Related gene-specific medical variations for Gene (Select 101927979) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109611	NM_001394789.1(INCA1):c.677C>T (p.Pro226Leu)	CAMTA2-AS1, INCA1 (P211L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109610	NM_001394789.1(INCA1):c.500A>T (p.Glu167Val)	CAMTA2-AS1, INCA1 (E152V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109609	NM_001394789.1(INCA1):c.496C>G (p.Leu166Val)	CAMTA2-AS1, INCA1 (L166V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109608	NM_001394789.1(INCA1):c.452G>A (p.Gly151Asp)	CAMTA2-AS1, INCA1 (G151D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
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)	not specified	GUncertain significance
Select item 2513592	NM_001394789.1(INCA1):c.187C>A (p.Pro63Thr)	CAMTA2-AS1, INCA1 (P63T)	Single nucleotide variant (missense variant)	not specified	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)	not specified	GUncertain significance
Select item 2459911	NM_001394789.1(INCA1):c.583C>T (p.Pro195Ser)	CAMTA2-AS1, INCA1 (P195S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455486	NM_001394789.1(INCA1):c.482A>G (p.Asn161Ser)	CAMTA2-AS1, INCA1 (N146S +1 more)	Single nucleotide variant (missense variant)	not specified	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)	not specified	GLikely benign
Select item 2377276	NM_001394789.1(INCA1):c.281G>A (p.Arg94Lys)	CAMTA2-AS1, INCA1 (R79K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315378	NM_001394789.1(INCA1):c.605G>A (p.Cys202Tyr)	CAMTA2-AS1, INCA1 (C187Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance