"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 142469	NM_004360.5(CDH1):c.8C>G (p.Pro3Arg)	CDH1 (P3R)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 987066	NM_004360.5(CDH1):c.583C>T (p.Gln195Ter)	CDH1 (Q195*)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GPathogenic
Select item 41787	NM_004360.5(CDH1):c.892G>A (p.Ala298Thr)	CDH1 (A298T)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 156499	NM_004360.5(CDH1):c.1137G>A (p.Thr379=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 127915	NM_004360.5(CDH1):c.1565+1G>A	CDH1	Single nucleotide variant (splice donor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 127921	NM_004360.5(CDH1):c.2104G>A (p.Glu702Lys)	CDH1 (E702K +3 more)	Single nucleotide variant (missense variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database

ClinVar