Fbxo18
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs585274728snpG/Tintron-variantFbxo18GRCm38.p32:11752705GCCTTGCTCAATCCC[G/T]AATAACACAAAAAGA50755
rs585340069snpA/Gintron-variantFbxo18GRCm38.p32:11765978ACTCTGTGTAACCCA[A/G]CCCCTCCCTATCCCC50755
rs585383130snpA/Gintron-variantFbxo18GRCm38.p32:11743508CCATAGAAAACTCTT[A/G]GGGAAGGAAGCATTA50755
rs585446867snpA/Gintron-variant, utr-variant-3-prime, nc-transcript-variantFbxo18GRCm38.p32:11744669TCCTGTGTCCACTGC[A/G]TATTCCTGTGTCCAC50755
rs585474428snpA/Gintron-variant, utr-variant-3-prime, nc-transcript-variantFbxo18GRCm38.p32:11744916TCCTGTGTCCACTGC[A/G]TATTCCTGTGTCCAC50755
rs585531167snpA/Tintron-variantFbxo18GRCm38.p32:11751216AGAAGAAGAAGAAGA[A/T]AAAGAGGAGGAGGAG50755
rs585696399snpA/Gintron-variantFbxo18GRCm38.p32:11751241GAGGAGGAGGAGGAA[A/G]AAGAAGAAGATGAGA50755
rs585757672snpC/Tintron-variantFbxo18GRCm38.p32:11754695ACATCCCTCCATGGC[C/T]TCTGCATCAGCTCCT50755
rs585791806snpC/Tintron-variantFbxo18GRCm38.p32:11750823ACAGTCAACACACAG[C/T]CAGGAGACCCTGGGG50755
rs585997475snpA/Gintron-variant, utr-variant-3-prime, nc-transcript-variantFbxo18GRCm38.p32:11744935TCCTGTGTCCACTGC[A/G]TATTCCTGTCTCCAC50755
rs586126227snpG/Tintron-variantFbxo18GRCm38.p32:11754662TTGAGCAAGCCAGGG[G/T]AAGCAAGCCAGTAAA50755
rs586132323snpA/Tintron-variant, downstream-variant-500BFbxo18GRCm38.p32:11744628TATTCCTGTGTCCAC[A/T]GCGTATTCCTGTCTC50755
rs586235970snpA/Cintron-variantFbxo18GRCm38.p32:11753748GTGATTAAGAAGAGA[A/C]CAGCATCATTGAGGT50755
rs586245668snpA/Gintron-variantFbxo18GRCm38.p32:11753981GCCTCAGTTGCAATC[A/G]ACGGCCCAGGACTGA50755
rs586246747snpA/Gintron-variant, downstream-variant-500BFbxo18GRCm38.p32:11744348CTGTCTCCACTGCGT[A/G]TTCCTGTCTCCACTG50755
rs586361833snpA/Gintron-variantFbxo18GRCm38.p32:11753407TGACAACCTGACCAT[A/G]TTTTGGGGAGGACTG50755
rs586412262snpA/Cintron-variantFbxo18GRCm38.p32:11771286ACACACACACACACA[A/C]ACACACACACACACA50755
rs586615489snpC/Tintron-variantFbxo18GRCm38.p32:11774982ATTTTTCTCCATTTC[C/T]CAGATTTACTATGAA50755
rs586616266snpC/Tintron-variant, utr-variant-3-prime, nc-transcript-variantFbxo18GRCm38.p32:11744751GTCCACTGCGTATTC[C/T]TGTCTCTACTGCGTA50755
rs586617694snpA/Gintron-variant, utr-variant-3-primeFbxo18GRCm38.p32:11745000CCACTGCGTATTCCT[A/G]TCTCCACTGCGTATT50755
rs586631394snpA/Tintron-variant, downstream-variant-500BFbxo18GRCm38.p32:11744400TATTCCTGTGTCCAC[A/T]GCGTATTCCTGTCTC50755
rs586719569snpA/Gintron-variantFbxo18GRCm38.p32:11758484GACTGTGACCCTCTG[A/G]TTAGGTAATTGTGCA50755
rs586725546snpA/Gintron-variant, utr-variant-3-prime, nc-transcript-variantFbxo18GRCm38.p32:11744688TCCTGTGTCCACTGC[A/G]TATTCCTGTCTCCAC50755
rs586739503snpA/Gintron-variantFbxo18GRCm38.p32:11752650CATGAGGATTTTTAG[A/G]CTGGGGATCCAGAGC50755
rs586918999snpA/Gintron-variantFbxo18GRCm38.p32:11772740CATTCTATGTTTGGA[A/G]CTATTGGTTATTGCA50755
rs587007411snpA/Cintron-variantFbxo18GRCm38.p32:11765140ACAACACAACTTAAC[A/C]GACACCGTGGAAACA50755
rs587110849snpC/Tintron-variantFbxo18GRCm38.p32:11751324ACTCCACAGGACTGT[C/T]TCACTAGCACAGAGT50755
rs587199008snpC/Gintron-variant, utr-variant-3-prime, nc-transcript-variantFbxo18GRCm38.p32:11744717ACTGCGTATTCCTGT[C/G]TCCACTGCGTATTCC50755
rs587291663snpA/Gintron-variant, downstream-variant-500BFbxo18GRCm38.p32:11744517TCCTGTGTCCACTGC[A/G]TATTCCTGTGTCCAC50755
rs587307726snpA/Gintron-variantFbxo18GRCm38.p32:11754373ATGTAAAGACTGTGG[A/G]ACGCTTAAAGTTATT50755
rs587324770snpA/Tintron-variant, utr-variant-3-primeFbxo18GRCm38.p32:11744970TATTCCTGTGTCCAC[A/T]GCGTATTCTTGTCTC50755
rs587457890snpA/Cintron-variantFbxo18GRCm38.p32:11754130GGGCATGGCTGGAGA[A/C]GTGACCCAAGCCCTT50755
rs587460932snpA/Gintron-variant, downstream-variant-500BFbxo18GRCm38.p32:11744441TCCTGTCTCCACTGC[A/G]TATTCCTGTCTCCAC50755
Page 1 | 2