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.2134T>C (p.Cys712Arg)RB1Pathogenic/Likely pathogenic134903789449037894TCcriteria provided, multiple submitters, no conflictsClinGen:CA026423,UniProtKB:P06400#VAR_005587,OMIM:614041.0024
single nucleotide variantNM_000321.3(RB1):c.607+1G>TRB1Pathogenic134892316048923160GTcriteria provided, multiple submitters, no conflictsClinGen:CA026463,OMIM:614041.0025
single nucleotide variantNM_000321.3(RB1):c.1818T>A (p.Tyr606Ter)RB1Pathogenic134903034349030343TAcriteria provided, single submitterClinGen:CA026402,OMIM:614041.0026
single nucleotide variantNM_000321.3(RB1):c.2490-1398A>GRB1Pathogenic134904609849046098AGcriteria provided, single submitterClinGen:CA026441,OMIM:614041.0028
single nucleotide variantNM_000321.3(RB1):c.1399C>T (p.Arg467Ter)RB1Pathogenic134895419848954198CTcriteria provided, multiple submitters, no conflictsClinGen:CA026376
DuplicationNM_000321.3(RB1):c.1585dup (p.Tyr529fs)RB1Pathogenic134895546448955465AATcriteria provided, single submitterClinGen:CA026382
IndelNM_000321.3(RB1):c.2067_2079delinsCAC (p.Gln689fs)RB1Pathogenic134903393049033942GAATGAGTATGAACACcriteria provided, single submitterClinGen:CA026419
single nucleotide variantNM_000321.3(RB1):c.1960G>A (p.Val654Met)RB1Pathogenic134903048549030485GAcriteria provided, single submitterClinGen:CA026413
single nucleotide variantNM_000321.3(RB1):c.1723C>T (p.Gln575Ter)RB1Pathogenic134902715649027156CTcriteria provided, single submitterClinGen:CA026397
single nucleotide variantNM_000321.3(RB1):c.1735C>T (p.Arg579Ter)RB1Pathogenic134902716849027168CTcriteria provided, multiple submitters, no conflictsClinGen:CA026398