"Ambry Genetics"[submitter] AND "CAMTA2-AS1"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2315378	NM_001394789.1(INCA1):c.605G>A (p.Cys202Tyr)	CAMTA2-AS1, INCA1 (C187Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2382043	NM_001394789.1(INCA1):c.590A>G (p.Asp197Gly)	CAMTA2-AS1, INCA1 (D182G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2459911	NM_001394789.1(INCA1):c.583C>T (p.Pro195Ser)	CAMTA2-AS1, INCA1 (P195S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612360	NM_001394789.1(INCA1):c.581G>C (p.Ser194Thr)	CAMTA2-AS1, INCA1 (S179T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2455486	NM_001394789.1(INCA1):c.482A>G (p.Asn161Ser)	INCA1, CAMTA2-AS1 (N146S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485443	NM_001394789.1(INCA1):c.424G>A (p.Gly142Arg)	CAMTA2-AS1, INCA1 (G142R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377276	NM_001394789.1(INCA1):c.281G>A (p.Arg94Lys)	CAMTA2-AS1, INCA1 (R79K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513592	NM_001394789.1(INCA1):c.187C>A (p.Pro63Thr)	CAMTA2-AS1, INCA1 (P63T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545807	NM_001394789.1(INCA1):c.77C>G (p.Pro26Arg)	CAMTA2-AS1, INCA1 (P26R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374228	NM_001394789.1(INCA1):c.76C>G (p.Pro26Ala)	INCA1, CAMTA2-AS1 (P26A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533212	NM_001394789.1(INCA1):c.61A>G (p.Ser21Gly)	CAMTA2-AS1, INCA1 (S21G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance