"PreventionGenetics, part of Exact Sciences"[submitter] AND "NDUFAF5"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 214195	NM_024120.5(NDUFAF5):c.-1G>C	LOC130065433, NDUFAF5	Single nucleotide variant (5 prime UTR variant +1 more)	NDUFAF5-related disorder +1 more	GLikely benign
Select item 1132460	NM_024120.5(NDUFAF5):c.7C>A (p.Arg3=)	LOC130065433, NDUFAF5	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 559166	NM_024120.5(NDUFAF5):c.222+8C>G	NDUFAF5	Single nucleotide variant (intron variant)	NDUFAF5-related disorder +2 more	GBenign/Likely benign
Select item 717045	NM_024120.5(NDUFAF5):c.531T>C (p.Ile177=)	NDUFAF5	Single nucleotide variant (synonymous variant +2 more)	NDUFAF5-related disorder +1 more	GBenign/Likely benign
Select item 383054	NM_024120.5(NDUFAF5):c.597T>C (p.Cys199=)	NDUFAF5	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 722513	NM_024120.5(NDUFAF5):c.752T>C (p.Met251Thr)	NDUFAF5 (M251T +3 more)	Single nucleotide variant (missense variant +1 more)	NDUFAF5-related disorder +2 more	GLikely benign
Select item 1568576	NM_024120.5(NDUFAF5):c.897T>C (p.Ala299=)	NDUFAF5	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign

ClinVar