SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs702965 | snp | A/G | 0.327445 | 0.237702 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611868 | CCCGGGCATGGCCCC[A/G]ATTCCCGCCACTCCC | 57661 |
rs702966 | snp | C/G | 0.398894 | 0.200825 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611919 | CCGACGGCAGGCATG[C/G]TGATGCCCCCCATTT | 57661 |
rs936468 | snp | C/T | 0.295923 | 0.245746 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607175 | TGGCCTGTTTCCTGA[C/T]GGGCCTTGGGCCGGG | 57661 |
rs936469 | snp | C/T | 0.304937 | 0.243889 | intron-variant | PHRF1 | GRCh38.p7 | 11:606749 | AACTGAGAAACTGCT[C/T]AAGAAGGGAAATCAA | 57661 |
rs936470 | snp | C/G | 0.302936 | 0.244331 | intron-variant | PHRF1 | GRCh38.p7 | 11:606656 | TGGGCTGAGTGCTTG[C/G]GAACAGCCTGAGGAC | 57661 |
rs936471 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PHRF1 | GRCh38.p7 | 11:594264 | AGGTCTATCATGCCA[C/T]GGTCTCTCAGGCCGT | 57661 |
rs936472 | snp | A/G | 0.470618 | 0.117591 | intron-variant | PHRF1 | GRCh38.p7 | 11:593453 | CTTCACCAGGAGCCC[A/G]TCCTCGGTGCGGCTC | 57661 |
rs1055382 | snp | C/T | 0.399073 | 0.200692 | utr-variant-3-prime, downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612182 | AGCTGCTGTGTACCT[C/T]TGGCTCTGAATTAGG | 57661 |
rs1802427 | snp | A/G | 1.65996e-05 | 0.00288089 | downstream-variant-500B, missense | PHRF1, IRF7 | GRCh38.p7 | 11:612686 | AACAGCCTCTATGAC[A/G]ACATCGAGTGCTTCC | 57661 |
rs2396545 | snp | A/G | 0.359998 | 0.2245 | intron-variant | PHRF1 | GRCh38.p7 | 11:601785 | GAGGGTGCCAAGGCC[A/G]GCGGGAGGCTTAGGC | 57661 |
rs3740648 | snp | A/C | 0.161596 | 0.233848 | intron-variant | PHRF1 | GRCh38.p7 | 11:596672 | CAGGTGAGGTCACAG[A/C]GGGGAGGCGGCCGTC | 57661 |
rs3740649 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHRF1 | GRCh38.p7 | 11:592825 | TGTAACAGGAAGGCC[C/T]GCAGGACTGAACCGC | 57661 |
rs3832719 | in-del | -/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:596638 | AAGTCAGGAAGGGGG[-/G]CCTCCCCAGGAACCA | 57661 |
rs4623937 | snp | A/G | 0.302184 | 0.244493 | intron-variant | PHRF1 | GRCh38.p7 | 11:605856 | GGCCGACTGATGAGC[A/G]TGACAGCTGAGGGGA | 57661 |
rs4963128 | snp | A/G | 0.415727 | 0.187175 | intron-variant | PHRF1 | GRCh38.p7 | 11:589564 | CCCCCGAGTGTGTCC[A/G]GGCCTCTTCTAAGCC | 57661 |
rs4963140 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | PHRF1 | GRCh38.p7 | 11:588654 | AAACTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 57661 |
rs4963177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:596194 | TCCCAAAGACCCCAG[A/T]CAGCCCTGAGTAAGG | 57661 |
rs4963178 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | PHRF1 | GRCh38.p7 | 11:593098 | CAGGGAGAGCAGCAG[A/G]TGCAGCATAACTGGA | 57661 |
rs6598010 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PHRF1 | GRCh38.p7 | 11:597318 | TCCCCCTGTGGCTGC[C/T]GGCCAAGTAGCAGCC | 57661 |
rs6598011 | snp | A/G | 0.426966 | 0.176587 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577809 | AAAAGGGCCTCTGGT[A/G]TCCGGGGTGCCTGCA | 57661 |
rs7101726 | snp | A/G | 0.399611 | 0.200291 | intron-variant | PHRF1 | GRCh38.p7 | 11:599313 | cagtgagccaagatc[A/G]tgccactgcactcca | 57661 |
rs7103762 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | PHRF1 | GRCh38.p7 | 11:589589 | ACCTGCCCCACAGGC[A/G]CCTCCTGCCCCCCCG | 57661 |
rs7107379 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:589076 | caatctcagctcact[A/G]caacctccaactccc | 57661 |
rs7112149 | snp | C/T | 0.305436 | 0.243776 | intron-variant | PHRF1 | GRCh38.p7 | 11:595890 | AGCAGAGGGGGGCGG[C/T]GGGTGGGGGCACTCC | 57661 |
rs7113728 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | PHRF1 | GRCh38.p7 | 11:578078 | CTTCCCTTCCCCATA[A/C]CCACCTCTGCCATGT | 57661 |
rs7113872 | snp | C/G | 0.151668 | 0.229849 | intron-variant | PHRF1 | GRCh38.p7 | 11:577908 | GATTAAAGAGGAAAA[C/G]AAAAAACTGGAAAGG | 57661 |
rs7115784 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | PHRF1 | GRCh38.p7 | 11:589647 | AGTCCGAGATCTTGA[A/C]TCCGTCCGGCATCGT | 57661 |
rs7115912 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | PHRF1 | GRCh38.p7 | 11:589597 | CCCAGCTGACCTGCC[C/T]CACAGGCGCCTCCTG | 57661 |
rs7116027 | snp | G/T | 0.00653559 | 0.0567898 | missense | PHRF1 | GRCh38.p7 | 11:609148 | TCGGCCGTAGCCACC[G/T]CCGGCGAGACATGTG | 57661 |
rs7116322 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | PHRF1 | GRCh38.p7 | 11:589246 | TGTCTTACACGTCTC[C/T]TTATGACTTATTTCT | 57661 |
rs7116433 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:589162 | ATTTTAACAGTTCAT[C/T]TGTAAGAGTTCTCCt | 57661 |
rs7117022 | snp | A/G | 0.333722 | 0.235565 | intron-variant | PHRF1 | GRCh38.p7 | 11:583787 | TGGCAACAGGGGACA[A/G]GGAAGGAGGTACCAC | 57661 |
rs7118452 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:596309 | TTCTATCGAGCCTTC[C/T]GGGAAGGTAGTTTGG | 57661 |
rs7118859 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:596005 | CTATGAGAAGGTGTC[C/T]GCTGTGTGGCCCTTG | 57661 |
rs7119844 | snp | A/G | 0.151668 | 0.229849 | intron-variant | PHRF1 | GRCh38.p7 | 11:577915 | TTTGGGGGATTAAAG[A/G]GGAAAACAAAAAACT | 57661 |
rs7119851 | snp | A/C | 0.151668 | 0.229849 | intron-variant | PHRF1 | GRCh38.p7 | 11:577903 | AAGAGGAAAACAAAA[A/C]ACTGGAAAGGCTATT | 57661 |
rs7120313 | snp | C/T | 0.498871 | 0.0237351 | intron-variant | PHRF1 | GRCh38.p7 | 11:584112 | AACTCTGGAAGGACA[C/T]GGCCAACACACATTG | 57661 |
rs7121828 | snp | A/T | 0.0850919 | 0.187897 | intron-variant | PHRF1 | GRCh38.p7 | 11:589595 | CAGCTGACCTGCCCC[A/T]CAGGCGCCTCCTGTC | 57661 |
rs7122021 | snp | C/T | 0.305685 | 0.24372 | intron-variant | PHRF1 | GRCh38.p7 | 11:595810 | GGACAAAGGCAAGGA[C/T]GAGCAGTACCTTCTT | 57661 |
rs7123948 | snp | A/G | 0.139932 | 0.224466 | missense | PHRF1 | GRCh38.p7 | 11:609577 | TGTACCCTCCCACTC[A/G]CAGAGGGGCTGTCTT | 57661 |
rs7124881 | snp | A/C | 0.0279272 | 0.11482 | intron-variant | PHRF1 | GRCh38.p7 | 11:587238 | GAGGAAACATGCCAG[A/C]TGGTGCAAGCAGGAT | 57661 |
rs7926440 | snp | A/G | 0.283947 | 0.247685 | intron-variant | PHRF1 | GRCh38.p7 | 11:589819 | CTCAGGCTGAGCCCC[A/G]CACGCTCTGTGCCCG | 57661 |
rs7928902 | snp | C/T | 0.36377 | 0.222613 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609068 | CCCCTGTGCAAGGGG[C/T]GCTGGGGAAGCCTCC | 57661 |
rs7929316 | snp | A/G | 0.134508 | 0.221724 | intron-variant | PHRF1 | GRCh38.p7 | 11:606399 | GTCACTGCCTCCCAC[A/G]GCCTGAGGGCCCGCA | 57661 |
rs7929655 | snp | A/G | 0.089084 | 0.191327 | intron-variant | PHRF1 | GRCh38.p7 | 11:606156 | CCAACTCCACCAACA[A/G]GTGGGAGGGGGCAGA | 57661 |
rs7931013 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | PHRF1 | GRCh38.p7 | 11:586334 | GAGGCAGCAGAAGAG[A/T]TTTAAGTTCCCATCT | 57661 |
rs7932229 | snp | C/T | 0.499218 | 0.0197529 | intron-variant | PHRF1 | GRCh38.p7 | 11:578759 | GTTATGAGACCAGCC[C/T]GGGCAACATGGCAAA | 57661 |
rs7935737 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:592406 | CTCCACGTGTACACA[A/G]GGATTTTTATGTTTT | 57661 |
rs7935754 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:592377 | TTCTACCATCTCAGG[A/G]TGGTGATCTAAGAGG | 57661 |
rs7936397 | snp | C/T | 0.370568 | 0.219005 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577534 | CATGATGCTGAGGTG[C/T]CATCCATCCACTAGC | 57661 |
rs7936642 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577357 | GCTGTTCTGCTGTTG[C/T]CGAAACAAGTAAAGC | 57661 |
rs7938382 | snp | A/C | | | missense | PHRF1 | GRCh38.p7 | 11:608151 | TGGACATGGCGGAGG[A/C]CGGTCCGAGAGGGGG | 57661 |
rs7938821 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:586417 | TGTTATCTGGCAAAG[A/G]GAAAGACACACCCAG | 57661 |
rs7940747 | snp | C/G | 0.170084 | 0.236883 | intron-variant | PHRF1 | GRCh38.p7 | 11:606224 | CTCGCAGCTCTGGCC[C/G]CAGGGAAACCAGGCG | 57661 |
rs7941547 | snp | C/T | 0.397271 | 0.202018 | intron-variant | PHRF1 | GRCh38.p7 | 11:611503 | CAGCACGCAGACAGA[C/T]GGCGGCAGAGGCCGC | 57661 |
rs7943546 | snp | A/G | 0.346811 | 0.230494 | utr-variant-3-prime, downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612148 | GGCGGGAGGCCACCT[A/G]GAGATTTATCAAGGA | 57661 |
rs7943961 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | PHRF1 | GRCh38.p7 | 11:605857 | GGGCCGACTGATGAG[C/T]GTGACAGCTGAGGGG | 57661 |
rs7947833 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:588289 | CAGACTTTGGGTGAC[A/G]TCACAGCCTGCCACC | 57661 |
rs7949750 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:586635 | TTCAACACGGCAGAG[C/G]CCATACGTGCACTGC | 57661 |
rs7952542 | snp | A/G | 0.0240604 | 0.107011 | intron-variant | PHRF1 | GRCh38.p7 | 11:592510 | ACCCAAACTCCCCGC[A/G]GTCACTTCCCAGCGT | 57661 |
rs9666658 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | PHRF1 | GRCh38.p7 | 11:599471 | ggccaggctggtctt[A/G]aactcccgacctcag | 57661 |
rs10736899 | snp | A/C | 0.199873 | 0.244923 | intron-variant | PHRF1 | GRCh38.p7 | 11:579256 | CCCAGCCCTGCTCCT[A/C]CCCCCAGCCCTGCTC | 57661 |
rs10902175 | snp | C/T | 0.33693 | 0.2344 | intron-variant | PHRF1 | GRCh38.p7 | 11:578996 | AGGTGCACGCCGCCA[C/T]GCCCGGCTCATTTTT | 57661 |
rs10902176 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:585026 | gacaggcatgagcca[A/C]cgcgcctggccAGGA | 57661 |
rs10902177 | snp | A/G | 0.294576 | 0.245994 | intron-variant | PHRF1 | GRCh38.p7 | 11:591083 | GACTTGAACAGGCTC[A/G]CCGCAGAGGGGCCTG | 57661 |
rs11246193 | snp | A/G | | | upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576031 | cagacgtgggggcgg[A/G]gctgcgggcgcgagg | 57661 |
rs11246194 | snp | A/G | 0.147656 | 0.228091 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577309 | ATGCTCCTTTTGACG[A/G]GGCTTGTGTTGCCCC | 57661 |
rs11246195 | snp | C/T | 0.118235 | 0.212457 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577354 | TGTGCTTTACTTGTT[C/T]CGACAACAGCAGAAC | 57661 |
rs11246196 | snp | C/T | 0.147321 | 0.227941 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577442 | CGAGCTGAGGTTTGA[C/T]TTCGGGTTTGGCATA | 57661 |
rs11246197 | snp | C/T | 0.119978 | 0.213528 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577454 | TGACTTCGGGTTTGG[C/T]ATAGTTGATCTCTCT | 57661 |
rs11246198 | snp | C/G | 0.118933 | 0.212888 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577670 | TTTGAGTTCTCCTAG[C/G]TGATACAGCAGATGG | 57661 |
rs11246199 | snp | A/G | 0.136506 | 0.222754 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577684 | GCTGATACAGCAGAT[A/G]GTGAATACAAGAATA | 57661 |
rs11246200 | snp | A/G | 0.183886 | 0.241099 | intron-variant | PHRF1 | GRCh38.p7 | 11:583107 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAG | 57661 |
rs11246201 | snp | C/G | 0.117537 | 0.212022 | intron-variant | PHRF1 | GRCh38.p7 | 11:583122 | GAGGCGGGCGGATCA[C/G]GAGGTCAGGAGATCG | 57661 |
rs11246202 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | PHRF1 | GRCh38.p7 | 11:584769 | tgagaccgagtttca[C/T]tcttgttgcccaggc | 57661 |
rs11246203 | snp | C/G | 0.198014 | 0.244535 | intron-variant | PHRF1 | GRCh38.p7 | 11:590605 | TTGTGTATGGTGTAC[C/G]TTAATAAAGCCAACA | 57661 |
rs11246204 | snp | A/T | 0.139903 | 0.224452 | intron-variant | PHRF1 | GRCh38.p7 | 11:595168 | TCTCTACTAAAAATA[A/T]AAAAATTGGCCGGGC | 57661 |
rs11246205 | snp | G/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:599753 | GACTCAGTGTCTGTG[G/T]GTCTGGTGCAGGGTC | 57661 |
rs11246206 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PHRF1 | GRCh38.p7 | 11:599774 | GTGCAGGGTCCTGGG[G/T]CTCCAGAGGACTCGG | 57661 |
rs11246207 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHRF1 | GRCh38.p7 | 11:599781 | GTCCTGGGTCTCCAG[A/G]GGACTCGGCGTCTGT | 57661 |
rs11246208 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHRF1 | GRCh38.p7 | 11:599788 | GTCTCCAGAGGACTC[A/G]GCGTCTGTGGGTCTG | 57661 |
rs11246209 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHRF1 | GRCh38.p7 | 11:599790 | CTCCAGAGGACTCGG[C/T]GTCTGTGGGTCTGGT | 57661 |
rs11246210 | snp | A/G | 0.103082 | 0.202275 | intron-variant | PHRF1 | GRCh38.p7 | 11:600474 | AGCCTGGGTGACAGA[A/G]TGAGACTCTGTCTCC | 57661 |
rs11246211 | snp | C/T | 0.118235 | 0.212457 | intron-variant | PHRF1 | GRCh38.p7 | 11:606294 | GAGCACCTCTTAGAA[C/T]AGCAGCCGGAGCCAG | 57661 |
rs11246212 | snp | C/T | 0.250934 | 0.249998 | missense | PHRF1 | GRCh38.p7 | 11:610277 | CAGGGGTCAGGCAGG[C/T]GTTCTCCGAGCTGCC | 57661 |
rs11539530 | snp | A/G | 0.318158 | 0.240538 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609353 | CACAGACTCTTCCCC[A/G]GAGCGAGACTTCCCA | 57661 |
rs11539531 | snp | A/G | | | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608987 | ACGGGAGCACAGGCG[A/G]CCTCGGTCCCGTGAG | 57661 |
rs11539532 | snp | C/G | | | missense | PHRF1 | GRCh38.p7 | 11:607969 | CCGACCCCACCGGCT[C/G]CGACTCCAGCGCCCC | 57661 |
rs11604252 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:602894 | cagcctcctgagtcg[C/T]tgggattataggcgt | 57661 |
rs11825714 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PHRF1 | GRCh38.p7 | 11:603413 | tcctggctcactgca[A/C]ccgccttgacctccc | 57661 |
rs11826379 | snp | G/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:603730 | CCATATTTAAGTTTG[G/T]TTTTTTTTTTTTTTT | 57661 |
rs12226533 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHRF1 | GRCh38.p7 | 11:592106 | atttttagtagagac[A/G]gggtttcactgtgtt | 57661 |
rs12272314 | snp | A/G | 0.354019 | 0.227333 | intron-variant | PHRF1 | GRCh38.p7 | 11:590648 | GTGGGTCAGAACACT[A/G]TTAATAAAGGCAAAA | 57661 |
rs12281144 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:599435 | tttgtatttttagta[A/G]agatggggcttcacc | 57661 |
rs12283876 | snp | A/G | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:581659 | GGAGCAGGGTGCCTG[A/G]TGTTTCCCTTTGGAG | 57661 |
rs12285890 | snp | C/T | 0.0876345 | 0.190099 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574754 | CCCTGGCCCCAGCGC[C/T]GCTGGCCCTCGGTGA | 57661 |
rs12285942 | snp | A/C | 0.287346 | 0.247195 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574813 | GGCTCCCTCCCCCGC[A/C]TGTGTGTGCACGCCC | 57661 |
rs12293073 | snp | C/T | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:581279 | ACCCTTCACGTGCTG[C/T]GGCGGTGGATGTGAC | 57661 |
rs12293369 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | PHRF1 | GRCh38.p7 | 11:581803 | TTGAACGAAAGGATG[C/T]TCCCTTTCCTTGCTT | 57661 |
rs12293832 | snp | C/T | 0.106382 | 0.204631 | intron-variant | PHRF1 | GRCh38.p7 | 11:606607 | GGCGGGTGAGTGCCT[C/T]CCCTGCCACGGCCCC | 57661 |
rs12295108 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | PHRF1 | GRCh38.p7 | 11:579546 | GGGAGAGGGGTCACC[C/T]TCCTGGATGGGCCGT | 57661 |
rs12295222 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | PHRF1 | GRCh38.p7 | 11:579676 | GCAGACTGCCTTGAG[C/T]GGGGATCATGACCAG | 57661 |
rs12295981 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:590512 | GGAGAGGGAAGGGCC[C/T]GAAGACCAGGGTGGG | 57661 |
rs12363567 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:603432 | ccttgacctcccagg[C/T]taaggtgatcctccc | 57661 |
rs12363914 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PHRF1 | GRCh38.p7 | 11:603816 | ctcagctcactgcaa[A/C]ctcggcctcccaaat | 57661 |
rs12419195 | snp | G/T | 0.0141837 | 0.08301 | intron-variant | PHRF1 | GRCh38.p7 | 11:610139 | TCCAGCCATGAAACA[G/T]CATTCTGGGCAGGGG | 57661 |
rs12419618 | snp | A/G | 0.304688 | 0.243945 | intron-variant | PHRF1 | GRCh38.p7 | 11:611531 | CTGCACCTAGGGCCT[A/G]CTCCTGAGCAGGGCA | 57661 |
rs12419694 | snp | C/T | 0.305436 | 0.243776 | intron-variant | PHRF1 | GRCh38.p7 | 11:598033 | CCTTGGCAAGCCTAA[C/T]GCTGAATTTGGAGTG | 57661 |
rs12419720 | snp | C/G | 0.305436 | 0.243776 | intron-variant | PHRF1 | GRCh38.p7 | 11:598205 | AGTGCTTGGCAGCCT[C/G]TGGCAGGGGAGAGGA | 57661 |
rs12420078 | snp | C/G | 0.0991586 | 0.199366 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577296 | CCCGACTCCTACCAT[C/G]CTCCTTTTGACGGGG | 57661 |
rs12420875 | snp | C/T | 0.322483 | 0.239262 | intron-variant | PHRF1 | GRCh38.p7 | 11:603776 | tttcgctcttgttgc[C/T]gaggctggagtgcag | 57661 |
rs12421158 | snp | C/T | 0.432797 | 0.170544 | intron-variant | PHRF1 | GRCh38.p7 | 11:609888 | AGCCCCCTGTGAATC[C/T]GACTCCTGTCAAGGA | 57661 |
rs12421174 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | PHRF1 | GRCh38.p7 | 11:606974 | TTTAAAGCGCACGAC[C/G]TCACAGAAAACCAGT | 57661 |
rs12421184 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | PHRF1 | GRCh38.p7 | 11:607050 | AATGATTGCCATTGA[A/C]TTTTTTGTTTTTTAG | 57661 |
rs12421646 | snp | C/G | 0.276267 | 0.248616 | intron-variant | PHRF1 | GRCh38.p7 | 11:578844 | GCATGAGCCACCACG[C/G]CCGGCTGATTCACAT | 57661 |
rs12577117 | snp | A/C | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575209 | taaacacagacaccc[A/C]cgatgagacgtgaac | 57661 |
rs12788887 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:599254 | TTTTtttttcttttc[C/T]ttttttttttttttt | 57661 |
rs12795572 | snp | A/G | 0.305186 | 0.243833 | intron-variant | PHRF1 | GRCh38.p7 | 11:590999 | tgagcccctgctccc[A/G]gccTATGAAAAGAAA | 57661 |
rs12797025 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:591837 | ctacagcctcaatct[C/G/T]ctgggctcaagcaat | 57661 |
rs12797113 | snp | C/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:591682 | ATATTGCCAGCTCCT[C/G]GGATATCCCTTCGAC | 57661 |
rs12797496 | snp | C/T | 0.275197 | 0.248727 | intron-variant | PHRF1 | GRCh38.p7 | 11:583767 | CAAGTCCGTGGGGTG[C/T]GCTGGTGGTACCTCC | 57661 |
rs12798732 | snp | A/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588682 | ccacgcccggccATT[A/T]TTATTTTTATTTTTT | 57661 |
rs12800061 | snp | A/C | 0.31072 | 0.242514 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:587425 | GCCGGAGAACTGTGC[A/C]CATTACTTCTGCCTG | 57661 |
rs12802486 | snp | C/G | 0.304438 | 0.244001 | intron-variant | PHRF1 | GRCh38.p7 | 11:592023 | tgggttcacgccatt[C/G]tcctgcctcagcctc | 57661 |
rs12803048 | snp | C/T | 0.251296 | 0.249997 | intron-variant | PHRF1 | GRCh38.p7 | 11:584243 | TCTGTAGTAGGTCTC[C/T]GCACCAGTTCTGGCG | 57661 |
rs12803132 | snp | A/G | 0.275464 | 0.2487 | intron-variant | PHRF1 | GRCh38.p7 | 11:586696 | AAGGTGTAGCCTCAG[A/G]ACCACTCCGAATTGG | 57661 |
rs12805435 | snp | C/T | 0.399073 | 0.200692 | downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612355 | TGCTGTCCCTGCCCT[C/T]GGCACAGCTGGTGGG | 57661 |
rs12806376 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:591824 | caatcacagcttact[A/C]cagcctcaatctcct | 57661 |
rs12806383 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:591826 | atcacagcttactac[A/C]gcctcaatctcctgg | 57661 |
rs12806523 | snp | A/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:591850 | ctcctgggctcaagc[A/T]atcctcatgcctcag | 57661 |
rs17155933 | snp | C/G | 0.14238 | 0.225679 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611802 | ATCACGGGCTATGCC[C/G]GGGGAGCTGTCGGGA | 57661 |
rs28393874 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:590055 | GGGCTCAGCCTGAGA[A/G]TGTCTGCAAACGGGC | 57661 |
rs28453218 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589993 | CGGGCACGGAGCGTG[C/T]GGGGCTCAGCCTCAG | 57661 |
rs28473244 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PHRF1 | GRCh38.p7 | 11:590019 | CTCAGAGAGTGTCTG[C/T]AAACGGGCATGGAGC | 57661 |
rs28510900 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHRF1 | GRCh38.p7 | 11:578634 | TTTGTTCACATACTA[C/T]GGCTCACTGCAGCCT | 57661 |
rs28513881 | snp | C/T | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589943 | GTCTGCAAACGGGCA[C/T]GGAGCGTGCGGGGCT | 57661 |
rs28520919 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589898 | GTCTGCAAACGGGCA[C/T]GGAGCGTGCAGGGTT | 57661 |
rs28537111 | snp | C/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589920 | TGCAGGGTTCAGCCT[C/G]AGAGGGTGTCTGCAA | 57661 |
rs28637203 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589925 | GGTTCAGCCTGAGAG[A/G]GTGTCTGCAAACGGG | 57661 |
rs34115587 | in-del | -/A | 0.439224 | 0.163383 | intron-variant | PHRF1 | GRCh38.p7 | 11:589580 | GACACACTCGGGGGG[-/A]GCAGGAGGCGCCTGT | 57661 |
rs34166836 | in-del | -/A | | | frameshift-variant | PHRF1 | GRCh38.p7 | 11:596987 | AGTGGTTCTGCCCGG[-/A]AATGTGCTGCGCCTG | 57661 |
rs34265491 | snp | C/T | 0.314544 | 0.241524 | intron-variant | PHRF1 | GRCh38.p7 | 11:587014 | AGCTGGTCTGGCACT[C/T]AGGACGCTCAGCTTC | 57661 |
rs34424470 | in-del | -/CCTC | | | intron-variant | PHRF1 | GRCh38.p7 | 11:606261 | CTCCCTCCCTCCCTC[-/CCTC]TGGGAGGCCCCGGTG | 57661 |
rs34515619 | in-del | -/T | 0.293037 | 0.246268 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574890 | ACCCCTAGCACCCCC[-/T]GTGCCCCTTCCTAGT | 57661 |
rs34610235 | in-del | -/A | 0.439224 | 0.163383 | intron-variant | PHRF1 | GRCh38.p7 | 11:589581 | ACACACTCGGGGGGG[-/A]CAGGAGGCGCCTGTG | 57661 |
rs34793529 | snp | G/T | 0.334871 | 0.235153 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575800 | CTCCGGCAGTGTTTG[G/T]TCAGAGGAGCGCGGC | 57661 |
rs34903620 | in-del | -/A | | | intron-variant | PHRF1 | GRCh38.p7 | 11:610364 | GGGTGTCTGGGCTGG[-/A]AGGGCTGTGGGCCGT | 57661 |
rs35482931 | snp | C/T | 0.0888142 | 0.1911 | missense | PHRF1 | GRCh38.p7 | 11:610724 | AGGAGAAGACCCCGG[C/T]CCCCAGGCTAGCTGC | 57661 |
rs35572525 | in-del | -/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:596631 | GCAGGCCTGGTTCCT[-/G]GGGGAGGCCCCCTTC | 57661 |
rs35607109 | in-del | -/C | | | frameshift-variant | PHRF1 | GRCh38.p7 | 11:609103 | AGGGCGGGAAGACCT[-/C]CCCCACCAGGTTGCC | 57661 |
rs35744807 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577849 | TAACAGTTGGGACTG[-/C]CCAATGCATTGGTTC | 57661 |
rs35825045 | in-del | -/AT | 0.488241 | 0.0757703 | intron-variant | PHRF1 | GRCh38.p7 | 11:600494 | ACTCTGTCTCCAAAA[-/AT]ATATATATATATATA | 57661 |
rs35865896 | snp | A/G | 0.372592 | 0.217879 | intron-variant | PHRF1 | GRCh38.p7 | 11:584591 | AGGCGGCAGGCCAGG[A/G]CGGGGGAGCTGTGAA | 57661 |
rs36060383 | snp | A/C | 0.305934 | 0.243663 | intron-variant | PHRF1 | GRCh38.p7 | 11:598723 | CATTGTGTCAGGGTG[A/C]TGCCGGCCTTCCCGC | 57661 |
rs55771159 | snp | C/G | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590102 | TCAGCCTGAGAATGT[C/G]TGCAAACGGGCACGG | 57661 |
rs55907139 | snp | C/T | 0.444444 | 0.157135 | intron-variant | PHRF1 | GRCh38.p7 | 11:589855 | GTCTGCAAACGGGCA[C/T]GGAGCGTGCGGGGCT | 57661 |
rs56004604 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:598509 | GGAAGACAAGTAAGC[A/C]TGAAGGGATGGACTC | 57661 |
rs56114630 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585283 | TGAGGTAGTAGCCCT[C/T]TCCAGCTTGAGGTAG | 57661 |
rs56137650 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585272 | CCTTTCCAGCTTGAG[A/G]TAGTAGCCCTTTCCA | 57661 |
rs56267241 | in-del | -/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588378 | TTTCTTTTTTTTTTT[-/T]GTTTTTTTGAGACGG | 57661 |
rs56322236 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHRF1 | GRCh38.p7 | 11:596102 | AGCCCGTGGTAAGTG[A/G]TAGTTAAGTTCAGTT | 57661 |
rs56333810 | snp | C/G | 0.363568 | 0.222716 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575408 | GCATCTACCGGGAGC[C/G]GGCACTTCCCACACC | 57661 |
rs56351744 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585265 | TAGTAGCCCTTTCCA[A/G]CTTGAGGTAGTAGCC | 57661 |
rs56379816 | snp | C/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589832 | TGCGGGGCTCAGCCT[C/G]AGAGAGAGTCTGCAA | 57661 |
rs56413249 | snp | A/G | 0.102014 | 0.201495 | intron-variant | PHRF1 | GRCh38.p7 | 11:604040 | ATTATTCGAACATCC[A/G]ATCTGTTTATTCATT | 57661 |
rs56695874 | snp | A/G | 0.089084 | 0.191327 | intron-variant | PHRF1 | GRCh38.p7 | 11:605393 | ATGCGGAGGCGTTAG[A/G]TTTTGTGTTTGAGAG | 57661 |
rs57038704 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | PHRF1 | GRCh38.p7 | 11:597868 | GCCCCATGCCAGCAC[C/T]GCTCCCTCTAGGCAC | 57661 |
rs57080334 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:590534 | CAGGGTGGGTACTCC[A/G]CAGGTTGTATATTTG | 57661 |
rs57223240 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:596866 | TCCCCTCACTTGAGG[A/C]GGTTTGGGAAAGCTG | 57661 |
rs57254644 | snp | A/G | 0.157642 | 0.232314 | intron-variant | PHRF1 | GRCh38.p7 | 11:609822 | AAGGCCCCGGCCTCC[A/G]CCGAGGACAGAGCCC | 57661 |
rs57379008 | in-del | -/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588475 | ACCTCCACCTTCCGG[-/G]TTCAAGCGATTCTCC | 57661 |
rs57490538 | snp | G/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:602770 | GTTTTTGTTTTTTTT[G/T]TTTTTTTTTTTGAGA | 57661 |
rs57504413 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | PHRF1 | GRCh38.p7 | 11:600846 | TGGCGGGCGCCTGTA[A/G]TCCCAGCTACACGGG | 57661 |
rs57585282 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:609800 | GAGGACAGAGCCCCC[A/C]GTGAGTAAGGCCCCG | 57661 |
rs57620348 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PHRF1 | GRCh38.p7 | 11:580770 | CTCGGCTCACTGCAA[C/T]CTCCGCCTCTCAGGT | 57661 |
rs57830193 | snp | A/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:592222 | GCCCAGCCTTTTTTT[A/T]TTTTTTTTTTAAGAG | 57661 |
rs57891886 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:600512 | TATATATATATATAT[A/G]TATATATGGTTTATT | 57661 |
rs57922029 | snp | A/G | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590082 | GGGCATGGAGCGTGC[A/G]GGGCTCAGCCTGAGA | 57661 |
rs57973687 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PHRF1 | GRCh38.p7 | 11:580732 | TTGCTCTTATTGCGC[A/G]GGCTGGAGTGCAGTG | 57661 |
rs58041097 | snp | G/T | 0.000693241 | 0.0186048 | intron-variant | PHRF1 | GRCh38.p7 | 11:609769 | GCCCCCAGTGAGTAA[G/T]GCCCTGGCCCCCGCC | 57661 |
rs58104786 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PHRF1 | GRCh38.p7 | 11:609774 | CAGTGAGTAAGGCCC[C/T]GGCCCCCGCCGAGGA | 57661 |
rs58228589 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:604230 | CCTGGGCGTCGTCCT[A/G]AGCTTTTTGTCCTGC | 57661 |
rs58383270 | in-del | -/CT | | | intron-variant | PHRF1 | GRCh38.p7 | 11:590103 | AGCCTGAGAATGTGT[-/CT]GCAAACGGGCACGGA | 57661 |
rs58391969 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | PHRF1 | GRCh38.p7 | 11:600790 | GCTAACACGGTGAAA[C/G]CCCGTCTCTACTAAA | 57661 |
rs58446691 | snp | A/C | 0.089084 | 0.191327 | intron-variant | PHRF1 | GRCh38.p7 | 11:604978 | CGGTCATCATGCCTG[A/C]GAAGCCCATTGACTT | 57661 |
rs58562994 | snp | C/G | 0.0898077 | 0.191933 | intron-variant | PHRF1 | GRCh38.p7 | 11:580480 | TGCCTCCTCAGCTCT[C/G]GGTACCACTGGGGAC | 57661 |
rs58607851 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:590129 | ACGGAGCGTGCAGGG[C/T]TCAGCAGCAGGGCTC | 57661 |
rs58696156 | in-del | -/AATAAATAAATA/AT | | | intron-variant | PHRF1 | GRCh38.p7 | 11:600496 | CTGTCTCCAAAAATA[-/AATAAATAAATA/AT]TATATATATATATAT | 57661 |
rs58860894 | in-del | -/TTTCCCCCCAGCCCTGCT | | | intron-variant | PHRF1 | GRCh38.p7 | 11:579270 | CCCCCCAGCCCTGCT[-/TTTCCCCCCAGCCCTGCT]CTGTTATCTCTTAGG | 57661 |
rs58875072 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:580290 | GACCAAAGTTTGAGG[A/C]CCTGGTGTGGAAGGA | 57661 |
rs59144823 | snp | C/T | 0.423257 | 0.180228 | intron-variant | PHRF1 | GRCh38.p7 | 11:590072 | GTCTGCAAACGGGCA[C/T]GGAGCGTGCGGGGCT | 57661 |
rs59180492 | snp | C/T | 0.00872033 | 0.0654532 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:592666 | GCTCTGCGACGGCTG[C/T]GATGCGGGGTAAGGG | 57661 |
rs59284754 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:596480 | ACCGCAGGAGCTCAG[C/T]GTGAGCCACTGTCGG | 57661 |
rs59362784 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:588504 | CCTGCCTCAGCCTCC[C/T]GCGTAGCTGGAACTG | 57661 |
rs59553365 | snp | C/T | 0.0262211 | 0.111459 | intron-variant | PHRF1 | GRCh38.p7 | 11:605767 | GGTGGGGGCAGCAGT[C/T]GGGCATCGGATGGGA | 57661 |
rs59646085 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | PHRF1 | GRCh38.p7 | 11:590775 | GTGGCGCCATCTCGG[C/G]TCACCGCAACCTCAG | 57661 |
rs59753810 | snp | C/T | 0.00461209 | 0.0477993 | intron-variant | PHRF1 | GRCh38.p7 | 11:592700 | GTTGGGACTGGCACA[C/T]GTGCCCTGCTGCGTG | 57661 |
rs59861558 | in-del | -/A | | | intron-variant | PHRF1 | GRCh38.p7 | 11:601446 | AAAAAAAAAAAAAAA[-/A]TTGCAAGCCGGTGCG | 57661 |
rs60083681 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:593008 | GGGGGAGGGGTGGCT[A/G]TGCCTGCGTCCATCA | 57661 |
rs60134547 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:580969 | GCTGGGGTTACAGGC[A/G]TGAGCAGCTATGCCT | 57661 |
rs60154196 | in-del | -/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:605979 | GCCCCTCTGCCCCCC[-/C]ACCCCGGCCTGAGAG | 57661 |
rs60291171 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:600693 | AAAATTAGGCCAGGC[A/G]TGGTGGCTTACACCT | 57661 |
rs60363043 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:609760 | GAGGACAGAGCCCCC[A/C]GTGAGTAAGGCCCTG | 57661 |
rs60421541 | snp | A/G | 0.089084 | 0.191327 | intron-variant | PHRF1 | GRCh38.p7 | 11:604344 | CCCTTGGGAGGGGCG[A/G]CGCCTGCCTTCAGGC | 57661 |
rs60477898 | snp | C/G/T | 0.00865533 | 0.0652242 | missense | PHRF1 | GRCh38.p7 | 11:608184 | CTCCGGGGTGCAGTG[C/G/T]CTGCCGAGGGGGCCT | 57661 |
rs60536731 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590086 | ATGGAGCGTGCGGGG[C/T]TCAGCCTGAGAATGT | 57661 |
rs60556309 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:609782 | AAGGCCCTGGCCCCC[A/G]CCGAGGACAGAGCCC | 57661 |
rs60568231 | snp | A/T | 0.308166 | 0.243139 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575553 | TCGCGAGTCCGCGCC[A/T]GCTCGGGATCCCCGG | 57661 |
rs60588515 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:590728 | TTTTTTTTGAGATGG[A/G]GTTTGGCTCTTGTCA | 57661 |
rs60676339 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:596499 | AGCCACTGTCGGCCT[C/G]TGGGTGTGTGTCGTG | 57661 |
rs60679095 | snp | A/G | 0.000690846 | 0.0185727 | intron-variant | PHRF1 | GRCh38.p7 | 11:609768 | AGCCCCCAGTGAGTA[A/G]GGCCCTGGCCCCCGC | 57661 |
rs60857733 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | PHRF1 | GRCh38.p7 | 11:596299 | GCAGCACTTCCCAAA[C/G]TACCTTCCCAGAAGG | 57661 |
rs60976049 | snp | C/T | 0.0241507 | 0.107201 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:605277 | TCTGTTTGGAGATCC[C/T]TATGAGCTGGATCCC | 57661 |
rs61170993 | snp | A/G/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:580309 | GGTGTGGAAGGAGGA[A/G/T]CGTGTCCAACTAGAT | 57661 |
rs61343338 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | PHRF1 | GRCh38.p7 | 11:580402 | AGGGGTCCCGGCTGA[C/T]GGGTCAGGGCCTTGA | 57661 |
rs61391789 | in-del | -/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:591929 | TTTTTTTTTTTTTTT[-/T]CCCGAGACAAGAGTC | 57661 |
rs61469439 | snp | A/G | 0.00485259 | 0.0490178 | intron-variant | PHRF1 | GRCh38.p7 | 11:605108 | ATCTTTTTCTTTGTT[A/G]CTGGATTCAGAGTGA | 57661 |
rs61577202 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:609742 | AGTGCCCCGGCCCCC[A/G]CCGAGGACAGAGCCC | 57661 |
rs61596393 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:601953 | GGTTGAGGGGTGGTC[A/G]TGTGCCCCCAAGGAA | 57661 |
rs61689080 | snp | A/G | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590125 | GGGCACGGAGCGTGC[A/G]GGGTTCAGCAGCAGG | 57661 |
rs61739487 | snp | A/T | 0.0425331 | 0.13949 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:592636 | CGGCAGGAGCGACCG[A/T]GAGGACAGGCTTTTG | 57661 |
rs61744675 | snp | A/G | 0.0253587 | 0.10971 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:581587 | ACAGGTCGGCCCTGC[A/G]GACCCGGCAGGTGAC | 57661 |
rs61746669 | snp | C/T | 0.00534636 | 0.0514256 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:587452 | CCTGGACTGCATTGT[C/T]GAATGGTCCAAGGTG | 57661 |
rs61877827 | snp | A/C | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576545 | CGACTCTCGGTCGTG[A/C]AGCGGCGGCGAGCGC | 57661 |
rs61877828 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | PHRF1 | GRCh38.p7 | 11:579078 | CTACGGAGCTCAGGC[C/T]GTCTGCCCACCTTGG | 57661 |
rs61877829 | snp | C/T | 0.275464 | 0.2487 | intron-variant | PHRF1 | GRCh38.p7 | 11:582727 | GATGGGGTTTCACCG[C/T]GTTAGCCAGGATGGT | 57661 |
rs61877830 | snp | A/C | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:584992 | ATCCACCCGCCTTGG[A/C]CTCCCAAAGTGCTGG | 57661 |
rs61877831 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585313 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs61877832 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585441 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs61877833 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585497 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCTCT | 57661 |
rs61877834 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585520 | GTAGCTCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs61877835 | snp | A/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585612 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs61877836 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | PHRF1 | GRCh38.p7 | 11:585658 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCTCT | 57661 |
rs67047074 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585451 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs67530061 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585464 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs68065134 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | PHRF1 | GRCh38.p7 | 11:585418 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs71022934 | in-del | -/T | 0.433963 | 0.169285 | intron-variant | PHRF1 | GRCh38.p7 | 11:582265 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTGTCGC | 57661 |
rs71022937 | in-del | -/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:603751 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 57661 |
rs71278582 | in-del | AGA/G | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589581 | GACACACTCGGGGGG[AGA/G]CAGGAGGCGCCTGTG | 57661 |
rs71283532 | snp | A/T | 0.46875 | 0.121031 | intron-variant | PHRF1 | GRCh38.p7 | 11:585474 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs71283533 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585487 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs71283534 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585510 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs71283535 | snp | C/T | 0.46875 | 0.121031 | intron-variant | PHRF1 | GRCh38.p7 | 11:585579 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs71462099 | in-del | -/CAAA | 0.275197 | 0.248727 | intron-variant | PHRF1 | GRCh38.p7 | 11:583732 | AGCGAGACGTTATCT[-/CAAA]ACAAAACAAAGGGGA | 57661 |
rs71462100 | in-del | -/AAAAC | 0.414741 | 0.188044 | intron-variant | PHRF1 | GRCh38.p7 | 11:594895 | AATTACTTGGCAGAT[-/AAAAC]AACGCAAGTACATAA | 57661 |
rs72479386 | snp | C/T | 0.158962 | 0.232835 | intron-variant | PHRF1 | GRCh38.p7 | 11:590201 | ACCCCTGGAGCTGGT[C/T]GGTAGGAGGGCACCC | 57661 |
rs72841254 | snp | C/T | 0.311859 | 0.242226 | intron-variant | PHRF1 | GRCh38.p7 | 11:579253 | CCCCCCAGCCCTGCT[C/T]CTCCCCCCAGCCCTG | 57661 |
rs72841255 | snp | C/T | 0.311859 | 0.242226 | intron-variant | PHRF1 | GRCh38.p7 | 11:579254 | CCCCCAGCCCTGCTC[C/T]TCCCCCCAGCCCTGC | 57661 |
rs72844710 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | PHRF1 | GRCh38.p7 | 11:604941 | CTTCACGGCCGATGT[A/G]TGCGGCATTGTTCCT | 57661 |
rs72844713 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | PHRF1 | GRCh38.p7 | 11:606770 | TTTCTCAGTTAGCTC[C/T]GAGTTCTTACCCAGC | 57661 |
rs73396303 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | PHRF1 | GRCh38.p7 | 11:589673 | GGACTAGAAAGCAAA[A/G]CTGAACCTTTGAAAA | 57661 |
rs73396305 | snp | G/T | 0.0678174 | 0.1712 | intron-variant | PHRF1 | GRCh38.p7 | 11:589748 | AAACAGTCTGAGAGA[G/T]TGTCTGCAAACGGGC | 57661 |
rs73396307 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | PHRF1 | GRCh38.p7 | 11:589752 | AGTCTGAGAGAGTGT[C/T]TGCAAACGGGCACGG | 57661 |
rs73396318 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PHRF1 | GRCh38.p7 | 11:593962 | TGCTGCCAGTTGCCC[C/T]GGCAGGCACTGAGTT | 57661 |
rs73396320 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:594329 | GCCCTCATCGCAGGC[C/T]AGGGCCGTGAGCCTT | 57661 |
rs73396324 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PHRF1 | GRCh38.p7 | 11:594535 | CAACCTCTGCAGCGA[A/G]TCACTGCAACCTCGG | 57661 |
rs73396327 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | PHRF1 | GRCh38.p7 | 11:595209 | ACACCTGTAACCCCC[A/G]ATCCTTGGGAGGCTG | 57661 |
rs73396328 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | PHRF1 | GRCh38.p7 | 11:595305 | TCCAGAGAGACTAAA[A/G]ACAAAAAACAAAAAA | 57661 |
rs73396333 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | PHRF1 | GRCh38.p7 | 11:596842 | TGCCATCGGAGGCCT[A/G]CTTTGTGGTCCCCTC | 57661 |
rs73396343 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:599542 | AGGCCTCTGAGCCAC[C/T]GCGCCTGGCCTGAAG | 57661 |
rs73396346 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | PHRF1 | GRCh38.p7 | 11:599654 | GCACAGAAATAGTTA[C/T]GAGACCACACTTCAG | 57661 |
rs73396347 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:599668 | ATGAGACCACACTTC[A/G]GCCCCACCAGCAGCC | 57661 |
rs73396351 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:602321 | ATGTTTGTGATGCTC[A/C]AACCGGGACTAAATG | 57661 |
rs73398375 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHRF1 | GRCh38.p7 | 11:606360 | CTCTCCCTGGCTCCC[A/G]CCTGCTGCGGGGCTC | 57661 |
rs73398385 | snp | C/T | 0.00666391 | 0.0573371 | intron-variant | PHRF1 | GRCh38.p7 | 11:611617 | AGGGCATTTGGTGAT[C/T]GCACCTCTTTCTCCA | 57661 |
rs73398389 | snp | A/C/T | 0.00152629 | 0.0275833 | missense | PHRF1 | GRCh38.p7 | 11:611740 | ACAAGAAACCAGAGG[A/C/T]CGGGGAGGAGCCGCC | 57661 |
rs73399091 | snp | C/T | 0.141596 | 0.225274 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574957 | CCCAGAGTTCAGGCA[C/T]TGGTCCCCAGTCACA | 57661 |
rs73401010 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | PHRF1 | GRCh38.p7 | 11:579568 | ATGGGCCGTGGCCCT[C/T]GTGTGTCTCTCAGAG | 57661 |
rs73401019 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:584395 | CAGCAGGGCCCCCAC[A/C]GTGTCTGCGCTCACC | 57661 |
rs73401029 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:587700 | GGGCAGGAGAGAGGA[C/T]GGCCGTGGGTCTCCC | 57661 |
rs74045033 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PHRF1 | GRCh38.p7 | 11:579596 | GAGCCAGTGTCTCTA[A/G]GATTCAGGTGCGGGA | 57661 |
rs74045035 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PHRF1 | GRCh38.p7 | 11:581189 | AGGATCTGGCTTTAT[A/G]GGTAGCTCTGTAAAT | 57661 |
rs74045049 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | PHRF1 | GRCh38.p7 | 11:593042 | TGGCTGCCTTGGTCC[C/G]TCACCTTTCACCCTG | 57661 |
rs74045052 | snp | C/T | 0.0108173 | 0.0727436 | missense | PHRF1 | GRCh38.p7 | 11:608959 | CCCGGTCCCCAAGCT[C/T]GGAGCACAGGGCACG | 57661 |
rs74426336 | snp | A/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:597907 | ACCTTCCTCTTGCAC[A/T]GGACCTGGTGCTCGG | 57661 |
rs74478509 | snp | G/T | 0.178144 | 0.239451 | intron-variant | PHRF1 | GRCh38.p7 | 11:604029 | GTTTTAAATGCATTA[G/T]TCGAACATCCGATCT | 57661 |
rs74607737 | snp | A/G | | | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610329 | GGAACCCGGGTTCCC[A/G]GACACAGACCCCTCT | 57661 |
rs74679147 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PHRF1 | GRCh38.p7 | 11:594909 | TAAAACAACGCAAGT[A/C]CATAAAAACCCTGGT | 57661 |
rs74794288 | snp | A/T | 0.444444 | 0.157135 | intron-variant | PHRF1 | GRCh38.p7 | 11:585566 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs75143012 | snp | A/G | 0.375 | 0.216506 | intron-variant | PHRF1 | GRCh38.p7 | 11:585640 | CCTTTCCAGCTTGAG[A/G]TAGTAGCCCTTTCCA | 57661 |
rs76072858 | snp | A/G | 0.355954 | 0.226437 | intron-variant | PHRF1 | GRCh38.p7 | 11:589581 | GACACACTCGGGGGG[A/G]CAGGAGGCGCCTGTG | 57661 |
rs76185932 | snp | A/G | 0.163564 | 0.234582 | intron-variant | PHRF1 | GRCh38.p7 | 11:602322 | TGTTTGTGATGCTCA[A/G]ACCGGGACTAAATGT | 57661 |
rs76369403 | snp | A/C | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:611421 | CCCCCCGCCCACCGA[A/C]ACCGTGGGACCCTCA | 57661 |
rs76680773 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577180 | AGTCCTCACAAGAGC[C/G]TCTCAGGTGTAGGTA | 57661 |
rs76898348 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PHRF1 | GRCh38.p7 | 11:583612 | AAAGGGCAGGTCTGC[A/G]CTGGGTGTGGTGGCC | 57661 |
rs76967430 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585326 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs77038558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:604468 | AGGAATAATGACAGC[A/G]CTTAAAATCTAAATT | 57661 |
rs77216638 | snp | C/G | | | missense | PHRF1 | GRCh38.p7 | 11:610328 | CGGAACCCGGGTTCC[C/G]AGACACAGACCCCTC | 57661 |
rs77377855 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PHRF1 | GRCh38.p7 | 11:592902 | CACAGAAGTGCAGGT[A/T]ATACATCAAGACAAA | 57661 |
rs77409873 | snp | C/T | 0.00032017 | 0.0126484 | missense | PHRF1 | GRCh38.p7 | 11:609217 | CAGCTGAGTGTGAGC[C/T]GGACGACCTGGACCT | 57661 |
rs77553935 | in-del | -/AACAA | | | intron-variant | PHRF1 | GRCh38.p7 | 11:594897 | TTACTTGGCAGATAA[-/AACAA]CGCAAGTACATAAAA | 57661 |
rs77946936 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:579188 | TCATCATCAAATGAG[C/G]ATTTGCACTCGGGAC | 57661 |
rs78082951 | snp | A/T | 0.160938 | 0.233598 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575461 | AGCCCAGGCAGCCCC[A/T]GCACGGGGAGCCCGC | 57661 |
rs78164018 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585556 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs78620810 | snp | A/G | | | missense | PHRF1 | GRCh38.p7 | 11:610330 | GAACCCGGGTTCCCA[A/G]ACACAGACCCCTCTC | 57661 |
rs79254735 | snp | C/T | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574890 | ACCCCTAGCACCCCC[C/T]GTGCCCCTTCCTAGT | 57661 |
rs79584545 | snp | A/G | 0.444444 | 0.157135 | intron-variant | PHRF1 | GRCh38.p7 | 11:591198 | CTTTCCTCCCCGCTA[A/G]GGCTGGCAGCTCTGC | 57661 |
rs79643522 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:610383 | GCTGTGGGCCGTGGG[C/T]AGTGGCCTGGCACCC | 57661 |
rs79762796 | snp | C/T | 0.375 | 0.216506 | intron-variant | PHRF1 | GRCh38.p7 | 11:603748 | TTTTTTTTTTTTTTT[C/T]TTTGAGATGGAGTTT | 57661 |
rs79852896 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PHRF1 | GRCh38.p7 | 11:583747 | CAAACAAAACAAAGG[A/G]GAGACAAGTCCGTGG | 57661 |
rs80220319 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | PHRF1 | GRCh38.p7 | 11:578976 | TCCGGAGTAGCTGGG[A/G]CTACAGGTGCACGCC | 57661 |
rs80340007 | snp | A/G | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:587749 | CCTGGTTGACATAGG[A/G]GCCATCTTGGCCTGC | 57661 |
rs111280373 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHRF1 | GRCh38.p7 | 11:598148 | GCCCTCTCGTGTGCC[C/T]CTGGGATGCTGTCTG | 57661 |
rs111285659 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589864 | CGGGCACGGAGCGTG[C/T]GGGGCTCAGCCTGAG | 57661 |
rs111314084 | snp | A/G | 0.0240643 | 0.107019 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574755 | CCTGGCCCCAGCGCC[A/G]CTGGCCCTCGGTGAG | 57661 |
rs111339543 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:586129 | GCCTCCCAAAGTACT[A/G]GGATTACAGGCTTGA | 57661 |
rs111357848 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | PHRF1 | GRCh38.p7 | 11:605999 | CGGCCTGAGAGCCAC[C/T]AGCACAGGGACACCG | 57661 |
rs111363951 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | PHRF1 | GRCh38.p7 | 11:580501 | CACTGGGGACTCAGC[A/C]GCACCCTGGTGGATG | 57661 |
rs111384263 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585290 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs111399015 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:582819 | GTGAGCCACCGCGCC[C/T]GGCCTTTTTTCAAGA | 57661 |
rs111406154 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | PHRF1 | GRCh38.p7 | 11:581256 | CTGTGGGTGATATCT[C/T]AGGGCTCACCCTTCA | 57661 |
rs111437303 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589952 | CGGGCACGGAGCGTG[C/T]GGGGCTCAGCCTGAG | 57661 |
rs111447606 | in-del | -/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:581112 | TACAGGCGTGACCAA[-/T]TTTTTTTTTTTTTTT | 57661 |
rs111450007 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611829 | GGGAGTGGCGGGAAT[C/T]GGGGCCATGCCCGGG | 57661 |
rs111487115 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | PHRF1 | GRCh38.p7 | 11:585257 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs111514492 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:578165 | ATTAACCCAGCATCC[C/T]AACTACAGGTCCTGG | 57661 |
rs111560769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:589747 | TAAACAGTCTGAGAG[A/G]GTGTCTGCAAACGGG | 57661 |
rs111659639 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | PHRF1 | GRCh38.p7 | 11:598595 | AGGCTGTGGGCATTT[C/G]CATTTCTTCTTTCTG | 57661 |
rs111688385 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:585744 | GGAGTGCAGCAGCAC[C/G]ATCTCAGTTCACTGC | 57661 |
rs111713669 | snp | C/G | | | upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576213 | GGCGGTACCAGCTGT[C/G]CCGGCCGCGGGGGGG | 57661 |
rs111729822 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585589 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs111737288 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | PHRF1 | GRCh38.p7 | 11:581290 | GCTGTGGCGGTGGAT[G/T]TGACACTGGGACACT | 57661 |
rs111761859 | in-del | -/G | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:577902 | AATAGCCTTTCCAGT[-/G]TTTTTGTTTTCCTCT | 57661 |
rs111830833 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PHRF1 | GRCh38.p7 | 11:586185 | ACTTTTAGTAGAGAC[A/G]GGGTTTCACTGTTAG | 57661 |
rs111831870 | snp | G/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:584594 | CGGCAGGCCAGGACG[G/T]GGGAGCTGTGAAGAG | 57661 |
rs111837717 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585359 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs111934797 | snp | G/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:594476 | CCAGGCTGGAGTGCA[G/T]TGGCGCCATCTTGGC | 57661 |
rs111939988 | snp | C/G | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:598736 | TGATGCCGGCCTTCC[C/G]GCATTGTTCCCCTCT | 57661 |
rs111980751 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589937 | GAGGGTGTCTGCAAA[C/T]GGGCACGGAGCGTGC | 57661 |
rs112055889 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:599287 | TGAGACAGAGTCTCG[C/T]TCTCCCAGGCTGGAG | 57661 |
rs112119506 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PHRF1 | GRCh38.p7 | 11:604663 | GGGATTACAGGCGTC[C/T]GCCACCAGGCCCAGC | 57661 |
rs112143693 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585267 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs112181236 | in-del | -/C | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590187 | GGGTGCTGCCGCACA[-/C]CCCTGGAGCTGGTCG | 57661 |
rs112378493 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585576 | CCAGCTTGAGGTAGT[A/C]GCCCTTTCCAGCTTG | 57661 |
rs112381778 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585303 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs112419341 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585221 | ACTGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs112464486 | in-del | -/C | 0.0644693 | 0.167566 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575410 | TCTACCGGGAGCCGG[-/C]CACTTCCCACACCTG | 57661 |
rs112472923 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:599079 | CTTGTCAGACACCCC[C/T]GGCGCTGGTGCGCGT | 57661 |
rs112481518 | snp | C/G | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590006 | TGTGGGGCTCAGCCT[C/G]AGAGAGTGTCTGTAA | 57661 |
rs112494810 | snp | C/T | 0.123105 | 0.215401 | upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576247 | GCCTGGACCAGCCCA[C/T]GGTCGCGGGTTAAAC | 57661 |
rs112646739 | snp | G/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585575 | TCCAGCTTGAGGTAG[G/T]AGCCCTTTCCAGCTT | 57661 |
rs112681023 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHRF1 | GRCh38.p7 | 11:583350 | TCAAAAAAAACAAAC[A/G]AAAAAACCCCACCAA | 57661 |
rs112735524 | snp | C/G | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575247 | TCAGTGAGCATTCTT[C/G]GGCAGTGCACAACCT | 57661 |
rs112770208 | snp | A/G | | | downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612284 | CGTTGCCTCCTGGAG[A/G]CAGGGTGCAGCAGTG | 57661 |
rs112771730 | snp | G/T | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:603729 | ACCATATTTAAGTTT[G/T]TTTTTTTTTTTTTTT | 57661 |
rs112776619 | snp | A/G | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:593097 | GTCCAGTTATGCTGC[A/G]CCTGCTGCTCTCCCT | 57661 |
rs112818794 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611923 | GGGGGGCATCACCAT[A/G]CCTGCCGTCGGGTTC | 57661 |
rs112855672 | snp | G/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:594698 | AACTCCTGGGCTCAA[G/T]TGATCCGCCCACCTC | 57661 |
rs112877118 | snp | A/C/G | 0.00639386 | 0.0561801 | missense | PHRF1 | GRCh38.p7 | 11:607356 | AGCCCCTGGTTCAAC[A/C/G]GCACCAACAAGCACA | 57661 |
rs112916079 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589849 | GAGAGAGTCTGCAAA[C/T]GGGCACGGAGCGTGC | 57661 |
rs112972906 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585336 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs112993401 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:589436 | CACCAAGAATTGCCA[A/G]GATAGCTTTGAAAAG | 57661 |
rs113060621 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:594609 | TGGGATTACAGGCAC[A/G]TGCCACCACACCTGG | 57661 |
rs113064640 | snp | A/C/G | 0.00223239 | 0.0333436 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611814 | GCCCGGGGAGCTGTC[A/C/G]GGAGTGGCGGGAATC | 57661 |
rs113069742 | snp | A/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585635 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs113096053 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612167 | TGGCCTCCCGCCAAC[A/C]GCTGCTGTGTACCTT | 57661 |
rs113172248 | snp | A/T | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585382 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs113201578 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:585857 | AGCTAATTTTTTGTA[C/T]ATTTATTTATTTATT | 57661 |
rs113207624 | snp | C/T | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585280 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs113221636 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | PHRF1 | GRCh38.p7 | 11:594481 | CTGGAGTGCAGTGGC[A/G]CCATCTTGGCTCACT | 57661 |
rs113269263 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590029 | GTCTGTAAACGGGCA[C/T]GGAGCGTGCGGGGCT | 57661 |
rs113299190 | snp | A/G | 0.0310518 | 0.120672 | utr-variant-3-prime, downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612176 | GCCAACAGCTGCTGT[A/G]TACCTTTGGCTCTGA | 57661 |
rs113330566 | in-del | -/AGAG | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:594273 | AGACCATGGCATGAT[-/AGAG]AGACCTGGTCCTGGT | 57661 |
rs113374870 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:590013 | CTCAGCCTCAGAGAG[A/T]GTCTGTAAACGGGCA | 57661 |
rs113403155 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | PHRF1 | GRCh38.p7 | 11:599779 | GGGTCCTGGGTCTCC[A/G]GAGGACTCGGCGTCT | 57661 |
rs113462066 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585395 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs113490019 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHRF1 | GRCh38.p7 | 11:585824 | TAGCTGGGACTATAG[A/G]CACCTGCCACCGCGT | 57661 |
rs113510345 | snp | A/G | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:594440 | ACTTATTTTTTTCAA[A/G]GCAGAGTCTTGGTCC | 57661 |
rs113525489 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PHRF1 | GRCh38.p7 | 11:598793 | GTTTATGGAAGCAGT[C/T]TTGTTATTTTTGCTG | 57661 |
rs113578318 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585372 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs113610080 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585543 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs113614874 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:581367 | TATCTCAGGGCTCAC[C/T]CTTCACGTGCTGTGG | 57661 |
rs113626448 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | PHRF1 | GRCh38.p7 | 11:589392 | GGGTGCTTGATGTGT[G/T]GTGAAGTCAACACAG | 57661 |
rs113691450 | snp | C/T | 0 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585602 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs113700134 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHRF1 | GRCh38.p7 | 11:582815 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTTTTTTC | 57661 |
rs113727061 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:589804 | GAGGGTGTCTGCAAA[C/T]GGGCACAGAGCGTGC | 57661 |
rs113779416 | snp | C/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585349 | GCTTGAGGTAGTAGC[C/T]CTTTCCAGCTTGAGG | 57661 |
rs113794548 | snp | A/G | 0.273318 | 0.24891 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576749 | GGCGCGCGCGCGCTG[A/G]GAGGCCCCGCCGAGA | 57661 |
rs113804454 | snp | A/C/T | 0.00119737 | 0.0244387 | synonymous-codon, missense | PHRF1 | GRCh38.p7 | 11:609720 | GAGGACAGAGCCCCC[A/C/T]GTGAGTAGTGCCCCG | 57661 |
rs113833477 | in-del | -/CTCC | 0.170733 | 0.237101 | intron-variant | PHRF1 | GRCh38.p7 | 11:606246 | AGCTGCGAGGTGGGG[-/CTCC]CTCCCTCCCTCCCTC | 57661 |
rs113889171 | snp | A/G | 0.0100208 | 0.0700714 | missense | PHRF1 | GRCh38.p7 | 11:607680 | GTGCCCCGGGAGCCC[A/G]GGGTGCACACGGGCA | 57661 |
rs113906292 | snp | A/C | 0.5 | 0 | missense | PHRF1 | GRCh38.p7 | 11:607827 | GCACATTCCAGCCAG[A/C]TCTCCAGCCCTGGCT | 57661 |
rs113948711 | snp | A/T | 0.5 | 0 | intron-variant | PHRF1 | GRCh38.p7 | 11:585405 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs114007857 | snp | C/G/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577238 | TGGAGCCCAGAAAGG[C/G/T]TAAGTAACTGGCCAG | 57661 |
rs114010389 | snp | A/G | 0.00108123 | 0.023226 | missense | PHRF1 | GRCh38.p7 | 11:591436 | AGTGCATTTGTATTC[A/G]AGCTCAATTTGGTGG | 57661 |
rs114013958 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PHRF1 | GRCh38.p7 | 11:595940 | TGTGCCCGGGGCAGT[C/T]GGCTTCTCTTCCTGC | 57661 |
rs114040080 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PHRF1 | GRCh38.p7 | 11:598288 | TGGCTGCCATTGTGG[C/G]CTGTGTTCTGGGCTC | 57661 |
rs114152632 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHRF1 | GRCh38.p7 | 11:599155 | TTAAGTCACTGTAGA[C/T]GCATGGACTCCTGCT | 57661 |
rs114206266 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | PHRF1 | GRCh38.p7 | 11:579354 | CTTTCAGATATGTTT[C/T]TCCAGGGCAGGGACT | 57661 |
rs114221314 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHRF1 | GRCh38.p7 | 11:594650 | TATTTTATGGAGAAA[C/T]GGGGTTTCACCATGT | 57661 |
rs114367277 | snp | A/G | 0.0047711 | 0.0486085 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608378 | AGCCCCACCCAGCCC[A/G]GACGTGCTGCAGGCT | 57661 |
rs114494824 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHRF1 | GRCh38.p7 | 11:586614 | GAGTTTGGTACAAAG[A/G]AGATAGCAGTGCACG | 57661 |
rs114519602 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PHRF1 | GRCh38.p7 | 11:588067 | GACCTCTGTACTCAG[A/G]GCTCAGCTCCGACAC | 57661 |
rs114595132 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHRF1 | GRCh38.p7 | 11:581769 | TTTTGTTTTATTTTT[A/G]ATGCAAACAACACAA | 57661 |
rs114608427 | snp | A/C/G | 0.00386396 | 0.0437848 | intron-variant | PHRF1 | GRCh38.p7 | 11:597349 | GCCGTTGGGGGAGGC[A/C/G]TGTGGCCTGTGAGTG | 57661 |
rs114641505 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PHRF1 | GRCh38.p7 | 11:595992 | TGTATGGCCCTAGCA[A/G]GGGCCACACAGCAGA | 57661 |
rs114687358 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | PHRF1 | GRCh38.p7 | 11:589794 | CTCAGCCTGAGAGGG[A/T]GTCTGCAAACGGGCA | 57661 |
rs114817139 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | PHRF1 | GRCh38.p7 | 11:586698 | GGTGTAGCCTCAGAA[C/G]CACTCCGAATTGGCC | 57661 |
rs114849320 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHRF1 | GRCh38.p7 | 11:593219 | TGGCTGTAAGCAGAT[A/G]CCCCCTTCCCCGTTA | 57661 |
rs114978447 | snp | G/T | 0.00832474 | 0.0639771 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609347 | CGAAAGCACAGACTC[G/T]TCCCCGGAGCGAGAC | 57661 |
rs114986234 | snp | A/G | 0.00632231 | 0.0558675 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608180 | CAAGCTCCGGGGTGC[A/G]GTGGCTGCCGAGGGG | 57661 |
rs115114670 | snp | A/G | 0.0356815 | 0.128715 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575832 | CTGGTAGCAGGCGAC[A/G]CCAGGACTCTTCTCC | 57661 |
rs115298815 | snp | A/G | 0.0329836 | 0.124112 | downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612430 | AGTCAAAGCTTGGCT[A/G]TGATGTGTGTGGTGA | 57661 |
rs115393484 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | PHRF1 | GRCh38.p7 | 11:589792 | GGCTCAGCCTGAGAG[A/G]GTGTCTGCAAACGGG | 57661 |
rs115691512 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHRF1 | GRCh38.p7 | 11:598879 | GGCCGAGTTGAGATC[A/G]GTGATTTCGCATCTT | 57661 |
rs115869213 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHRF1 | GRCh38.p7 | 11:586564 | CCTCTTCCCATGTGA[A/G]CTTGTGTTCTGTTTA | 57661 |
rs115920222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:579785 | CAGGCAGTAGTAAGA[C/T]TTGGCAGTTGACAGT | 57661 |
rs115977880 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PHRF1 | GRCh38.p7 | 11:594196 | TTTACCTGTGGCTGC[A/G]GCCACTCTGGGCATG | 57661 |
rs115984244 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PHRF1 | GRCh38.p7 | 11:604900 | TGACACTGCAATGCC[C/T]GAGAGCCTCTGGTAG | 57661 |
rs116024930 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589811 | TCTGCAAACGGGCAC[A/G]GAGCGTGCGGGGCTC | 57661 |
rs116085718 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | PHRF1 | GRCh38.p7 | 11:590107 | CTGAGAATGTGTGCA[A/C]ACGGGCACGGAGCGT | 57661 |
rs116136736 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:588306 | TCACCCAAAGTCTGG[C/T]TCTGGTACTTCCTGT | 57661 |
rs116220115 | snp | C/T | 0.078151 | 0.181571 | intron-variant | PHRF1 | GRCh38.p7 | 11:589639 | GCACACACACGATGC[C/T]GGACGGAGTCAAGAT | 57661 |
rs116254170 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:592873 | CTTTCCCCAAAAAAC[A/G]TTCTGAGGCTGCCCA | 57661 |
rs116284225 | snp | C/T | 0.00870305 | 0.0653895 | missense | PHRF1 | GRCh38.p7 | 11:609145 | AAGCACATGTCTCGC[C/T]GGAGGTGGCTACGGC | 57661 |
rs116371715 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHRF1 | GRCh38.p7 | 11:582504 | TGACCTCAAGTGAGC[C/T]GCTGTGCCTGGCCTG | 57661 |
rs116653428 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHRF1 | GRCh38.p7 | 11:594005 | TCTGAAGGGCAGGGC[C/T]GCTGCCTTGACTATC | 57661 |
rs116736285 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PHRF1 | GRCh38.p7 | 11:601479 | TGGTCCCGCTGTACC[A/G]GCTCCTTGGGCTCCG | 57661 |
rs116828268 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PHRF1 | GRCh38.p7 | 11:597074 | TTCTCACTGTCCACT[C/T]TGCGGTCCCCGGGGT | 57661 |
rs116858691 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHRF1 | GRCh38.p7 | 11:587190 | AGCGCAGCCTGGGCC[C/T]GCTTGCCTCCAGTGC | 57661 |
rs117067147 | snp | A/G | 3.73881e-05 | 0.0043235 | intron-variant | PHRF1 | GRCh38.p7 | 11:597048 | CTCCCGTCCCAAGGC[A/G]CACATGGGCCTTCTC | 57661 |
rs117211719 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:598715 | GCCTCTGGCATTGTG[C/T]CAGGGTGATGCCGGC | 57661 |
rs117454583 | snp | A/T | 0.00239304 | 0.0345079 | intron-variant | PHRF1 | GRCh38.p7 | 11:606629 | CACGGCCCCTTCCTC[A/T]GTGGGCTGCTGGTCC | 57661 |
rs117610358 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHRF1 | GRCh38.p7 | 11:594414 | CCTGTTAGCTTTTAT[C/T]TTACTCATTTACTTA | 57661 |
rs117611145 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHRF1 | GRCh38.p7 | 11:587161 | GGGCTGTGCATTGCC[A/G]ACCTGGTGTCCTGAG | 57661 |
rs117660271 | snp | A/G | 0.00960815 | 0.0686423 | synonymous-codon, intron-variant | PHRF1 | GRCh38.p7 | 11:582056 | CGAGGGGGCGTCTGA[A/G]GAGGAAGACCTGGAA | 57661 |
rs117818025 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PHRF1 | GRCh38.p7 | 11:599588 | TTAAGTGAATGCACT[C/T]GCTTTAGTGTGTAGT | 57661 |
rs117952887 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574696 | AAGAGAAGTTGGTGT[A/T]CACAGCCCCTGCGTG | 57661 |
rs118042921 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PHRF1 | GRCh38.p7 | 11:579736 | GAAAGGTTAATTACT[A/G]ATTTGGCAAAACTAC | 57661 |
rs118082193 | snp | C/G | 0.000228354 | 0.0106829 | missense | PHRF1 | GRCh38.p7 | 11:609591 | GCGAGTGGGAGGGTA[C/G]AGGAGGCAGCCCGGC | 57661 |
rs118136288 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHRF1 | GRCh38.p7 | 11:601145 | GACAGAGCAAGACTC[C/T]GTCTCAGAAAAAAAT | 57661 |
rs118187319 | snp | C/T | 0.0356815 | 0.128715 | downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612382 | TGGGAGTGGCTTTGG[C/T]GGCCACTGGCCTGTC | 57661 |
rs137873910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:599032 | TCCCTTAAAATTAAC[A/G]GGCCGCTCCTGGGGA | 57661 |
rs137970833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:589187 | TAAAATGCTGCTTAG[C/T]GAGATTATTGGATAC | 57661 |
rs138030319 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHRF1 | GRCh38.p7 | 11:603369 | ACAAAGTCTGGTTCT[A/G]TTACCCGGGCTGGAG | 57661 |
rs138142657 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHRF1 | GRCh38.p7 | 11:579280 | CCTGCTCTGTTATCT[C/T]TTAGGTGGTCTCTTT | 57661 |
rs138144082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:593847 | CAGACACCTCGCCGT[C/G]CCTCCTTTCTCACGA | 57661 |
rs138267517 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PHRF1 | GRCh38.p7 | 11:584514 | CCATGGACCTGGGGT[G/T]GGGAGAGGCTTCTGG | 57661 |
rs138357016 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PHRF1 | GRCh38.p7 | 11:603822 | TCACTGCAACCTCGG[C/T]CTCCCAAATAGCTGG | 57661 |
rs138408584 | snp | A/C/G | 0.00677811 | 0.0578226 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607394 | CCTTGCCTCTGCCGC[A/C/G]TCTAAGATCTCAAGC | 57661 |
rs138419215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:593225 | TAAGCAGATGCCCCC[C/T]TCCCCGTTAGCCTCC | 57661 |
rs138710315 | snp | A/G | 0.00171484 | 0.0292315 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608297 | TGAGGAGGATGGGGC[A/G]TCTTGCAGCACCTTC | 57661 |
rs138962305 | snp | A/G | 0.0130921 | 0.0798413 | downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612307 | CAGCAGTGGCAGCCT[A/G]AGGGCTGGCGACAGG | 57661 |
rs139042730 | snp | C/T | 0.000105176 | 0.00725101 | intron-variant | PHRF1 | GRCh38.p7 | 11:610791 | CTCCCACTTTCCCCA[C/T]GTTCCCATCTTACTT | 57661 |
rs139163146 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577168 | CTTAACTCTTGCAGT[C/G]CTCACAAGAGCCTCT | 57661 |
rs139303343 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | PHRF1 | GRCh38.p7 | 11:589643 | ACACACGATGCCGGA[C/T]GGAGTCAAGATCTCG | 57661 |
rs139356679 | snp | G/T | 0.00189218 | 0.0307003 | intron-variant | PHRF1 | GRCh38.p7 | 11:605557 | TGGGCTGGGGTTTCT[G/T]GGAGCTGGGAGTCAC | 57661 |
rs139365947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590517 | GGGAAGGGCCCGAAG[A/T]CCAGGGTGGGTACTC | 57661 |
rs139443706 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:586550 | ACACCGAGTCTGCTC[C/G]TCTTCCCATGTGAAC | 57661 |
rs139460704 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:581235 | GGCTTACTGGTGAGG[C/G]TTGTTCTGTGGGTGA | 57661 |
rs139638126 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PHRF1 | GRCh38.p7 | 11:591180 | CGCGTTCATGGAGCT[G/T]CTCTTTCCTCCCCGC | 57661 |
rs139741487 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHRF1 | GRCh38.p7 | 11:595570 | AGCTGGGCAGGTCTC[A/G]GCAGCCCTCCTTGTC | 57661 |
rs139793524 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PHRF1 | GRCh38.p7 | 11:585175 | ATTGCTTTTCCCACC[C/T]TGGTGTTTCCTGCTG | 57661 |
rs139846982 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PHRF1 | GRCh38.p7 | 11:606260 | GCTCCCTCCCTCCCT[C/G]CCTCTGGGAGGCCCC | 57661 |
rs140129115 | snp | C/G | 0.0232847 | 0.105357 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575402 | CCTTCAGCATCTACC[C/G]GGAGCCGGCACTTCC | 57661 |
rs140162417 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:579768 | TCTACAATCGCTGTT[G/T]CCAGGCAGTAGTAAG | 57661 |
rs140229568 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHRF1 | GRCh38.p7 | 11:596248 | AGACTCCCGAGCCTC[A/G]GCTGCTTGGAGGGGC | 57661 |
rs140451033 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PHRF1 | GRCh38.p7 | 11:611558 | GGCAGGCGAGGGAGC[C/G]CAGCTTTGGCCCTGG | 57661 |
rs140470055 | snp | C/T | 3.32734e-05 | 0.00407868 | downstream-variant-500B, missense | PHRF1, IRF7 | GRCh38.p7 | 11:612650 | AGACTGGGTTCTAGG[C/T]GGGCTGCTCCAGCTC | 57661 |
rs140512737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:588203 | TCCTCCTGTTCTGTT[A/T]CACTGAGTAGCTGAA | 57661 |
rs140802650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:602497 | GCCAGCCTGGCCAAC[A/T]TGGTGAAACCCCATC | 57661 |
rs140942386 | snp | A/G | 0.114387 | 0.210022 | intron-variant | PHRF1 | GRCh38.p7 | 11:583158 | ATTGTGGCTAACATG[A/G]TGAAACCCCGTCTCT | 57661 |
rs141010415 | snp | A/G/T | 0.000232156 | 0.0107719 | missense | PHRF1 | GRCh38.p7 | 11:587384 | CCAATCTGTCTCAAC[A/G/T]CATTCAGAGACCAGG | 57661 |
rs141336233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577864 | GCCAATGCATTGGTT[C/T]CCCTGAATTTGAAAA | 57661 |
rs141387654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:590425 | GTCCATGCTGCGGCT[C/T]CAATCCTGAGAAACC | 57661 |
rs141399439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:581782 | TTAATGCAAACAACA[C/T]AAATGTTGAACGAAA | 57661 |
rs141420909 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589281 | AAGAGCTTTTCTAAC[A/C]CAGCCGTGACTGAAG | 57661 |
rs141452520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:578377 | GGCCCGTGGAGTCTT[C/T]CCTCACCAGCTGTGG | 57661 |
rs141565712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:604963 | ATTGTTCCTGCTTGT[C/T]GGTCATCATGCCTGA | 57661 |
rs141828365 | snp | C/T | 3.3325e-05 | 0.00408184 | intron-variant | PHRF1 | GRCh38.p7 | 11:592712 | ACACGTGCCCTGCTG[C/T]GTGCAAGGCGGGCCA | 57661 |
rs141915736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:594705 | GGGCTCAATTGATCC[A/G]CCCACCTCGGCCTCC | 57661 |
rs141948484 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585726 | CGCTCTGTTGCCCAG[A/G]CTGGAGTGCAGCAGC | 57661 |
rs142110692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:592978 | GGTGGGACGTGTCCT[A/G]GTCCCGGCCTTTGTG | 57661 |
rs142159030 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:579823 | AGTTGACATTCTTCA[C/T]TGTTTTATAAGGCAT | 57661 |
rs142161594 | in-del | -/C | 0.0329836 | 0.124112 | intron-variant | PHRF1 | GRCh38.p7 | 11:605973 | GAGGTGGCCCCTCTG[-/C]CCCCCCACCCCGGCC | 57661 |
rs142177874 | snp | C/T | 0.00013614 | 0.00824933 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:587281 | GGATTCTGAAGACGA[C/T]GGGGAGACATTGCTG | 57661 |
rs142180184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:607001 | CAGTTGTGATAAAAA[A/T]TAAACCACTGACATT | 57661 |
rs142224276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:584125 | CCGTGTCCTTCCAGA[A/G]TTCGATGTTTAGCTC | 57661 |
rs142383152 | snp | C/T | 0.000373783 | 0.0136657 | missense | PHRF1 | GRCh38.p7 | 11:597398 | GGTTCTTCCCAGATG[C/T]GGGTCCCGTGAGTGA | 57661 |
rs142474495 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHRF1 | GRCh38.p7 | 11:611184 | CATGAGTGCAGGCCC[A/G]AGGTCAGCCAGCCAG | 57661 |
rs142555368 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | PHRF1 | GRCh38.p7 | 11:581092 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 57661 |
rs142772730 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHRF1 | GRCh38.p7 | 11:589113 | TGCACTCCAGCCCGG[C/T]GACAGAGCAAGACAC | 57661 |
rs142972371 | snp | C/T | 0.155656 | 0.231515 | intron-variant | PHRF1 | GRCh38.p7 | 11:609814 | CCGTGAGTAAGGCCC[C/T]GGCCTCCACCGAGGA | 57661 |
rs143047321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590169 | CCCCAGTCCCACCAT[A/G]GGGGGTGCTGCCGCA | 57661 |
rs143180015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577455 | GACTTCGGGTTTGGC[A/G]TAGTTGATCTCTCTC | 57661 |
rs143197172 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PHRF1 | GRCh38.p7 | 11:606359 | ACTCTCCCTGGCTCC[C/T]GCCTGCTGCGGGGCT | 57661 |
rs143260428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:610012 | GGGCAGAACAGGTCA[C/T]GGTCGGGGATCAGTG | 57661 |
rs143356597 | snp | A/G | 0.046775 | 0.145601 | intron-variant | PHRF1 | GRCh38.p7 | 11:588659 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 57661 |
rs143434497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:589477 | GCCTACTGGATATTA[C/T]GATTTATAAAACTAC | 57661 |
rs143500370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590148 | GCAGCAGGGCTCCTC[G/T]GGGAACCCCAGTCCC | 57661 |
rs143602567 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:606675 | GCACTCAGCCCATGT[C/G]TCAGTCACGGAAGAT | 57661 |
rs143687332 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:587628 | TTGCTTTGTGAGCAC[C/T]ATGGCTCTTGGGGGT | 57661 |
rs143852248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:604146 | GGTCCCCTGGGCTCT[C/T]CCTTTGCTTTGCGGG | 57661 |
rs143901631 | snp | C/T | 0.000786993 | 0.0198211 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607649 | CACACGGGCAGAGAG[C/T]GAGGCCAGCAGCAGG | 57661 |
rs143953206 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHRF1 | GRCh38.p7 | 11:584572 | GGAGGAGGTGGCTGG[A/G]CAGAGGCGGCAGGCC | 57661 |
rs144036793 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHRF1 | GRCh38.p7 | 11:601803 | CCTTGGCACCCTCGC[A/G]CGGTTATGGAGCAGG | 57661 |
rs144154176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:587005 | GCTTAGAGGAGCTGG[G/T]CTGGCACTCAGGACG | 57661 |
rs144218558 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:584931 | TTATTCGAGATGGGG[C/T]TTCACCATGTTGGCC | 57661 |
rs144437378 | snp | A/G | 0.000249254 | 0.0111609 | downstream-variant-500B, synonymous-codon | PHRF1, IRF7 | GRCh38.p7 | 11:612705 | ATAGAGGCTGTTGGC[A/G]CTGGACAGGCAGAGG | 57661 |
rs144439467 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PHRF1 | GRCh38.p7 | 11:611138 | GGGCGGTACGTCGCT[A/G]CTGTCTCGTCAGCAT | 57661 |
rs144534225 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHRF1 | GRCh38.p7 | 11:599700 | TGTGGCCATGTGCAT[C/T]ACTGTGTGTCGGTCG | 57661 |
rs144569915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:602720 | AACTGAGTTGCAGCC[A/G]TTGTTCAAGTGTTTG | 57661 |
rs144571139 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | PHRF1 | GRCh38.p7 | 11:589641 | ACACACACGATGCCG[C/G]ACGGAGTCAAGATCT | 57661 |
rs144630030 | in-del | -/GGACGCGCTCTG | 0.104868 | 0.20356 | cds-indel | PHRF1 | GRCh38.p7 | 11:608515 | GACGGACGCGCTCTG[-/GGACGCGCTCTG]AATCCAGGGACAGGA | 57661 |
rs144630408 | in-del | -/TG | | | intron-variant | PHRF1 | GRCh38.p7 | 11:602754 | AATCTTTTTTGGTTT[-/TG]TTTTTGTTTTTTTTG | 57661 |
rs144636218 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | PHRF1 | GRCh38.p7 | 11:586661 | TGAACTCGGAGCATC[-/T]TCCCTGCTCCCTGCT | 57661 |
rs144658894 | snp | C/G/T | 0.0331039 | 0.125034 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574324 | TGCTGCCTTCTCTCT[C/G/T]TGCTTCGGCTGCCTA | 57661 |
rs144841481 | snp | C/T | 5.82004e-05 | 0.00539415 | missense | PHRF1 | GRCh38.p7 | 11:609067 | GGGAGGCTTCCCCAG[C/T]GCCCCTTGCACAGGG | 57661 |
rs144882236 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577269 | CGCCGGCAGCCGGGG[A/G]TCCGCGCCAGCCCCG | 57661 |
rs144955824 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHRF1 | GRCh38.p7 | 11:583324 | CCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 57661 |
rs144980548 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHRF1 | GRCh38.p7 | 11:586611 | TTGGAGTTTGGTACA[A/G]AGAAGATAGCAGTGC | 57661 |
rs145110193 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:610851 | TGGGCGGAAGCTGGT[C/T]GCTGTGCCTCTGGAA | 57661 |
rs145216464 | snp | A/G | 0.00187596 | 0.030569 | intron-variant | PHRF1 | GRCh38.p7 | 11:591480 | AAGGTGAGTGTGGAC[A/G]CTGCCGTGGAGGCCC | 57661 |
rs145272389 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:598852 | CCATCTGGGCCTGGG[C/G]TTTTCTGTGGGGGCC | 57661 |
rs145655008 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHRF1 | GRCh38.p7 | 11:596387 | CAGTGGCTTGGTGTG[A/T]GGTGCAATGTTTGAA | 57661 |
rs145800608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:601358 | CACGTGAGCCCAGGA[A/G]TTGGAGGCTGCTGTG | 57661 |
rs145990638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590849 | GCTGGGGTTACAGGT[A/G]TGCGCCACCACACCT | 57661 |
rs146070268 | in-del | -/GA | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589579 | GGACACACTCGGGGG[-/GA]GGCAGGAGGCGCCTG | 57661 |
rs146115442 | snp | C/T | 0.144632 | 0.226711 | intron-variant | PHRF1 | GRCh38.p7 | 11:609819 | AGTAAGGCCCCGGCC[C/T]CCACCGAGGACAGAG | 57661 |
rs146135948 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612265 | TCGAGTTTGCACTCA[A/G]CACCGTTGCCTCCTG | 57661 |
rs146151880 | in-del | -/TT | 0.0111196 | 0.0737302 | intron-variant | PHRF1 | GRCh38.p7 | 11:596580 | AACCGCAGGTCTTCC[-/TT]TTCTTGGTTTTGGAA | 57661 |
rs146355616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:580205 | CTTTCCTCCGAGAGT[C/T]GCCTGGGAAACAAGG | 57661 |
rs146375049 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHRF1 | GRCh38.p7 | 11:584458 | TGGGGGACAGGGTCA[C/T]AGACACTGAGAGCTG | 57661 |
rs146438334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:601876 | GCTGATGGAAATGAA[C/T]ATTTCTGTAGCACAG | 57661 |
rs146455916 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:606100 | TTTCGCCACAAGAAC[A/G]AAAAATTAACCAAAA | 57661 |
rs146631537 | in-del | -/GGGG | | | intron-variant | PHRF1 | GRCh38.p7 | 11:594065 | CAGTGCTTATTGGCT[-/GGGG]GTTGATTACTGACTT | 57661 |
rs146801817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:587903 | GACTGTCCTTAAAAC[A/G]GGTGAATAGAGTTTA | 57661 |
rs146818931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:589710 | ATGGGTAGCTCTGTG[A/G]TAAGAAAAGAGAAGG | 57661 |
rs146958536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:589184 | TGTTAAAATGCTGCT[C/T]AGCGAGATTATTGGA | 57661 |
rs147237414 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHRF1 | GRCh38.p7 | 11:604158 | TCTCCCTTTGCTTTG[C/T]GGGGTGCCCTGAGCC | 57661 |
rs147344307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:585158 | TGGGAGCTTTCGTTC[C/T]CATTGCTTTTCCCAC | 57661 |
rs147361109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:586415 | TTCTGGGTGTGTCTT[C/T]CCCTTTGCCAGATAA | 57661 |
rs147451758 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:596118 | TAGTTAAGTTCAGTT[G/T]AATTCAGGCTCAATT | 57661 |
rs147468612 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | PHRF1 | GRCh38.p7 | 11:600222 | GCTCATTTTCTGTGT[C/G]TCTCCCCGATAGGAA | 57661 |
rs147716183 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:592929 | CAAAAAAGAAAACAG[C/G]CGGACAGGAGGCTGT | 57661 |
rs147732257 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:596833 | AGACTTGGGTGCCAT[C/T]GGAGGCCTGCTTTGT | 57661 |
rs147819611 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHRF1 | GRCh38.p7 | 11:611145 | ACGTCGCTGCTGTCT[C/T]GTCAGCATGGACTTT | 57661 |
rs147836092 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577727 | AGTTGAGGTGTTGGA[C/T]TTGGCTGCAGGCTTG | 57661 |
rs147961370 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PHRF1 | GRCh38.p7 | 11:592250 | GAGGCAGATCTTGCT[C/T]TTCCGTGGCAGTCCA | 57661 |
rs148101702 | snp | C/T | 0.108755 | 0.206276 | intron-variant | PHRF1 | GRCh38.p7 | 11:583156 | CCATTGTGGCTAACA[C/T]GGTGAAACCCCGTCT | 57661 |
rs148191792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:590316 | CCCACACGAAGACAC[A/G]TCCATCGATGTTCAC | 57661 |
rs148312667 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHRF1 | GRCh38.p7 | 11:611513 | CCGCCGTCTGTCTGC[A/G]TGCTGCACCTAGGGC | 57661 |
rs148332379 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHRF1 | GRCh38.p7 | 11:599711 | GCATCACTGTGTGTC[A/G]GTCGTGCTGGTCCTG | 57661 |
rs148437607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:601745 | TCCTGCTGGCCACAG[C/T]ACCCTCGCGTGGTTA | 57661 |
rs148575043 | snp | C/G | 0.00303102 | 0.0388114 | missense | PHRF1 | GRCh38.p7 | 11:609081 | GCGCCCCTTGCACAG[C/G]GGGAGCCAGGGCGGG | 57661 |
rs148590891 | snp | C/T | 0.031825 | 0.122064 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574384 | CGTGACTTGCTTCAC[C/T]TTATCACTTAGAAGA | 57661 |
rs148681741 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:587172 | TGCCGACCTGGTGTC[C/T]TGAGCGCAGCCTGGG | 57661 |
rs148804283 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:604825 | TTACTGTCAGTCATC[A/G]GTTGAATTTTTTGTT | 57661 |
rs148825912 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:593243 | CCCGTTAGCCTCCTG[A/C/T]GAGGGGCTTTCCCTG | 57661 |
rs148913741 | snp | C/T | 1.83048e-05 | 0.00302524 | intron-variant | PHRF1 | GRCh38.p7 | 11:606609 | CGGGTGAGTGCCTTC[C/T]CTGCCACGGCCCCTT | 57661 |
rs149443419 | snp | A/G | 0.0754912 | 0.179016 | missense | PHRF1 | GRCh38.p7 | 11:608593 | GCCCCAGGAGGCAGC[A/G]GTCCAAGGCCAAGAG | 57661 |
rs149495935 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHRF1 | GRCh38.p7 | 11:584516 | ATGGACCTGGGGTGG[A/G]GAGAGGCTTCTGGAG | 57661 |
rs149653232 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:579450 | TGGGGTCTGTTGTCA[C/G]GGTGGTCACAGCTAT | 57661 |
rs149778022 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | PHRF1 | GRCh38.p7 | 11:596035 | GGTGCAGGACTCTTG[A/G]GAGAATGGGTTTACT | 57661 |
rs149830497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:601309 | TGGTGCCTACCTGTA[G/T]TTCCAGCTGCTTGGG | 57661 |
rs149868322 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PHRF1 | GRCh38.p7 | 11:610840 | GGCTGAGTTTATGGG[C/T]GGAAGCTGGTCGCTG | 57661 |
rs149881784 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577139 | GCCTGTGTGGCTGGC[-/G]GGTTTTCCTATTCCT | 57661 |
rs150005519 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHRF1 | GRCh38.p7 | 11:591193 | CTGCTCTTTCCTCCC[C/T]GCTAGGGCTGGCAGC | 57661 |
rs150074788 | in-del | -/CCCCCC | | | intron-variant | PHRF1 | GRCh38.p7 | 11:579953 | CAGCAGTGGCGCTGA[-/CCCCCC]CAGCCACTTTCCCCC | 57661 |
rs150114009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:593201 | ATCCCTGCTTTGTGT[C/T]GTTGGCTGTAAGCAG | 57661 |
rs150201351 | snp | A/G | 0.00557141 | 0.0524849 | missense | PHRF1 | GRCh38.p7 | 11:608248 | AGGGCCTGGCTGCCC[A/G]GCTGCGGAGGCCATC | 57661 |
rs150359061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:603228 | GCCCGGCTAGTTTTT[A/G]TATTTTTCGTAGACA | 57661 |
rs150393275 | snp | A/G | 0.00112716 | 0.023713 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:611693 | CAACCTGGTGAAGGC[A/G]TACGTGGACAAGTAC | 57661 |
rs150409727 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHRF1 | GRCh38.p7 | 11:579278 | GCCCTGCTCTGTTAT[C/T]TCTTAGGTGGTCTCT | 57661 |
rs150479813 | in-del | -/TTTCCCCCCAGCCCTGCT | | | intron-variant | PHRF1 | GRCh38.p7 | 11:579253 | CCCCCAGCCCTGCTC[-/TTTCCCCCCAGCCCTGCT]CTCCCCCCAGCCCTG | 57661 |
rs150502157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:589554 | GTTTTGCAGGGGCTT[A/G]GAAGAGGCCTGGACA | 57661 |
rs150641410 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PHRF1 | GRCh38.p7 | 11:595184 | AAAAATTGGCCGGGC[C/G]TGGTGGTTCACACCT | 57661 |
rs150657453 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:585768 | TCACTGCAAGCTCTG[C/T]GTCCCAGGTTCACGC | 57661 |
rs150731199 | snp | C/T | 1.87668e-05 | 0.00306318 | missense | PHRF1 | GRCh38.p7 | 11:610526 | CCGGCCTGCCGCCTG[C/T]CCCGGCCCAGCCCTC | 57661 |
rs150799342 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHRF1 | GRCh38.p7 | 11:590513 | GAGAGGGAAGGGCCC[A/G]AAGACCAGGGTGGGT | 57661 |
rs150933146 | in-del | -/CTC | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:603558 | CAAGCTGGTCTTGAA[-/CTC]CTAGGCTCAAATGAT | 57661 |
rs150941591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:581213 | TGTAAATGTGAATCA[C/T]GTGTAAGGCTTACTG | 57661 |
rs151190592 | snp | A/G | 0.0022203 | 0.0332449 | missense | PHRF1 | GRCh38.p7 | 11:587372 | GCAGAGAGCTGCCCA[A/G]TCTGTCTCAACGCAT | 57661 |
rs180943343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:583264 | GAATTGCTGGAACCC[A/G]GGAGTCGGAGGTTGC | 57661 |
rs180963984 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | PHRF1, IRF7 | GRCh38.p7 | 11:612145 | GCGTCCTTGATAAAT[C/G]TCTAGGTGGCCTCCC | 57661 |
rs180970745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:596680 | CCTCCCCGCTGTGAC[C/T]TCACCTGGCCTTCCC | 57661 |
rs181011093 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588617 | CTCCCAACCTCAGGT[A/G]ATCCACCCGTCTCGG | 57661 |
rs181051292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577666 | CAATTTTGAGTTCTC[C/T]TAGCTGATACAGCAG | 57661 |
rs181125236 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:579948 | TCCAGACAGCAGTGG[C/T]GCTGACAGCCACTTT | 57661 |
rs181245966 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:586011 | GGATTACAGGCACAC[A/G]CCACCACACCCGGCT | 57661 |
rs181305543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:600601 | TTTGGGAGGCTGAGG[C/T]GGGTGTGTCACCTGA | 57661 |
rs181353870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:578294 | ACTTTTGTGTGATAT[C/T]GAGGAAGGATGTTGT | 57661 |
rs181354079 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PHRF1 | GRCh38.p7 | 11:589029 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 57661 |
rs181477137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:603819 | AGCTCACTGCAACCT[C/T]GGCCTCCCAAATAGC | 57661 |
rs181682848 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574348 | CTGCCTAAGAGGGAA[A/G]GGCCCCCTGTCCTAT | 57661 |
rs181690520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:580208 | TCCTCCGAGAGTCGC[A/C]TGGGAAACAAGGTCA | 57661 |
rs181851887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:601148 | AGAGCAAGACTCCGT[C/G]TCAGAAAAAAATTTG | 57661 |
rs181892127 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:589276 | ATTTAAAGAGCTTTT[C/G]TAACACAGCCGTGAC | 57661 |
rs181895633 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:604359 | ACGCCTGCCTTCAGG[C/T]GATGAAGTCCCAGCC | 57661 |
rs181899851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:578910 | AGTGGCATGTAGTGG[C/T]GCGATCTCAGCTCAC | 57661 |
rs181915117 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:585014 | AAGTGCTGGGATGAC[A/T]GGCATGAGCCACCGC | 57661 |
rs181937777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:583167 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 57661 |
rs182129445 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:586110 | AGGTGATCCACCTGC[A/C/G]TCAGCCTCCCAAAGT | 57661 |
rs182144037 | snp | A/G/T | 0.00762544 | 0.0612799 | missense | PHRF1 | GRCh38.p7 | 11:598481 | ACGCCGCGCACTCCC[A/G/T]CCCGACGGAAGAGGA | 57661 |
rs182150991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:584117 | TGTGTTGGCCGTGTC[C/T]TTCCAGAGTTCGATG | 57661 |
rs182207558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:592754 | GATGCAGAGCCTCTT[C/T]GCTCTGTGAAGTCTG | 57661 |
rs182362829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:595978 | TCTCCTGTCTTTCTT[A/G]TATGGCCCTAGCAAG | 57661 |
rs182417771 | snp | C/T | 0.00124827 | 0.0249514 | missense | PHRF1 | GRCh38.p7 | 11:608871 | AGGCACAAGCATCAG[C/T]GGGAACGCAGCCACG | 57661 |
rs182435474 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHRF1 | GRCh38.p7 | 11:604718 | TGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT | 57661 |
rs182471981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:580668 | GCCGTTTTGTTCGTA[C/T]ATGGTGTTGCGATTC | 57661 |
rs182484268 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PHRF1 | GRCh38.p7 | 11:580813 | CCTGCCTCAGCTTCC[C/G]GAGTAGCTGGGATTA | 57661 |
rs182519010 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHRF1 | GRCh38.p7 | 11:593572 | TGTTAGCCACATACC[C/G]AGGCCTCTGCTCCAC | 57661 |
rs182522052 | snp | C/T | 3.38949e-05 | 0.00411659 | missense | PHRF1 | GRCh38.p7 | 11:609366 | CCGGAGCGAGACTTC[C/T]CACTGAAGCCTGCGT | 57661 |
rs182565389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590121 | AAACGGGCACGGAGC[A/G]TGCAGGGTTCAGCAG | 57661 |
rs182571688 | snp | G/T | 8.35261e-05 | 0.0064619 | missense | PHRF1 | GRCh38.p7 | 11:605209 | TCAGTGTTGAAGCCA[G/T]TGGAGCCCTCTTTGG | 57661 |
rs182714224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:579017 | GCTCATTTTTTCTAT[G/T]TTAGTAGAGATGGGG | 57661 |
rs182774944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:594117 | TGCTTAAAAAGAAAA[A/G]AAAAGGTGGAGGGGT | 57661 |
rs182971394 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:586922 | GAAATGAACCTGATG[G/T]TCTCTGGGACCTGTG | 57661 |
rs182984730 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHRF1 | GRCh38.p7 | 11:589619 | TCAGCTGGGGGCTGC[C/T]CACAGCACACACACG | 57661 |
rs183021335 | snp | C/T | 0.000108052 | 0.00734943 | intron-variant | PHRF1 | GRCh38.p7 | 11:597037 | TAAGGACACTGCTCC[C/T]GTCCCAAGGCGCACA | 57661 |
rs183157550 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:605915 | CCTGTGTCAGAGGCC[A/G]CGGCCTGCCTGTGAG | 57661 |
rs183188872 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:602392 | AATATGTAAAAACTT[C/G]AATTACGGCCGAGCG | 57661 |
rs183266269 | snp | A/C | 0.00716266 | 0.059414 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575423 | CGGCACTTCCCACAC[A/C]TGCGCAGACCCACCC | 57661 |
rs183291538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:583364 | CAAAAAAACCCCACC[A/G]AAATTAGCCGGGCGT | 57661 |
rs183374737 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:586629 | AAGATAGCAGTGCAC[A/G/T]TATGGGCTCTGCCGT | 57661 |
rs183376034 | snp | A/G | 3.49004e-05 | 0.0041772 | intron-variant | PHRF1 | GRCh38.p7 | 11:601743 | TCTCCTGCTGGCCAC[A/G]GCACCCTCGCGTGGT | 57661 |
rs183390497 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574408 | TAGAAGATTCACCCT[C/G]CTTACCCTGCCCCCT | 57661 |
rs183470068 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:585095 | AACTGGTGGGAAACA[C/T]GTTGAGGAGGGAGTT | 57661 |
rs183474462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:600553 | AAAATCTTTGACGCC[A/G]GGCACAGTGGCTCGC | 57661 |
rs183571614 | snp | C/T | 1.77985e-05 | 0.00298311 | missense | PHRF1 | GRCh38.p7 | 11:581591 | GTCGGCCCTGCGGAC[C/T]CGGCAGGTGACTTTG | 57661 |
rs183851954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:583432 | TGAGGTTGGAGGATC[A/G]CTTGAGCCCAAGAGG | 57661 |
rs183929453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:594715 | GATCCGCCCACCTCG[G/T]CCTCCCAAAGTGCTG | 57661 |
rs184073754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:595008 | ATTTGCAGTCTGCCA[A/G]ATTTTCAGTTAAGTC | 57661 |
rs184089481 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:582595 | AGTGGCGCGATCTCG[A/G]CTCACTGCAAGCTCT | 57661 |
rs184090243 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHRF1 | GRCh38.p7 | 11:610450 | TCACAGCTCCTGGGC[A/G]CAGAGCTGCTAGCTG | 57661 |
rs184097568 | snp | C/T | 0.00131911 | 0.0256479 | intron-variant | PHRF1 | GRCh38.p7 | 11:582126 | TGTGTTTCCTCTTGT[C/T]GTGATGGGGACAGCC | 57661 |
rs184108923 | snp | C/T | 5.04698e-05 | 0.00502318 | intron-variant | PHRF1 | GRCh38.p7 | 11:610945 | GCATCACACACATGT[C/T]CCCTCTAGTACATGA | 57661 |
rs184181499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:606850 | GCCCCTGGTTAATAT[C/T]GTGTCCTGATGGCCT | 57661 |
rs184206149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:579751 | AATTTGGCAAAACTA[C/T]TTCTACAATCGCTGT | 57661 |
rs184215929 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHRF1 | GRCh38.p7 | 11:587885 | ATAACTGGCATCAAA[A/G]GAGACTGTCCTTAAA | 57661 |
rs184310274 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PHRF1 | GRCh38.p7 | 11:591980 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCACTGCA | 57661 |
rs184327851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:580166 | TGCCTCGCTGGATTC[C/T]TGACTCACTCTCCTA | 57661 |
rs184353006 | snp | A/G | 0.000447603 | 0.0149533 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:591416 | AGTTGATCGAACTCT[A/G]TTTAAGTGCATTTGT | 57661 |
rs184360268 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHRF1 | GRCh38.p7 | 11:611256 | GGGGTCAAGCCTGTT[A/C]GCCTGTGGCTGCCCC | 57661 |
rs184621366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:584857 | ATTCTCCTGCCTCAG[C/T]CTCTCGAGTAGCTCG | 57661 |
rs184623036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590806 | CCTCTCGGGTTCAAA[C/T]GATTCTCCTGCCTCA | 57661 |
rs184696554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:588756 | GAGGAACAAGATACA[A/G]TGTTTGCTATGTATT | 57661 |
rs184732075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577492 | CATCCGGTTTTCTTT[C/T]TTATTGGAAGAATGT | 57661 |
rs184800096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:577886 | ATTTGAAAAGAGAGA[A/G]AAATAGCCTTTCCAG | 57661 |
rs184804132 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:598851 | GCCATCTGGGCCTGG[G/T]CTTTTCTGTGGGGGC | 57661 |
rs184814950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:603620 | GATTACAGGTGTGAG[C/T]GCCAAGTCTGCTGCA | 57661 |
rs184847958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:588138 | GCAGCCCGTGCTGTC[C/T]CCGGCTCTCTTCAGG | 57661 |
rs184851891 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:603191 | TTCCTGAGTAGCTGG[A/G]ACTACAGGCATAGCC | 57661 |
rs184912249 | snp | A/C | 0.030665 | 0.119967 | intron-variant | PHRF1 | GRCh38.p7 | 11:584767 | TTTGAGACCGAGTTT[A/C]ACTCTTGTTGCCCAG | 57661 |
rs185053145 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PHRF1 | GRCh38.p7 | 11:582927 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG | 57661 |
rs185068682 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHRF1 | GRCh38.p7 | 11:602893 | TCAGCCTCCTGAGTC[A/G]CTGGGATTATAGGCG | 57661 |
rs185149596 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:596712 | CATCTAAGGACACCA[A/G]TCCTATAACCTTAAA | 57661 |
rs185164532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:595496 | GTCAGATCTGAGCAC[C/T]TTCAGCTGCAGGGCC | 57661 |
rs185400383 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHRF1 | GRCh38.p7 | 11:583270 | CTGGAACCCGGGAGT[C/T]GGAGGTTGCAGTGAG | 57661 |
rs185586226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:593744 | CCTTGCAGTGCGCTC[C/T]GCCGGCCCTTCCAGG | 57661 |
rs185626939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:599832 | GGGCTCCGGGGGTCT[C/T]GGCGTCTGTGGGTCT | 57661 |
rs185645961 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:580837 | GGGATTACAGGCGCC[C/G]GCCACCACGCCTGGC | 57661 |
rs185665202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:579421 | AGGTGTTGGAGCAGG[C/T]GTCCTGGAAGATGTG | 57661 |
rs185727418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:610398 | CAGTGGCCTGGCACC[C/T]GTGCCACACACACCA | 57661 |
rs185803201 | snp | A/G | 0.000147474 | 0.00858577 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608984 | GGCACGGGAGCACAG[A/G]CGGCCTCGGTCCCGT | 57661 |
rs185893637 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:592808 | TCACCACCCTCAGCA[A/G]CGCGGTTCAGTCCTG | 57661 |
rs185908654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:604107 | CCAGGTGTTGGATAA[A/G]GACCTGCTATTTCCC | 57661 |
rs185916718 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:589114 | GCACTCCAGCCCGGC[A/G]ACAGAGCAAGACACT | 57661 |
rs185917857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:578348 | TCCTGCTGCTGTGGT[A/G]GAGGAGTGTAAGAGG | 57661 |
rs186145161 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHRF1 | GRCh38.p7 | 11:601470 | CGGTGCGTGTGGTCC[C/T]GCTGTACCGGCTCCT | 57661 |
rs186155513 | snp | C/T | 0.000428556 | 0.014632 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608678 | AGCCAAGGACAAGAG[C/T]AGGGAGCACAGGCGG | 57661 |
rs186161741 | snp | A/C | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574354 | AAGAGGGAAGGGCCC[A/C]CTGTCCTATGATCAC | 57661 |
rs186165486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:586245 | GATCTGCCCACCTCA[C/G]CCTCCCAAAGATGCC | 57661 |
rs186174505 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHRF1 | GRCh38.p7 | 11:604813 | CATCAAGGGGTTTTA[C/T]TGTCAGTCATCAGTT | 57661 |
rs186520739 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHRF1 | GRCh38.p7 | 11:600906 | GGGAGGCAGAGATTG[C/T]AGTGAGCTGAGATCA | 57661 |
rs186527406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:604365 | GCCTTCAGGCGATGA[A/C]GTCCCAGCCACAGCG | 57661 |
rs186582196 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:583382 | ATTAGCCGGGCGTGG[A/T]GGTGCGTGCCTGTAA | 57661 |
rs186628687 | snp | C/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:586661 | TTGAACTCGGAGCAT[C/G]TCCCTGCTCCCTGCT | 57661 |
rs186631263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:602300 | GGTGGTGTGTCATTC[A/G]TGTGCATGTTTGTGA | 57661 |
rs186754253 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PHRF1 | GRCh38.p7 | 11:586050 | ATTTTTTGTAGAGAC[A/G]GGGTTTCACCATGTT | 57661 |
rs186768427 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:582505 | GACCTCAAGTGAGCC[A/G]CTGTGCCTGGCCTGT | 57661 |
rs186820466 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:597075 | TCTCACTGTCCACTC[G/T]GCGGTCCCCGGGGTT | 57661 |
rs186876977 | snp | G/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:598797 | ATGGAAGCAGTCTTG[G/T]TATTTTTGCTGTAAA | 57661 |
rs186885980 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:584129 | GTCCTTCCAGAGTTC[A/G]ATGTTTAGCTCTGCA | 57661 |
rs187132299 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PHRF1 | GRCh38.p7 | 11:592136 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 57661 |
rs187331752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:580603 | CGTGTCACTGAGGCC[A/C]CTCTTGTGCCCAGCT | 57661 |
rs187341009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590335 | ATCGATGTTCACCAC[A/G]GGGGAATGGACACGT | 57661 |
rs187343915 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:605381 | GCCCCGAGGTGCATG[C/T]GGAGGCGTTAGGTTT | 57661 |
rs187397295 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHRF1 | GRCh38.p7 | 11:602920 | GGCGTGTGCCACCAC[A/G]CCCAGCTAATTTTTG | 57661 |
rs187412799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:578949 | CCGCCTGCCAGGTTC[A/C]AGCAATTCTCCTCCG | 57661 |
rs187446135 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:587961 | TCAAAATGAACTTTT[A/T]GAAGCAGTCAGCTCC | 57661 |
rs187449581 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576953 | GGCGGACGTCCTGGG[C/T]TTGCGAGGACGCGGC | 57661 |
rs187562964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:610826 | ACTAAAGTTGTTGGG[G/T]CTGAGTTTATGGGCG | 57661 |
rs187630163 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PHRF1 | GRCh38.p7 | 11:583168 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57661 |
rs187646263 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | PHRF1 | GRCh38.p7 | 11:589659 | GGAGTCAAGATCTCG[A/G]ACTAGAAAGCAAAGC | 57661 |
rs187670695 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611930 | ATCACCATGCCTGCC[A/G]TCGGGTTCCTGCGCT | 57661 |
rs187727522 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574421 | CTCCTTACCCTGCCC[C/G]CTTGTCTTGTATGCA | 57661 |
rs187823420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:594914 | CAACGCAAGTACATA[A/G]AAACCCTGGTGGATC | 57661 |
rs187884370 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHRF1 | GRCh38.p7 | 11:606089 | CAGTTCTTTTGTTTC[A/G]CCACAAGAACAAAAA | 57661 |
rs187922810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:579052 | ACTGTGTTGCCTAGG[C/T]TGGTCTTGAACTACG | 57661 |
rs188015085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:583546 | TTCTCAGCTCACTTA[C/G]AATTGGCTGATGGTT | 57661 |
rs188067748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:596344 | TTAAAACATAGTTTC[C/T]TTTCAGCAAAGAAAC | 57661 |
rs188096569 | snp | A/C | 0.0228947 | 0.104514 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:575571 | TCGGGATCCCCGGAG[A/C]CTCCCCTGGTGCGCT | 57661 |
rs188116799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:602434 | ACCTGTGATCCCACC[A/G]CTTTGGGGGGCTGAG | 57661 |
rs188134283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:603216 | ATAGCCCACCGTGCC[C/T]GGCTAGTTTTTGTAT | 57661 |
rs188141213 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHRF1 | GRCh38.p7 | 11:583223 | ACGCGCCTGTAATCC[C/T]AGCTACTTGGGAGGC | 57661 |
rs188198883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:600558 | CTTTGACGCCGGGCA[C/T]AGTGGCTCGCACCTG | 57661 |
rs188373855 | snp | C/T | 0.000132661 | 0.00814328 | missense | PHRF1 | GRCh38.p7 | 11:587385 | CAATCTGTCTCAACG[C/T]ATTCAGAGACCAGGC | 57661 |
rs188474772 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:594422 | CTTTTATTTTACTCA[A/T]TTACTTATTTTTTTC | 57661 |
rs188547907 | snp | C/T | 0.000164193 | 0.00905923 | intron-variant | PHRF1 | GRCh38.p7 | 11:611126 | GCTCGGGGTCACGGG[C/T]GGTACGTCGCTGCTG | 57661 |
rs188651933 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:598874 | GTGGGGGCCGAGTTG[A/C]GATCAGTGATTTCGC | 57661 |
rs188736063 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:609808 | AGCCCCCCGTGAGTA[A/G]GGCCCCGGCCTCCAC | 57661 |
rs188752500 | snp | C/T | 0.00119056 | 0.0243693 | intron-variant | PHRF1 | GRCh38.p7 | 11:581623 | TGAGCTGCCTAGCGC[C/T]GGGTAGGGGCGTCCC | 57661 |
rs188799981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:595093 | CACAGTAGGCCGAGG[C/T]GGGTGGATCACCTGA | 57661 |
rs188820147 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PHRF1 | GRCh38.p7 | 11:582803 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 57661 |
rs188875184 | snp | A/G | | | missense | PHRF1 | GRCh38.p7 | 11:597445 | CTCTTGGCTGATGTG[A/G]TGCCCACCACCAGCA | 57661 |
rs188879557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:579439 | CCTGGAAGATGTGGG[A/G]TCTGTTGTCAGGGTG | 57661 |
rs188990843 | snp | A/G | 0.000310174 | 0.0124495 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608150 | ACCCCCTCTCGGACC[A/G]TCCTCCGCCATGTCC | 57661 |
rs189049336 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:592080 | GCCACCACGCCCGGC[A/T]AATTTTTTGTATTTT | 57661 |
rs189061540 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHRF1 | GRCh38.p7 | 11:580199 | ACAGGCCTTTCCTCC[A/G]AGAGTCGCCTGGGAA | 57661 |
rs189094654 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611982 | TGTTGCTCACAGTTG[A/G]AAACTGGACACTTTT | 57661 |
rs189162583 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHRF1 | GRCh38.p7 | 11:588459 | ATCTTGGCTCACCAC[A/G]ACCTCCACCTTCCGG | 57661 |
rs189192286 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:591811 | GAGTGCAGTAGCACA[A/G]TCACAGCTTACTACA | 57661 |
rs189195699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:600084 | AGTCTCAAGCAGTCC[A/G]CCTGCCTCGGCCTCC | 57661 |
rs189205538 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:590964 | TGCCTCGGCCTCCCA[A/T]AGTGCTGGGATTACA | 57661 |
rs189408818 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577502 | TCTTTCTTATTGGAA[A/C/G]AATGTTAAGTCAGAG | 57661 |
rs189424371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:603675 | ATTATTGTTTATTTC[C/T]TAGTAAATATAAACT | 57661 |
rs189440616 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:578230 | CCAGAGGGTACCTGC[A/G]GAGGCTTCCTGGGTT | 57661 |
rs189455806 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:584999 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATGACA | 57661 |
rs189466293 | snp | C/T | 0.000254145 | 0.0112698 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607154 | CCGAGCACTGCCCTC[C/T]GGGAGCCCGGCCCAA | 57661 |
rs189478863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:579855 | ATCTTAGAATCTAGG[G/T]TTTTGCACTGTCTTG | 57661 |
rs189719087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:589020 | ACGTACCTGTAGTCC[C/T]AGCTACTCGGGAGGC | 57661 |
rs189748488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:580776 | TCACTGCAACCTCCG[C/T]CTCTCAGGTGCAAGC | 57661 |
rs189774430 | snp | C/T | 0.00116559 | 0.024113 | intron-variant | PHRF1 | GRCh38.p7 | 11:598368 | CACCACCCCTTTGCC[C/T]GTAGCACACACCAGG | 57661 |
rs189938662 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PHRF1 | GRCh38.p7 | 11:584790 | TTGCCCAGGCTGGAG[C/T]GTAGTGGCGCAATCT | 57661 |
rs189966372 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHRF1 | GRCh38.p7 | 11:583293 | GCAGTGAGCCAAGAT[C/T]GCCACTGCACTCCAG | 57661 |
rs189993624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:579175 | TTCTATGTGAAATTC[A/G]TCATCAAATGAGGAT | 57661 |
rs189994832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:595931 | GGCGTGTCGTGTGCC[C/T]GGGGCAGTCGGCTTC | 57661 |
rs190009721 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:596740 | AAAGGTTCCATGTCT[A/G]TCTGCTGTCACATTG | 57661 |
rs190244687 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHRF1 | GRCh38.p7 | 11:583111 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCAGGAGG | 57661 |
rs190254729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:580628 | CCAGCTGATAAAGCC[C/T]GGCTCTGCCTCAGCT | 57661 |
rs190277395 | snp | A/G | 0.000232752 | 0.0107853 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608786 | GAGTAGGAAGAAGAA[A/G]AAAAGGAGATCAGCG | 57661 |
rs190286770 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHRF1 | GRCh38.p7 | 11:611476 | ACAGGACGGGGGTCT[C/T]ACATAGGTGGGGCGG | 57661 |
rs190403153 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHRF1 | GRCh38.p7 | 11:581455 | TTCTTTGCAGCCTGG[C/G]ACAGTTTGGAAGTTG | 57661 |
rs190438886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:593987 | TGAGTTGGTTGCTGT[A/G]AGTCTGAAGGGCAGG | 57661 |
rs190497170 | snp | A/G | 3.31609e-05 | 0.00407177 | intron-variant | PHRF1 | GRCh38.p7 | 11:592546 | GTGGTGGTGACCGAC[A/G]ATTCTGTCCTAGATC | 57661 |
rs190666752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:589138 | AGACACTGTCTCAAA[A/T]AAAAAAAAAGGAGAA | 57661 |
rs190668449 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:604108 | CAGGTGTTGGATAAG[G/T]ACCTGCTATTTCCCA | 57661 |
rs190685423 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:578842 | AAGCATGAGCCACCA[C/T]GCCCGGCTGATTCAC | 57661 |
rs190694198 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:589538 | GAAACCAGTCCCAGG[A/G]GTTTTGCAGGGGCTT | 57661 |
rs190917929 | snp | C/T | 0.00026676 | 0.0115459 | missense | PHRF1 | GRCh38.p7 | 11:601610 | GAAGAAAGAAAACCC[C/T]GTCCGGACCATCCGC | 57661 |
rs190930653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:586377 | CACTTCTCCCAGCCT[C/T]TTTAACAGTGTAAAT | 57661 |
rs190930857 | snp | C/T | 0.0023933 | 0.0345097 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574359 | GGAAGGGCCCCCTGT[C/T]CTATGATCACGTGAC | 57661 |
rs190946394 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PHRF1 | GRCh38.p7 | 11:593223 | TGTAAGCAGATGCCC[A/C]CTTCCCCGTTAGCCT | 57661 |
rs190949341 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PHRF1 | GRCh38.p7 | 11:578997 | GGTGCACGCCGCCAT[G/T]CCCGGCTCATTTTTT | 57661 |
rs190972167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:602354 | TCACCTTGTCCACTC[A/G]GACTGCACATTTAAA | 57661 |
rs191003484 | snp | A/T | 1.67399e-05 | 0.00289304 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:605175 | CCTGCGCAGGCCTGT[A/T]CACAGCAGCTGCATC | 57661 |
rs191179401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:586837 | GGTCCTCATGCTTTG[A/G]GAAGGGGGCGTTGGA | 57661 |
rs191375233 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHRF1 | GRCh38.p7 | 11:584019 | CATAGCCCTGTGGTT[A/T]TCAGGGTTAGAATGT | 57661 |
rs191504661 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:586096 | AAACCCCTGACCTCA[A/G]GTGATCCACCTGCCT | 57661 |
rs191599287 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:594950 | CATTAAAACTGATCA[A/G]TATAACGATTCTCAT | 57661 |
rs191602878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:610934 | CCTTCCTGGCCGCAT[C/T]ACACACATGTCCCCT | 57661 |
rs191605950 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHRF1 | GRCh38.p7 | 11:582587 | CTGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 57661 |
rs191620858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:598809 | TTGTTATTTTTGCTG[C/T]AAACATTTGTCAGAA | 57661 |
rs191638333 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PHRF1 | GRCh38.p7 | 11:591932 | TTTTTTTTTTTTTCC[C/T]GAGACAAGAGTCTCG | 57661 |
rs191739729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:601093 | GAGGCGGAGGTTGCA[A/G]TGAGGTAAGATCGCA | 57661 |
rs191742029 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHRF1 | GRCh38.p7 | 11:597239 | GGGGTTCCGGTCCTC[A/G]GTGTTAGGAGCACCA | 57661 |
rs191817269 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574248 | TAGCGGTAGAAGAAA[C/T]AGTGAAAGTCTTAAA | 57661 |
rs191833935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:595179 | AATAAAAAAATTGGC[C/T]GGGCGTGGTGGTTCA | 57661 |
rs191854352 | snp | A/G | 0.00130133 | 0.0254749 | intron-variant | PHRF1 | GRCh38.p7 | 11:611132 | GGTCACGGGCGGTAC[A/G]TCGCTGCTGTCTCGT | 57661 |
rs192050609 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHRF1 | GRCh38.p7 | 11:583404 | TGCCTGTAATCCCCA[C/T]TACTCAGGAGGCTGA | 57661 |
rs192249722 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHRF1 | GRCh38.p7 | 11:579322 | TGGTAGATTCATGTG[A/C]GAGAGTCTGCCTCCC | 57661 |
rs192288806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:590461 | GAAGACGTACCTAAC[C/T]ACACCCCTGAGACAA | 57661 |
rs192294553 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:605799 | TTCTAGGGTGGGGCC[A/G]TGATAGCCTGGCTCT | 57661 |
rs192308584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:577022 | TGCCCCCTGCGAGTC[C/T]GCCCTGCCGCGTTTG | 57661 |
rs192340626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:588077 | CTCAGGGCTCAGCTC[C/T]GACACCACTACCTCT | 57661 |
rs192343886 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:603087 | TTTGAGATGGTATCA[C/T]TCTGTGGCCCAGGCT | 57661 |
rs192529084 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:584688 | CACTGGAGAGGTGTT[C/G]GTATAGCCACTGTGA | 57661 |
rs192557368 | snp | C/G/T | 6.68912e-05 | 0.00578288 | missense | PHRF1 | GRCh38.p7 | 11:607431 | TCTAAGCCCCCATGT[C/G/T]GCAGTGTGGTGCCGG | 57661 |
rs192660020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:579522 | CTGCTAGGTCTCAGT[G/T]CATGCTGTGGGAGAG | 57661 |
rs192870743 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:587684 | GTGGTGTATTGGTCA[A/G]GGGCAGGAGAGAGGA | 57661 |
rs192944856 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | PHRF1 | GRCh38.p7 | 11:602750 | GCTGAATCTTTTTTG[G/T]TTTTGTTTTTGTTTT | 57661 |
rs192947568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:582804 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 57661 |
rs192961551 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHRF1 | GRCh38.p7 | 11:599530 | TGCTGGGATTACAGG[C/T]CTCTGAGCCACTGCG | 57661 |
rs193006652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:609948 | CACCACAGGGAGCTT[C/T]TGGAGCCAGGGAACA | 57661 |
rs193011839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:581638 | CGGGTAGGGGCGTCC[C/T]CAGGAGGAGCAGGGT | 57661 |
rs193080797 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576297 | TATTGGTCTCCCCGG[A/G]CGGCAGTCCTGCATT | 57661 |
rs193116909 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHRF1 | GRCh38.p7 | 11:591174 | ATGCTACGCGTTCAT[A/G]GAGCTGCTCTTTCCT | 57661 |
rs193141727 | snp | C/T | 0.00156189 | 0.0279017 | intron-variant | PHRF1 | GRCh38.p7 | 11:605774 | GCAGCAGTTGGGCAT[C/T]GGATGGGAGTTCTAG | 57661 |
rs193201055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:584822 | GGCTCACTGCAGCCT[C/T]TGCCTCCCGGGTTCA | 57661 |
rs193209531 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHRF1 | GRCh38.p7 | 11:594480 | GCTGGAGTGCAGTGG[C/T]GCCATCTTGGCTCAC | 57661 |
rs193266055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:606201 | CCAGAGGTGACTTCT[C/T]CCAAAAACGCCTGGT | 57661 |
rs199621048 | snp | C/T | 0.00882876 | 0.0658516 | intron-variant | PHRF1 | GRCh38.p7 | 11:581476 | TTGGAAGTTGCTTGG[C/T]TCTTCTTTCTTTCAG | 57661 |
rs199627499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:591494 | CGCTGCCGTGGAGGC[C/T]CCAGCCGTGCTTCTA | 57661 |
rs199628151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:611104 | TGTGTGCGAGCCTGT[A/G]TGTGGGGCTCGGGGT | 57661 |
rs199646190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:599148 | TGGGGATTTAAGTCA[C/G]TGTAGACGCATGGAC | 57661 |
rs199667414 | snp | C/G/T | 0.000167491 | 0.00914984 | intron-variant | PHRF1 | GRCh38.p7 | 11:596907 | CCGGATGCTTTGGCC[C/G/T]TGCTCTCTCCTGTAG | 57661 |
rs199734108 | snp | A/C/G | 0.000176858 | 0.00940212 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:598429 | CATCGAGGCTGTGGC[A/C/G]ACTGGCCTGAGCACT | 57661 |
rs199744691 | snp | C/G | 0.000570613 | 0.0168814 | intron-variant | PHRF1 | GRCh38.p7 | 11:582107 | TGGTGTTCACGCCGG[C/G]TCCTGTGTTTCCTCT | 57661 |
rs199791071 | snp | A/G | 1.67573e-05 | 0.00289454 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610980 | GCTGCACATGCAGGA[A/G]CGTGCTGTGGAGGAG | 57661 |
rs199793786 | snp | A/G/T | 5.07828e-05 | 0.00503877 | missense | PHRF1 | GRCh38.p7 | 11:607965 | CCATCCGACCCCACC[A/G/T]GCTCCGACTCCAGCG | 57661 |
rs199793906 | snp | C/T | 0.00416851 | 0.045463 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609521 | CGCGGCTGAGAAGGC[C/T]GAGGCACCCAGTTCC | 57661 |
rs199818767 | snp | A/G | 0.000987741 | 0.0222012 | missense | PHRF1 | GRCh38.p7 | 11:607630 | CCGGGCAGCCAGGGC[A/G]AGGCACACGGGCAGA | 57661 |
rs199824125 | snp | C/T | 9.93986e-05 | 0.00704907 | intron-variant | PHRF1 | GRCh38.p7 | 11:610377 | TGGAGGGCTGTGGGC[C/T]GTGGGCAGTGGCCTG | 57661 |
rs199865524 | snp | A/G | 0.000260548 | 0.0114108 | synonymous-codon, intron-variant | PHRF1 | GRCh38.p7 | 11:581975 | AGAAGAAAGCAGCGT[A/G]GGCAGCAGTGGGGAC | 57661 |
rs199878253 | snp | C/T | 0.000115567 | 0.00760066 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608351 | GACCTGTGTGACTGT[C/T]GTGGAGCCGGAAGCC | 57661 |
rs199899831 | snp | C/T | 0.000239934 | 0.0109503 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608238 | ACAGAGAGCCAGGGC[C/T]TGGCTGCCCGGCTGC | 57661 |
rs199904786 | snp | C/T | 0.000285175 | 0.0119376 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610956 | ATGTCCCCTCTAGTA[C/T]ATGAAGAAGCTGCAC | 57661 |
rs199922330 | snp | C/G | 0.00188343 | 0.0306295 | missense | PHRF1 | GRCh38.p7 | 11:609351 | AGCACAGACTCTTCC[C/G]CGGAGCGAGACTTCC | 57661 |
rs199939943 | snp | A/G | 0.000102861 | 0.00717078 | missense | PHRF1 | GRCh38.p7 | 11:607767 | AGAGGGAAAGGGGTC[A/G]GGTCGACCTTTGAGA | 57661 |
rs199984677 | snp | C/T | 0.00018437 | 0.00959954 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609278 | CGTCTTTGATGATTT[C/T]TCAAGCGACGCCGTT | 57661 |
rs200082715 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589881 | GGGCTCAGCCTGAGA[A/G]TGTCTGCAAACGGGC | 57661 |
rs200089387 | snp | C/T | 0.000198998 | 0.00997294 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:592657 | CAGGCTTTTGCTCTG[C/T]GACGGCTGCGATGCG | 57661 |
rs200089483 | snp | C/G/T | 0.00134601 | 0.0259078 | missense | PHRF1 | GRCh38.p7 | 11:611752 | AGGCCGGGGAGGAGC[C/G/T]GCCCACGCAGGGGGC | 57661 |
rs200091823 | snp | G/T | | | stop-gained, splice-acceptor-variant, intron-variant | PHRF1 | GRCh38.p7 | 11:581964 | CCCTGGTGTCTAGAA[G/T]AAAGCAGCGTGGGCA | 57661 |
rs200116286 | snp | C/G | 0.0215843 | 0.101618 | intron-variant | PHRF1 | GRCh38.p7 | 11:606392 | GCCTGGGTGCGGGCC[C/G]TCAGGCCGTGGGAGG | 57661 |
rs200148178 | in-del | -/CT | 0.0126979 | 0.078662 | intron-variant | PHRF1 | GRCh38.p7 | 11:583328 | GGCAACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA | 57661 |
rs200183606 | snp | C/T | 0.000670175 | 0.0182931 | missense | PHRF1 | GRCh38.p7 | 11:608299 | AGGAGGATGGGGCGT[C/T]TTGCAGCACCTTCTT | 57661 |
rs200188468 | snp | A/G | 0.000737327 | 0.0191865 | intron-variant | PHRF1 | GRCh38.p7 | 11:605319 | AGTGAACTGGTGATG[A/G]TCCTGCCTGGGCACC | 57661 |
rs200203047 | snp | C/G | 0.00013363 | 0.00817294 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607373 | CACCAACAAGCACAC[C/G]TTGCCCCTTGCCTCT | 57661 |
rs200204469 | snp | C/T | 0.000648018 | 0.0179886 | missense | PHRF1 | GRCh38.p7 | 11:598449 | GCCTGAGCACTGCCG[C/T]GTATCAGCGCCCCCT | 57661 |
rs200253242 | snp | A/G/T | 3.44259e-05 | 0.00414873 | missense | PHRF1 | GRCh38.p7 | 11:608521 | CGCGCTCTGGGACGC[A/G/T]CTCTGAATCCAGGGA | 57661 |
rs200279414 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588650 | TCCCAAACTGCTGGG[A/C]TTACAGGCGTGAGCC | 57661 |
rs200290962 | snp | A/G/T | 0.000418614 | 0.0144614 | missense | PHRF1 | GRCh38.p7 | 11:608890 | AACGCAGCCACGAGC[A/G/T]GCCAGACAGGAAGGA | 57661 |
rs200303644 | in-del | -/TCG | | | intron-variant | PHRF1 | GRCh38.p7 | 11:585439 | AGCTTGAGGTAGTAG[-/TCG]CCCTTTCCAGCTTGA | 57661 |
rs200305178 | snp | G/T | | | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574225 | TCCTCTTTGAAGTTC[G/T]TAGTAGATAGCGGTA | 57661 |
rs200310178 | snp | A/G | 0.000370612 | 0.0136077 | missense | PHRF1 | GRCh38.p7 | 11:610513 | CAGGTTTACAGCCCC[A/G]GCCTGCCGCCTGCCC | 57661 |
rs200328357 | in-del | -/T | 0.0584853 | 0.160693 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574880 | TCCGGCCCCCACCCC[-/T]AGCACCCCCTGTGCC | 57661 |
rs200365637 | snp | C/T | 0.000219737 | 0.0104795 | intron-variant | PHRF1 | GRCh38.p7 | 11:596879 | GGAGGTTTGGGAAAG[C/T]TGTGAGCAGCACCCG | 57661 |
rs200410941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:581926 | CTGCATGGTCTTGAC[A/G]CCGCCCTGCGGCCTG | 57661 |
rs200469735 | snp | C/T | 0.000526639 | 0.0162186 | synonymous-codon, intron-variant | PHRF1 | GRCh38.p7 | 11:582011 | GGACGACAGTGACAG[C/T]GAGCATGGAGATGGC | 57661 |
rs200483337 | snp | C/G | 1.70295e-05 | 0.00291796 | missense | PHRF1 | GRCh38.p7 | 11:609375 | GACTTCCCACTGAAG[C/G]CTGCGTTGCCCCCAG | 57661 |
rs200491500 | snp | C/T | 8.68108e-05 | 0.00658771 | missense | PHRF1 | GRCh38.p7 | 11:608877 | AAGCATCAGCGGGAA[C/T]GCAGCCACGAGCGGC | 57661 |
rs200505264 | snp | A/C | 0.000925591 | 0.0214928 | missense | PHRF1 | GRCh38.p7 | 11:607819 | GAAACATGGCACATT[A/C]CAGCCAGCTCTCCAG | 57661 |
rs200569537 | snp | A/C/G/T | 0.000117487 | 0.00766361 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609248 | GGATTATGGCGACTC[A/C/G/T]GTGGAGGCCGGACAC | 57661 |
rs200601092 | snp | G/T | 0.000333739 | 0.0129135 | intron-variant | PHRF1 | GRCh38.p7 | 11:601565 | CAGACTTCAACCTCT[G/T]TTCCTTAGGAAGACG | 57661 |
rs200615051 | snp | A/G | 1.8592e-05 | 0.00304888 | splice-donor-variant, intron-variant | PHRF1 | GRCh38.p7 | 11:581607 | CGGCAGGTGACTTTG[A/G]TGAGCTGCCTAGCGC | 57661 |
rs200618070 | snp | A/G/T | 0.0039919 | 0.0444974 | missense | PHRF1 | GRCh38.p7 | 11:587282 | GATTCTGAAGACGAC[A/G/T]GGGAGACATTGCTGG | 57661 |
rs200629708 | snp | C/T | 0.00110015 | 0.0234279 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607679 | GGTGCCCCGGGAGCC[C/T]GGGGTGCACACGGGC | 57661 |
rs200637009 | snp | C/G/T | 0.000192219 | 0.00980166 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:597531 | GAGAGTGAGAGCAAC[C/G/T]GTGAACCGGAACCGG | 57661 |
rs200687895 | snp | C/T | 0.00310974 | 0.039309 | missense | PHRF1 | GRCh38.p7 | 11:608997 | AGGCGGCCTCGGTCC[C/T]GTGAGAAGTGGCCGC | 57661 |
rs200720688 | snp | A/G/T | 4.30656e-05 | 0.00464018 | intron-variant | PHRF1 | GRCh38.p7 | 11:587223 | CGGTTCACGCTGCCC[A/G/T]TCCTGCTTGCACCAG | 57661 |
rs200726235 | snp | C/G/T | 0.00124631 | 0.0249323 | intron-variant | PHRF1 | GRCh38.p7 | 11:611098 | GTGGGCTGTGTGCGA[C/G/T]CCTGTGTGTGGGGCT | 57661 |
rs200735580 | snp | C/T | 0.000101475 | 0.00712229 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607961 | CGACCCATCCGACCC[C/T]ACCGGCTCCGACTCC | 57661 |
rs200753321 | snp | A/G | 6.83761e-05 | 0.00584665 | missense | PHRF1 | GRCh38.p7 | 11:607237 | CCCGCACCCCCGCCC[A/G]CACCGCGGGGGCGCC | 57661 |
rs200765861 | snp | A/G | 0.0019323 | 0.0310228 | missense | PHRF1 | GRCh38.p7 | 11:607183 | AAGGCCCGTCAGGAA[A/G]CAGGCCACAGAGCAC | 57661 |
rs200779817 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:604307 | CACAGCCTGGGGGCC[C/G/T]GATGGCACGTGAGGG | 57661 |
rs200787809 | snp | A/G | 9.33716e-05 | 0.00683206 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609452 | CGATGAAGACCCTTC[A/G]CAGCCCCCACCCCTG | 57661 |
rs200796858 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588657 | CTGCTGGGATTACAG[A/G]CGTGAGCCACCACGC | 57661 |
rs200814156 | snp | A/G | 0.000473157 | 0.0153738 | intron-variant | PHRF1 | GRCh38.p7 | 11:610792 | TCCCACTTTCCCCAT[A/G]TTCCCATCTTACTTT | 57661 |
rs200817338 | snp | A/C/G | 0.000150823 | 0.00868289 | missense | PHRF1 | GRCh38.p7 | 11:611667 | GGAGAGATCAACCCC[A/C/G]TGAAGGTGGCCAACC | 57661 |
rs200851835 | snp | A/G | 0.000149134 | 0.00863392 | missense | PHRF1 | GRCh38.p7 | 11:592578 | CAGTGGAGAACACCA[A/G]AGCGAGCGAGGAGGA | 57661 |
rs200857527 | snp | G/T | | | missense | PHRF1 | GRCh38.p7 | 11:611747 | ACCAGAGGCCGGGGA[G/T]GAGCCGCCCACGCAG | 57661 |
rs200880236 | snp | A/G | 1.67494e-05 | 0.00289386 | missense | PHRF1 | GRCh38.p7 | 11:601654 | TCAGCGACAAGATCT[A/G]AGAAACGCCAACATC | 57661 |
rs200911468 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PHRF1 | GRCh38.p7 | 11:585244 | GTAGCCCTTTCCAGC[A/T]TGAGGTAGTAGCCCT | 57661 |
rs200913383 | snp | C/T | 0.00202695 | 0.0317706 | synonymous-codon, intron-variant | PHRF1 | GRCh38.p7 | 11:581999 | TGGGGACTCTGGGGA[C/T]GACAGTGACAGCGAG | 57661 |
rs200915859 | snp | A/G | 1.79142e-05 | 0.00299279 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608207 | GGGGGCCTCTGACAC[A/G]GAGCGAGAGGAGCCC | 57661 |
rs200926442 | snp | C/T | 0.000636627 | 0.01783 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610680 | AGCCTCAGAGCCAGC[C/T]AGTCAAGCCACTGCA | 57661 |
rs200929014 | snp | C/T | 0.000215394 | 0.0103755 | missense | PHRF1 | GRCh38.p7 | 11:592602 | AGGAGGAGGAGGACC[C/T]GACCTTCTGTGAGGT | 57661 |
rs200951448 | snp | C/T | 0.031825 | 0.122064 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574887 | CCCACCCCTAGCACC[C/T]CCTGTGCCCCTTCCT | 57661 |
rs200966018 | snp | A/G | 0.000467344 | 0.0152792 | intron-variant | PHRF1 | GRCh38.p7 | 11:592722 | TGCTGCGTGCAAGGC[A/G]GGCCAGGCGCAGGAG | 57661 |
rs201016370 | snp | A/G | 1.6703e-05 | 0.00288985 | missense | PHRF1 | GRCh38.p7 | 11:607366 | TCAACGGCACCAACA[A/G]GCACACCTTGCCCCT | 57661 |
rs201019570 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:594897 | TTACTTGGCAGATAA[A/C]ACAACGCAAGTACAT | 57661 |
rs201041084 | snp | A/G | 0.000422601 | 0.01453 | missense | PHRF1 | GRCh38.p7 | 11:609358 | ACTCTTCCCCGGAGC[A/G]AGACTTCCCACTGAA | 57661 |
rs201056875 | snp | C/T | 0.000166911 | 0.00913389 | intron-variant | PHRF1 | GRCh38.p7 | 11:592721 | CTGCTGCGTGCAAGG[C/T]GGGCCAGGCGCAGGA | 57661 |
rs201063264 | snp | G/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588652 | CCAAACTGCTGGGAT[G/T]ACAGGCGTGAGCCAC | 57661 |
rs201081599 | snp | A/G | 7.81464e-05 | 0.00625037 | intron-variant | PHRF1 | GRCh38.p7 | 11:582127 | GTGTTTCCTCTTGTC[A/G]TGATGGGGACAGCCT | 57661 |
rs201084702 | snp | A/C/G | 0.000456519 | 0.0151023 | intron-variant | PHRF1 | GRCh38.p7 | 11:611096 | AGGTGGGCTGTGTGC[A/C/G]AGCCTGTGTGTGGGG | 57661 |
rs201121933 | snp | C/T | 0.000620375 | 0.0176012 | missense | PHRF1 | GRCh38.p7 | 11:608800 | AGAAAAGGAGATCAG[C/T]GTCCAGACCTCGGGG | 57661 |
rs201189901 | snp | A/T | 0.000248767 | 0.0111499 | missense | PHRF1 | GRCh38.p7 | 11:587433 | ACTGTGCCCATTACT[A/T]CTGCCTGGACTGCAT | 57661 |
rs201225978 | snp | C/T | 0.000410256 | 0.0143164 | missense | PHRF1 | GRCh38.p7 | 11:610529 | GCCTGCCGCCTGCCC[C/T]GGCCCAGCCCTCAAG | 57661 |
rs201232704 | snp | C/T | 0.00024781 | 0.0111285 | missense | PHRF1 | GRCh38.p7 | 11:608359 | TGACTGTCGTGGAGC[C/T]GGAAGCCCCACCCAG | 57661 |
rs201234343 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:579343 | TCTGCCTCCCTCTTT[C/T]AGATATGTTTCTCCA | 57661 |
rs201244128 | snp | A/G | 0.00571185 | 0.0531347 | missense | PHRF1 | GRCh38.p7 | 11:610300 | GAGCTGCCCTTTCCC[A/G]GTCACGTGCTTCCGG | 57661 |
rs201301017 | snp | A/G | | | missense | PHRF1 | GRCh38.p7 | 11:610753 | GCGGAGAAAACCAAG[A/G]AGGAGGAGGTGAGTC | 57661 |
rs201315084 | snp | A/G | 0.000399281 | 0.0141238 | missense | PHRF1 | GRCh38.p7 | 11:609036 | TCCCATTCCCCAGAG[A/G]GGAAGGGGGCTGTGA | 57661 |
rs201348815 | snp | A/G | 1.70188e-05 | 0.00291704 | missense | PHRF1 | GRCh38.p7 | 11:607093 | TTCAGCGAAACTCAG[A/G]CAGTCTGTCCAGAGG | 57661 |
rs201355756 | snp | C/T | 0.00299553 | 0.0385849 | missense | PHRF1 | GRCh38.p7 | 11:610969 | TACATGAAGAAGCTG[C/T]ACATGCAGGAGCGTG | 57661 |
rs201370286 | snp | A/G | | | nc-transcript-variant | LOC143666 | GRCh38.p7 | 11:574335 | CTCTTTGCTTCGGCT[A/G]CCTAAGAGGGAAGGG | 57661 |
rs201479751 | snp | C/T | 1.68182e-05 | 0.00289979 | missense | PHRF1 | GRCh38.p7 | 11:607921 | TCTCCATCAAGAAGA[C/T]GAAGCAGCTGCGGAG | 57661 |
rs201482450 | snp | C/T | 0.00198167 | 0.0314151 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609719 | CGAGGACAGAGCCCC[C/T]CGTGAGTAGTGCCCC | 57661 |
rs201485720 | snp | C/T | 0.00010347 | 0.00719195 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609401 | CCCAGCCAGCCTGGC[C/T]GTGGCCGCCATCCAG | 57661 |
rs201489397 | snp | A/G | 0.00124917 | 0.0249605 | missense | PHRF1 | GRCh38.p7 | 11:608929 | CGTGGCCCCGAGACC[A/G]GAGGAAGCGGAGGTC | 57661 |
rs201496622 | snp | C/T | 0.00697544 | 0.0586435 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610545 | GGCCCAGCCCTCAAG[C/T]ATCCCACCCTGCGCA | 57661 |
rs201508784 | snp | C/T | 3.65905e-05 | 0.00427714 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611795 | CCAGGCAATCACGGG[C/T]TATGCCCGGGGAGCT | 57661 |
rs201520162 | snp | A/G | 0.000134546 | 0.00820092 | missense | PHRF1 | GRCh38.p7 | 11:581522 | GCAGCAATGGATGAC[A/G]ACAGCCTGGATGAGC | 57661 |
rs201529946 | snp | A/G | 0.000228004 | 0.0106747 | missense | PHRF1 | GRCh38.p7 | 11:608812 | CAGCGTCCAGACCTC[A/G]GGGAAGGGAGTGCTC | 57661 |
rs201538268 | snp | A/G/T | 9.32437e-05 | 0.0068275 | missense | PHRF1 | GRCh38.p7 | 11:597506 | CGATAGCCAGGACAC[A/G/T]GCAGAGTGAGAGAGT | 57661 |
rs201540824 | snp | A/T | 0.0766824 | 0.180169 | intron-variant | PHRF1 | GRCh38.p7 | 11:600495 | CTCTGTCTCCAAAAA[A/T]ATATATATATATATA | 57661 |
rs201564523 | snp | C/T | 8.87414e-05 | 0.00666054 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609429 | CAGAGGGAGGTGTCA[C/T]TGATGCACGATGAAG | 57661 |
rs201571276 | snp | C/T | 0.000183178 | 0.00956846 | missense | PHRF1 | GRCh38.p7 | 11:609553 | CGGATGTGGCGCCTG[C/T]GGGGAAGGAAGACAG | 57661 |
rs201589784 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:582264 | TGTAGTACTTCATTT[C/T]TTTTTTTTTTTTTTT | 57661 |
rs201614026 | snp | C/G | 0.000467969 | 0.0152894 | missense | PHRF1 | GRCh38.p7 | 11:596996 | TGCCCGGAATGTGCT[C/G]CGCCTGGTGTTGTCC | 57661 |
rs201641830 | snp | A/G/T | 0.000249382 | 0.0111643 | missense | PHRF1 | GRCh38.p7 | 11:587343 | CCGCTGGCTCTTTCA[A/G/T]TTCTGATGATGATGC | 57661 |
rs201645397 | snp | A/G | 0.00265283 | 0.0363232 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608333 | CTCTGAGGAGCGGAC[A/G]GTGACCTGTGTGACT | 57661 |
rs201648834 | snp | C/T | 0.00031597 | 0.0125652 | intron-variant | PHRF1 | GRCh38.p7 | 11:598528 | AGGGATGGACTCTCC[C/T]GCCAGCCACAGGCTG | 57661 |
rs201661078 | snp | A/G | 0.000348747 | 0.0132005 | missense | PHRF1 | GRCh38.p7 | 11:587352 | CTTTCAATTCTGATG[A/G]TGATGCAGAGAGCTG | 57661 |
rs201670892 | snp | G/T | 1.70595e-05 | 0.00292052 | missense | PHRF1 | GRCh38.p7 | 11:608129 | CATCTTTGGTACAGA[G/T]CCCGAACCCCCTCTC | 57661 |
rs201679778 | snp | A/G | 0.000190825 | 0.00976606 | missense | PHRF1 | GRCh38.p7 | 11:598386 | AGCACACACCAGGGC[A/G]CCTCGGGTCTTCCCT | 57661 |
rs201707369 | in-del | -/CTGTT | 0.0119091 | 0.0762411 | intron-variant | PHRF1 | GRCh38.p7 | 11:588198 | CTGGGTCCTCCTGTT[-/CTGTT]TCACTGAGTAGCTGA | 57661 |
rs201757461 | snp | G/T | 0.0039921 | 0.0444985 | intron-variant | PHRF1 | GRCh38.p7 | 11:592551 | GGTGACCGACGATTC[G/T]GTCCTAGATCCCAGT | 57661 |
rs201763155 | snp | C/G | 1.69035e-05 | 0.00290714 | missense | PHRF1 | GRCh38.p7 | 11:607269 | GTGAGGCTGGACTTG[C/G]CAGCAGCCCCTGGGG | 57661 |
rs201796525 | snp | C/T | 0.000849183 | 0.0205881 | missense | PHRF1 | GRCh38.p7 | 11:608554 | GGAGCTCGAGGTCAG[C/T]GTCACCATCAGTGGG | 57661 |
rs201810294 | snp | A/G | 1.74534e-05 | 0.00295405 | missense | PHRF1 | GRCh38.p7 | 11:608499 | GTGTCCAGGGAGCAC[A/G]GACGGACGCGCTCTG | 57661 |
rs201862192 | snp | A/G | 0.000237244 | 0.0108888 | missense | PHRF1 | GRCh38.p7 | 11:608013 | GAGAGGTCTGGCCCC[A/G]GCCTCCTGCCCTCTG | 57661 |
rs201973740 | snp | G/T | 3.32011e-05 | 0.00407424 | intron-variant | PHRF1 | GRCh38.p7 | 11:592680 | GCGATGCGGGGTAAG[G/T]GACGGTTGGGACTGG | 57661 |
rs201999507 | snp | C/G/T | 0.00119366 | 0.0244013 | intron-variant | PHRF1 | GRCh38.p7 | 11:592529 | GGGAGTTTGGGTCCT[C/G/T]TGTGGTGGTGACCGA | 57661 |
rs202001290 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588669 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCATTTTT | 57661 |
rs202005033 | snp | A/C/G | 0.00133729 | 0.0258239 | missense | PHRF1 | GRCh38.p7 | 11:607687 | GGGAGCCCGGGGTGC[A/C/G]CACGGGCAGCTCCCG | 57661 |
rs202013178 | snp | C/T | 0.000161676 | 0.00898954 | missense | PHRF1 | GRCh38.p7 | 11:609502 | CACATTTGCTCAGGC[C/T]GGACGCGGCTGAGAA | 57661 |
rs202034943 | snp | C/G/T | 0.000103422 | 0.00719028 | missense | PHRF1 | GRCh38.p7 | 11:607082 | TCCAGTTTCTTTTCA[C/G/T]CGAAACTCAGGCAGT | 57661 |
rs202054727 | snp | A/G | 0.000122865 | 0.00783693 | synonymous-codon, intron-variant | PHRF1 | GRCh38.p7 | 11:581996 | CAGTGGGGACTCTGG[A/G]GACGACAGTGACAGC | 57661 |
rs202082756 | snp | A/C/G | 0.000124515 | 0.0078895 | missense, intron-variant | PHRF1 | GRCh38.p7 | 11:581994 | AGCAGTGGGGACTCT[A/C/G]GGGACGACAGTGACA | 57661 |
rs202085724 | snp | C/T | 1.76571e-05 | 0.00297123 | missense | PHRF1 | GRCh38.p7 | 11:610664 | CCGCTGCCCTGACCC[C/T]AGCCTCAGAGCCAGC | 57661 |
rs202141408 | snp | C/T | 4.83781e-05 | 0.004918 | missense | PHRF1 | GRCh38.p7 | 11:611758 | GGGAGGAGCCGCCCA[C/T]GCAGGGGGCCGAGGG | 57661 |
rs202144590 | snp | A/G | 0.00521654 | 0.0508041 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609002 | GCCTCGGTCCCGTGA[A/G]AAGTGGCCGCAGACC | 57661 |
rs202208436 | snp | A/C | 0.000407436 | 0.0142672 | missense | PHRF1 | GRCh38.p7 | 11:607560 | GCCCCGGCCCACGGG[A/C]AGAGCATTGAGATCC | 57661 |
rs202209293 | snp | A/C/G | 0.000282508 | 0.0118818 | missense | PHRF1 | GRCh38.p7 | 11:610651 | CTGGCCCCAGTGCCC[A/C/G]CTGCCCTGACCCCAG | 57661 |
rs202241158 | snp | C/G/T | 0.000152497 | 0.00873097 | synonymous-codon, missense | PHRF1 | GRCh38.p7 | 11:609365 | CCCGGAGCGAGACTT[C/G/T]CCACTGAAGCCTGCG | 57661 |
rs367549915 | snp | A/G | | | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608000 | TGGCAGCAGCCCCGA[A/G]AGGTCTGGCCCCGGC | 57661 |
rs367623294 | snp | C/T | 0.000401816 | 0.0141685 | missense | PHRF1 | GRCh38.p7 | 11:610313 | CCAGTCACGTGCTTC[C/T]GGAACCCGGGTTCCC | 57661 |
rs367659936 | snp | A/G | 3.40983e-05 | 0.00412892 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607220 | CAGCTGTCAAGGCAG[A/G]TCCCGCACCCCCGCC | 57661 |
rs367662812 | snp | A/G | 0.000156148 | 0.00883458 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608555 | GAGCTCGAGGTCAGC[A/G]TCACCATCAGTGGGT | 57661 |
rs367666385 | snp | C/T | 0.000106082 | 0.00728214 | intron-variant | PHRF1 | GRCh38.p7 | 11:587230 | CGCTGCCCATCCTGC[C/T]TGCACCAGCTGGCAT | 57661 |
rs367666673 | snp | C/T | 1.77552e-05 | 0.00297948 | missense | PHRF1 | GRCh38.p7 | 11:605134 | AGTGAAGCCACCACT[C/T]GCTCTCGAATCGCGC | 57661 |
rs367670551 | snp | C/G/T | 0.00106196 | 0.0230203 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:598480 | GACGCCGCGCACTCC[C/G/T]GCCCGACGGAAGAGG | 57661 |
rs367680854 | snp | G/T | 1.68986e-05 | 0.00290672 | intron-variant | PHRF1 | GRCh38.p7 | 11:596878 | AGGAGGTTTGGGAAA[G/T]CTGTGAGCAGCACCC | 57661 |
rs367734268 | snp | A/C | 1.81417e-05 | 0.00301173 | intron-variant | PHRF1 | GRCh38.p7 | 11:605742 | GTGTGAGGGCAGAGG[A/C]TTCTGGGGAGGTGGG | 57661 |
rs367747625 | snp | A/G/T | 0.000242351 | 0.0110054 | missense | PHRF1 | GRCh38.p7 | 11:608839 | GCTCCCCCACCAGCA[A/G/T]CCTGGAGAGGCTCTG | 57661 |
rs367751800 | snp | C/T | 1.68403e-05 | 0.0029017 | missense | PHRF1 | GRCh38.p7 | 11:581544 | TGGATGAGCTTGTGG[C/T]CCGGAGCCCAGGGCC | 57661 |
rs367758132 | snp | A/G | 0.00807278 | 0.0630176 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:597477 | GCTTCGGCCTCGAGC[A/G]GGTAGGACCCGGGCG | 57661 |
rs367759306 | snp | A/G | 1.75674e-05 | 0.00296368 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610629 | GGGCTGTGGGGCAGC[A/G]CAGACCCTGGCCCCA | 57661 |
rs367803474 | snp | C/T | 5.02913e-05 | 0.00501429 | missense | PHRF1 | GRCh38.p7 | 11:607477 | CAGCGCCCAGAAGAA[C/T]AGACATCTCTGAGCT | 57661 |
rs367813947 | snp | C/T | 1.89536e-05 | 0.00307838 | stop-gained | PHRF1 | GRCh38.p7 | 11:591435 | AAGTGCATTTGTATT[C/T]GAGCTCAATTTGGTG | 57661 |
rs367848709 | snp | A/C/G | 0.000711436 | 0.0188473 | missense | PHRF1 | GRCh38.p7 | 11:607155 | CGAGCACTGCCCTCC[A/C/G]GGAGCCCGGCCCAAG | 57661 |
rs367849960 | snp | A/G | 5.00914e-05 | 0.00500432 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:596986 | CGAGTGGTTCTGCCC[A/G]GAATGTGCTGCGCCT | 57661 |
rs367910054 | snp | C/T | 1.66618e-05 | 0.00288628 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:605263 | GCTGCCTCTCTGTCT[C/T]TGTTTGGAGATCCTT | 57661 |
rs367936214 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:587756 | GACATAGGGGCCATC[C/T]TGGCCTGCAAGCCAG | 57661 |
rs367942411 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:604873 | TCACTTAATGCTACT[A/G]CGACGTGATGGTGAC | 57661 |
rs367956094 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:583029 | ACAGAGCGAGACTCC[A/G]TCTCAAAGGAAGAAA | 57661 |
rs367991634 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, nc-transcript-variant | PHRF1, LOC143666 | GRCh38.p7 | 11:574479 | GGGCCACTACCGGTC[G/T]CCACGTCTTGATGGT | 57661 |
rs368062320 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:606082 | TTTTGGCCAGTTCTT[C/T]TGTTTCGCCACAAGA | 57661 |
rs368081392 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHRF1 | GRCh38.p7 | 11:584099 | TCATGGCCTGAGCCA[A/G]TGTGTGTTGGCCGTG | 57661 |
rs368121230 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHRF1 | GRCh38.p7 | 11:603119 | AAGTGCAATGGCTCA[A/G]TCCCAGCTCACTGCA | 57661 |
rs368142717 | snp | C/T | 5.03065e-05 | 0.00501505 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:611678 | CCCCGTGAAGGTGGC[C/T]AACCTGGTGAAGGCG | 57661 |
rs368146749 | in-del | -/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:582264 | TGTAGTACTTCATTT[-/C]TTTTTTTTTTTTTTT | 57661 |
rs368164827 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:596241 | TTTGCATAGACTCCC[A/G]AGCCTCGGCTGCTTG | 57661 |
rs368184624 | snp | A/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:590824 | TTCTCCTGCCTCAGC[A/C]TCCCGAGTAGCTGGG | 57661 |
rs368209975 | snp | C/T | 0.00169456 | 0.0290587 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609242 | GGACCTGGATTATGG[C/T]GACTCCGTGGAGGCC | 57661 |
rs368253631 | snp | C/T | 7.34093e-05 | 0.00605799 | missense | PHRF1 | GRCh38.p7 | 11:597466 | ACCACCAGCAGGCTT[C/T]GGCCTCGAGCAGGTA | 57661 |
rs368265669 | snp | A/C | 1.68207e-05 | 0.00290001 | missense | PHRF1 | GRCh38.p7 | 11:581520 | GTGCAGCAATGGATG[A/C]CGACAGCCTGGATGA | 57661 |
rs368273584 | snp | A/G | 3.88229e-05 | 0.00440567 | missense | PHRF1 | GRCh38.p7 | 11:608938 | GAGACCGGAGGAAGC[A/G]GAGGTCCCGGTCCCC | 57661 |
rs368282503 | snp | A/G/T | 6.77052e-05 | 0.00581796 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607544 | TGGCAGACGGGATGC[A/G/T]GCCCCGGCCCACGGG | 57661 |
rs368318260 | snp | C/T | 0.00262455 | 0.0361301 | intron-variant | PHRF1 | GRCh38.p7 | 11:604920 | GCCTCTGGTAGCCTG[C/T]AGGAGCTTCACGGCC | 57661 |
rs368366418 | snp | C/T | 0.000102622 | 0.00716243 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:611058 | GGAGGAGTACAAGGA[C/T]ATCCTGCGCAAGGCC | 57661 |
rs368379321 | snp | C/T | 8.53162e-05 | 0.00653076 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:605710 | GGCCAGGCCCGTCTC[C/T]GTGGGGCTTTCCAGG | 57661 |
rs368381846 | snp | C/T | 0.000938133 | 0.0216376 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:611666 | TGGAGAGATCAACCC[C/T]GTGAAGGTGGCCAAC | 57661 |
rs368384146 | snp | A/G | 0.000271928 | 0.0116572 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607250 | CCGCACCGCGGGGGC[A/G]CCTGTGAGGCTGGAC | 57661 |
rs368385785 | snp | A/G | 3.87634e-05 | 0.0044023 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609467 | GCAGCCCCCACCCCT[A/G]CCAGAGGGCACCCAG | 57661 |
rs368390703 | snp | A/G/T | 0.000310562 | 0.0124575 | missense | PHRF1 | GRCh38.p7 | 11:609162 | GAGGTGGCTACGGCC[A/G/T]ACAAGGCCCCCCTGC | 57661 |
rs368390894 | snp | C/T | 1.97315e-05 | 0.00314091 | missense | PHRF1 | GRCh38.p7 | 11:598487 | CGCACTCCCGCCCGA[C/T]GGAAGAGGAAGACAA | 57661 |
rs368400216 | snp | A/T | 3.37764e-05 | 0.00410938 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607952 | CGAGGTCTACGACCC[A/T]TCCGACCCCACCGGC | 57661 |
rs368433431 | snp | A/G | 0.000159987 | 0.00894249 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:596941 | CCACATGGAATGCTT[A/G]GACCCCCCTCTCCAG | 57661 |
rs368485876 | snp | A/G/T | 6.71609e-05 | 0.00579455 | missense | PHRF1 | GRCh38.p7 | 11:607500 | TCTGAGCTACCCAGG[A/G/T]TACCAAAGATCAGGA | 57661 |
rs368487709 | snp | C/T | 2.29597e-05 | 0.00338812 | intron-variant | PHRF1 | GRCh38.p7 | 11:591485 | GAGTGTGGACGCTGC[C/T]GTGGAGGCCCCAGCC | 57661 |
rs368560706 | in-del | -/AAAAC | 0.00676609 | 0.0577691 | intron-variant | PHRF1 | GRCh38.p7 | 11:602683 | CAAAACTCTGCCTCA[-/AAAAC]AAAACAAAACAAAAC | 57661 |
rs368580858 | snp | A/G | 1.68457e-05 | 0.00290216 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:605154 | TCGAATCGCGCGGAC[A/G]CTGGGCCTGCGCAGG | 57661 |
rs368606522 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:592489 | ATTCTGGATTAACTG[C/T]GTTTCACGCTGGGAA | 57661 |
rs368725133 | in-del | -/C | | | intron-variant | PHRF1 | GRCh38.p7 | 11:599604 | GCTTTAGTGTGTAGT[-/C]CTAGGTTTGACAGAC | 57661 |
rs368740302 | snp | A/G | 5.02559e-05 | 0.00501253 | intron-variant | PHRF1 | GRCh38.p7 | 11:605316 | GTGAGTGAACTGGTG[A/G]TGGTCCTGCCTGGGC | 57661 |
rs368743365 | snp | C/T | 3.35267e-05 | 0.00409417 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609263 | CGTGGAGGCCGGACA[C/T]GTCTTTGATGATTTC | 57661 |
rs368751287 | snp | A/C/G/T | 0.000304648 | 0.0123384 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608024 | CCCCGGCCTCCTGCC[A/C/G/T]TCTGAGATCACACGA | 57661 |
rs368757796 | snp | C/T | 0.000168745 | 0.0091839 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:597016 | TGGTGTTGTCCTTGC[C/T]GCTGGTAAGGACACT | 57661 |
rs368778978 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:604975 | TGTCGGTCATCATGC[C/T]TGAGAAGCCCATTGA | 57661 |
rs368788772 | snp | C/T | 0.000376078 | 0.0137076 | missense | PHRF1 | GRCh38.p7 | 11:608914 | GGAAGGAGAGTGTGG[C/T]GTGGCCCCGAGACCG | 57661 |
rs368798093 | snp | C/T | 0.000163987 | 0.00905352 | missense | PHRF1 | GRCh38.p7 | 11:610706 | CTGCAGCCAGCAACT[C/T]GGAGGAGAAGACCCC | 57661 |
rs368798135 | snp | G/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:599635 | GTAACTTCCATTCCA[G/T]CCAGCACAGAAATAG | 57661 |
rs368805766 | snp | C/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:586080 | TGGCCAGGCTGGTCT[C/G]AAACCCCTGACCTCA | 57661 |
rs368811571 | snp | A/G | 3.51327e-05 | 0.00419108 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:609578 | AGACAGCCCCTCTGC[A/G]AGTGGGAGGGTACAG | 57661 |
rs368814376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHRF1, LOC143666 | GRCh38.p7 | 11:576972 | CGAGGACGCGGCGAG[A/G]GCCCACTCGCCTCGC | 57661 |
rs368829404 | snp | C/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:588262 | GACCCAGACATTCCT[C/T]ATGCTGCTGGTGGTG | 57661 |
rs368863354 | snp | A/G | 0.0341408 | 0.126114 | utr-variant-3-prime | PHRF1 | GRCh38.p7 | 11:611830 | GGAGTGGCGGGAATC[A/G]GGGCCATGCCCGGGG | 57661 |
rs368901146 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:602440 | GATCCCACCACTTTG[C/G]GGGGCTGAGGCGGAC | 57661 |
rs368921476 | snp | A/G/T | 7.44664e-05 | 0.00610153 | missense | PHRF1 | GRCh38.p7 | 11:608725 | GCCGGAGGACGTCCC[A/G/T]GTCGCGGTCGGGGAG | 57661 |
rs368945407 | snp | A/C | 0.000159987 | 0.00894248 | missense | PHRF1 | GRCh38.p7 | 11:608413 | CCCACAGAGTCGTGG[A/C]GCTCAGGCCCCCTTC | 57661 |
rs368956303 | snp | C/G | 0.000447728 | 0.0149554 | intron-variant | PHRF1 | GRCh38.p7 | 11:609733 | CCCGTGAGTAGTGCC[C/G]CGGCCCCCACCGAGG | 57661 |
rs368961072 | snp | C/G | 0.000155988 | 0.00883004 | intron-variant | PHRF1 | GRCh38.p7 | 11:598361 | CTGACGGCACCACCC[C/G]TTTGCCTGTAGCACA | 57661 |
rs368972802 | snp | C/T | 0.000123445 | 0.00785539 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:606583 | CGACGGCTCCCTCAG[C/T]GCCAAGAGGGCGGGT | 57661 |
rs369016795 | snp | C/T | 0.000159987 | 0.00894248 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607589 | CCCCAGTGCCTGCAT[C/T]AGCCGACTGACTGGC | 57661 |
rs369047912 | snp | C/G | 1.87327e-05 | 0.00306039 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:610527 | CGGCCTGCCGCCTGC[C/G]CCGGCCCAGCCCTCA | 57661 |
rs369087485 | snp | C/T | 4.97434e-05 | 0.00498691 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:587401 | ATTCAGAGACCAGGC[C/T]GTGGGGACGCCGGAG | 57661 |
rs369136949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:605454 | GGTGCAGGTGGGTGG[C/T]GTGGAACTCAGAGGT | 57661 |
rs369155682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHRF1 | GRCh38.p7 | 11:588670 | AGGCGTGAGCCACCA[C/T]GCCCGGCCATTTTTA | 57661 |
rs369159246 | in-del | -/GTTTTGTTTTT | | | intron-variant | PHRF1 | GRCh38.p7 | 11:602750 | GCTGAATCTTTTTTG[-/GTTTTGTTTTT]GTTTTTTTTGTTTTT | 57661 |
rs369165619 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589043 | CGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 57661 |
rs369170553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHRF1 | GRCh38.p7 | 11:583253 | CTGAGGCAGGAGAAT[C/T]GCTGGAACCCGGGAG | 57661 |
rs369191333 | in-del | -/GAGA | | | intron-variant | PHRF1 | GRCh38.p7 | 11:594276 | CCATGGCATGATAGA[-/GAGA]CCTGGTCCTGGTCGC | 57661 |
rs369236190 | snp | A/T | | | intron-variant | PHRF1 | GRCh38.p7 | 11:594849 | ATTTACAAACTTGAT[A/T]TATTGATTTTCTTTC | 57661 |
rs369282695 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:589932 | CCTGAGAGGGTGTCT[A/G]CAAACGGGCACGGAG | 57661 |
rs369359432 | snp | A/G | 0.000161987 | 0.00899817 | missense | PHRF1 | GRCh38.p7 | 11:610507 | CCCTCCCAGGTTTAC[A/G]GCCCCGGCCTGCCGC | 57661 |
rs369368409 | snp | C/T | 3.34135e-05 | 0.00408725 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:607355 | CAGCCCCTGGTTCAA[C/T]GGCACCAACAAGCAC | 57661 |
rs369457513 | snp | A/G | 7.30994e-05 | 0.00604519 | intron-variant | PHRF1 | GRCh38.p7 | 11:611127 | CTCGGGGTCACGGGC[A/G]GTACGTCGCTGCTGT | 57661 |
rs369472188 | snp | A/G | 0.00059943 | 0.0173019 | intron-variant | PHRF1 | GRCh38.p7 | 11:606415 | GTGGGAGGCAGTGAC[A/G]GCAGGGCCTTGGGTC | 57661 |
rs369473896 | snp | A/G | 8.2968e-05 | 0.00644027 | intron-variant | PHRF1 | GRCh38.p7 | 11:597591 | TGGCCCAGCCCTGAC[A/G]CCAGTCGTAGAACCC | 57661 |
rs369483906 | snp | C/G | 0.000163987 | 0.00905353 | intron-variant | PHRF1 | GRCh38.p7 | 11:581645 | GGGCGTCCCCAGGAG[C/G]AGCAGGGTGCCTGGT | 57661 |
rs369527374 | in-del | -/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:598247 | GGCTGCTGCAGTGGC[-/G]GGGTGGGGAGGCTGT | 57661 |
rs369581601 | snp | C/T | 6.83492e-05 | 0.0058455 | synonymous-codon | PHRF1 | GRCh38.p7 | 11:608132 | CTTTGGTACAGAGCC[C/T]GAACCCCCTCTCGGA | 57661 |
rs369595775 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | PHRF1 | GRCh38.p7 | 11:598554 | GGCTGGGACCCACGC[C/T]CGAGGTCCACTCACT | 57661 |
rs369651404 | snp | A/G | | | intron-variant | PHRF1 | GRCh38.p7 | 11:583589 | TTCTTTTGAGAGAAC[A/G]ATGTTCCAAAGGGCA | 57661 |
rs369674579 | snp | C/T | 0.000165986 | 0.00910855 | missense | PHRF1 | GRCh38.p7 | 11:609667 | TGGTGAAGCGGGTCA[C/T]CTGGAACCTGCAGGA | 57661 |