Knowledge base for genomic medicine in Japanese
カテコラミン誘発性多形性心室頻拍
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_001743.6(CALM2):c.293A>T (p.Asn98Ile)CALM2Pathogenic24738899047388990TAcriteria provided, single submitterClinGen:CA186027,UniProtKB:P62158#VAR_073277,OMIM:114182.0004
single nucleotide variantNM_001743.6(CALM2):c.293A>G (p.Asn98Ser)CALM2Pathogenic24738899047388990TCcriteria provided, multiple submitters, no conflictsClinGen:CA186025,UniProtKB:P62158#VAR_069223,OMIM:114182.0003
single nucleotide variantNM_001743.6(CALM2):c.396T>G (p.Asp132Glu)CALM2Pathogenic24738888747388887ACcriteria provided, single submitterClinGen:CA186030,UniProtKB:P62158#VAR_073279,OMIM:114182.0005
single nucleotide variantNM_001743.6(CALM2):c.414C>G (p.Asn138Lys)CALM2Pathogenic24738886947388869GCcriteria provided, single submitterClinGen:CA346719008
single nucleotide variantNM_001743.6(CALM2):c.434T>G (p.Met145Arg)CALM2Likely pathogenic24738793147387931ACcriteria provided, single submitter-
single nucleotide variantNM_005184.4(CALM3):c.422A>G (p.Glu141Gly)CALM3Likely pathogenic194711238247112382AGcriteria provided, single submitterClinGen:CA406473868
single nucleotide variantNM_005184.4(CALM3):c.396T>A (p.Asp132Glu)CALM3Pathogenic194711221347112213TAcriteria provided, single submitterClinGen:CA16620863
single nucleotide variantNM_005184.4(CALM3):c.395A>G (p.Asp132Gly)CALM3Likely pathogenic194711221247112212AGcriteria provided, single submitterClinGen:CA16608277
single nucleotide variantNM_005184.4(CALM3):c.286G>C (p.Asp96His)CALM3Pathogenic194711210347112103GCcriteria provided, single submitterClinGen:CA16616292
single nucleotide variantNM_005184.4(CALM3):c.281A>C (p.Asp94Ala)CALM3Pathogenic194711184147111841ACcriteria provided, single submitterClinGen:CA16616071