"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "NDUFAF5"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559164	NM_024120.5(NDUFAF5):c.213G>C (p.Leu71=)	NDUFAF5	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 377595	NM_024120.5(NDUFAF5):c.216G>A (p.Lys72=)	NDUFAF5	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 214198	NM_024120.5(NDUFAF5):c.222+8_222+15del	NDUFAF5	Deletion (intron variant)	Mitochondrial complex 1 deficiency, nuclear type 16 +1 more	GBenign
Select item 559166	NM_024120.5(NDUFAF5):c.222+8C>G	NDUFAF5	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 136597	NM_024120.5(NDUFAF5):c.486T>C (p.His162=)	NDUFAF5	Single nucleotide variant (synonymous variant +2 more)	not specified +1 more	GBenign
Select item 129694	NM_024120.5(NDUFAF5):c.582C>T (p.Leu194=)	NDUFAF5	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign

ClinVar