"Laboratory of Genetics and Molecular Cardiology, University of São Pa - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 217461	NM_000257.4(MYH7):c.4992C>A (p.Asn1664Lys)	LOC126861897, MHRT +1 more (N1664K)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 43039	NM_000257.4(MYH7):c.4817G>A (p.Arg1606His)	LOC126861897, MHRT +1 more (R1606H)	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiomyopathy +7 more	GUncertain significance