"Revvity Omics, Revvity"[submitter] AND "CTNNA3"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1153884	NM_013266.4(CTNNA3):c.2404G>T (p.Asp802Tyr)	CTNNA3 (D802Y)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GConflicting classifications of pathogenicity
Select item 2440605	NM_013266.4(CTNNA3):c.1561T>G (p.Cys521Gly)	CTNNA3 (C521G)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance
Select item 2440608	NM_013266.4(CTNNA3):c.1496A>C (p.Asp499Ala)	CTNNA3 (D499A)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance
Select item 2440607	NM_013266.4(CTNNA3):c.1321G>A (p.Gly441Arg)	CTNNA3 (G441R)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance
Select item 220977	NM_013266.4(CTNNA3):c.1303A>G (p.Met435Val)	CTNNA3 (M435V)	Single nucleotide variant (missense variant)	CTNNA3-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 541665	NM_013266.4(CTNNA3):c.1247C>T (p.Ala416Val)	CTNNA3 (A416V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance
Select item 220976	NM_013266.4(CTNNA3):c.1231A>G (p.Ile411Val)	CTNNA3 (I411V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13 +1 more	GConflicting classifications of pathogenicity
Select item 581999	NM_013266.4(CTNNA3):c.952T>C (p.Ser318Pro)	CTNNA3 (S318P +1 more)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance
Select item 240873	NM_013266.4(CTNNA3):c.578A>G (p.Gln193Arg)	CTNNA3 (Q193R +1 more)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance
Select item 2440606	NM_013266.4(CTNNA3):c.466A>G (p.Arg156Gly)	CTNNA3 (R156G +1 more)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 13	GUncertain significance