"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 184065	NM_004360.5(CDH1):c.27G>A (p.Ser9=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	CDH1-related condition +4 more	GConflicting classifications of pathogenicity
Select item 136692	NM_004360.5(CDH1):c.48+6C>T	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 127931	NM_004360.5(CDH1):c.532-18C>T	CDH1	Single nucleotide variant (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 136694	NM_004360.5(CDH1):c.833-16C>G	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 136057	NM_004360.5(CDH1):c.1224G>A (p.Ala408=)	CDH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +4 more	GBenign/Likely benign
Select item 136695	NM_004360.5(CDH1):c.1272C>T (p.Val424=)	CDH1	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +5 more	GBenign/Likely benign
Select item 136697	NM_004360.5(CDH1):c.1680G>C (p.Thr560=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 136698	NM_004360.5(CDH1):c.1744C>T (p.Leu582=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Breast and/or ovarian cancer +4 more	GBenign/Likely benign
Select item 41783	NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr)	CDH1 (A592T +2 more)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 12241	NM_004360.5(CDH1):c.1792C>T (p.Arg598Ter)	CDH1 (R598* +2 more)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 142770	NM_004360.5(CDH1):c.2076T>C (p.Ala692=)	CDH1	Single nucleotide variant (synonymous variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 136699	NM_004360.5(CDH1):c.2292C>T (p.Asp764=)	CDH1	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign/Likely benign
Select item 136066	NM_004360.5(CDH1):c.2439+10C>T	CDH1	Single nucleotide variant (intron variant)	not provided +6 more	GBenign/Likely benign
Select item 182386	NM_004360.5(CDH1):c.2520C>T (p.Ser840=)	CDH1	Single nucleotide variant (synonymous variant)	CDH1-related condition +5 more	GBenign/Likely benign