| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs762602365 | snp | C/T | 1.78768e-05 | 0.00298966 | intron-variant | RNF114 | GRCh38.p7 | 20:49946121 | TTTTCTTTTTTCCTG[C/T]GTTTCACCTTCCAGG | 55905 |
| rs762717450 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49948904 | TGGGACATTGCTCAT[C/T]GGCTTATTTTCTTAG | 55905 |
| rs762719657 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49948683 | CCTCAGGTGATCTAC[C/T]GCTTTGGCCTCCCAA | 55905 |
| rs762804263 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49945794 | CCTCAACCTCCCAAG[C/T]AGCTGGGATTACAGG | 55905 |
| rs762916154 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946368 | CTAGATTGACAGATT[A/G]TTAACATTTTACCAT | 55905 |
| rs762982255 | snp | G/T | 8.23852e-05 | 0.00641762 | missense | RNF114 | GRCh38.p7 | 20:49945412 | ATCCGGTCCCACGTG[G/T]CTACTTGTTCCAAAT | 55905 |
| rs763103613 | snp | A/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49938787 | GTGAACATTTGATAG[A/T]TGAGCTGTACCTGTG | 55905 |
| rs763120260 | snp | C/G | 1.67987e-05 | 0.00289811 | intron-variant | RNF114 | GRCh38.p7 | 20:49941554 | TTCTCTGTATGTCTT[C/G]TTCTAGCTTTTGCTC | 55905 |
| rs763213917 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49950457 | AGGCTGAGGCAGGTG[A/G]ATCGCTTGAGCTCAG | 55905 |
| rs763352615 | snp | C/G | 0.000195332 | 0.00988067 | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936405 | GCGCGGCGCAGAGCG[C/G]CAGCAAGATGGCGGC | 55905 |
| rs763371110 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | RNF114 | GRCh38.p7 | 20:49952122 | ATCAGGTGTTGCAGC[A/G]CTCCATCATCGACCA | 55905 |
| rs763400605 | snp | A/G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943448 | TTTGAGAGCAGCCTG[A/G/T]GGAATATAGTGGACC | 55905 |
| rs763457619 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942717 | TAGTCTCAACTGTTC[A/G]GGAGGCTGAGGTGAG | 55905 |
| rs763518307 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49941925 | TTAAGTATATATTTT[A/G]GGTTTGAAAGCCATA | 55905 |
| rs763606188 | snp | C/T | 1.65504e-05 | 0.00287662 | missense | RNF114 | GRCh38.p7 | 20:49946162 | ACCGTTACACCTTTC[C/T]TTGTCCTTACTGTCC | 55905 |
| rs763623692 | snp | C/G | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952434 | CCTGTGGAAGATAAT[C/G]TAGCTTCTCCACCTC | 55905 |
| rs763810738 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49945073 | TAGTATAGAAAACTT[G/T]TAAAAACATCCTAGA | 55905 |
| rs763848788 | snp | G/T | 1.65466e-05 | 0.00287628 | intron-variant | RNF114 | GRCh38.p7 | 20:49949207 | AGGGCTGGTGCAAGC[G/T]TGGAAATTGGGTGCC | 55905 |
| rs763891100 | in-del | -/AGA | 1.65121e-05 | 0.00287329 | cds-indel | RNF114 | GRCh38.p7 | 20:49946180 | GTCCTTACTGTCCTG[-/AGA]AGAACTTTGATCAGG | 55905 |
| rs764056847 | snp | A/G | 3.30175e-05 | 0.00406296 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49941597 | GGAATGTCTGAAGCC[A/G]AAGAAGCCTGTCTGT | 55905 |
| rs764103217 | snp | C/T | 1.73939e-05 | 0.00294901 | missense | RNF114 | GRCh38.p7 | 20:49936462 | CGCAGCTGGCGGGGC[C/T]GGCGGCGGAGGCTGA | 55905 |
| rs764478993 | snp | A/G | 3.29582e-05 | 0.00405931 | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952160 | GAGTCCGTGCTTGCT[A/G]TCTGTCTCATGTTAC | 55905 |
| rs765001604 | snp | A/C/G | 0.000936412 | 0.0216206 | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936399 | GCCGTTGCGCGGCGC[A/C/G]GAGCGGCAGCAAGAT | 55905 |
| rs765096002 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946317 | CTTGGAGAAAAATGA[C/T]GGGATTAGTAGAATG | 55905 |
| rs765194645 | in-del | -/AGGCA | 1.64936e-05 | 0.00287168 | frameshift-variant | RNF114 | GRCh38.p7 | 20:49941618 | CCTGTCTGTGGGGTG[-/AGGCA]TGTCGCAGCGCTCTG | 55905 |
| rs765356724 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49949062 | ACCCAGTCCCACGTG[G/T]CATTTGACTTGAGCT | 55905 |
| rs765388682 | snp | A/G | 1.68755e-05 | 0.00290473 | intron-variant | RNF114 | GRCh38.p7 | 20:49941547 | ACAGAGGTTCTCTGT[A/G]TGTCTTGTTCTAGCT | 55905 |
| rs765435663 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49951500 | TTACAAATGTTCTGA[A/G]CACTTGGTCTGTGCC | 55905 |
| rs765449692 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49936582 | CGGGCCTGGTCGGGG[A/G]GCGCTTAACTGGGAA | 55905 |
| rs765702335 | snp | C/T | | | synonymous-codon | RNF114 | GRCh38.p7 | 20:49941711 | TGGCTGCCGTAAGAA[C/T]GTATGTGGAAGTGAT | 55905 |
| rs765828484 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942793 | CGTGCCACTGCACTC[C/T]ATCCTGGGTGATAGA | 55905 |
| rs765946103 | snp | G/T | 0.000394607 | 0.0140409 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49936439 | ACAGCGGGACTGCGG[G/T]GGTGCTGCGCAGCTG | 55905 |
| rs766171378 | snp | C/T | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49936250 | TGGATTTGGCTTCCA[C/T]GTTTTCCAGATTTCC | 55905 |
| rs766277855 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946401 | TTGCTTAACCATGCT[C/G]TATAGTACACATTTT | 55905 |
| rs766294421 | snp | C/T | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49934454 | GTGGAAATTTACACA[C/T]TCTTAAAAGAACCAA | 55905 |
| rs766365837 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49948712 | AAAGTGCTGGGATTA[C/T]AAGTGTGAGCCACTG | 55905 |
| rs766561339 | snp | A/T | 1.65468e-05 | 0.00287631 | missense | RNF114 | GRCh38.p7 | 20:49941581 | GCTCTGCATGCCTGC[A/T]GGAATGTCTGAAGCC | 55905 |
| rs766573191 | snp | C/T | 4.94629e-05 | 0.00497283 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49941651 | ACCTGGCGTCCGAGC[C/T]GTGGAGCTCGAGCGG | 55905 |
| rs766711493 | snp | C/T | 9.3569e-05 | 0.00683928 | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936409 | GGCGCAGAGCGGCAG[C/T]AAGATGGCGGCGCAA | 55905 |
| rs766819838 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | RNF114 | GRCh38.p7 | 20:49949260 | AAGGTTTGTCCGATA[C/T]GTGCCTCGATGCCCT | 55905 |
| rs766875670 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49950479 | TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 55905 |
| rs766907785 | snp | A/G | 1.65416e-05 | 0.00287586 | intron-variant | RNF114 | GRCh38.p7 | 20:49949371 | GTAAGTCTGGAGCCT[A/G]GGCTCTGATCCCTCC | 55905 |
| rs767090487 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49939425 | AAGTGTTCAGAAGAT[C/G]GCCTTTCATTATATA | 55905 |
| rs767099535 | in-del | -/C | | | downstream-variant-500B | RNF114 | GRCh38.p7 | 20:49953895 | TCTAAGTGGTAAGCT[-/C]ATGGTTCTTGTTTTC | 55905 |
| rs767151700 | snp | A/C | 1.67756e-05 | 0.00289612 | missense | RNF114 | GRCh38.p7 | 20:49946138 | TTTCACCTTCCAGGA[A/C]TGTTCCAAACCGTTA | 55905 |
| rs767598432 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49940262 | GCCTAGAATAGTCTT[C/T]CCTTCCTCTGCTAGC | 55905 |
| rs767658174 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant | RNF114 | GRCh38.p7 | 20:49941739 | GATGTGGAAGAGTCC[A/G]TGTCTTTCCATGATA | 55905 |
| rs767851964 | snp | C/T | 0.000156165 | 0.00883504 | missense | RNF114 | GRCh38.p7 | 20:49936420 | GCAGCAAGATGGCGG[C/T]GCAACAGCGGGACTG | 55905 |
| rs768023083 | snp | A/C/G | 1.64754e-05 | 0.00287009 | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952151 | CAGTGAGCAGAGTCC[A/C/G]TGCTTGCTATCTGTC | 55905 |
| rs768038100 | snp | A/C | 3.29544e-05 | 0.00405908 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49949325 | AGAGCACATCCAGCG[A/C]CGGCACCGGTTTTCT | 55905 |
| rs768133750 | snp | C/T | 0.000354589 | 0.0133105 | missense | RNF114 | GRCh38.p7 | 20:49936456 | GTGCTGCGCAGCTGG[C/T]GGGGCCGGCGGCGGA | 55905 |
| rs768255029 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946018 | TGAAGTGATCATCAG[C/T]ATCCTTATCATTACA | 55905 |
| rs768338664 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49941114 | TCCTGTAGCGCTTTG[C/T]CTTCACCTGTAATGA | 55905 |
| rs768438686 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49938682 | AAGGGCGCATAAGTA[C/G]GAAATAGAAACTGAA | 55905 |
| rs768438722 | snp | A/C | 2.08644e-05 | 0.00322983 | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936391 | CATCGGCCGCCGTTG[A/C]GCGGCGCAGAGCGGC | 55905 |
| rs768653137 | snp | C/G | 0.000139733 | 0.00835745 | missense | RNF114 | GRCh38.p7 | 20:49936431 | GCGGCGCAACAGCGG[C/G]ACTGCGGGGGTGCTG | 55905 |
| rs768719503 | snp | C/G | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49953313 | TTGCTTTAGGAACAG[C/G]TCAAGAACCTTGGAG | 55905 |
| rs768749333 | snp | A/G | | | missense | RNF114 | GRCh38.p7 | 20:49941665 | CCGTGGAGCTCGAGC[A/G]GCAGATCGAGAGCAC | 55905 |
| rs768887804 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942668 | GCTCTACTGAAAATA[C/T]AAAAAACTAGCAGGG | 55905 |
| rs769113613 | snp | C/T | 1.64914e-05 | 0.00287149 | missense | RNF114 | GRCh38.p7 | 20:49941632 | TGTGTCGCAGCGCTC[C/T]GGCACCTGGCGTCCG | 55905 |
| rs769185142 | in-del | -/CCCCCCCC | | | intron-variant | RNF114 | GRCh38.p7 | 20:49947216 | CAGAACAAAACTGCC[-/CCCCCCCC]CCCCCCCCCCCCCAA | 55905 |
| rs769236622 | snp | A/G | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935589 | GGCCAGGCTGCTCTA[A/G]TACTCCTAGGCTCAA | 55905 |
| rs769389069 | snp | A/C | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935972 | CCTGTGGTCCAGCTA[A/C]GCAGGAGGCTGAGGT | 55905 |
| rs769482316 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | RNF114 | GRCh38.p7 | 20:49952118 | ATGAATCAGGTGTTG[C/G]AGCGCTCCATCATCG | 55905 |
| rs769521870 | snp | A/G | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935768 | TGGCTGGGTACTGTG[A/G]CTCACCGCTGTAATC | 55905 |
| rs769534499 | in-del | -/AC/ATATAC | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943833 | CAGCTATATATATAT[-/AC/ATATAC]ACACACACACACACA | 55905 |
| rs769540202 | snp | A/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49949468 | TTTGTCGCTGTTGTG[A/T]TGGGCTTCCAGTCTG | 55905 |
| rs769611423 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | RNF114 | GRCh38.p7 | 20:49945409 | AAGATCCGGTCCCAC[A/G]TGGCTACTTGTTCCA | 55905 |
| rs769814354 | snp | A/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49941213 | GTATCCTCCCAGCAG[A/T]CCTAGAGGTAGGTAC | 55905 |
| rs770175404 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49944101 | TGAGACAGGGTCTGG[C/G]TTTGTTGCCCGGGCT | 55905 |
| rs770477534 | snp | C/G | 0.000284374 | 0.0119208 | missense | RNF114 | GRCh38.p7 | 20:49941698 | AGACTTCTTGCCATG[C/G]CTGCCGTAAGAATGT | 55905 |
| rs770498899 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49950947 | TAATTATCTTCAAAA[A/G]TACTTCAGGTCAAAT | 55905 |
| rs770527066 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49937173 | CCTGAATATTGTGAA[C/T]AGAGTGGTTATAATG | 55905 |
| rs770608082 | snp | A/G | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952415 | CCTGGAGCTTCTGCC[A/G]CCTCCTGTGGAAGAT | 55905 |
| rs770625286 | snp | A/G | 5.37244e-05 | 0.0051826 | missense | RNF114 | GRCh38.p7 | 20:49936524 | TTAGAGGTGTACGAG[A/G]AGCCGGTACAGGTGC | 55905 |
| rs770839644 | snp | A/T | 1.8931e-05 | 0.00307654 | intron-variant | RNF114 | GRCh38.p7 | 20:49946267 | TGAGTAACCTTTTTT[A/T]TTTTTTTTAAACTTC | 55905 |
| rs770928665 | in-del | -/TC | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935870 | GTGAGACCCGCCCGC[-/TC]TCTGCACCACTCCTT | 55905 |
| rs770945468 | snp | A/C | 1.71678e-05 | 0.00292978 | intron-variant | RNF114 | GRCh38.p7 | 20:49946128 | TTTTCCTGTGTTTCA[A/C]CTTCCAGGAATGTTC | 55905 |
| rs771000291 | in-del | -/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946054 | GGTGAGCTTTGCTCC[-/T]TTTTGGAGTGTACTG | 55905 |
| rs771144216 | snp | A/G | | | downstream-variant-500B | RNF114 | GRCh38.p7 | 20:49954160 | TTCTGCTACGTGCGG[A/G]TAACAGCAGCAGTGC | 55905 |
| rs771300568 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | RNF114 | GRCh38.p7 | 20:49945378 | CTGATTCTTCCTATT[C/T]GAGTTCTTCCTGTCC | 55905 |
| rs771342518 | snp | C/T | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49953135 | GTTTTCCTTATGACA[C/T]TGGTTTCGACATGTA | 55905 |
| rs771394615 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49944748 | TAGCTGGGCCTGATG[A/G]CACACACCTGTAATC | 55905 |
| rs772052403 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942423 | TTCCAAGAGATATAC[A/G]CAGCCTTGTTGATTT | 55905 |
| rs772096696 | snp | C/T | 9.13159e-05 | 0.00675645 | intron-variant | RNF114 | GRCh38.p7 | 20:49946282 | TTTTTTTTTAAACTT[C/T]ATTAAGGGAAAGGAT | 55905 |
| rs772101827 | in-del | -/T | 1.65932e-05 | 0.00288034 | intron-variant | RNF114 | GRCh38.p7 | 20:49949388 | CTCTGATCCCTCCCC[-/T]TGGGGGAGTGGCACG | 55905 |
| rs772133859 | snp | A/T | 1.67047e-05 | 0.00288999 | intron-variant | RNF114 | GRCh38.p7 | 20:49945520 | CCCCTTAGGTGGAGG[A/T]CATCTCTTGCTATTA | 55905 |
| rs772178867 | in-del | -/CA | | | intron-variant | RNF114 | GRCh38.p7 | 20:49938389 | GAAGACAGATGGAAG[-/CA]CACCTCTGTGAGGGC | 55905 |
| rs772186536 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | RNF114 | GRCh38.p7 | 20:49949315 | CCAACTTCAGAGAGC[A/G]CATCCAGCGCCGGCA | 55905 |
| rs772266914 | snp | C/T | | | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936385 | CCTCCTCATCGGCCG[C/T]CGTTGCGCGGCGCAG | 55905 |
| rs772338253 | snp | C/G | 1.64827e-05 | 0.00287073 | missense | RNF114 | GRCh38.p7 | 20:49945392 | TTGAGTTCTTCCTGT[C/G]CAAGATCCGGTCCCA | 55905 |
| rs772392514 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49941439 | CTTAGTATTTGAACT[C/G]GGAGGAGAGAGCAAG | 55905 |
| rs772538037 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49937130 | GTAGGAGGTTTGTTT[C/G]TTTCAGTTTTCAATT | 55905 |
| rs772836455 | snp | G/T | 1.64776e-05 | 0.00287028 | missense | RNF114 | GRCh38.p7 | 20:49945410 | AGATCCGGTCCCACG[G/T]GGCTACTTGTTCCAA | 55905 |
| rs772840531 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946367 | CCTAGATTGACAGAT[G/T]GTTAACATTTTACCA | 55905 |
| rs772904387 | snp | A/C/G | 0.000134418 | 0.008197 | missense | RNF114 | GRCh38.p7 | 20:49936437 | CAACAGCGGGACTGC[A/C/G]GGGGTGCTGCGCAGC | 55905 |
| rs773087855 | snp | C/T | 4.01929e-05 | 0.00448273 | intron-variant | RNF114 | GRCh38.p7 | 20:49946110 | TCACAGAAAAGTTTT[C/T]TTTTTTCCTGTGTTT | 55905 |
| rs773173342 | snp | C/T | 1.64893e-05 | 0.0028713 | stop-gained | RNF114 | GRCh38.p7 | 20:49941646 | CTGGCACCTGGCGTC[C/T]GAGCCGTGGAGCTCG | 55905 |
| rs773379722 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49951771 | TTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55905 |
| rs773382858 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49938721 | CCAGGATATTTGAGT[G/T]GTTCAAAAGCAGGCT | 55905 |
| rs773420761 | in-del | -/G | 1.64751e-05 | 0.00287007 | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952150 | CAGTGAGCAGAGTCC[-/G]GTGCTTGCTATCTGT | 55905 |
| rs773514262 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943407 | CCTTGGGAGGCTGAG[G/T]TGGGAAGATTGCTTG | 55905 |
| rs773585709 | snp | C/T | 3.29674e-05 | 0.00405988 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49949343 | GCACCGGTTTTCTTA[C/T]GACACTTTTGTGGTA | 55905 |
| rs773760905 | snp | A/G | 8.24205e-05 | 0.00641899 | missense | RNF114 | GRCh38.p7 | 20:49941704 | CTTGCCATGGCTGCC[A/G]TAAGAATGTATGTGG | 55905 |
| rs773782731 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943462 | GGGGAATATAGTGGA[C/T]CCAGTTTCTACAAAA | 55905 |
| rs773898709 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49939216 | ACTATCTGAAATTAA[C/T]ATTTGTGTTTCCCTT | 55905 |
| rs773986175 | snp | C/T | 0.000147823 | 0.00859592 | missense | RNF114 | GRCh38.p7 | 20:49936531 | TGTACGAGAAGCCGG[C/T]ACAGGTGCCCTGCGG | 55905 |
| rs774079668 | snp | C/T | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49936349 | CCGCTCACCGCCCCG[C/T]GAGCCCCGCCCCCTC | 55905 |
| rs774081913 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49949789 | AGCTGGGACTACAGG[C/T]GCATGCCACCATGCC | 55905 |
| rs774169482 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49937256 | GGGCTTTCGAGGTTG[A/G]TCAGGTTGGTCGATT | 55905 |
| rs774233928 | snp | G/T | 1.90442e-05 | 0.00308573 | intron-variant | RNF114 | GRCh38.p7 | 20:49946268 | GAGTAACCTTTTTTT[G/T]TTTTTTTAAACTTCA | 55905 |
| rs774275973 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49948816 | ACCTTTTGTGTGAGG[C/G]CTTTTCAGCCTGATC | 55905 |
| rs774345517 | snp | C/G | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935871 | TGAGACCCGCCCGCT[C/G]TCTGCACCACTCCTT | 55905 |
| rs774437061 | snp | C/T | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49953369 | TATAAGTCCAAGAGC[C/T]GTCAGCCTAATCTGT | 55905 |
| rs774522387 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49939962 | GGGAGTCTGAAGCAG[A/G]AGAATCGCTTGGACC | 55905 |
| rs774708503 | snp | C/T | 0.000124401 | 0.00788576 | missense | RNF114 | GRCh38.p7 | 20:49936444 | GGGACTGCGGGGGTG[C/T]TGCGCAGCTGGCGGG | 55905 |
| rs774715168 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49952135 | GCGCTCCATCATCGA[C/T]CAGTGAGCAGAGTCC | 55905 |
| rs774762810 | in-del | -/A | 2.17193e-05 | 0.00329533 | intron-variant | RNF114 | GRCh38.p7 | 20:49946276 | TTTTTTTTTTTTTTT[-/A]AACTTCATTAAGGGA | 55905 |
| rs774913732 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49944780 | CAGCTACTCAGGAGG[C/T]TGAGGTGGGAGAATC | 55905 |
| rs775076155 | snp | C/T | 3.32552e-05 | 0.00407756 | missense | RNF114 | GRCh38.p7 | 20:49946149 | AGGAATGTTCCAAAC[C/T]GTTACACCTTTCCTT | 55905 |
| rs775094421 | snp | A/C | | | intron-variant | RNF114 | GRCh38.p7 | 20:49945034 | GTGGTTTTTGGCTTG[A/C]TGTAAGGAGACTAGT | 55905 |
| rs775164035 | snp | A/G | 2.3038e-05 | 0.00339389 | intron-variant | RNF114 | GRCh38.p7 | 20:49946283 | TTTTTTTTAAACTTC[A/G]TTAAGGGAAAGGATC | 55905 |
| rs775568613 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49941510 | TTGATCCATATTTGT[C/T]GTCTTGTCTCCATGA | 55905 |
| rs775616402 | snp | G/T | 0.000419551 | 0.0144776 | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936387 | TCCTCATCGGCCGCC[G/T]TTGCGCGGCGCAGAG | 55905 |
| rs775686162 | snp | A/G | 1.648e-05 | 0.0028705 | missense | RNF114 | GRCh38.p7 | 20:49945401 | TCCTGTCCAAGATCC[A/G]GTCCCACGTGGCTAC | 55905 |
| rs775700523 | in-del | -/G | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935588 | GGCCAGGCTGCTCTA[-/G]GTACTCCTAGGCTCA | 55905 |
| rs775722244 | snp | C/T | 3.4132e-05 | 0.00413096 | intron-variant | RNF114 | GRCh38.p7 | 20:49941518 | TATTTGTCGTCTTGT[C/T]TCCATGATGCGTGAC | 55905 |
| rs775883199 | snp | C/T | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49953505 | GCTGCTGTGGGGCTC[C/T]GCGCCTGCCGGTGAA | 55905 |
| rs775948948 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49947385 | CTCTTGAACTACATA[C/T]TCTGTTGTATGGGCA | 55905 |
| rs776148672 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | RNF114 | GRCh38.p7 | 20:49949326 | GAGCACATCCAGCGC[C/T]GGCACCGGTTTTCTT | 55905 |
| rs776211914 | snp | A/G | 0.000297575 | 0.0121942 | utr-variant-5-prime | RNF114 | GRCh38.p7 | 20:49936394 | CGGCCGCCGTTGCGC[A/G]GCGCAGAGCGGCAGC | 55905 |
| rs776313885 | snp | C/G | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935737 | CTGTTATTAGAATTT[C/G]CTTAAATTTAAGAAA | 55905 |
| rs776346359 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946063 | TGCTCCTTTTTGGAG[C/T]GTACTGTGGTTGAAG | 55905 |
| rs776420674 | snp | G/T | 5.27514e-05 | 0.00513546 | missense | RNF114 | GRCh38.p7 | 20:49936435 | CGCAACAGCGGGACT[G/T]CGGGGGTGCTGCGCA | 55905 |
| rs776420736 | snp | C/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49939857 | GTCAGGAGTTCGAGA[C/G]CAGCCTGGCTAACGT | 55905 |
| rs776424061 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | RNF114 | GRCh38.p7 | 20:49941742 | GTGGAAGAGTCCATG[C/T]CTTTCCATGATAAGT | 55905 |
| rs776715438 | snp | A/T | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49953445 | GGTTTTTTGATGTCA[A/T]ATGTCTCTGATGGGG | 55905 |
| rs777021008 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942687 | AAACTAGCAGGGCAT[A/G]GTGGTGTGTGCCCGT | 55905 |
| rs777207053 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49950857 | CTATGGAAATGCAGG[C/T]GCAGCATTGCCTAGC | 55905 |
| rs777211100 | snp | A/G | 1.85414e-05 | 0.00304472 | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952232 | GTACCTTACCTGTTC[A/G]ACAGACCTGAAAATG | 55905 |
| rs777275509 | snp | C/T | 1.70493e-05 | 0.00291965 | intron-variant | RNF114 | GRCh38.p7 | 20:49941528 | CTTGTCTCCATGATG[C/T]GTGACAGAGGTTCTC | 55905 |
| rs777328791 | snp | C/T | 3.29794e-05 | 0.00406061 | missense | RNF114 | GRCh38.p7 | 20:49941638 | GCAGCGCTCTGGCAC[C/T]TGGCGTCCGAGCCGT | 55905 |
| rs777369599 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49938074 | AATGAACTAATAAGT[C/T]GTGTAAGCAAGCTTC | 55905 |
| rs777477948 | in-del | -/TCTT | | | intron-variant | RNF114 | GRCh38.p7 | 20:49944552 | CTCTGGGTTTTCTTC[-/TCTT]TCTGTTTTACTGTTG | 55905 |
| rs777670545 | snp | G/T | 1.67231e-05 | 0.00289159 | intron-variant | RNF114 | GRCh38.p7 | 20:49936600 | GCTTAACTGGGAAGG[G/T]AATGGAGCCGAGGAG | 55905 |
| rs777837503 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942202 | AGTTTGGGATTACAG[G/T]GATCTATGATCATGC | 55905 |
| rs778042618 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49945674 | GAGCTATATTCTTTT[C/T]TTCTTTTTTGAGACA | 55905 |
| rs778095478 | snp | C/T | 1.80218e-05 | 0.00300176 | stop-gained | RNF114 | GRCh38.p7 | 20:49936422 | AGCAAGATGGCGGCG[C/T]AACAGCGGGACTGCG | 55905 |
| rs778120599 | snp | C/T | 1.67987e-05 | 0.00289811 | intron-variant | RNF114 | GRCh38.p7 | 20:49949405 | GGGGGAGTGGCACGG[C/T]TACTTCACTCTTCTC | 55905 |
| rs778196092 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946686 | GGCAGGGATGGTACA[C/T]GAGTTCTCTGTCCTC | 55905 |
| rs778206078 | snp | A/T | 1.64798e-05 | 0.00287047 | stop-gained | RNF114 | GRCh38.p7 | 20:49945466 | GTGAAGGCCACCATT[A/T]AGGATGCATCTCTTC | 55905 |
| rs778212669 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49944257 | TGTATTTTCAGTAGA[A/G]ACGAGTTTTGCATGT | 55905 |
| rs778525784 | snp | A/G | | | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952594 | CTTTGGCAGCCGTGC[A/G]CCTGACCAGAGCTGA | 55905 |
| rs778583284 | snp | A/G | 1.70723e-05 | 0.00292162 | intron-variant | RNF114 | GRCh38.p7 | 20:49941511 | TGATCCATATTTGTC[A/G]TCTTGTCTCCATGAT | 55905 |
| rs778643204 | in-del | -/ATCT | | | intron-variant | RNF114 | GRCh38.p7 | 20:49939479 | GGTTATACTGTCTTA[-/ATCT]ATCTATCAGGTTGGG | 55905 |
| rs778885194 | snp | C/T | 0.000164728 | 0.00907398 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49949298 | CCCCAACTACCGCAG[C/T]GCCAACTTCAGAGAG | 55905 |
| rs779054182 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49945384 | CTTCCTATTTGAGTT[C/T]TTCCTGTCCAAGATC | 55905 |
| rs779296372 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49950117 | ATTAGCCAGGTGTGG[C/T]GGTGGGCACCTGTAA | 55905 |
| rs779370692 | snp | C/G | 1.65277e-05 | 0.00287464 | intron-variant | RNF114 | GRCh38.p7 | 20:49945503 | GGTAAATGACTCAGT[C/G]TCCCCTTAGGTGGAG | 55905 |
| rs779614930 | snp | C/T | 8.24232e-05 | 0.0064191 | synonymous-codon | RNF114 | GRCh38.p7 | 20:49941678 | GCGGCAGATCGAGAG[C/T]ACAGAGACTTCTTGC | 55905 |
| rs779671543 | snp | A/G | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49935321 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 55905 |
| rs779743787 | snp | A/G | 1.64933e-05 | 0.00287165 | missense | RNF114 | GRCh38.p7 | 20:49941626 | GTGGGGTGTGTCGCA[A/G]CGCTCTGGCACCTGG | 55905 |
| rs779825842 | snp | C/T | 4.94311e-05 | 0.00497123 | missense | RNF114 | GRCh38.p7 | 20:49949323 | AGAGAGCACATCCAG[C/T]GCCGGCACCGGTTTT | 55905 |
| rs779931633 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49939578 | TTCAGGATAGGAACT[C/T]GGTCATCTTTGACTT | 55905 |
| rs780098387 | snp | A/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943420 | AGGTGGGAAGATTGC[A/T]TGAGCCCAGAAGTTT | 55905 |
| rs780110015 | snp | G/T | 1.65078e-05 | 0.00287291 | stop-gained | RNF114 | GRCh38.p7 | 20:49946222 | TGGAACACTGCAAAT[G/T]ATTCCATAGCACGGA | 55905 |
| rs780311292 | snp | C/T | 1.80198e-05 | 0.0030016 | intron-variant | RNF114 | GRCh38.p7 | 20:49945527 | GGTGGAGGTCATCTC[C/T]TGCTATTAATACAAA | 55905 |
| rs780503825 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49949158 | ATGTCAGGAAAGCTG[C/T]CCTGGAAGAAAGGAG | 55905 |
| rs780587983 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49936708 | GCCGTGAAAGCTGCC[A/G]GGGCGCTCTTCTGTC | 55905 |
| rs780596561 | snp | A/G | 1.64762e-05 | 0.00287016 | splice-acceptor-variant | RNF114 | GRCh38.p7 | 20:49952075 | CTCTTTTTGCCCTTA[A/G]GATTATGATGTTGAT | 55905 |
| rs780694036 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49947088 | AGCCAGGCATGGTGG[C/T]GGGCGCCTTTAATCC | 55905 |
| rs780874648 | snp | A/C/G | 0.000144464 | 0.00849788 | intron-variant | RNF114 | GRCh38.p7 | 20:49936593 | GGGGGGCGCTTAACT[A/C/G]GGAAGGGAATGGAGC | 55905 |
| rs780927181 | in-del | -/AA | | | intron-variant | RNF114 | GRCh38.p7 | 20:49942270 | TCTTAAAAAAAAGTC[-/AA]TATGAAATCATTGGA | 55905 |
| rs780939153 | snp | A/G | 1.65064e-05 | 0.00287279 | intron-variant | RNF114 | GRCh38.p7 | 20:49945358 | TCCTCACTAACTTAT[A/G]GGCTCTGATTCTTCC | 55905 |
| rs781014788 | in-del | -/CCCCCCCCC | | | intron-variant | RNF114 | GRCh38.p7 | 20:49947215 | GCAGAACAAAACTGC[-/CCCCCCCCC]CCCCCCCCCCCCCAA | 55905 |
| rs781163734 | snp | C/T | 1.81115e-05 | 0.00300922 | utr-variant-3-prime | RNF114 | GRCh38.p7 | 20:49952225 | GACTCCTGTACCTTA[C/T]CTGTTCAACAGACCT | 55905 |
| rs781233035 | snp | C/T | 9.59647e-05 | 0.00692626 | missense | RNF114 | GRCh38.p7 | 20:49936480 | CGGCGGAGGCTGACC[C/T]CCTAGGACGCTTCAC | 55905 |
| rs781360718 | snp | G/T | 2.5155e-05 | 0.00354639 | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49936365 | GAGCCCCGCCCCCTC[G/T]GCCTCCTCCTCATCG | 55905 |
| rs781379961 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943126 | CCATCTCCTTTTCAG[C/T]GTGATTTAGTATTAG | 55905 |
| rs781538958 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | RNF114 | GRCh38.p7 | 20:49949288 | CCTGGGGAGACCCCA[A/G]CTACCGCAGCGCCAA | 55905 |
| rs781703504 | snp | A/G | | | downstream-variant-500B | RNF114 | GRCh38.p7 | 20:49954270 | TGTGGGGCATCTAGC[A/G]AATATTTTCTGAACC | 55905 |
| rs781760917 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49936851 | TGATAGTGGACTCGT[G/T]CCCTGCGGGGACTTT | 55905 |
| rs796304852 | multinucleotide-polymorphism | AA/CC | | | intron-variant | RNF114 | GRCh38.p7 | 20:49947235 | CCCCCCCCCCCCCCC[AA/CC]AAAAAGTATTTGTTC | 55905 |
| rs796420182 | in-del | -/TT | | | intron-variant | RNF114 | GRCh38.p7 | 20:49946261 | CTGTGGTGAGTAACC[-/TT]TTTTTTTTTTTTTAA | 55905 |
| rs796736530 | snp | A/G | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943319 | GGGCAACATAGTGGG[A/G]CTCTGTATATACCAA | 55905 |
| rs796767761 | snp | C/T | | | upstream-variant-2KB | RNF114 | GRCh38.p7 | 20:49934593 | TCACTTGAGGTCAGG[C/T]GTTTGAGACCAGCCT | 55905 |
| rs796790727 | snp | C/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49943837 | CTATATATATATACA[C/T]ACACACACACACACA | 55905 |
| rs796926877 | snp | G/T | | | intron-variant | RNF114 | GRCh38.p7 | 20:49947784 | GTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 55905 |