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Variants search result for All species
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21 records found for search term Fam155a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582606CV117159single nucleotide variantNM_001080396.2(FAM155A):c.916-48619C>GLung cancer [RCV000097680]uncertain significance13107259374107259374Humanname
8582607CV117160single nucleotide variantNM_001080396.2(FAM155A):c.916-52907G>TLung cancer [RCV000097681]uncertain significance13107263662107263662Humanname
8582608CV117161single nucleotide variantNM_001080396.2(FAM155A):c.916-97116A>TLung cancer [RCV000097682]uncertain significance13107307871107307871Humanname
8582622CV117175single nucleotide variantNM_001080396.2(FAM155A):c.915+99287G>ALung cancer [RCV000097696]uncertain significance13107766395107766395Humanname
8582623CV117176single nucleotide variantNM_001080396.2(FAM155A):c.915+49267C>ALung cancer [RCV000097697]uncertain significance13107816415107816415Humanname
8582624CV117177single nucleotide variantNM_001080396.2(FAM155A):c.915+45341G>TLung cancer [RCV000097698]uncertain significance13107820341107820341Humanname
8582605CV117158single nucleotide variantNM_001080396.2(FAM155A):c.1087+15811T>CLung cancer [RCV000097679]uncertain significance13107194773107194773Humanname
8582609CV117162single nucleotide variantNM_001080396.2(FAM155A):c.916-111296C>ALung cancer [RCV000097683]uncertain significance13107322051107322051Humanname
8582610CV117163single nucleotide variantNM_001080396.2(FAM155A):c.916-123797A>TLung cancer [RCV000097684]uncertain significance13107334552107334552Humanname
8582611CV117164single nucleotide variantNM_001080396.2(FAM155A):c.916-130497G>TLung cancer [RCV000097685]uncertain significance13107341252107341252Humanname
8582612CV117165single nucleotide variantNM_001080396.2(FAM155A):c.916-142126C>GLung cancer [RCV000097686]uncertain significance13107352881107352881Humanname
8582613CV117166single nucleotide variantNM_001080396.2(FAM155A):c.916-168912C>TLung cancer [RCV000097687]uncertain significance13107379667107379667Humanname
8582614CV117167single nucleotide variantNM_001080396.2(FAM155A):c.916-222753G>TLung cancer [RCV000097688]uncertain significance13107433508107433508Humanname
8582615CV117168single nucleotide variantNM_001080396.2(FAM155A):c.916-249870C>GLung cancer [RCV000097689]uncertain significance13107460625107460625Humanname
8582616CV117169single nucleotide variantNM_001080396.2(FAM155A):c.916-290983A>TLung cancer [RCV000097690]uncertain significance13107501738107501738Humanname
8582617CV117170single nucleotide variantNM_001080396.2(FAM155A):c.916-311279C>GLung cancer [RCV000097691]uncertain significance13107522034107522034Humanname
8582618CV117171single nucleotide variantNM_001080396.2(FAM155A):c.915+245629A>GLung cancer [RCV000097692]uncertain significance13107620053107620053Humanname
8582619CV117172single nucleotide variantNM_001080396.2(FAM155A):c.915+226320C>GLung cancer [RCV000097693]uncertain significance13107639362107639362Humanname
8582620CV117173single nucleotide variantNM_001080396.2(FAM155A):c.915+155206T>ALung cancer [RCV000097694]uncertain significance13107710476107710476Humanname
8582621CV117174single nucleotide variantNM_001080396.2(FAM155A):c.915+122976C>GLung cancer [RCV000097695]uncertain significance13107742706107742706Humanname
8627414CV82558single nucleotide variantNM_001080396.2(FAM155A):c.144C>T (p.Phe48=)Malignant melanoma [RCV000062637]not provided13107866453107866453Humanname