"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "NDUFB9"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 214763	NM_005005.3(NDUFB9):c.201C>T (p.Ala67=)	NDUFB9	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 138469	NM_005005.3(NDUFB9):c.436C>T (p.Pro146Ser)	NDUFB9 (P146S +3 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 214765	NM_005005.3(NDUFB9):c.472C>G (p.Arg158Gly)	NDUFB9 (R158G +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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