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)
single nucleotide variantNM_000321.3(RB1):c.2325+1G>ARB1Pathogenic134903924849039248GAcriteria provided, multiple submitters, no conflictsClinGen:CA388167737
DeletionNM_000321.3(RB1):c.2299_2302del (p.Asn767fs)RB1Pathogenic134903922049039223CAAATCcriteria provided, single submitterClinGen:CA645369595
single nucleotide variantNM_000321.3(RB1):c.2284C>T (p.Gln762Ter)RB1Pathogenic134903920649039206CTcriteria provided, single submitter-
InsertionNM_000321.3(RB1):c.2247_2248insAA (p.Asp750fs)RB1Pathogenic134903916949039170TTAAcriteria provided, single submitterClinGen:CA658798152
single nucleotide variantNM_000321.3(RB1):c.2242G>T (p.Glu748Ter)RB1Pathogenic134903916449039164GTcriteria provided, single submitterClinGen:CA026433,OMIM:614041.0010
DeletionNC_000013.11:g.(?_48464992)_(48465374_?)delRB1Pathogenic134903912849039510nanacriteria provided, single submitter-
single nucleotide variantNM_000321.3(RB1):c.2211G>T (p.Glu737Asp)RB1Pathogenic134903797149037971GTcriteria provided, single submitterClinGen:CA388167239
single nucleotide variantNM_000321.3(RB1):c.2211G>A (p.Glu737=)RB1Pathogenic134903797149037971GAcriteria provided, single submitterClinGen:CA026429,OMIM:614041.0021
single nucleotide variantNM_000321.3(RB1):c.2206C>T (p.Gln736Ter)RB1Pathogenic134903796649037966CTcriteria provided, single submitter-
DeletionNM_000321.3(RB1):c.2194_2197del (p.Pro732fs)RB1Pathogenic134903795449037957TCCTCTcriteria provided, single submitterClinGen:CA16614023