"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "GNB4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1098934	NM_021629.4(GNB4):c.918T>G (p.Gly306=)	GNB4	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 941789	NM_021629.4(GNB4):c.826G>A (p.Val276Ile)	GNB4 (V276I)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease dominant intermediate F +1 more	GUncertain significance
Select item 2059644	NM_021629.4(GNB4):c.724G>A (p.Ala242Thr)	GNB4 (A242T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 3379515	NM_021629.4(GNB4):c.596_598delinsATA (p.Phe199_Val200delinsTyrIle)	GNB4	Indel (missense variant)	not provided	GUncertain significance
Select item 1693880	NM_021629.4(GNB4):c.157G>A (p.Gly53Ser)	GNB4 (G53S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1163830	NM_021629.4(GNB4):c.113A>G (p.Asp38Gly)	GNB4 (D38G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

ClinVar