"Ambry Genetics"[submitter] AND "NDUFB6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3187926	NM_002493.5(NDUFB6):c.352C>G (p.Pro118Ala)	NDUFB6, SMIM27 (P103A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343388	NM_002493.5(NDUFB6):c.316C>T (p.Pro106Ser)	NDUFB6, SMIM27 (P75S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187920	NM_002493.5(NDUFB6):c.308G>T (p.Arg103Ile)	NDUFB6, SMIM27 (R103I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517135	NM_002493.5(NDUFB6):c.266A>G (p.His89Arg)	NDUFB6 (H89R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299060	NM_002493.5(NDUFB6):c.194A>G (p.Tyr65Cys)	NDUFB6 (Y65C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187933	NM_002493.5(NDUFB6):c.62G>T (p.Arg21Leu)	LOC130001631, NDUFB6 (R21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar