RNF41
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs773308555snpA/Gupstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variantRNF41, NABP2GRCh38.p712:56221844CTGCCCTGGTGCCGG[A/G]TCCCAGCCTCTCCCG10193
rs773431925snpA/Cintron-variant, upstream-variant-2KBRNF41, NABP2GRCh38.p712:56220958TGCCCTATTGTCAGA[A/C]TCTAAAACCCCTGTA10193
rs773517056snpC/T1.6483e-050.00287076intron-variantRNF41GRCh38.p712:56208144AGGGATATGTTCTCC[C/T]CCGTGTCTTGGGGCC10193
rs773662119in-del-/AAAintron-variantRNF41GRCh38.p712:56215718GCACGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA10193
rs773719764snpC/T1.65021e-050.00287241synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56208247CTGTACCACTGAGCG[C/T]AGGTGCTTAATGCAG10193
rs774073863snpC/Tintron-variant, upstream-variant-2KBRNF41GRCh38.p712:56217957TGCTTTCACATAAAT[C/T]ATTATTATTATTTCG10193
rs774161113snpA/Gintron-variantRNF41GRCh38.p712:56208668CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG10193
rs774190140snpA/G3.15981e-050.00397467intron-variantRNF41GRCh38.p712:56206850ATCTCCTTTCTCTGT[A/G]TTGGCTTTTTCTGCT10193
rs774559826snpA/G1.65395e-050.00287567synonymous-codon, utr-variant-5-prime, nc-transcript-variantRNF41GRCh38.p712:56210530AGAGAACCACTGGGT[A/G]ATGCAGGCGTTGCAG10193
rs774588272snpA/Gintron-variantRNF41GRCh38.p712:56213412ACCATGTTGGCCAGG[A/G]TGGCTCTTGAACTCG10193
rs774809907snpA/Gintron-variantRNF41GRCh38.p712:56214379TACAAAAATTAGCTG[A/G]GTGTGGTATGCGCAT10193
rs774897383snpC/Tupstream-variant-2KB, intron-variantRNF41, NABP2GRCh38.p712:56221724CCCCTCCCACACCCT[C/T]TTTTAGGTGGAAGAT10193
rs774953461snpC/T1.64727e-050.00286986missense, nc-transcript-variantRNF41GRCh38.p712:56207725TTGCACGCATGTATG[C/T]CTTTAGCAGCTGGAT10193
rs775004661snpG/T1.64876e-050.00287116intron-variantRNF41GRCh38.p712:56208131TTATCTGCATATGAG[G/T]GATATGTTCTCCCCC10193
rs775031054snpC/Gutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56204661GACAGGACAGTATGA[C/G]CCTTGGTTAAGGCAG10193
rs775086939snpC/T3.29571e-050.00405924intron-variantRNF41GRCh38.p712:56213944CCACCAAACCTGCCA[C/T]CAGACCAACTCACCT10193
rs775127855snpA/Tintron-variantRNF41GRCh38.p712:56212766GAGTAGTACTGGGAG[A/T]AAAAATAAAGGCTCA10193
rs775270365snpC/T1.64743e-050.00287synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56206549CATCACGACAACAGC[C/T]TGCTTGCCAGGGATG10193
rs775468696snpC/G1.67711e-050.00289573intron-variantRNF41GRCh38.p712:56208310CAGGCTGCAGACCAG[C/G]GTGGGGAAAGAGCAG10193
rs775582891snpC/Tintron-variantRNF41GRCh38.p712:56208927TGGAGTGCAATGGCA[C/T]GGTCTCAGCTCACTG10193
rs775735983snpC/T3.31472e-050.00407093missense, nc-transcript-variantRNF41GRCh38.p712:56210346GGTTGTGCTCACAGT[C/T]GCTGAGGTGAGACAT10193
rs776121028snpA/Cintron-variant, upstream-variant-2KBRNF41GRCh38.p712:56216881CGTGGTGGCTCACGC[A/C]TGTAATCCCAGCTCT10193
rs776149944snpC/T1.64754e-050.00287009intron-variantRNF41GRCh38.p712:56207603TCCTTTCAGGCCTTG[C/T]TGTCAGGACATGAAA10193
rs776260977snpG/Tintron-variantRNF41GRCh38.p712:56211364ATAAATATATATATA[G/T]ATATTCCCTGTGCTC10193
rs776343820snpC/T1.64727e-050.00286986missense, nc-transcript-variantRNF41GRCh38.p712:56207719TGCGGATTGCACGCA[C/T]GTATGCCTTTAGCAG10193
rs776381579snpC/Gintron-variantRNF41GRCh38.p712:56214086CTGAAAGGACAACAG[C/G]AAAAAGAGGCCAGTT10193
rs776402446snpC/Tintron-variantRNF41GRCh38.p712:56212452CTCAGAAGATAAAGC[C/T]TGGAGGTAGATGGGT10193
rs776479109snpC/Tupstream-variant-2KB, utr-variant-5-primeRNF41, NABP2GRCh38.p712:56222090GTCTAGTCTAGAGTC[C/T]ATATGGTCCCAGCCA10193
rs776808054snpC/Tutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56205107CTTAGAACCCAGCTA[C/T]ACAGCTCCAAGGAAA10193
rs776849265snpA/G1.65693e-050.00287826synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56208276AGTTATGGTTGGGCA[A/G]CTCATCTTTGGGCAT10193
rs776921587snpA/Gutr-variant-5-prime, nc-transcript-variantRNF41GRCh38.p712:56216507AGTGCCACTGAAGAG[A/G]TTCTCCCAGTAACCC10193
rs777045424snpC/T4.97673e-050.00498811missense, nc-transcript-variantRNF41GRCh38.p712:56210327CAGGTCACAGGCCGC[C/T]TCGGGTTGTGCTCAC10193
rs777198394snpC/Tintron-variant, upstream-variant-2KBRNF41GRCh38.p712:56217446CAGCTACTCAGGAGG[C/T]TGAGGCAGGGAGAAT10193
rs777204332snpA/Gintron-variantRNF41GRCh38.p712:56214623GAGCTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG10193
rs777315691snpC/Gintron-variant, upstream-variant-2KBRNF41, NABP2GRCh38.p712:56221284ATGGAGGGCTGGGAG[C/G]GGGTGAGGAGCGGGG10193
rs777423759in-del-/A/TAintron-variantRNF41GRCh38.p712:56219198TTTATTTATTTATTT[-/A/TA]ATTTTTTTTTTGAGA10193
rs777452893snpC/Tintron-variant, upstream-variant-2KBRNF41GRCh38.p712:56218322TGGAGTACAGTGGCA[C/T]GATCATAGCTCACTA10193
rs777483024snpC/G3.29457e-050.00405854intron-variantRNF41GRCh38.p712:56207785AGGAATAATGGTTAA[C/G]GCAGACAGCAGAAAA10193
rs777483595snpA/G1.64727e-050.00286986synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56207696GTTCTGAAGGTTGGG[A/G]TTGACACTGCGGATT10193
rs777962986snpC/Gupstream-variant-2KB, intron-variantRNF41, NABP2GRCh38.p712:56223596CAGGTTCCATTTCTT[C/G]CAAGAAGGGTGAGCC10193
rs778065480snpC/T1.65081e-050.00287293splice-acceptor-variantRNF41GRCh38.p712:56214071ACTGAAACCCAGGTC[C/T]TGAAAGGACAACAGG10193
rs778144429snpC/T0.000232980.0107905missense, nc-transcript-variantRNF41GRCh38.p712:56210306TCTCACCCACAGCCC[C/T]GTTCACAGGTCACAG10193
rs778162442snpC/Gintron-variantRNF41GRCh38.p712:56207958ATGTGATAACTGGTA[C/G]GTGAATTAATGCTAT10193
rs778162723snpA/Cdownstream-variant-500BRNF41GRCh38.p712:56202032CTACCTAAGAGGCTG[A/C]GGTAGGAGGATCACT10193
rs778333547snpA/Gintron-variant, upstream-variant-2KBRNF41GRCh38.p712:56218010CTAGGCTAGAGTGCA[A/G]TGGCGCGATCTTGGC10193
rs778541493snpA/G6.60437e-050.00574608synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56210404ACAGCCGAACACAGC[A/G]TTGTCACAGGCAATC10193
rs778568033snpA/Cintron-variantRNF41GRCh38.p712:56209855GTGACTTGCCCACTT[A/C]GGCCTCCCAAAGTGC10193
rs778798724in-del-/TGTGintron-variantRNF41GRCh38.p712:56219662GTGTGTGTGTATATA[-/TGTG]TATATACACGCGCGC10193
rs778799698snpA/G4.94173e-050.00497053synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56207657TCACTCTAGGATCTC[A/G]TTGTATTCAATTGTC10193
rs778814117snpC/Tutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56202559TACAAAAGCAGGCAG[C/T]GGGGTTGTAACCTGT10193
rs778867163snpC/Tutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56204172CAAAGGAAAAAGATA[C/T]ATACATATCTTCTGT10193
rs778930429snpA/Gintron-variantRNF41GRCh38.p712:56218767GGAGTACAGTGGCAC[A/G]ATCTTGGCTCACTGC10193
rs779027557in-del-/A0.0007099580.0188275intron-variantRNF41GRCh38.p712:56214087TGAAAGGACAACAGG[-/A]AAAAGAGGCCAGTTC10193
rs779214645snpA/Gintron-variantRNF41GRCh38.p712:56211845GGCGTGGTGGCGGGT[A/G]CCTGTAGTCTCAGCT10193
rs779256471snpA/G6.78346e-050.00582346synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56206462TTATATCTCTTCCAC[A/G]CCATGCGCAAATATC10193
rs779316077snpC/Tupstream-variant-2KB, intron-variantRNF41, NABP2GRCh38.p712:56222836GTTTATACACAACAA[C/T]ACAGAGCTAGCTACC10193
rs779365423snpG/Tutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56205930TGCTTGGCACAGAGG[G/T]CCAGTCTTTCCCTAA10193
rs779596851snpA/Gintron-variantRNF41GRCh38.p712:56213487TGAGCCACTGTGCCC[A/G]GCCTTCCTATTTGTT10193
rs779627739snpC/Gutr-variant-3-prime, nc-transcript-variant, downstream-variant-500BRNF41GRCh38.p712:56203030AAACATACCTTGTGT[C/G]CATAGAAGCGCAGAC10193
rs779940450snpA/G/T6.58896e-050.00573943synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56207651TGACACTCACTCTAG[A/G/T]ATCTCGTTGTATTCA10193
rs780074577snpA/G4.0235e-050.00448507intron-variantRNF41GRCh38.p712:56206805TTCACCCACCTGTGT[A/G]GAGGTGGTTAAAGAT10193
rs780128243in-del-/Tupstream-variant-2KB, intron-variantRNF41, NABP2GRCh38.p712:56223820TACATATTTTTTGTC[-/T]TTTTTTCCCTTTTTG10193
rs780145933snpA/G1.6489e-050.00287128missense, utr-variant-5-prime, nc-transcript-variantRNF41GRCh38.p712:56210477CGCAGATGGGCGACC[A/G]TCACAACACTACGGT10193
rs780170511snpA/Gintron-variantRNF41GRCh38.p712:56209584TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA10193
rs780288436in-del-/Cintron-variantRNF41GRCh38.p712:56211796GCTAACATAGCGAAA[-/C]CCTGTCTCTACTAAA10193
rs780792583snpA/Gintron-variantRNF41GRCh38.p712:56215227AGCAAGGGCCATGCT[A/G]TGAAAAGTCTGTGAG10193
rs780893150snpA/Gutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56204452TAAGGTGAGAGAAAG[A/G]CAAAAGCAGAGGGGA10193
rs780961663snpA/Gupstream-variant-2KB, intron-variantRNF41, NABP2GRCh38.p712:56222616GATGTGGGCGGTAGA[A/G]AACGTGGGATCCAAG10193
rs781015009snpC/Gutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56205643TATCAAAGTAACTAA[C/G]TACAGTCACAGGGCT10193
rs781025263snpC/T1.64784e-050.00287035synonymous-codon, nc-transcript-variantRNF41GRCh38.p712:56208205AGCTGACGTCTTCTC[C/T]AGCTCTGCGATGCGT10193
rs781220038snpC/Tintron-variant, utr-variant-5-prime, nc-transcript-variantRNF41GRCh38.p712:56213117TCAAAATGCAGAGTG[C/T]ATGGCTGTATCAAAA10193
rs781243134snpC/T1.68801e-050.00290512missense, nc-transcript-variantRNF41GRCh38.p712:56206763ATCATCCCTCCCCAG[C/T]GGGTCACTCTTGCTG10193
rs781563996in-del-/AAintron-variantRNF41GRCh38.p712:56214521CGAGCCTCAGTCTCT[-/AA]AAAAAAAAAAAAAAT10193
rs781645291snpA/G1.64882e-050.00287121synonymous-codon, utr-variant-5-prime, nc-transcript-variantRNF41GRCh38.p712:56210467AGGTACTGGGCGCAG[A/G]TGGGCGACCGTCACA10193
rs781689655snpC/T0.0001357270.0082368intron-variantRNF41GRCh38.p712:56210596ACAAGGCAAAAGGGG[C/T]GCAAGGGAATTAGCA10193
rs781700266snpC/Tintron-variantRNF41GRCh38.p712:56210080CACAAATTTACTAAA[C/T]TGCTGTGCCCCTTCT10193
rs796126131in-del-/Aintron-variantRNF41GRCh38.p712:56211184ATCTCGAAAAAAAAA[-/A]GCTGGGCCTGGTGGC10193
rs796226237in-del-/Cutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56205574AAAAAAAAGAGGGGG[-/C]GGGGGCAGTAGGTGG10193
rs796231451snpA/Gintron-variantRNF41GRCh38.p712:56215741AAAAAAAAAAAAAGA[A/G]AGGTCCAAAAGAGCA10193
rs796248392in-del-/TTutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56203188CCTTTTTCTTTTCTT[-/TT]CTTTTTTTTTTTTGA10193
rs796258832in-del-/Tintron-variantRNF41GRCh38.p712:56213205TCCTATTTGTTTTTG[-/T]TTTTTTTTTTTTTGA10193
rs796264790in-del-/TAintron-variantRNF41GRCh38.p712:56219198ATTTATTTATTTATT[-/TA]TTTTTTTTTTGAGAC10193
rs796314078snpC/Tutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56205552ATAGCCATGATCAGG[C/T]CATTCTTAAAAAAAA10193
rs796362219snpG/Tintron-variantRNF41GRCh38.p712:56215905GGTGGGTGGATCACC[G/T]GAGGTCAGGAGTTCA10193
rs796549473snpA/Gintron-variantRNF41GRCh38.p712:56211635GATAATTCAGATGAT[A/G]GATTTAGAGAGGAGG10193
rs796642921in-del-/GGutr-variant-3-prime, nc-transcript-variantRNF41GRCh38.p712:56203399ATACTTATGAAGACT[-/GG]TTTTTTTTTTTTTTT10193
rs796908541snpC/Tintron-variant, upstream-variant-2KBRNF41GRCh38.p712:56218336ATGATCATAGCTCAC[C/T]ACAGCCTCGCCTTCC10193
rs796980194in-del-/Cintron-variantRNF41GRCh38.p712:56215946GCCAACATGGTGAAA[-/C]CCCCATCTCTACTAA10193
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