"ITMI"[submitter] AND "CDH1"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 133844	NM_004360.5(CDH1):c.24_25delinsGC (p.Ser9Pro)	CDH1 (S9P)	Indel (missense variant +1 more)	not specified	Gnot provided
Select item 127933	NM_004360.5(CDH1):c.88C>A (p.Pro30Thr)	CDH1 (P30T)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 133850	NM_004360.5(CDH1):c.113C>T (p.Thr38Met)	CDH1 (T38M)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 132769	NM_004360.5(CDH1):c.164T>G (p.Val55Gly)	CDH1 (V55G)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 133852	NM_004360.5(CDH1):c.289C>G (p.His97Asp)	CDH1 (H97D)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 133851	NM_004360.5(CDH1):c.322A>G (p.Arg108Gly)	CDH1 (R108G)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 133853	NM_004360.5(CDH1):c.604G>A (p.Val202Ile)	CDH1 (V202I)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 127906	NM_004360.5(CDH1):c.1162G>A (p.Glu388Lys)	CDH1 (E388K)	Single nucleotide variant (5 prime UTR variant +2 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 133854	NM_004360.5(CDH1):c.1214A>G (p.Asn405Ser)	CDH1 (N405S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 133855	NM_004360.5(CDH1):c.1225T>C (p.Trp409Arg)	CDH1 (W409R)	Single nucleotide variant (5 prime UTR variant +2 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 133845	NM_004360.5(CDH1):c.1370C>T (p.Thr457Met)	CDH1 (T457M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GConflicting classifications of pathogenicity
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 12232	NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)	CDH1 (A617T +2 more)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 133846	NM_004360.5(CDH1):c.1888C>G (p.Leu630Val)	CDH1 (L630V +2 more)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 133847	NM_004360.5(CDH1):c.2053G>A (p.Val685Met)	CDH1 (V685M +3 more)	Single nucleotide variant (missense variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 133848	NM_004360.5(CDH1):c.2074G>A (p.Ala692Thr)	CDH1 (A692T +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 133849	NM_004360.5(CDH1):c.2246G>A (p.Arg749Gln)	CDH1 (R749Q +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma +4 more	GConflicting classifications of pathogenicity
Select item 127922	NM_004360.5(CDH1):c.2329G>A (p.Asp777Asn)	CDH1 (D777N +3 more)	Single nucleotide variant (missense variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 127925	NM_004360.5(CDH1):c.2413G>A (p.Asp805Asn)	CDH1 (D805N +3 more)	Single nucleotide variant (missense variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 12246	NM_004360.5(CDH1):c.2494G>A (p.Val832Met)	CDH1 (V832M +3 more)	Single nucleotide variant (missense variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database

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Items: 20