Knowledge base for genomic medicine in Japanese
網膜芽細胞腫
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_000321.2(RB1):c.1402_1412dup (p.Gln471Hisfs)RB1Pathogenic134895419948954200GGATTATCCATTCcriteria provided, single submitterClinGen:CA275022
single nucleotide variantNM_000321.3(RB1):c.1696-1G>ARB1Pathogenic134902712849027128GAcriteria provided, multiple submitters, no conflictsClinGen:CA026395
single nucleotide variantNM_000321.3(RB1):c.2370C>A (p.Tyr790Ter)RB1Pathogenic134903938549039385CAcriteria provided, single submitterClinGen:CA026439
single nucleotide variantNM_000321.3(RB1):c.297G>A (p.Trp99Ter)RB1Pathogenic134891676748916767GAcriteria provided, multiple submitters, no conflictsClinGen:CA026447
single nucleotide variantNM_000321.3(RB1):c.1154T>G (p.Leu385Ter)RB1Pathogenic134894756748947567TGcriteria provided, single submitterClinGen:CA10583158
single nucleotide variantNM_000321.3(RB1):c.1814+3A>CRB1Pathogenic134902725049027250ACcriteria provided, single submitterClinGen:CA10583159
single nucleotide variantNM_000321.3(RB1):c.2053C>T (p.Gln685Ter)RB1Pathogenic134903391649033916CTcriteria provided, multiple submitters, no conflictsClinGen:CA10583160
DeletionNM_000321.3(RB1):c.376del (p.Ile126fs)RB1Pathogenic134891684448916844GAGcriteria provided, multiple submitters, no conflictsClinGen:CA10604120
single nucleotide variantNM_000321.3(RB1):c.2548C>T (p.Gln850Ter)RB1Pathogenic134905086449050864CTcriteria provided, single submitterClinGen:CA10604891
single nucleotide variantNM_000321.3(RB1):c.1510C>T (p.Gln504Ter)RB1Pathogenic134895539448955394CTcriteria provided, multiple submitters, no conflictsClinGen:CA10605288