Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 343070 |
| ensemblid | ENSG00000204505.5 |
| hgncid | 27996 |
| symbol | PRAMEF9 |
| name | PRAME family member 9 |
| refseq_nuc | NM_001010890.3 |
| refseq_prot | NP_001010890.2 |
| ensembl_nuc | ENST00000415919.3 |
| ensembl_prot | ENSP00000485258.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 13171848 |
| end | 13179459 |
| strand | + |
| ver | v1.2 |
| region | chr1:13171848-13179459 |
| region5000 | chr1:13166848-13184459 |
| regionname0 | PRAMEF9_chr1_13171848_13179459 |
| regionname5000 | PRAMEF9_chr1_13166848_13184459 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 478 | 82 | 3 | 29 | 37 | 4 | 9 | 31 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0002 | 0/0 | 478 | 35 | 1 | 6 | 26 | 0 | 2 | 19 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0003 | 1/0 | 478 | 22 | 0 | 3 | 17 | 0 | 1 | 13 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0004 | 0/1 | 478 | 19 | 2 | 2 | 11 | 1 | 2 | 11 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0005 | 0/0 | 478 | 8 | 2 | 1 | 2 | 1 | 2 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0006 | 0/0 | 478 | 6 | 1 | 1 | 4 | 0 | 0 | 3 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0007 | 0/0 | 167 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(162): Show |
chr1 | 13166848 | 13184459 |
| a0008 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0009 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0010 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0011 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0012 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0013 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0014 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0015 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0016 | 0/0 | 215 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(210): Show |
chr1 | 13166848 | 13184459 |
| a0017 | 0/0 | 478 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0018 | 0/0 | 478 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0019 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0020 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0021 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0022 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0023 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0024 | 0/0 | 344 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(339): Show |
chr1 | 13166848 | 13184459 |
| a0025 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0026 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0027 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0028 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| a0029 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | MKMSI others(473): Show |
chr1 | 13166848 | 13184459 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1434 | 81 | 3 | 29 | 36 | 4 | 9 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0001c0033 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0002c0002 | 0/0 | 1434 | 33 | 1 | 6 | 24 | 0 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0002c0023 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0002c0024 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0003c0003 | 1/0 | 1434 | 20 | 0 | 3 | 15 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0003c0008 | 0/0 | 1434 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0004c0004 | 0/1 | 1434 | 19 | 2 | 2 | 11 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0005c0005 | 0/0 | 1434 | 8 | 2 | 1 | 2 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0006c0006 | 0/0 | 1434 | 6 | 1 | 1 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0007c0014 | 0/0 | 1434 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0007c0029 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0008c0015 | 0/0 | 1434 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0009c0011 | 0/0 | 1434 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0010c0013 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0011c0009 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0012c0012 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0013c0010 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0014c0007 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0015c0030 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0016c0034 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0017c0017 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0018c0018 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0019c0016 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0020c0021 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0021c0032 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0022c0020 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0023c0019 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0024c0022 | 0/0 | 1756 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1751): Show |
chr1 | 13166848 | 13184459 | ||
| a0025c0025 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0026c0026 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0027c0027 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0028c0028 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 | ||
| a0029c0031 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | ATGAA others(1429): Show |
chr1 | 13166848 | 13184459 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2460 | 69 | 3 | 23 | 31 | 4 | 8 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0008 | 0/0 | 2460 | 3 | 0 | 1 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0012 | 0/0 | 2460 | 2 | 0 | 1 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0013 | 0/0 | 2460 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0015 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0018 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0019 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0022 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0001t0027 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0001c0033t0001 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0002c0002t0002 | 0/0 | 2458 | 25 | 0 | 0 | 24 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2453): Show |
chr1 | 13166848 | 13184459 |
| a0002c0002t0007 | 0/0 | 2458 | 5 | 0 | 4 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2453): Show |
chr1 | 13166848 | 13184459 |
| a0002c0002t0011 | 0/0 | 2460 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0002c0002t0026 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2453): Show |
chr1 | 13166848 | 13184459 |
| a0002c0023t0002 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2453): Show |
chr1 | 13166848 | 13184459 |
| a0002c0024t0007 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2453): Show |
chr1 | 13166848 | 13184459 |
| a0003c0003t0003 | 1/0 | 2465 | 20 | 0 | 3 | 15 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0003c0008t0003 | 0/0 | 2465 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0004c0004t0004 | 0/0 | 2465 | 17 | 1 | 2 | 11 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0004c0004t0024 | 0/1 | 2464 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2459): Show |
chr1 | 13166848 | 13184459 |
| a0004c0004t0025 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0005c0005t0005 | 0/0 | 2460 | 8 | 2 | 1 | 2 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0006c0006t0006 | 0/0 | 2465 | 4 | 0 | 0 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0006c0006t0010 | 0/0 | 2465 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0007c0014t0001 | 0/0 | 2460 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0007c0029t0001 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0008c0015t0001 | 0/0 | 2460 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0009c0011t0004 | 0/0 | 2465 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0010c0013t0008 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0011c0009t0006 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0011c0009t0014 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0012c0012t0009 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0013c0010t0004 | 0/0 | 2465 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0014c0007t0020 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0014c0007t0021 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0015c0030t0001 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0016c0034t0016 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0017c0017t0003 | 0/0 | 2465 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0018c0018t0003 | 0/0 | 2465 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0019c0016t0003 | 0/0 | 2465 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0020c0021t0009 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0021c0032t0001 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0022c0020t0006 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0023c0019t0006 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0024c0022t0017 | 0/0 | 2782 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2777): Show |
chr1 | 13166848 | 13184459 |
| a0025c0025t0023 | 0/0 | 2465 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0026c0026t0004 | 0/0 | 2465 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2460): Show |
chr1 | 13166848 | 13184459 |
| a0027c0027t0005 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0028c0028t0005 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| a0029c0031t0001 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | TGTAG others(2455): Show |
chr1 | 13166848 | 13184459 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 40 | 1 | 15 | 17 | 1 | 6 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0008g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0012g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0013g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0013g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0019g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0022g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0001t0027g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0001c0033t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0007g0003 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0011g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0002t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0023t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0002c0024t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0003c0003t0003g0004 | 1/0 | 10 | 0 | 2 | 6 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0003c0003t0003g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0003c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0003c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0003c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0003c0008t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0004g0002 | 0/0 | 13 | 0 | 2 | 9 | 0 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0024g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0004c0004t0025g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0005c0005t0005g0006 | 0/0 | 6 | 2 | 0 | 2 | 0 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0005c0005t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0005c0005t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0006c0006t0006g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0006c0006t0006g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0006c0006t0010g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0007c0014t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0007c0014t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0007c0029t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0008c0015t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0009c0011t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0010c0013t0008g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0010c0013t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0011c0009t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0011c0009t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0012c0012t0009g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0013c0010t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0014c0007t0020g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0014c0007t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0015c0030t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0016c0034t0016g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0017c0017t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0018c0018t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0019c0016t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0020c0021t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0021c0032t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0022c0020t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0023c0019t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0024c0022t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0025c0025t0023g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0026c0026t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0027c0027t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0028c0028t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| a0029c0031t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00140 | hp2 | a0005 | c0005 | t0005 | g0038 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00323 | hp1 | a0004 | c0004 | t0004 | g0042 | EUR | FIN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00438 | hp1 | a0015 | c0030 | t0001 | g0001 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00438 | hp2 | a0001 | c0033 | t0001 | g0001 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00597 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00609 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00642 | hp2 | a0016 | c0034 | t0016 | g0061 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0068 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01070 | hp1 | a0001 | c0001 | t0018 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0065 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0064 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01167 | hp1 | a0006 | c0006 | t0010 | g0009 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01168 | hp1 | a0005 | c0005 | t0005 | g0037 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01168 | hp2 | a0007 | c0014 | t0001 | g0063 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01175 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01256 | hp2 | a0009 | c0011 | t0004 | g0002 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01258 | hp1 | a0009 | c0011 | t0004 | g0002 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01346 | hp1 | a0008 | c0015 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01361 | hp2 | a0001 | c0001 | t0027 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01433 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01433 | hp2 | a0017 | c0017 | t0003 | g0028 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01891 | hp1 | a0010 | c0013 | t0008 | g0001 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01891 | hp2 | a0010 | c0013 | t0008 | g0048 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01934 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01934 | hp2 | a0001 | c0001 | t0012 | g0060 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01952 | hp1 | a0018 | c0018 | t0003 | g0004 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01952 | hp2 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01975 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01978 | hp1 | a0002 | c0002 | t0011 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01978 | hp2 | a0002 | c0002 | t0011 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02004 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02015 | hp2 | a0019 | c0016 | t0003 | g0029 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02071 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02074 | hp2 | a0003 | c0008 | t0003 | g0004 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02148 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02155 | hp1 | a0006 | c0006 | t0006 | g0009 | EAS | CDX | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | CDX | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02273 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02451 | hp1 | a0002 | c0002 | t0026 | g0005 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02451 | hp2 | a0020 | c0021 | t0009 | g0058 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02615 | hp1 | a0021 | c0032 | t0001 | g0057 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02615 | hp2 | a0022 | c0020 | t0006 | g0023 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02717 | hp1 | a0023 | c0019 | t0006 | g0024 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02717 | hp2 | a0007 | c0029 | t0001 | g0066 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02735 | hp2 | a0004 | c0004 | t0004 | g0002 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03139 | hp1 | a0013 | c0010 | t0004 | g0015 | AFR | ESN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03139 | hp2 | a0004 | c0004 | t0025 | g0045 | AFR | ESN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03453 | hp1 | a0024 | c0022 | t0017 | g0039 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03486 | hp1 | a0011 | c0009 | t0014 | g0021 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03486 | hp2 | a0012 | c0012 | t0009 | g0019 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03490 | hp2 | a0005 | c0005 | t0005 | g0006 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03579 | hp1 | a0014 | c0007 | t0020 | g0016 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03579 | hp2 | a0004 | c0004 | t0004 | g0040 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03654 | hp2 | a0025 | c0025 | t0023 | g0002 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03704 | hp2 | a0004 | c0004 | t0004 | g0002 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03831 | hp1 | a0026 | c0026 | t0004 | g0041 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03831 | hp2 | a0002 | c0002 | t0007 | g0003 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG04184 | hp1 | a0027 | c0027 | t0005 | g0006 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG04184 | hp2 | a0005 | c0005 | t0005 | g0006 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG04199 | hp1 | a0001 | c0001 | t0012 | g0059 | SAS | STU | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG04199 | hp2 | a0028 | c0028 | t0005 | g0006 | SAS | STU | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18942 | hp1 | a0002 | c0024 | t0007 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18942 | hp2 | a0001 | c0001 | t0022 | g0010 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18945 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18949 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18953 | hp2 | a0006 | c0006 | t0006 | g0013 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18954 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18954 | hp2 | a0003 | c0003 | t0003 | g0026 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18959 | hp1 | a0004 | c0004 | t0004 | g0043 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18960 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18962 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18962 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18968 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18970 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18975 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18975 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18976 | hp1 | a0006 | c0006 | t0006 | g0009 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18976 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18977 | hp2 | a0006 | c0006 | t0006 | g0013 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18980 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18981 | hp2 | a0003 | c0008 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18983 | hp1 | a0029 | c0031 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18990 | hp2 | a0002 | c0023 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18992 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18994 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18995 | hp1 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18995 | hp2 | a0005 | c0005 | t0005 | g0006 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19004 | hp1 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19004 | hp2 | a0005 | c0005 | t0005 | g0006 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19064 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19067 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19070 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19077 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19079 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19082 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19084 | hp2 | a0004 | c0004 | t0004 | g0044 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19240 | hp1 | a0013 | c0010 | t0004 | g0015 | AFR | YRI | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA19240 | hp2 | a0006 | c0006 | t0010 | g0009 | AFR | YRI | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01123 | hp1 | a0008 | c0015 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02486 | hp1 | a0011 | c0009 | t0006 | g0022 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG02486 | hp2 | a0012 | c0012 | t0009 | g0019 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG06807 | hp1 | a0005 | c0005 | t0005 | g0006 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| HG06807 | hp2 | a0014 | c0007 | t0021 | g0016 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA20300 | hp1 | a0007 | c0014 | t0001 | g0011 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| NA20300 | hp2 | a0005 | c0005 | t0005 | g0006 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| homoSapiens | chm13v2 | a0004 | c0004 | t0024 | g0002 | REF | REF | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0003 | g0004 | REF | REF | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:13175324 | C | T | 1 | a0020 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.44C>T | p.Ala15Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 745/2465 | 44/1437 | 15/478 | chr1 | 13175324 | |||
| chr1:13175335 | C | G | 1 | a0020 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.55C>G | p.Leu19Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 756/2465 | 55/1437 | 19/478 | chr1 | 13175335 | |||
| chr1:13175357 | C | T | 5 | a0004 a0009 a0013 others(2): Show |
24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
missense_variant | MODERATE | c.77C>T | p.Ala26Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 778/2465 | 77/1437 | 26/478 | chr1 | 13175357 | |||
| chr1:13175471 | G | A | 3 | a0005 a0027 a0028 |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
missense_variant | MODERATE | c.191G>A | p.Arg64His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 892/2465 | 191/1437 | 64/478 | chr1 | 13175471 | |||
| chr1:13175474 | G | A | 1 | a0027 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.194G>A | p.Arg65His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 895/2465 | 194/1437 | 65/478 | chr1 | 13175474 | |||
| chr1:13175500 | A | T | 1 | a0016 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.220A>T | p.Met74Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 921/2465 | 220/1437 | 74/478 | chr1 | 13175500 | |||
| chr1:13175535 | T | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.255T>G | p.Asp85Glu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 956/2465 | 255/1437 | 85/478 | chr1 | 13175535 | |||
| chr1:13175555 | C | A | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.275C>A | p.Thr92Asn | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 976/2465 | 275/1437 | 92/478 | chr1 | 13175555 | |||
| chr1:13175558 | A | T | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.278A>T | p.Gln93Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 979/2465 | 278/1437 | 93/478 | chr1 | 13175558 | |||
| chr1:13175561 | G | A | 3 | a0005 a0027 a0028 |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
missense_variant | MODERATE | c.281G>A | p.Gly94Glu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 982/2465 | 281/1437 | 94/478 | chr1 | 13175561 | |||
| chr1:13175566 | T | C | 3 | a0016 a0019 a0024 |
3 | HG00642.hp2 HG02015.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.286T>C | p.Cys96Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 987/2465 | 286/1437 | 96/478 | chr1 | 13175566 | |||
| chr1:13176318 | G | A | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.371G>A | p.Arg124His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1072/2465 | 371/1437 | 124/478 | chr1 | 13176318 | |||
| chr1:13176324 | C | G | 15 | a0001 a0006 a0007 others(12): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
missense_variant | MODERATE | c.377C>G | p.Ser126Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1078/2465 | 377/1437 | 126/478 | chr1 | 13176324 | |||
| chr1:13176351 | C | A | 2 | a0010 a0024 |
3 | HG01891.hp1 HG01891.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.404C>A | p.Thr135Lys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1105/2465 | 404/1437 | 135/478 | chr1 | 13176351 | |||
| chr1:13176384 | A | G | 20 | a0001 a0002 a0005 others(17): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
missense_variant | MODERATE | c.437A>G | p.Gln146Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1138/2465 | 437/1437 | 146/478 | chr1 | 13176384 | |||
| chr1:13176415 | G | A | 1 | a0007 | 1 | HG02717.hp2 | stop_gained | HIGH | c.468G>A | p.Trp156* | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1169/2465 | 468/1437 | 156/478 | chr1 | 13176415 | |||
| chr1:13176440 | T | C | 3 | a0011 a0014 a0023 |
5 | HG02486.hp1 HG02717.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.493T>C | p.Tyr165His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1194/2465 | 493/1437 | 165/478 | chr1 | 13176440 | |||
| chr1:13176450 | A | G | 3 | a0011 a0014 a0024 |
5 | HG02486.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.503A>G | p.Tyr168Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1204/2465 | 503/1437 | 168/478 | chr1 | 13176450 | |||
| chr1:13176451 | C | A | 1 | a0007 | 2 | HG01168.hp2 NA20300.hp1 |
stop_gained | HIGH | c.504C>A | p.Tyr168* | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1205/2465 | 504/1437 | 168/478 | chr1 | 13176451 | |||
| chr1:13176517 | G | C | 1 | a0015 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.570G>C | p.Leu190Phe | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1271/2465 | 570/1437 | 190/478 | chr1 | 13176517 | |||
| chr1:13176595 | C | A | 1 | a0016 | 1 | HG00642.hp2 | stop_gained | HIGH | c.648C>A | p.Cys216* | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1349/2465 | 648/1437 | 216/478 | chr1 | 13176595 | |||
| chr1:13176728 | C | A | 4 | a0004 a0009 a0025 others(1): Show |
22 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(19): Show |
missense_variant | MODERATE | c.781C>A | p.Gln261Lys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1482/2465 | 781/1437 | 261/478 | chr1 | 13176728 | |||
| chr1:13176756 | A | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.809A>G | p.His270Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1510/2465 | 809/1437 | 270/478 | chr1 | 13176756 | |||
| chr1:13176774 | A | C | 3 | a0002 a0013 a0024 |
38 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(35): Show |
missense_variant | MODERATE | c.827A>C | p.Tyr276Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1528/2465 | 827/1437 | 276/478 | chr1 | 13176774 | |||
| chr1:13176776 | A | ATGAACTC others(315): Show |
1 | a0024 | 1 | HG03453.hp1 | frameshift_variant&stop_gained | HIGH | c.840_841insCCTTTTTT others(314): Show |
p.Ser281fs | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1542/2465 | 841/1437 | 281/478 | INFO_REALIGN_3_PRIME | chr1 | 13176776 | ||
| chr1:13176821 | A | G | 1 | a0016 | 1 | HG00642.hp2 | missense_variant&splice_region_variant | MODERATE | c.874A>G | p.Ser292Gly | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1575/2465 | 874/1437 | 292/478 | chr1 | 13176821 | |||
| chr1:13178614 | G | A | 1 | a0028 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.919G>A | p.Val307Met | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1620/2465 | 919/1437 | 307/478 | chr1 | 13178614 | |||
| chr1:13178639 | A | G | 1 | a0021 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.944A>G | p.His315Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1645/2465 | 944/1437 | 315/478 | chr1 | 13178639 | |||
| chr1:13178665 | C | G | 1 | a0018 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.970C>G | p.Gln324Glu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1671/2465 | 970/1437 | 324/478 | chr1 | 13178665 | |||
| chr1:13178750 | C | T | 10 | a0001 a0007 a0008 others(7): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
missense_variant | MODERATE | c.1055C>T | p.Ala352Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1756/2465 | 1055/1437 | 352/478 | chr1 | 13178750 | |||
| chr1:13178789 | T | C | 1 | a0029 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.1094T>C | p.Ile365Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1795/2465 | 1094/1437 | 365/478 | chr1 | 13178789 | |||
| chr1:13178833 | T | A | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1138T>A | p.Phe380Ile | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1839/2465 | 1138/1437 | 380/478 | chr1 | 13178833 | |||
| chr1:13178835 | T | G | 11 | a0001 a0007 a0008 others(8): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
missense_variant | MODERATE | c.1140T>G | p.Phe380Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1841/2465 | 1140/1437 | 380/478 | chr1 | 13178835 | |||
| chr1:13178845 | G | A | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1150G>A | p.Ala384Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1851/2465 | 1150/1437 | 384/478 | chr1 | 13178845 | |||
| chr1:13178873 | C | G | 2 | a0024 a0026 |
2 | HG03453.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.1178C>G | p.Ser393Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1879/2465 | 1178/1437 | 393/478 | chr1 | 13178873 | |||
| chr1:13178912 | T | C | 2 | a0012 a0020 |
3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1217T>C | p.Ile406Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1918/2465 | 1217/1437 | 406/478 | chr1 | 13178912 | |||
| chr1:13178929 | G | C | 2 | a0008 a0025 |
3 | HG01123.hp1 HG01346.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.1234G>C | p.Val412Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1935/2465 | 1234/1437 | 412/478 | chr1 | 13178929 | |||
| chr1:13178935 | G | C | 2 | a0024 a0025 |
2 | HG03453.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.1240G>C | p.Val414Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1941/2465 | 1240/1437 | 414/478 | chr1 | 13178935 | |||
| chr1:13178951 | G | A | 13 | a0001 a0005 a0007 others(10): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
missense_variant | MODERATE | c.1256G>A | p.Arg419Gln | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1957/2465 | 1256/1437 | 419/478 | chr1 | 13178951 | |||
| chr1:13178963 | G | A | 4 | a0006 a0011 a0022 others(1): Show |
10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
missense_variant | MODERATE | c.1268G>A | p.Gly423Asp | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1969/2465 | 1268/1437 | 423/478 | chr1 | 13178963 | |||
| chr1:13179021 | C | G | 1 | a0017 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1326C>G | p.Asn442Lys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2027/2465 | 1326/1437 | 442/478 | chr1 | 13179021 | |||
| chr1:13179030 | G | T | 1 | a0008 | 2 | HG01123.hp1 HG01346.hp1 |
missense_variant | MODERATE | c.1335G>T | p.Arg445Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2036/2465 | 1335/1437 | 445/478 | chr1 | 13179030 | |||
| chr1:13179065 | T | C | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1370T>C | p.Ile457Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2071/2465 | 1370/1437 | 457/478 | chr1 | 13179065 | |||
| chr1:13179070 | A | T | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1375A>T | p.Asn459Tyr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2076/2465 | 1375/1437 | 459/478 | chr1 | 13179070 | |||
| chr1:13179071 | A | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1376A>G | p.Asn459Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2077/2465 | 1376/1437 | 459/478 | chr1 | 13179071 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:13175322 | G | T | 25 | a0001c0001 a0001c0033 a0002c0002 others(22): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
synonymous_variant | LOW | c.42G>T | p.Leu14Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 743/2465 | 42/1437 | 14/478 | chr1 | 13175322 | |||
| chr1:13175325 | G | A | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.45G>A | p.Ala15Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 746/2465 | 45/1437 | 15/478 | chr1 | 13175325 | |||
| chr1:13175352 | C | T | 15 | a0001c0001 a0001c0033 a0005c0005 others(12): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
synonymous_variant | LOW | c.72C>T | p.Ala24Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 773/2465 | 72/1437 | 24/478 | chr1 | 13175352 | |||
| chr1:13175454 | G | A | 1 | a0012c0012 | 2 | HG02486.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.174G>A | p.Val58Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 875/2465 | 174/1437 | 58/478 | chr1 | 13175454 | |||
| chr1:13176367 | T | C | 1 | a0002c0023 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.420T>C | p.Cys140Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1121/2465 | 420/1437 | 140/478 | chr1 | 13176367 | |||
| chr1:13176625 | T | C | 3 | a0002c0002 a0002c0023 a0002c0024 |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
synonymous_variant | LOW | c.678T>C | p.Phe226Phe | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1379/2465 | 678/1437 | 226/478 | chr1 | 13176625 | |||
| chr1:13176673 | C | T | 1 | a0001c0033 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.726C>T | p.Ser242Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1427/2465 | 726/1437 | 242/478 | chr1 | 13176673 | |||
| chr1:13178643 | A | C | 3 | a0005c0005 a0027c0027 a0028c0028 |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
synonymous_variant | LOW | c.948A>C | p.Leu316Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1649/2465 | 948/1437 | 316/478 | chr1 | 13178643 | |||
| chr1:13178682 | C | T | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.987C>T | p.Asp329Asp | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1688/2465 | 987/1437 | 329/478 | chr1 | 13178682 | |||
| chr1:13178703 | C | A | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1008C>A | p.Thr336Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1709/2465 | 1008/1437 | 336/478 | chr1 | 13178703 | |||
| chr1:13178764 | T | C | 16 | a0001c0001 a0001c0033 a0005c0005 others(13): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
synonymous_variant | LOW | c.1069T>C | p.Leu357Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1770/2465 | 1069/1437 | 357/478 | chr1 | 13178764 | |||
| chr1:13178805 | C | T | 15 | a0001c0001 a0001c0033 a0005c0005 others(12): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
synonymous_variant | LOW | c.1110C>T | p.Asn370Asn | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1811/2465 | 1110/1437 | 370/478 | chr1 | 13178805 | |||
| chr1:13178812 | C | T | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1117C>T | p.Leu373Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1818/2465 | 1117/1437 | 373/478 | chr1 | 13178812 | |||
| chr1:13178820 | C | A | 1 | a0002c0023 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1125C>A | p.Ala375Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1826/2465 | 1125/1437 | 375/478 | chr1 | 13178820 | |||
| chr1:13178820 | C | G | 2 | a0002c0002 a0002c0024 |
34 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(31): Show |
synonymous_variant | LOW | c.1125C>G | p.Ala375Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1826/2465 | 1125/1437 | 375/478 | chr1 | 13178820 | |||
| chr1:13178823 | G | C | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1128G>C | p.Leu376Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1829/2465 | 1128/1437 | 376/478 | chr1 | 13178823 | |||
| chr1:13178844 | T | C | 3 | a0002c0024 a0024c0022 a0029c0031 |
3 | HG03453.hp1 NA18942.hp1 NA18983.hp1 |
synonymous_variant | LOW | c.1149T>C | p.Asn383Asn | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1850/2465 | 1149/1437 | 383/478 | chr1 | 13178844 | |||
| chr1:13178949 | G | C | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1254G>C | p.Pro418Pro | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1955/2465 | 1254/1437 | 418/478 | chr1 | 13178949 | |||
| chr1:13179030 | G | A | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1335G>A | p.Arg445Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2036/2465 | 1335/1437 | 445/478 | chr1 | 13179030 | |||
| chr1:13179057 | T | C | 1 | a0024c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1362T>C | p.Phe454Phe | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2063/2465 | 1362/1437 | 454/478 | chr1 | 13179057 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:13171863 | C | G | 1 | a0001c0001t0027 | 1 | HG01361.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-686C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13171863 | |||||||
| chr1:13171870 | T | C | 6 | a0006c0006t0006 a0006c0006t0010 a0011c0009t0006 others(3): Show |
10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-679T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3411 | chr1 | 13171870 | ||||||
| chr1:13171876 | TTC | T | 5 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0026 others(2): Show |
33 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-671_-670delCT | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3402 | INFO_REALIGN_3_PRIME | chr1 | 13171876 | |||||
| chr1:13171877 | TC | T | 1 | a0002c0002t0011 | 2 | HG01978.hp1 HG01978.hp2 |
5_prime_UTR_variant | MODIFIER | c.-671delC | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3403 | chr1 | 13171877 | ||||||
| chr1:13171878 | CT | C | 30 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(27): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
5_prime_UTR_variant | MODIFIER | c.-650delT | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3382 | INFO_REALIGN_3_PRIME | chr1 | 13171878 | |||||
| chr1:13171879 | T | G | 1 | a0002c0002t0011 | 2 | HG01978.hp1 HG01978.hp2 |
5_prime_UTR_variant | MODIFIER | c.-670T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3402 | chr1 | 13171879 | ||||||
| chr1:13171880 | T | G | 5 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0026 others(2): Show |
33 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(30): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-669T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13171880 | |||||||
| chr1:13171882 | T | C | 1 | a0001c0001t0015 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-667T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3399 | chr1 | 13171882 | ||||||
| chr1:13171883 | T | C | 23 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(20): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-666T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3398 | chr1 | 13171883 | ||||||
| chr1:13171884 | T | C | 2 | a0001c0001t0022 a0014c0007t0021 |
2 | HG06807.hp2 NA18942.hp2 |
5_prime_UTR_variant | MODIFIER | c.-665T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3397 | chr1 | 13171884 | ||||||
| chr1:13171885 | T | C | 1 | a0025c0025t0023 | 1 | HG03654.hp2 | 5_prime_UTR_variant | MODIFIER | c.-664T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3396 | chr1 | 13171885 | ||||||
| chr1:13171887 | T | C | 2 | a0001c0001t0012 a0001c0001t0027 |
3 | HG01361.hp2 HG01934.hp2 HG04199.hp1 |
5_prime_UTR_variant | MODIFIER | c.-662T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3394 | chr1 | 13171887 | ||||||
| chr1:13171898 | T | G | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-651T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13171898 | |||||||
| chr1:13171899 | T | A | 3 | a0012c0012t0009 a0016c0034t0016 a0020c0021t0009 |
4 | HG00642.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-650T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3382 | chr1 | 13171899 | ||||||
| chr1:13171948 | C | T | 26 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(23): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-601C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3333 | chr1 | 13171948 | ||||||
| chr1:13171977 | G | C | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-572G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3304 | chr1 | 13171977 | ||||||
| chr1:13171978 | G | C | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-571G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3303 | chr1 | 13171978 | ||||||
| chr1:13172018 | G | T | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-531G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3263 | chr1 | 13172018 | ||||||
| chr1:13172020 | G | T | 19 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(16): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-529G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3261 | chr1 | 13172020 | ||||||
| chr1:13172068 | T | A | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-481T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3213 | chr1 | 13172068 | ||||||
| chr1:13172089 | T | C | 27 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(24): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-460T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3192 | chr1 | 13172089 | ||||||
| chr1:13172090 | G | C | 4 | a0005c0005t0005 a0024c0022t0017 a0027c0027t0005 others(1): Show |
11 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-459G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3191 | chr1 | 13172090 | ||||||
| chr1:13172161 | C | G | 26 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(23): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-388C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3120 | chr1 | 13172161 | ||||||
| chr1:13172196 | T | G | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-353T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3085 | chr1 | 13172196 | ||||||
| chr1:13172209 | C | A | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-340C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3072 | chr1 | 13172209 | ||||||
| chr1:13172233 | G | C | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-316G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13172233 | |||||||
| chr1:13172305 | C | G | 6 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0011 others(3): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-244C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2976 | chr1 | 13172305 | ||||||
| chr1:13172322 | GGTGGA | G | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(29): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-220_-216delTGGAG | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2948 | INFO_REALIGN_3_PRIME | chr1 | 13172322 | |||||
| chr1:13172343 | T | G | 1 | a0004c0004t0025 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2938 | chr1 | 13172343 | ||||||
| chr1:13172405 | G | A | 1 | a0001c0001t0018 | 1 | HG01070.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2876 | chr1 | 13172405 | ||||||
| chr1:13172410 | A | G | 44 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(41): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-139A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13172410 | |||||||
| chr1:13172488 | G | C | 26 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(23): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-61G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2793 | chr1 | 13172488 | ||||||
| chr1:13179149 | A | G | 1 | a0016c0034t0016 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 17 | chr1 | 13179149 | ||||||
| chr1:13179153 | G | A | 1 | a0016c0034t0016 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 21 | chr1 | 13179153 | ||||||
| chr1:13179194 | C | T | 1 | a0024c0022t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 62 | chr1 | 13179194 | ||||||
| chr1:13179199 | T | A | 3 | a0001c0001t0008 a0001c0001t0013 a0010c0013t0008 |
7 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*67T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 67 | chr1 | 13179199 | ||||||
| chr1:13179235 | A | G | 1 | a0011c0009t0014 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 103 | chr1 | 13179235 | ||||||
| chr1:13179245 | T | C | 1 | a0001c0001t0019 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 113 | chr1 | 13179245 | ||||||
| chr1:13179246 | A | G | 1 | a0011c0009t0014 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 114 | chr1 | 13179246 | ||||||
| chr1:13179269 | A | T | 23 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(20): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*137A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 137 | chr1 | 13179269 | ||||||
| chr1:13179287 | A | C | 2 | a0002c0002t0026 a0024c0022t0017 |
2 | HG02451.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*155A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 155 | chr1 | 13179287 | ||||||
| chr1:13179319 | T | C | 17 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(14): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*187T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 187 | chr1 | 13179319 | ||||||
| chr1:13179338 | A | G | 1 | a0002c0002t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 206 | chr1 | 13179338 | ||||||
| chr1:13179394 | A | C | 3 | a0002c0002t0007 a0002c0002t0011 a0002c0024t0007 |
8 | HG01952.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*262A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 262 | chr1 | 13179394 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:13172570 | C | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-17+38C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172570 | |||||||
| chr1:13172574 | C | G | 10 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(7): Show |
24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17+42C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172574 | |||||||
| chr1:13172583 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17+51A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172583 | |||||||
| chr1:13172610 | A | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(72): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-17+78A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172610 | |||||||
| chr1:13172618 | G | C | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+86G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172618 | |||||||
| chr1:13172641 | TATA | T | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+110_-17+112del others(3): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172641 | |||||||
| chr1:13172646 | A | T | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+114A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172646 | |||||||
| chr1:13172648 | A | T | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+116A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172648 | |||||||
| chr1:13172649 | T | C | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+117T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172649 | |||||||
| chr1:13172662 | T | G | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+130T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172662 | |||||||
| chr1:13172665 | A | G | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+133A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172665 | |||||||
| chr1:13172675 | G | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(56): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17+143G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172675 | |||||||
| chr1:13172695 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-17+163C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172695 | |||||||
| chr1:13172885 | A | G | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+353A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172885 | |||||||
| chr1:13172935 | C | T | 10 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(7): Show |
24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17+403C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172935 | |||||||
| chr1:13172943 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+411A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172943 | |||||||
| chr1:13172947 | C | A | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+415C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172947 | |||||||
| chr1:13172960 | A | C | 31 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(28): Show |
70 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-17+428A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172960 | |||||||
| chr1:13172965 | T | C | 6 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(3): Show |
11 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+433T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172965 | |||||||
| chr1:13173014 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-17+482T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173014 | |||||||
| chr1:13173044 | T | G | 1 | a0011c0009t0014g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17+512T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173044 | |||||||
| chr1:13173084 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0019g0007 others(1): Show |
11 | HG00558.hp2 HG02004.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17+552C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173084 | |||||||
| chr1:13173091 | G | T | 1 | a0019c0016t0003g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-17+559G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173091 | |||||||
| chr1:13173132 | C | T | 6 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(3): Show |
11 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+600C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173132 | |||||||
| chr1:13173155 | C | T | 1 | a0001c0001t0008g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-17+623C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173155 | |||||||
| chr1:13173220 | T | C | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+688T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173220 | |||||||
| chr1:13173231 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(83): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-17+699C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173231 | |||||||
| chr1:13173265 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-17+733T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173265 | |||||||
| chr1:13173298 | C | CCAAAAA | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(72): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-17+772_-17+777dup others(6): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 13173298 | ||||||
| chr1:13173310 | T | C | 4 | a0011c0009t0006g0022 a0011c0009t0014g0021 a0022c0020t0006g0023 others(1): Show |
4 | HG02486.hp1 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+778T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173310 | |||||||
| chr1:13173344 | C | T | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+812C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173344 | |||||||
| chr1:13173384 | G | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(46): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.-17+852G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173384 | |||||||
| chr1:13173431 | C | A | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+899C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173431 | |||||||
| chr1:13173453 | CAATCTT | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17+922_-17+927del others(6): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173453 | |||||||
| chr1:13173460 | G | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17+928G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173460 | |||||||
| chr1:13173481 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+949T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173481 | |||||||
| chr1:13173542 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(46): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.-17+1010A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173542 | |||||||
| chr1:13173644 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(49): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17+1112T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173644 | |||||||
| chr1:13173682 | A | G | 3 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 |
6 | HG01167.hp1 HG02155.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+1150A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173682 | |||||||
| chr1:13173687 | C | A | 3 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 |
6 | HG01167.hp1 HG02155.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+1155C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173687 | |||||||
| chr1:13173778 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1246G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173778 | |||||||
| chr1:13173779 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1247G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173779 | |||||||
| chr1:13173804 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1272G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173804 | |||||||
| chr1:13173808 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-17+1276A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173808 | |||||||
| chr1:13173836 | T | G | 10 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(7): Show |
24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17+1304T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173836 | |||||||
| chr1:13173858 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1326T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173858 | |||||||
| chr1:13173870 | C | T | 3 | a0002c0002t0002g0005 a0002c0002t0026g0005 a0002c0023t0002g0005 |
11 | HG00597.hp2 HG02071.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+1338C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173870 | |||||||
| chr1:13173880 | T | A | 6 | a0004c0004t0004g0040 a0006c0006t0006g0009 a0006c0006t0006g0013 others(3): Show |
9 | HG01167.hp1 HG01891.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17+1348T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173880 | |||||||
| chr1:13173893 | C | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1361C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173893 | |||||||
| chr1:13173919 | G | A | 9 | a0004c0004t0004g0002 a0004c0004t0004g0042 a0004c0004t0004g0043 others(6): Show |
23 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.-16-1346G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173919 | |||||||
| chr1:13173940 | C | A | 5 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 others(2): Show |
8 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16-1325C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173940 | |||||||
| chr1:13173964 | A | T | 6 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(3): Show |
11 | HG00140.hp2 HG01168.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-1301A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173964 | |||||||
| chr1:13173982 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0013g0064 others(7): Show |
11 | HG00140.hp1 HG00642.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-1283C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173982 | |||||||
| chr1:13173985 | C | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1280C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173985 | |||||||
| chr1:13174001 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-16-1264A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174001 | |||||||
| chr1:13174024 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-16-1241C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174024 | |||||||
| chr1:13174139 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.-16-1126T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174139 | |||||||
| chr1:13174166 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1099C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174166 | |||||||
| chr1:13174174 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-16-1091C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174174 | |||||||
| chr1:13174247 | T | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1018T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174247 | |||||||
| chr1:13174255 | T | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(71): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-16-1010T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174255 | |||||||
| chr1:13174261 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1004T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174261 | |||||||
| chr1:13174270 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-995G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174270 | |||||||
| chr1:13174272 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-993G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174272 | |||||||
| chr1:13174275 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-990G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174275 | |||||||
| chr1:13174280 | T | C | 1 | a0026c0026t0004g0041 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-16-985T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174280 | |||||||
| chr1:13174292 | A | G | 1 | a0004c0004t0025g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16-973A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174292 | |||||||
| chr1:13174322 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0022g0010 |
4 | HG02132.hp1 NA18942.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-943T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174322 | |||||||
| chr1:13174324 | G | A | 10 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(7): Show |
24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.-16-941G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174324 | |||||||
| chr1:13174357 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-908C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174357 | |||||||
| chr1:13174368 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-897C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174368 | |||||||
| chr1:13174369 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-16-896A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174369 | |||||||
| chr1:13174404 | G | T | 7 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 others(4): Show |
10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16-861G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174404 | |||||||
| chr1:13174481 | A | C | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-16-784A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174481 | |||||||
| chr1:13174492 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(77): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-16-773C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174492 | |||||||
| chr1:13174518 | T | A | 1 | a0016c0034t0016g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-747T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174518 | |||||||
| chr1:13174543 | G | C | 1 | a0016c0034t0016g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-722G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174543 | |||||||
| chr1:13174555 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-710G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174555 | |||||||
| chr1:13174586 | C | G | 1 | a0012c0012t0009g0019 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-679C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174586 | |||||||
| chr1:13174615 | C | G | 2 | a0001c0001t0013g0064 a0001c0001t0013g0065 |
2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-16-650C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174615 | |||||||
| chr1:13174632 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-633G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174632 | |||||||
| chr1:13174641 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-624C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174641 | |||||||
| chr1:13174699 | T | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-566T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174699 | |||||||
| chr1:13174743 | A | G | 1 | a0001c0001t0001g0012 | 3 | HG00558.hp2 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-16-522A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174743 | |||||||
| chr1:13174855 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-410T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174855 | |||||||
| chr1:13174876 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-389A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174876 | |||||||
| chr1:13174921 | C | T | 2 | a0021c0032t0001g0057 a0024c0022t0017g0039 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-16-344C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174921 | |||||||
| chr1:13174955 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-16-310C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174955 | |||||||
| chr1:13174958 | T | C | 1 | a0003c0003t0003g0008 | 7 | HG00597.hp1 NA18954.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16-307T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174958 | |||||||
| chr1:13175055 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-210A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175055 | |||||||
| chr1:13175065 | C | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-200C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175065 | |||||||
| chr1:13175076 | G | A | 1 | a0005c0005t0005g0037 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-16-189G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175076 | |||||||
| chr1:13175110 | G | C | 5 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(2): Show |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16-155G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175110 | |||||||
| chr1:13175159 | G | A | 2 | a0001c0001t0001g0067 a0024c0022t0017g0039 |
2 | HG03453.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-16-106G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175159 | |||||||
| chr1:13175162 | G | C | 2 | a0001c0001t0001g0067 a0024c0022t0017g0039 |
2 | HG03453.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-16-103G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175162 | |||||||
| chr1:13175164 | T | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-101T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175164 | |||||||
| chr1:13175186 | G | C | 6 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 others(3): Show |
9 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-79G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175186 | |||||||
| chr1:13175202 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-63A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175202 | |||||||
| chr1:13175223 | G | T | 6 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0021c0032t0001g0057 others(3): Show |
11 | HG01168.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-42G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175223 | |||||||
| chr1:13175226 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-39T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175226 | |||||||
| chr1:13175232 | T | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-33T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175232 | |||||||
| chr1:13175583 | C | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.293+10C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175583 | |||||||
| chr1:13175635 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.293+62G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175635 | |||||||
| chr1:13175641 | T | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.293+68T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175641 | |||||||
| chr1:13175683 | C | T | 1 | a0004c0004t0004g0044 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.293+110C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175683 | |||||||
| chr1:13175734 | G | C | 10 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(7): Show |
24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.293+161G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175734 | |||||||
| chr1:13175745 | G | A | 1 | a0022c0020t0006g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293+172G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175745 | |||||||
| chr1:13175766 | T | C | 2 | a0021c0032t0001g0057 a0022c0020t0006g0023 |
2 | HG02615.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.293+193T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175766 | |||||||
| chr1:13175783 | G | C | 3 | a0011c0009t0006g0022 a0011c0009t0014g0021 a0016c0034t0016g0061 |
3 | HG00642.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.293+210G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175783 | |||||||
| chr1:13175786 | C | G | 3 | a0011c0009t0006g0022 a0011c0009t0014g0021 a0016c0034t0016g0061 |
3 | HG00642.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.293+213C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175786 | |||||||
| chr1:13175831 | A | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.293+258A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175831 | |||||||
| chr1:13175906 | A | C | 1 | a0002c0002t0002g0036 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.293+333A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175906 | |||||||
| chr1:13175913 | T | A | 1 | a0016c0034t0016g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.294-328T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175913 | |||||||
| chr1:13175939 | C | T | 2 | a0002c0002t0002g0036 a0016c0034t0016g0061 |
2 | HG00642.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.294-302C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175939 | |||||||
| chr1:13175973 | A | G | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.294-268A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175973 | |||||||
| chr1:13175989 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-252C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175989 | |||||||
| chr1:13175992 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.294-249A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175992 | |||||||
| chr1:13176036 | T | C | 1 | a0012c0012t0009g0019 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.294-205T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176036 | |||||||
| chr1:13176044 | G | T | 1 | a0004c0004t0004g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.294-197G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176044 | |||||||
| chr1:13176050 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-191G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176050 | |||||||
| chr1:13176050 | G | C | 1 | a0001c0001t0015g0062 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.294-191G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176050 | |||||||
| chr1:13176061 | G | T | 9 | a0004c0004t0004g0002 a0004c0004t0004g0042 a0004c0004t0004g0043 others(6): Show |
23 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-180G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176061 | |||||||
| chr1:13176065 | TC | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.294-175delC | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176065 | |||||||
| chr1:13176066 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.294-175C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176066 | |||||||
| chr1:13176067 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.294-174A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176067 | |||||||
| chr1:13176074 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0056 |
3 | HG00323.hp2 HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.294-167A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176074 | |||||||
| chr1:13176083 | A | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-158A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176083 | |||||||
| chr1:13176098 | T | C | 1 | a0011c0009t0006g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.294-143T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176098 | |||||||
| chr1:13176105 | C | G | 14 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0030 others(11): Show |
33 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.294-136C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176105 | |||||||
| chr1:13176113 | A | G | 4 | a0003c0003t0003g0025 a0003c0003t0003g0026 a0003c0003t0003g0027 others(1): Show |
4 | HG01433.hp1 HG01433.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-128A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176113 | |||||||
| chr1:13176171 | A | C | 1 | a0019c0016t0003g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.294-70A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176171 | |||||||
| chr1:13176191 | A | G | 12 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0031 others(9): Show |
24 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.294-50A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176191 | |||||||
| chr1:13176208 | T | G | 7 | a0002c0002t0002g0031 a0005c0005t0005g0006 a0005c0005t0005g0037 others(4): Show |
12 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.294-33T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176208 | |||||||
| chr1:13176222 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(51): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.294-19C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176222 | |||||||
| chr1:13176871 | T | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+49T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176871 | |||||||
| chr1:13176874 | C | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+52C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176874 | |||||||
| chr1:13176876 | A | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+54A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176876 | |||||||
| chr1:13176880 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+58G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176880 | |||||||
| chr1:13176918 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(66): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.875+96A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176918 | |||||||
| chr1:13176948 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+126A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176948 | |||||||
| chr1:13176988 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+166T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176988 | |||||||
| chr1:13176995 | A | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+173A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176995 | |||||||
| chr1:13177011 | C | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+189C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177011 | |||||||
| chr1:13177012 | G | A | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.875+190G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177012 | |||||||
| chr1:13177013 | G | C | 1 | a0004c0004t0004g0044 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.875+191G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177013 | |||||||
| chr1:13177024 | G | C | 9 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(6): Show |
22 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.875+202G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177024 | |||||||
| chr1:13177036 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+214A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177036 | |||||||
| chr1:13177043 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+221T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177043 | |||||||
| chr1:13177046 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+224T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177046 | |||||||
| chr1:13177050 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+228A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177050 | |||||||
| chr1:13177062 | G | C | 7 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 others(4): Show |
10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.875+240G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177062 | |||||||
| chr1:13177065 | A | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+243A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177065 | |||||||
| chr1:13177116 | C | T | 1 | a0001c0001t0008g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.875+294C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177116 | |||||||
| chr1:13177146 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+324G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177146 | |||||||
| chr1:13177154 | A | G | 25 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(22): Show |
58 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.875+332A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177154 | |||||||
| chr1:13177179 | T | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.875+357T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177179 | |||||||
| chr1:13177196 | G | C | 5 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(2): Show |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.875+374G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177196 | |||||||
| chr1:13177206 | T | C | 5 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(2): Show |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.875+384T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177206 | |||||||
| chr1:13177208 | G | A | 1 | a0002c0002t0002g0032 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.875+386G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177208 | |||||||
| chr1:13177239 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+417G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177239 | |||||||
| chr1:13177246 | C | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+424C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177246 | |||||||
| chr1:13177265 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+443G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177265 | |||||||
| chr1:13177270 | G | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(40): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.875+448G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177270 | |||||||
| chr1:13177274 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+452T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177274 | |||||||
| chr1:13177318 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+496A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177318 | |||||||
| chr1:13177320 | T | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+498T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177320 | |||||||
| chr1:13177325 | A | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+503A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177325 | |||||||
| chr1:13177334 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+512A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177334 | |||||||
| chr1:13177337 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+515C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177337 | |||||||
| chr1:13177341 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+519G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177341 | |||||||
| chr1:13177344 | A | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+522A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177344 | |||||||
| chr1:13177344 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+522A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177344 | |||||||
| chr1:13177351 | C | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+529C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177351 | |||||||
| chr1:13177358 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+536C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177358 | |||||||
| chr1:13177369 | G | C | 2 | a0012c0012t0009g0019 a0020c0021t0009g0058 |
3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.875+547G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177369 | |||||||
| chr1:13177374 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+552A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177374 | |||||||
| chr1:13177390 | G | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+568G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177390 | |||||||
| chr1:13177395 | A | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+573A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177395 | |||||||
| chr1:13177398 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(36): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.875+576G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177398 | |||||||
| chr1:13177413 | G | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+591G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177413 | |||||||
| chr1:13177418 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+596T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177418 | |||||||
| chr1:13177440 | A | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+618A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177440 | |||||||
| chr1:13177445 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+623T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177445 | |||||||
| chr1:13177448 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+626G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177448 | |||||||
| chr1:13177507 | A | T | 8 | a0006c0006t0006g0009 a0006c0006t0006g0013 a0006c0006t0010g0009 others(5): Show |
11 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.875+685A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177507 | |||||||
| chr1:13177508 | T | G | 9 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(6): Show |
22 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.875+686T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177508 | |||||||
| chr1:13177537 | C | T | 1 | a0006c0006t0006g0013 | 2 | NA18953.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.875+715C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177537 | |||||||
| chr1:13177538 | G | A | 25 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(22): Show |
58 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.875+716G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177538 | |||||||
| chr1:13177540 | C | A | 24 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(21): Show |
57 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.875+718C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177540 | |||||||
| chr1:13177545 | T | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+723T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177545 | |||||||
| chr1:13177547 | G | A | 2 | a0003c0003t0003g0025 a0003c0003t0003g0026 |
2 | NA18954.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.875+725G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177547 | |||||||
| chr1:13177553 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.875+731C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177553 | |||||||
| chr1:13177574 | C | T | 15 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(12): Show |
35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.875+752C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177574 | |||||||
| chr1:13177586 | C | T | 14 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(11): Show |
34 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.875+764C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177586 | |||||||
| chr1:13177610 | AAGC | A | 2 | a0012c0012t0009g0019 a0020c0021t0009g0058 |
3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.875+791_875+793del others(3): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 13177610 | ||||||
| chr1:13177613 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.875+791C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177613 | |||||||
| chr1:13177614 | A | G | 2 | a0014c0007t0020g0016 a0014c0007t0021g0016 |
2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.875+792A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177614 | |||||||
| chr1:13177622 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+800T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177622 | |||||||
| chr1:13177623 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+801A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177623 | |||||||
| chr1:13177643 | G | T | 1 | a0021c0032t0001g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.875+821G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177643 | |||||||
| chr1:13177661 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+839C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177661 | |||||||
| chr1:13177692 | C | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(35): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.875+870C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177692 | |||||||
| chr1:13177704 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-867T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177704 | |||||||
| chr1:13177710 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-861G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177710 | |||||||
| chr1:13177754 | G | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-817G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177754 | |||||||
| chr1:13177780 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-791C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177780 | |||||||
| chr1:13177784 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(69): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.876-787A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177784 | |||||||
| chr1:13177872 | G | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-699G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177872 | |||||||
| chr1:13177884 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-687A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177884 | |||||||
| chr1:13177894 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-677C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177894 | |||||||
| chr1:13177944 | A | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(36): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.876-627A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177944 | |||||||
| chr1:13177959 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.876-612T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177959 | |||||||
| chr1:13177963 | T | C | 1 | a0002c0002t0002g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.876-608T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177963 | |||||||
| chr1:13177996 | G | A | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-575G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177996 | |||||||
| chr1:13178055 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-516A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178055 | |||||||
| chr1:13178067 | C | G | 1 | a0003c0003t0003g0026 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.876-504C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178067 | |||||||
| chr1:13178071 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.876-500T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178071 | |||||||
| chr1:13178078 | A | AT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.876-485dupT | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 13178078 | ||||||
| chr1:13178085 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-486T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178085 | |||||||
| chr1:13178091 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-480C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178091 | |||||||
| chr1:13178159 | T | G | 1 | a0004c0004t0004g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876-412T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178159 | |||||||
| chr1:13178184 | A | G | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-387A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178184 | |||||||
| chr1:13178186 | G | A | 1 | a0004c0004t0004g0042 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.876-385G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178186 | |||||||
| chr1:13178220 | T | C | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-351T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178220 | |||||||
| chr1:13178271 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(65): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.876-300C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178271 | |||||||
| chr1:13178290 | G | C | 5 | a0005c0005t0005g0006 a0005c0005t0005g0037 a0005c0005t0005g0038 others(2): Show |
10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.876-281G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178290 | |||||||
| chr1:13178294 | G | A | 12 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0030 others(9): Show |
24 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.876-277G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178294 | |||||||
| chr1:13178316 | C | G | 2 | a0012c0012t0009g0019 a0020c0021t0009g0058 |
3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.876-255C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178316 | |||||||
| chr1:13178328 | C | A | 3 | a0012c0012t0009g0019 a0016c0034t0016g0061 a0020c0021t0009g0058 |
4 | HG00642.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-243C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178328 | |||||||
| chr1:13178348 | T | G | 15 | a0004c0004t0004g0002 a0004c0004t0004g0040 a0004c0004t0004g0042 others(12): Show |
33 | HG00140.hp2 HG00323.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.876-223T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178348 | |||||||
| chr1:13178380 | C | G | 3 | a0001c0001t0012g0060 a0016c0034t0016g0061 a0024c0022t0017g0039 |
3 | HG00642.hp2 HG01934.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.876-191C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178380 | |||||||
| chr1:13178381 | T | C | 1 | a0001c0001t0012g0060 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.876-190T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178381 | |||||||
| chr1:13178386 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.876-185G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178386 | |||||||
| chr1:13178429 | C | T | 23 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0014 others(20): Show |
56 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.876-142C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178429 | |||||||
| chr1:13178474 | C | T | 1 | a0024c0022t0017g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-97C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178474 | |||||||
| chr1:13178479 | T | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(69): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.876-92T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178479 | |||||||
| chr1:13178481 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.876-90G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178481 | |||||||
| chr1:13178489 | C | A | 1 | a0007c0014t0001g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.876-82C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178489 | |||||||
| chr1:13178497 | A | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(76): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.876-74A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178497 | |||||||
| chr1:13178567 | C | A | 12 | a0001c0001t0008g0017 a0001c0001t0008g0068 a0001c0001t0013g0064 others(9): Show |
16 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.876-4C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178567 |