Knowledge base for genomic medicine in Japanese
膵臓がん・悪性黒色腫症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000077.5(CDKN2A):c.377T>A (p.Val126Asp)CDKN2APathogenic92197098121970981ATcriteria provided, multiple submitters, no conflictsClinGen:CA120398,UniProtKB:P42771#VAR_001479,OMIM:600160.0013
IndelNM_000077.5(CDKN2A):c.381_393delinsGATGCG (p.Arg128fs)CDKN2ALikely pathogenic92197096521970977GCGCAGGTACCGTCGCATCcriteria provided, single submitterClinGen:CA658656022
single nucleotide variantNM_000077.5(CDKN2A):c.457G>T (p.Asp153Tyr)CDKN2APathogenic/Likely pathogenic92197090121970901CAcriteria provided, multiple submitters, no conflictsClinGen:CA337714
single nucleotide variantNM_000077.5(CDKN2A):c.458-105A>GCDKN2APathogenic/Likely pathogenic92196834621968346TCcriteria provided, multiple submitters, no conflictsClinGen:CA16612773,OMIM:600160.0014