ClinVar for MedGen (Select 64634) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 234528	NM_004360.5(CDH1):c.1493A>C (p.Asp498Ala)	CDH1 (D498A +1 more)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 12234	NM_004360.5(CDH1):c.781G>T (p.Glu261Ter)	CDH1 (E261*)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database