 | a0001c0001t0002g0309a0001c0002t0001g0272 | 2 | HG02004.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1367+1282_1367+130 others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
G | GAAGAAGA | 1 | a0001c0001t0003g0175 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1367+1246_1367+124 others(11): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
GAAGA | G | 30 | a0001c0001t0001g0115a0001c0001t0001g0208a0001c0001t0002g0028others(27): Show | 30 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1367+1302_1367+130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
GAAGAAAG others(1): Show |
G | 13 | a0001c0001t0001g0171a0001c0001t0001g0277a0001c0001t0002g0065others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1367+1298_1367+130 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
GAAGAAAG others(5): Show |
G | 13 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0054others(10): Show | 13 | HG01358.hp1 HG01975.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+1294_1367+130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
GAAGAAAG others(9): Show |
G | 2 | a0001c0001t0001g0127a0001c0001t0002g0211 | 2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1367+1290_1367+130 others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757796
|
GAAGAAAG others(113): Show |
G | 1 | a0001c0001t0002g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1367+1288_1368-121 others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | |||||
| chrX:129757797
|
AAG | A | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1367+1244_1367+124 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757797 | |||||
| chrX:129757799
|
GA | G | 1 | a0001c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1367+1247delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757799 | |||||
| chrX:129757800
|
A | G | 1 | a0001c0001t0003g0003 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1367+1245A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757800 | ||||||
| chrX:129757803
|
GA | G | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1251delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757803 | |||||
| chrX:129757804
|
A | C | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1249A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757804 | ||||||
| chrX:129757808
|
A | AAG | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1367+1254_1367+125 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757808 | |||||
| chrX:129757811
|
G | GAA | 1 | a0001c0001t0001g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1367+1258_1367+125 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757811 | |||||
| chrX:129757811
|
GA | G | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1259delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757811 | |||||
| chrX:129757815
|
GA | G | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1263delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757815 | |||||
| chrX:129757819
|
G | GAAAGA | 1 | a0001c0001t0012g0167 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1367+1267_1367+127 others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757819 | |||||
| chrX:129757819
|
G | GAAAGAAA others(2): Show |
1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+1267_1367+127 others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757819 | |||||
| chrX:129757821
|
A | AG | 1 | a0001c0001t0003g0103 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1367+1266_1367+126 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757821 | ||||||
| chrX:129757825
|
AAG | A | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1272_1367+127 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757825 | |||||
| chrX:129757826
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1271A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757826 | ||||||
| chrX:129757827
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1272G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757827 | ||||||
| chrX:129757832
|
AAAG | A | 1 | a0007c0022t0003g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1367+1280_1367+128 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757832 | |||||
| chrX:129757833
|
A | AAGAAG | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1367+1282_1367+128 others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757833 | |||||
| chrX:129757835
|
G | GA | 1 | a0001c0001t0012g0167 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1367+1283dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757835 | |||||
| chrX:129757839
|
GA | G | 1 | a0001c0002t0001g0235 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1367+1287delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757839 | |||||
| chrX:129757839
|
GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0002g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1367+1286_1367+129 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757839 | |||||
| chrX:129757843
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1367+1291dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757843 | |||||
| chrX:129757843
|
GAAA | G | 1 | a0001c0001t0003g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1367+1289_1367+129 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757843 | ||||||
| chrX:129757849
|
AAG | A | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1296_1367+129 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757849 | |||||
| chrX:129757849
|
AAGAAAG | A | 2 | a0001c0001t0002g0014a0003c0004t0006g0280 | 2 | HG02572.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1367+1296_1367+130 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757849 | |||||
| chrX:129757849
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0002g0223 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1367+1297_1367+130 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757849 | |||||
| chrX:129757851
|
G | GAA | 1 | a0001c0001t0010g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1367+1298_1367+129 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757851 | |||||
| chrX:129757855
|
GA | G | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1367+1303delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757855 | |||||
| chrX:129757856
|
A | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0191a0003c0004t0006g0280 | 3 | HG02572.hp1 HG02886.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1367+1301A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757856 | ||||||
| chrX:129757857
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1367+1302A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757857 | ||||||
| chrX:129757857
|
AAGAGGGA others(1): Show |
A | 14 | a0001c0001t0002g0192a0001c0001t0003g0104a0001c0001t0006g0206others(11): Show | 14 | HG00099.hp2 HG00735.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1367+1307_1368-131 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757857 | |||||
| chrX:129757857
|
AAGAGGGA others(5): Show |
A | 5 | a0001c0001t0003g0082a0001c0001t0003g0304a0001c0001t0005g0197others(2): Show | 5 | HG00597.hp2 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+1306_1368-130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757857 | |||||
| chrX:129757858
|
AGAGG | A | 24 | a0001c0001t0001g0120a0001c0001t0002g0020a0001c0001t0002g0094others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1367+1307_1367+131 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757858 | |||||
| chrX:129757859
|
G | GAA | 11 | a0001c0001t0001g0053a0001c0001t0001g0121a0001c0001t0001g0123others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+1305_1367+130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757859 | |||||
| chrX:129757859
|
G | GAAAGAA | 1 | a0001c0001t0001g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1367+1305_1367+130 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757859 | |||||
| chrX:129757859
|
G | GAAAGAAA others(7): Show |
1 | a0020c0014t0004g0030 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1367+1305_1367+130 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757859 | |||||
| chrX:129757860
|
AGG | A | 11 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0002g0019others(8): Show | 11 | HG00673.hp1 HG01346.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+1307_1367+130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757860 | |||||
| chrX:129757861
|
G | A | 80 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0116others(77): Show | 80 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1367+1306G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757861 | ||||||
| chrX:129757862
|
G | A | 92 | a0001c0001t0001g0053a0001c0001t0001g0095a0001c0001t0001g0096others(89): Show | 92 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1367+1307G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757862 | ||||||
| chrX:129757862
|
G | GAA | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1307_1367+130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757862 | ||||||
| chrX:129757863
|
G | A | 24 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0121others(21): Show | 24 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1367+1308G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757863 | ||||||
| chrX:129757864
|
AG | A | 2 | a0001c0002t0001g0097a0026c0023t0003g0001 | 2 | NA19074.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1367+1310delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757864 | ||||||
| chrX:129757865
|
G | A | 83 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0116others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1367+1310G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757865 | ||||||
| chrX:129757866
|
A | AGAAGAG | 1 | a0001c0001t0004g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1368-1312_1368-131 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757866 | |||||
| chrX:129757866
|
A | G | 19 | a0001c0001t0001g0118a0001c0001t0001g0126a0001c0001t0001g0145others(16): Show | 19 | HG00735.hp1 HG01081.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1367+1311A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757866 | ||||||
| chrX:129757867
|
G | A | 12 | a0001c0001t0001g0087a0001c0001t0001g0121a0001c0001t0001g0123others(9): Show | 12 | HG00673.hp1 HG01346.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1367+1312G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757867 | ||||||
| chrX:129757868
|
A | G | 12 | a0001c0001t0001g0053a0001c0001t0001g0161a0001c0001t0002g0022others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1312A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757868 | ||||||
| chrX:129757868
|
AG | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0097 | 2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1368-1311delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757868 | ||||||
| chrX:129757869
|
G | A | 70 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0128others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1368-1311G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757869 | ||||||
| chrX:129757869
|
GAGAA | G | 1 | a0001c0001t0003g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1368-1307_1368-130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757869 | |||||
| chrX:129757870
|
A | G | 26 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0116others(23): Show | 26 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1368-1310A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757870 | ||||||
| chrX:129757871
|
G | A | 2 | a0001c0001t0001g0087a0001c0002t0001g0059 | 2 | NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1368-1309G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757871 | ||||||
| chrX:129757871
|
GA | G | 1 | a0001c0002t0001g0215 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1368-1306delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757871 | |||||
| chrX:129757872
|
A | G | 9 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(6): Show | 9 | HG00673.hp1 HG01346.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1368-1308A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757872 | ||||||
| chrX:129757873
|
A | AAG | 1 | a0001c0001t0002g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AAGAAAGA others(13): Show |
1 | a0001c0002t0001g0266 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AAGAAAGA others(7): Show |
1 | a0019c0015t0002g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0128 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AAGAG | 1 | a0014c0018t0004g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1368-1287_1368-128 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AAGAGGG | 1 | a0001c0002t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1368-1303_1368-130 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AAGAGGGA others(1): Show |
2 | a0001c0002t0001g0156a0001c0002t0001g0263 | 2 | HG02293.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1368-1303_1368-130 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
A | AG | 1 | a0001c0001t0004g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1368-1307_1368-130 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757873 | ||||||
| chrX:129757873
|
A | G | 95 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0095others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1368-1307A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757873 | ||||||
| chrX:129757873
|
AAG | A | 13 | a0001c0001t0001g0062a0001c0001t0001g0171a0001c0001t0001g0279others(10): Show | 13 | HG01496.hp2 HG01934.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1368-1285_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757873
|
AAGAG | A | 1 | a0001c0002t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1368-1287_1368-128 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | |||||
| chrX:129757874
|
A | AGAAAGAG others(1): Show |
2 | a0001c0001t0004g0148a0001c0002t0001g0256 | 2 | HG01346.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1368-1304_1368-130 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757874 | |||||
| chrX:129757874
|
A | AGAGG | 4 | a0001c0001t0003g0159a0001c0002t0001g0248a0001c0002t0001g0270others(1): Show | 4 | HG00621.hp1 HG01258.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-1303_1368-130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757874 | |||||
| chrX:129757874
|
A | ATGAG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-1306_1368-130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757874 | ||||||
| chrX:129757874
|
A | G | 18 | a0001c0001t0003g0072a0001c0001t0003g0073a0001c0001t0003g0103others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.1368-1306A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757874 | ||||||
| chrX:129757875
|
G | GAA | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757875 | |||||
| chrX:129757876
|
A | AAAGAGG | 2 | a0022c0016t0001g0117a0028c0030t0001g0178 | 2 | NA19067.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1368-1304_1368-130 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757876 | ||||||
| chrX:129757876
|
A | AG | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1368-1303dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757876 | |||||
| chrX:129757876
|
A | AGG | 2 | a0001c0001t0001g0164a0001c0002t0001g0017 | 2 | NA18957.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1368-1303_1368-130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757876 | |||||
| chrX:129757876
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0136a0001c0002t0001g0059 | 3 | NA18939.hp2 NA18960.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1368-1304A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757876 | ||||||
| chrX:129757876
|
AG | A | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1368-1303delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757876 | ||||||
| chrX:129757877
|
G | A | 26 | a0001c0001t0001g0118a0001c0001t0001g0126a0001c0001t0001g0145others(23): Show | 26 | HG00597.hp2 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1368-1303G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757877 | ||||||
| chrX:129757877
|
G | GGGAGAGA others(5): Show |
2 | a0001c0001t0003g0067a0001c0002t0013g0281 | 2 | NA18948.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1368-1303_1368-130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757877 | ||||||
| chrX:129757878
|
A | G | 30 | a0001c0001t0001g0120a0001c0001t0002g0055a0001c0001t0002g0094others(27): Show | 30 | HG00099.hp2 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1368-1302A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757878 | ||||||
| chrX:129757879
|
G | A | 12 | a0001c0001t0001g0053a0001c0001t0001g0161a0001c0001t0002g0022others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1301G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757879 | ||||||
| chrX:129757880
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-1300A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757880 | ||||||
| chrX:129757881
|
G | A | 33 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0116others(30): Show | 33 | HG00597.hp2 HG00741.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1368-1299G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757881 | ||||||
| chrX:129757882
|
A | G | 6 | a0001c0001t0003g0304a0001c0001t0023g0205a0001c0002t0001g0060others(3): Show | 6 | HG01175.hp2 HG01255.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-1298A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757882 | ||||||
| chrX:129757883
|
G | A | 12 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(9): Show | 12 | HG00673.hp1 HG01346.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1297G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757883 | ||||||
| chrX:129757883
|
G | GAGAGA | 1 | a0001c0002t0001g0048 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1368-1296_1368-129 others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | |||||
| chrX:129757883
|
GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0007g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1368-1293_1368-128 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | |||||
| chrX:129757883
|
GAGAGAGA others(11): Show |
G | 3 | a0001c0001t0005g0007a0001c0001t0005g0153a0001c0001t0007g0284 | 3 | HG02615.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1368-1293_1368-127 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | |||||
| chrX:129757883
|
GAGAGAGA others(15): Show |
G | 2 | a0001c0001t0005g0006a0001c0001t0007g0285 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1368-1293_1368-127 others(26): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | |||||
| chrX:129757883
|
GAGAGAGA others(19): Show |
G | 1 | a0001c0001t0005g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1368-1293_1368-126 others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | |||||
| chrX:129757885
|
G | A | 24 | a0001c0001t0003g0072a0001c0001t0003g0073a0001c0001t0003g0103others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1368-1295G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757885 | ||||||
| chrX:129757885
|
GAGAGAGA others(13): Show |
G | 2 | a0001c0001t0005g0202a0001c0001t0005g0204 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1368-1291_1368-127 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757885 | |||||
| chrX:129757885
|
GAGAGAGA others(17): Show |
G | 5 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0203others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1368-1291_1368-126 others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757885 | |||||
| chrX:129757886
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0003g0082a0001c0002t0001g0075 | 3 | HG00597.hp2 NA18949.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1368-1294A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757886 | ||||||
| chrX:129757887
|
G | A | 7 | a0001c0001t0001g0087a0001c0001t0001g0136a0001c0001t0001g0164others(4): Show | 7 | NA18939.hp2 NA18957.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1293G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757887 | ||||||
| chrX:129757887
|
GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0002g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1368-1289_1368-127 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757887 | |||||
| chrX:129757887
|
GAGAGAGA others(11): Show |
G | 7 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(4): Show | 7 | HG01496.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1289_1368-127 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757887 | |||||
| chrX:129757887
|
GAGAGAGA others(15): Show |
G | 1 | a0001c0001t0002g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1368-1289_1368-126 others(26): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757887 | |||||
| chrX:129757888
|
AG | A | 1 | a0001c0001t0001g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1368-1291delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757888 | ||||||
| chrX:129757889
|
G | A | 27 | a0001c0001t0002g0055a0001c0001t0002g0094a0001c0001t0002g0192others(24): Show | 27 | HG00099.hp2 HG00597.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1368-1291G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757889 | ||||||
| chrX:129757889
|
G | GAA | 1 | a0001c0001t0002g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1368-1290_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | |||||
| chrX:129757889
|
G | GAGAAGAA others(4): Show |
1 | a0001c0001t0004g0032 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1368-1288_1368-128 others(15): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | |||||
| chrX:129757889
|
GAGAGAGA others(5): Show |
G | 1 | a0001c0002t0001g0297 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1368-1287_1368-127 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | |||||
| chrX:129757889
|
GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0003g0112a0001c0001t0006g0185a0001c0001t0010g0177 | 3 | NA19030.hp1 NA19056.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1368-1287_1368-127 others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | |||||
| chrX:129757889
|
GAGAGAGA others(13): Show |
G | 1 | a0001c0001t0006g0125 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1368-1287_1368-126 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | |||||
| chrX:129757890
|
AGAG | A | 1 | a0001c0001t0002g0099 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1368-1289_1368-128 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757890 | ||||||
| chrX:129757891
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-1289G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757891 | ||||||
| chrX:129757891
|
GAGAGAA | G | 7 | a0001c0001t0001g0115a0001c0001t0001g0160a0001c0001t0002g0065others(4): Show | 7 | HG00639.hp1 HG02015.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-1285_1368-128 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | |||||
| chrX:129757891
|
GAGAGAAA others(3): Show |
G | 17 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0002g0058others(14): Show | 17 | HG00408.hp2 HG00544.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1368-1285_1368-127 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | |||||
| chrX:129757891
|
GAGAGAAA others(7): Show |
G | 8 | a0001c0001t0001g0250a0001c0001t0002g0012a0001c0001t0002g0302others(5): Show | 8 | HG03130.hp1 HG03239.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-1285_1368-127 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | |||||
| chrX:129757891
|
GAGAGAAA others(11): Show |
G | 6 | a0001c0001t0001g0143a0001c0001t0001g0277a0001c0001t0002g0093others(3): Show | 6 | HG03098.hp1 HG03927.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-1285_1368-126 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | |||||
| chrX:129757891
|
GAGAGAAA others(15): Show |
G | 1 | a0001c0001t0002g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-126 others(26): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | |||||
| chrX:129757891
|
GAGAGAAA others(19): Show |
G | 1 | a0001c0001t0001g0239 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-126 others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | |||||
| chrX:129757893
|
G | A | 12 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0165others(9): Show | 12 | HG01175.hp2 HG01255.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1287G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757893 | ||||||
| chrX:129757893
|
G | GAA | 1 | a0001c0001t0012g0241 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1368-1286_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
G | GAGAA | 2 | a0001c0001t0003g0132a0001c0002t0001g0155 | 2 | NA18945.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1368-1221_1368-121 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGA | G | 1 | a0001c0001t0002g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-128 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGAA | G | 17 | a0001c0001t0001g0174a0001c0001t0003g0024a0001c0001t0003g0070others(14): Show | 17 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1368-1221_1368-121 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGAAAGA others(1): Show |
G | 11 | a0001c0001t0003g0021a0001c0001t0003g0105a0001c0001t0003g0147others(8): Show | 11 | HG01071.hp2 HG01884.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1368-1225_1368-121 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGAAAGA others(4): Show |
G | 1 | a0001c0001t0012g0167 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-127 others(15): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGAAAGA others(5): Show |
G | 19 | a0001c0001t0002g0176a0001c0001t0003g0011a0001c0001t0003g0036others(16): Show | 19 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1368-1229_1368-121 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGAAAGA others(9): Show |
G | 7 | a0001c0001t0003g0003a0001c0002t0001g0013a0001c0002t0001g0133others(4): Show | 7 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1233_1368-121 others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757893
|
GAGAAAGA others(13): Show |
G | 2 | a0001c0001t0001g0086a0001c0002t0001g0154 | 2 | HG03710.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1368-1237_1368-121 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | |||||
| chrX:129757895
|
GAA | G | 10 | a0001c0001t0002g0094a0001c0001t0002g0111a0001c0001t0008g0195others(7): Show | 10 | HG00597.hp1 HG02135.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1368-1283_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | |||||
| chrX:129757895
|
GAAA | G | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-1284_1368-128 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757895 | ||||||
| chrX:129757895
|
GAAAGA | G | 1 | a0001c0001t0001g0208 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1368-1282_1368-127 others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | |||||
| chrX:129757895
|
GAAAGAA | G | 15 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0055others(12): Show | 15 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1368-1283_1368-127 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | |||||
| chrX:129757895
|
GAAAGAAA others(3): Show |
G | 10 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0126others(7): Show | 10 | HG01175.hp1 HG01891.hp2 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.1368-1283_1368-127 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | |||||
| chrX:129757895
|
GAAAGAAA others(7): Show |
G | 4 | a0001c0001t0001g0145a0001c0001t0001g0172a0001c0001t0003g0084others(1): Show | 4 | HG01081.hp1 HG02723.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-1283_1368-127 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | |||||
| chrX:129757895
|
GAAAGAAA others(11): Show |
G | 2 | a0001c0001t0002g0042a0013c0025t0001g0274 | 2 | HG03041.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1368-1283_1368-126 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | |||||
| chrX:129757896
|
A | AAG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1283_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757896 | |||||
| chrX:129757897
|
A | G | 102 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0120others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1368-1283A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757897 | ||||||
| chrX:129757899
|
GAA | G | 1 | a0001c0001t0002g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1368-1279_1368-127 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757899 | |||||
| chrX:129757901
|
A | G | 85 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0121others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1368-1279A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757901 | ||||||
| chrX:129757905
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1275_1368-127 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757905 | ||||||
| chrX:129757905
|
A | G | 77 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0096others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1368-1275A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757905 | ||||||
| chrX:129757907
|
G | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1273G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757907 | ||||||
| chrX:129757907
|
GAAAGA | G | 1 | a0001c0002t0001g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1368-1270_1368-126 others(9): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757907 | |||||
| chrX:129757908
|
A | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1272A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757908 | ||||||
| chrX:129757909
|
A | G | 33 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0122others(30): Show | 33 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1368-1271A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757909 | ||||||
| chrX:129757913
|
A | G | 8 | a0001c0001t0002g0020a0001c0001t0003g0082a0001c0002t0001g0060others(5): Show | 8 | HG00597.hp2 HG01175.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-1267A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757913 | ||||||
| chrX:129757917
|
A | G | 3 | a0001c0001t0003g0082a0001c0002t0001g0075a0013c0025t0001g0274 | 3 | HG00597.hp2 HG03490.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1368-1263A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757917 | ||||||
| chrX:129757921
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1368-1259A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757921 | ||||||
| chrX:129757931
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1246dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757931 | |||||
| chrX:129757959
|
GAAAA | G | 1 | a0001c0001t0024g0283 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1368-1219_1368-121 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757959 | |||||
| chrX:129758000
|
T | C | 41 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(38): Show | 41 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1368-1180T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758000 | ||||||
| chrX:129758088
|
T | G | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1368-1092T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758088 | ||||||
| chrX:129758088
|
T | TG | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1368-1089dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758088 | |||||
| chrX:129758089
|
G | T | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1368-1091G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758089 | ||||||
| chrX:129758093
|
CA | C | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-1083delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758093 | |||||
| chrX:129758106
|
G | A | 5 | a0001c0001t0004g0032a0001c0001t0004g0061a0001c0001t0004g0173others(2): Show | 5 | HG01891.hp2 HG02155.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-1074G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758106 | ||||||
| chrX:129758121
|
AG | A | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-1057delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758121 | |||||
| chrX:129758165
|
A | G | 1 | a0001c0001t0018g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1368-1015A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758165 | ||||||
| chrX:129758212
|
A | AG | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1368-966dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758212 | |||||
| chrX:129758263
|
CT | C | 1 | a0001c0001t0012g0167 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1368-915delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758263 | |||||
| chrX:129758300
|
T | TG | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1368-875dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758300 | |||||
| chrX:129758369
|
CT | C | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-809delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758369 | |||||
| chrX:129758428
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-749dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758428 | |||||
| chrX:129758432
|
TG | T | 1 | a0001c0001t0012g0167 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1368-745delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758432 | |||||
| chrX:129758439
|
A | AT | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1368-738dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758439 | |||||
| chrX:129758446
|
C | T | 41 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(38): Show | 41 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1368-734C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758446 | ||||||
| chrX:129758522
|
TG | T | 2 | a0001c0001t0001g0136a0001c0001t0012g0167 | 2 | NA18947.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1368-655delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758522 | |||||
| chrX:129758571
|
TC | T | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1368-607delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758571 | |||||
| chrX:129758635
|
AG | A | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-543delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758635 | |||||
| chrX:129758697
|
A | AG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-481dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758697 | |||||
| chrX:129758736
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1368-444G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758736 | ||||||
| chrX:129758807
|
T | TC | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-369dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758807 | |||||
| chrX:129758816
|
G | GGT | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-364_1368-363i others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758816 | ||||||
| chrX:129758817
|
T | A | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-363T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758817 | ||||||
| chrX:129758822
|
A | AG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-354dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758822 | |||||
| chrX:129758841
|
GC | G | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-337delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758841 | |||||
| chrX:129758844
|
TC | T | 2 | a0026c0023t0003g0001a0027c0007t0020g0015 | 2 | NA18987.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1368-333delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758844 | |||||
| chrX:129758856
|
T | TG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-322dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758856 | |||||
| chrX:129758907
|
A | AC | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-272dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758907 | |||||
| chrX:129758931
|
TG | T | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-244delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758931 | |||||
| chrX:129758942
|
T | TG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-237dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758942 | |||||
| chrX:129758947
|
A | AG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-230dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129758947 | |||||
| chrX:129759032
|
A | AG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-144dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129759032 | |||||
| chrX:129759068
|
C | T | 1 | a0001c0001t0006g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1368-112C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129759068 | ||||||
| chrX:129759128
|
GC | G | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1368-48delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129759128 | |||||
| chrX:129759141
|
G | GC | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1368-35dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129759141 | |||||
| chrX:129759169
|
CT | C | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1368-9delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129759169 | |||||
| chrX:129759248
|
TG | T | 1 | a0020c0014t0004g0030 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1428+11delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759248 | |||||
| chrX:129759273
|
T | C | 36 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(33): Show | 36 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.1428+33T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759273 | ||||||
| chrX:129759274
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1428+39delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759274 | |||||
| chrX:129759281
|
A | AG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1428+46dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759281 | |||||
| chrX:129759404
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1428+168dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759404 | |||||
| chrX:129759408
|
CG | C | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1428+172delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759408 | |||||
| chrX:129759415
|
AT | A | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1428+178delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759415 | |||||
| chrX:129759423
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1428+183C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759423 | ||||||
| chrX:129759440
|
GC | G | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1428+203delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759440 | |||||
| chrX:129759441
|
C | T | 75 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(72): Show | 75 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1428+201C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759441 | ||||||
| chrX:129759457
|
TC | T | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1428+219delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759457 | |||||
| chrX:129759510
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1428+272dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759510 | |||||
| chrX:129759519
|
A | AC | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1428+280dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759519 | |||||
| chrX:129759578
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1428+338C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759578 | ||||||
| chrX:129759582
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1428+342G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759582 | ||||||
| chrX:129759616
|
T | G | 134 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(131): Show | 134 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.1428+376T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759616 | ||||||
| chrX:129759632
|
TG | T | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1428+396delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759632 | |||||
| chrX:129759675
|
TG | T | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1428+440delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759675 | |||||
| chrX:129759691
|
A | AT | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1428+451_1428+452i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759691 | ||||||
| chrX:129759755
|
A | AG | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1428+519dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759755 | |||||
| chrX:129759794
|
G | GT | 1 | a0001c0001t0003g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1428+557dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759794 | |||||
| chrX:129759833
|
A | C | 37 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(34): Show | 37 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1428+593A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759833 | ||||||
| chrX:129759942
|
G | A | 3 | a0001c0001t0006g0125a0003c0004t0006g0088a0003c0004t0006g0130 | 3 | NA18975.hp1 NA19065.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1429-570G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759942 | ||||||
| chrX:129759995
|
TCAGCAGC others(11): Show |
T | 2 | a0001c0002t0001g0106a0001c0002t0001g0222 | 2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1429-513_1429-496d others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759995 | |||||
| chrX:129760001
|
GC | G | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1429-509delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760001 | |||||
| chrX:129760013
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0042a0001c0001t0002g0055others(1): Show | 4 | HG03041.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429-499A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760013 | ||||||
| chrX:129760042
|
A | G | 8 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0197others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-470A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760042 | ||||||
| chrX:129760048
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1429-464C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760048 | ||||||
| chrX:129760097
|
CA | C | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1429-413delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760097 | |||||
| chrX:129760125
|
TC | T | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1429-384delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760125 | |||||
| chrX:129760181
|
T | TC | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1429-330dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760181 | |||||
| chrX:129760237
|
C | T | 8 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0197others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-275C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760237 | ||||||
| chrX:129760248
|
T | TG | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1429-263dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760248 | |||||
| chrX:129760300
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1429-212G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760300 | ||||||
| chrX:129760358
|
A | AC | 2 | a0001c0001t0001g0136a0020c0014t0004g0030 | 2 | HG02523.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1429-151dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760358 | |||||
| chrX:129760387
|
T | TC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1429-119dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760387 | |||||
| chrX:129760409
|
A | AC | 1 | a0020c0014t0004g0030 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1429-100dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760409 | |||||
| chrX:129760430
|
C | T | 1 | a0001c0006t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1429-82C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760430 | ||||||
| chrX:129760479
|
G | A | 8 | a0001c0001t0002g0046a0001c0001t0008g0195a0001c0001t0008g0196others(5): Show | 8 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-33G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760479 | ||||||
| chrX:129760502
|
T | TC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.1429-6dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129760502 | |||||
| chrX:129760583
|
T | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | splice_donor_variant&intron_variant | HIGH | c.1498+2T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760583 | ||||||
| chrX:129760590
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+10delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760590 | ||||||
| chrX:129760592
|
G | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+11G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760592 | ||||||
| chrX:129760594
|
A | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+13A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760594 | ||||||
| chrX:129760649
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+71dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760649 | |||||
| chrX:129760649
|
TG | T | 1 | a0020c0014t0004g0030 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1498+71delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760649 | |||||
| chrX:129760670
|
AT | A | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1498+93delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760670 | |||||
| chrX:129760679
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+99dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760679 | |||||
| chrX:129760683
|
C | CG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+102_1498+103i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760683 | ||||||
| chrX:129760715
|
T | TACG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+135_1498+136i others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760715 | |||||
| chrX:129760719
|
G | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+138G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760719 | ||||||
| chrX:129760725
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+144_1498+145i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760725 | ||||||
| chrX:129760747
|
C | CT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+166_1498+167i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760747 | ||||||
| chrX:129760756
|
A | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+175A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760756 | ||||||
| chrX:129760796
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+215_1498+216i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760796 | ||||||
| chrX:129760832
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+252dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760832 | |||||
| chrX:129760851
|
G | GA | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1498+270_1498+271i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760851 | ||||||
| chrX:129760917
|
G | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0054a0001c0001t0002g0278 | 3 | HG00544.hp2 HG00673.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1499-255G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760917 | ||||||
| chrX:129760918
|
AG | A | 1 | a0001c0001t0005g0247 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1499-252delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760918 | |||||
| chrX:129760948
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-224_1499-223i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760948 | ||||||
| chrX:129760949
|
T | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-223T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760949 | ||||||
| chrX:129760985
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-187_1499-186i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760985 | ||||||
| chrX:129760989
|
A | AC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-181dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129760989 | |||||
| chrX:129760999
|
C | CT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-173_1499-172i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760999 | ||||||
| chrX:129761004
|
C | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-168C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129761004 | ||||||
| chrX:129761014
|
C | T | 37 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(34): Show | 37 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1499-158C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129761014 | ||||||
| chrX:129761052
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-120_1499-119i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129761052 | ||||||
| chrX:129761058
|
G | GC | 1 | a0015c0012t0004g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1499-112dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129761058 | |||||
| chrX:129761087
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-84dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129761087 | |||||
| chrX:129761129
|
CG | C | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1499-41delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129761129 | |||||
| chrX:129761142
|
T | TGA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-29_1499-28dup others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 129761142 | |||||
| chrX:129761278
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.1603+2_1603+3insC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761278 | ||||||
| chrX:129761293
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+18dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761293 | |||||
| chrX:129761308
|
C | A | 1 | a0001c0002t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1603+32C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761308 | ||||||
| chrX:129761311
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1603+35C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761311 | ||||||
| chrX:129761314
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+38_1603+39ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761314 | ||||||
| chrX:129761329
|
A | G | 2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1603+53A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761329 | ||||||
| chrX:129761340
|
G | A | 2 | a0002c0003t0002g0292a0002c0003t0002g0295 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603+64G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761340 | ||||||
| chrX:129761352
|
TA | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+77delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761352 | ||||||
| chrX:129761378
|
AT | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+103delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761378 | ||||||
| chrX:129761387
|
T | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+111T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761387 | ||||||
| chrX:129761388
|
C | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+112C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761388 | ||||||
| chrX:129761389
|
T | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+113T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761389 | ||||||
| chrX:129761437
|
A | AG | 1 | a0020c0014t0004g0030 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1603+163dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761437 | |||||
| chrX:129761457
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+181_1603+182i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761457 | ||||||
| chrX:129761510
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+234_1603+235i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761510 | ||||||
| chrX:129761512
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+236_1603+237i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761512 | ||||||
| chrX:129761536
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+261delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761536 | ||||||
| chrX:129761538
|
C | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+262C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761538 | ||||||
| chrX:129761577
|
T | TCG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+301_1603+302i others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761577 | ||||||
| chrX:129761579
|
T | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+303T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761579 | ||||||
| chrX:129761580
|
G | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+304G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761580 | ||||||
| chrX:129761594
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+318_1603+319i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761594 | ||||||
| chrX:129761597
|
G | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+321G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761597 | ||||||
| chrX:129761599
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+324dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761599 | |||||
| chrX:129761642
|
C | CT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-364_1604-363i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761642 | ||||||
| chrX:129761646
|
A | AC | 1 | a0001c0001t0002g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1604-356dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761646 | |||||
| chrX:129761672
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-332dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761672 | |||||
| chrX:129761705
|
T | TC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1604-299dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761705 | |||||
| chrX:129761708
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-296delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761708 | |||||
| chrX:129761718
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-288_1604-287i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761718 | ||||||
| chrX:129761741
|
A | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-265A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761741 | ||||||
| chrX:129761742
|
G | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-264G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761742 | ||||||
| chrX:129761745
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-261_1604-260i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761745 | ||||||
| chrX:129761748
|
C | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-258C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761748 | ||||||
| chrX:129761749
|
A | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-257A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761749 | ||||||
| chrX:129761751
|
G | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-255G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761751 | ||||||
| chrX:129761772
|
C | T | 1 | a0002c0003t0005g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1604-234C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761772 | ||||||
| chrX:129761814
|
CA | C | 2 | a0001c0001t0015g0150a0026c0023t0003g0001 | 2 | NA18987.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1604-190delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chrX | 129761814 | |||||
| chrX:129761842
|
A | C | 37 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(34): Show | 37 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1604-164A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761842 | ||||||
| chrX:129761862
|
G | GCCA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-144_1604-143i others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761862 | ||||||
| chrX:129761912
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-94_1604-93ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761912 | ||||||
| chrX:129761913
|
G | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-93G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761913 | ||||||
| chrX:129761995
|
T | G | 5 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-11T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761995 | ||||||
| chrX:129762070
|
G | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.1663+5G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762070 | ||||||
| chrX:129762072
|
C | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.1663+7C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762072 | ||||||
| chrX:129762095
|
A | AC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1663+34dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762095 | |||||
| chrX:129762117
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1663+55delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762117 | |||||
| chrX:129762180
|
CG | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1663+118delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762180 | |||||
| chrX:129762181
|
G | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 5 | NA18951.hp2 NA19059.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663+116G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762181 | ||||||
| chrX:129762191
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1663+130delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762191 | |||||
| chrX:129762232
|
C | CCA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1663+169_1663+170d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762232 | |||||
| chrX:129762240
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1663+175_1663+176i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762240 | ||||||
| chrX:129762248
|
TC | T | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1663+187delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762248 | |||||
| chrX:129762256
|
G | GC | 1 | a0001c0001t0005g0247 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1663+194dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762256 | |||||
| chrX:129762262
|
A | AC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1663+200dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762262 | |||||
| chrX:129762278
|
TG | T | 2 | a0001c0001t0005g0247a0021c0028t0001g0049 | 2 | HG02897.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1663+216delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762278 | |||||
| chrX:129762289
|
T | TC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1663+227dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762289 | |||||
| chrX:129762314
|
C | T | 2 | a0001c0001t0003g0036a0001c0001t0003g0175 | 2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1663+249C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762314 | ||||||
| chrX:129762372
|
G | A | 74 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(71): Show | 74 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1663+307G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762372 | ||||||
| chrX:129762382
|
G | A | 3 | a0001c0001t0002g0111a0001c0001t0002g0191a0001c0001t0002g0211 | 3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1664-312G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762382 | ||||||
| chrX:129762396
|
GT | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-297delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762396 | ||||||
| chrX:129762417
|
G | GTA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-276_1664-275d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762417 | |||||
| chrX:129762432
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-262_1664-261i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762432 | ||||||
| chrX:129762461
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1664-233C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762461 | ||||||
| chrX:129762508
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-184delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762508 | |||||
| chrX:129762510
|
GC | G | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1664-182delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762510 | |||||
| chrX:129762534
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-159dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762534 | |||||
| chrX:129762540
|
C | T | 1 | a0002c0003t0005g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1664-154C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762540 | ||||||
| chrX:129762555
|
C | T | 3 | a0001c0001t0002g0098a0001c0001t0002g0137a0001c0001t0009g0198 | 3 | HG01891.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1664-139C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762555 | ||||||
| chrX:129762562
|
TG | T | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1664-128delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762562 | |||||
| chrX:129762577
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-115dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762577 | |||||
| chrX:129762621
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-72dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762621 | |||||
| chrX:129762641
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1664-50delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762641 | |||||
| chrX:129762688
|
TC | T | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | splice_region_variant&intron_variant | LOW | c.1664-3delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 129762688 | |||||
| chrX:129762864
|
AG | A | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+97delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129762864 | |||||
| chrX:129762877
|
T | TG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+108dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129762877 | |||||
| chrX:129763029
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+262dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763029 | |||||
| chrX:129763064
|
C | T | 74 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(71): Show | 74 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1740+294C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763064 | ||||||
| chrX:129763068
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+302delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763068 | |||||
| chrX:129763107
|
G | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0170a0001c0001t0002g0302 | 3 | HG02735.hp1 HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1740+337G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763107 | ||||||
| chrX:129763224
|
T | TC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+454_1740+455i others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763224 | ||||||
| chrX:129763268
|
A | G | 2 | a0002c0003t0002g0292a0002c0003t0002g0295 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+498A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763268 | ||||||
| chrX:129763281
|
C | G | 74 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(71): Show | 74 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1740+511C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763281 | ||||||
| chrX:129763341
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+574dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763341 | |||||
| chrX:129763371
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+606dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763371 | |||||
| chrX:129763374
|
AAAG | A | 1 | a0001c0001t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1740+609_1740+611d others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763374 | |||||
| chrX:129763425
|
TG | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+658delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763425 | |||||
| chrX:129763475
|
C | T | 1 | a0001c0002t0001g0246 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1740+705C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763475 | ||||||
| chrX:129763501
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+733delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763501 | |||||
| chrX:129763504
|
C | CA | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1740+740dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763504 | |||||
| chrX:129763513
|
C | CA | 2 | a0021c0028t0001g0049a0026c0023t0003g0001 | 2 | NA19075.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1740+752dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763513 | |||||
| chrX:129763513
|
CA | C | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+752delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763513 | |||||
| chrX:129763522
|
AT | A | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1740+754delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763522 | |||||
| chrX:129763523
|
T | A | 73 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(70): Show | 73 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1740+753T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763523 | ||||||
| chrX:129763532
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1740+762C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763532 | ||||||
| chrX:129763553
|
T | TC | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1740+786dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763553 | |||||
| chrX:129763553
|
TC | T | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+786delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763553 | |||||
| chrX:129763564
|
C | T | 2 | a0002c0003t0002g0292a0002c0003t0002g0295 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+794C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763564 | ||||||
| chrX:129763564
|
CG | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+797delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763564 | |||||
| chrX:129763588
|
T | TC | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1740+819dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763588 | |||||
| chrX:129763671
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+910dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763671 | |||||
| chrX:129763688
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+922dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763688 | |||||
| chrX:129763794
|
GA | G | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+1026delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763794 | |||||
| chrX:129763854
|
T | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1084T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763854 | ||||||
| chrX:129763857
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1093dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763857 | |||||
| chrX:129763871
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1101_1740+110 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763871 | ||||||
| chrX:129763886
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1116_1740+111 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763886 | ||||||
| chrX:129763920
|
TG | T | 2 | a0001c0001t0004g0035a0027c0007t0020g0015 | 2 | NA18986.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1740+1156delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763920 | |||||
| chrX:129763929
|
TA | T | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1740+1162delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763929 | |||||
| chrX:129763936
|
A | AT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1166_1740+116 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763936 | ||||||
| chrX:129763963
|
G | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0194 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1740+1193G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763963 | ||||||
| chrX:129763967
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1200delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129763967 | |||||
| chrX:129764063
|
CA | C | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1295delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764063 | |||||
| chrX:129764070
|
AG | A | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1301delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764070 | ||||||
| chrX:129764110
|
GA | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1344delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764110 | |||||
| chrX:129764124
|
T | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1354T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764124 | ||||||
| chrX:129764125
|
GT | G | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+1358delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764125 | |||||
| chrX:129764144
|
TA | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1377delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764144 | |||||
| chrX:129764186
|
G | GT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1419dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764186 | |||||
| chrX:129764231
|
C | CT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1466dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764231 | |||||
| chrX:129764245
|
G | A | 134 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(131): Show | 134 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.1740+1475G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764245 | ||||||
| chrX:129764265
|
A | G | 2 | a0001c0001t0004g0034a0001c0001t0004g0043 | 2 | NA18970.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1740+1495A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764265 | ||||||
| chrX:129764301
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1740+1531T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764301 | ||||||
| chrX:129764377
|
C | CG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1610dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764377 | |||||
| chrX:129764414
|
G | GC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1644_1740+164 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764414 | ||||||
| chrX:129764463
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1693_1740+169 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764463 | ||||||
| chrX:129764511
|
C | T | 3 | a0002c0003t0002g0292a0002c0003t0002g0295a0002c0003t0005g0213 | 3 | HG01243.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+1741C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764511 | ||||||
| chrX:129764517
|
T | C | 203 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(200): Show | 203 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1740+1747T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764517 | ||||||
| chrX:129764536
|
T | TC | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1740+1769dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764536 | |||||
| chrX:129764572
|
T | A | 3 | a0002c0003t0002g0292a0002c0003t0002g0295a0002c0003t0005g0213 | 3 | HG01243.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+1802T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764572 | ||||||
| chrX:129764586
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1740+1816C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764586 | ||||||
| chrX:129764655
|
C | CA | 13 | a0001c0001t0003g0023a0001c0001t0003g0132a0001c0001t0005g0005others(10): Show | 13 | HG00099.hp2 HG01243.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1740+1901dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764655 | |||||
| chrX:129764655
|
C | CAAA | 1 | a0002c0003t0005g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1740+1899_1740+190 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764655 | |||||
| chrX:129764655
|
CA | C | 116 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(113): Show | 116 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.1740+1901delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764655 | |||||
| chrX:129764655
|
CAA | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0042a0001c0001t0002g0055others(1): Show | 4 | HG03041.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1740+1900_1740+190 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764655 | |||||
| chrX:129764656
|
A | AC | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1886_1740+188 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764656 | ||||||
| chrX:129764707
|
T | TA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1939dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764707 | |||||
| chrX:129764866
|
AG | A | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+2098delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764866 | |||||
| chrX:129764893
|
G | GA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+2123_1740+212 others(5): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764893 | ||||||
| chrX:129764951
|
G | A | 2 | a0001c0001t0001g0086a0012c0024t0001g0249 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1740+2181G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764951 | ||||||
| chrX:129764977
|
A | C | 17 | a0001c0001t0002g0046a0001c0001t0003g0084a0001c0001t0003g0112others(14): Show | 17 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1740+2207A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764977 | ||||||
| chrX:129764988
|
GA | G | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1740+2222delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764988 | |||||
| chrX:129765012
|
T | TCTTTCTT others(10): Show |
1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+2246_1740+226 others(21): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765012 | |||||
| chrX:129765060
|
G | A | 1 | a0001c0001t0004g0025 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1740+2290G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765060 | ||||||
| chrX:129765082
|
AT | A | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1740+2316delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765082 | |||||
| chrX:129765143
|
GC | G | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1740+2377delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765143 | |||||
| chrX:129765178
|
G | T | 7 | a0001c0001t0003g0084a0001c0001t0003g0112a0001c0001t0003g0113others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1740+2408G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765178 | ||||||
| chrX:129765311
|
AT | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-2289delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765311 | |||||
| chrX:129765371
|
C | A | 7 | a0001c0001t0003g0084a0001c0001t0003g0112a0001c0001t0003g0113others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1741-2232C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765371 | ||||||
| chrX:129765451
|
C | CA | 1 | a0017c0013t0003g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1741-2149dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765451 | |||||
| chrX:129765503
|
G | C | 1 | a0001c0001t0005g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1741-2100G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765503 | ||||||
| chrX:129765554
|
A | C | 1 | a0001c0001t0002g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1741-2049A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765554 | ||||||
| chrX:129765615
|
CT | C | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1741-1981delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765615 | |||||
| chrX:129765619
|
T | C | 3 | a0001c0001t0002g0111a0001c0001t0002g0191a0001c0001t0002g0211 | 3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1741-1984T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765619 | ||||||
| chrX:129765619
|
T | TTTTC | 1 | a0001c0002t0001g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1741-1968_1741-196 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765619 | |||||
| chrX:129765635
|
C | CT | 27 | a0001c0001t0002g0111a0001c0001t0002g0309a0001c0001t0005g0005others(24): Show | 27 | HG00323.hp1 HG01123.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741-1946dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | |||||
| chrX:129765635
|
C | CTT | 15 | a0001c0001t0003g0084a0001c0001t0003g0112a0001c0001t0003g0113others(12): Show | 15 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1741-1947_1741-194 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | |||||
| chrX:129765635
|
CT | C | 67 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(64): Show | 67 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1741-1946delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | |||||
| chrX:129765635
|
CTT | C | 63 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0095others(60): Show | 63 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1741-1947_1741-194 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | |||||
| chrX:129765635
|
CTTT | C | 4 | a0001c0001t0001g0087a0001c0020t0005g0209a0003c0004t0006g0280others(1): Show | 4 | HG02280.hp1 HG04184.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1741-1948_1741-194 others(7): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | |||||
| chrX:129765649
|
T | C | 1 | a0001c0002t0019g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1741-1954T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765649 | ||||||
| chrX:129765651
|
T | A | 25 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0019others(22): Show | 25 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1741-1952T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765651 | ||||||
| chrX:129765692
|
C | CA | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1741-1910dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765692 | |||||
| chrX:129765714
|
T | C | 217 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(214): Show | 217 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1741-1889T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765714 | ||||||
| chrX:129765783
|
A | G | 165 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(162): Show | 165 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1741-1820A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765783 | ||||||
| chrX:129765913
|
A | AG | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-1688dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765913 | |||||
| chrX:129766011
|
T | C | 1 | a0001c0001t0005g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1741-1592T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766011 | ||||||
| chrX:129766144
|
T | TG | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-1457dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766144 | |||||
| chrX:129766324
|
C | T | 1 | a0001c0001t0003g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1741-1279C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766324 | ||||||
| chrX:129766396
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1741-1207G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766396 | ||||||
| chrX:129766512
|
C | CT | 4 | a0001c0001t0001g0143a0001c0001t0002g0168a0001c0001t0002g0169others(1): Show | 4 | NA18972.hp1 NA18977.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1741-1078dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766512 | |||||
| chrX:129766512
|
CT | C | 3 | a0001c0001t0017g0212a0016c0027t0001g0182a0027c0007t0020g0015 | 3 | HG02896.hp2 NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1741-1078delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766512 | |||||
| chrX:129766579
|
G | GC | 1 | a0001c0002t0013g0281 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1741-1021dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766579 | |||||
| chrX:129766583
|
G | A | 5 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0011g0307others(2): Show | 5 | HG02109.hp1 HG06807.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1741-1020G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766583 | ||||||
| chrX:129766759
|
TA | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1741-842delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766759 | |||||
| chrX:129766761
|
AT | A | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1741-837delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766761 | |||||
| chrX:129766807
|
TG | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-792delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766807 | |||||
| chrX:129766865
|
C | T | 19 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0005g0186others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1741-738C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766865 | ||||||
| chrX:129766960
|
TC | T | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1741-640delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129766960 | |||||
| chrX:129767038
|
AC | A | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-563delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767038 | |||||
| chrX:129767041
|
T | G | 14 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0007g0284others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741-562T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767041 | ||||||
| chrX:129767198
|
A | AG | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1741-402dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767198 | |||||
| chrX:129767213
|
C | CA | 14 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0007g0284others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741-382dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767213 | |||||
| chrX:129767234
|
A | T | 8 | a0001c0001t0007g0284a0001c0001t0007g0285a0001c0001t0007g0286others(5): Show | 8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1741-369A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767234 | ||||||
| chrX:129767254
|
G | GC | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1741-346dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767254 | |||||
| chrX:129767259
|
GC | G | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-341delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767259 | |||||
| chrX:129767264
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1741-339A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767264 | ||||||
| chrX:129767265
|
A | G | 1 | a0013c0025t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1741-338A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767265 | ||||||
| chrX:129767281
|
T | C | 6 | a0001c0001t0008g0195a0001c0001t0008g0196a0001c0001t0008g0207others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741-322T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767281 | ||||||
| chrX:129767297
|
GC | G | 1 | a0027c0007t0020g0015 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1741-303delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767297 | |||||
| chrX:129767353
|
G | GA | 1 | a0001c0002t0013g0281 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1741-245dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767353 | |||||
| chrX:129767361
|
CA | C | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1741-239delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767361 | |||||
| chrX:129767373
|
TA | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1741-227delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767373 | |||||
| chrX:129767379
|
TC | T | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1741-222delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767379 | |||||
| chrX:129767446
|
A | AG | 1 | a0021c0028t0001g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1741-154dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767446 | |||||
| chrX:129767455
|
A | G | 14 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0007g0284others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741-148A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767455 | ||||||
| chrX:129767471
|
G | GC | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1741-130dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767471 | |||||
| chrX:129767474
|
A | AG | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1741-126dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767474 | |||||
| chrX:129767495
|
G | C | 1 | a0001c0002t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1741-108G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767495 | ||||||
| chrX:129767495
|
GC | G | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1741-105delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767495 | |||||
| chrX:129767515
|
C | G | 1 | a0001c0001t0017g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1741-88C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767515 | ||||||
| chrX:129767516
|
G | C | 1 | a0001c0001t0017g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1741-87G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767516 | ||||||
| chrX:129767742
|
C | CT | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1830+51dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129767742 | |||||
| chrX:129767769
|
TC | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1830+80delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129767769 | |||||
| chrX:129767774
|
GC | G | 1 | a0001c0001t0017g0212 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1830+86delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129767774 | |||||
| chrX:129767833
|
TC | T | 1 | a0026c0023t0003g0001 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1830+145delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129767833 | |||||
| chrX:129767976
|
C | T | 1 | a0001c0020t0005g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1830+284C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | chrX | 129767976 | ||||||
| chrX:129768047
|
TC | T | 1 | a0025c0011t0014g0008 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1831-241delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129768047 | |||||
| chrX:129768051
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1831-240G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | chrX | 129768051 | ||||||
| chrX:129768112
|
AG | A | 1 | a0001c0001t0015g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1831-175delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129768112 | |||||
| chrX:129768163
|
T | TG | 1 | a0001c0002t0013g0281 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1831-123dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 129768163 | |||||
| chrX:129768259
|
A | G | 14 | a0001c0001t0002g0306a0001c0001t0002g0309a0001c0001t0007g0284others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1831-32A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | chrX | 129768259 |