"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 127848	NM_002354.3(EPCAM):c.267G>C (p.Gln89His)	EPCAM (Q89H)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1285057	NM_002354.3(EPCAM):c.307G>A (p.Gly103Arg)	EPCAM (G103R)	Single nucleotide variant (missense variant)	not provided	GPathogenic/Likely pathogenic
Select item 132761	NM_002354.3(EPCAM):c.492-5T>C	EPCAM	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign

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ClinVar