"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "NDUFB3"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 252575	NM_002491.3(NDUFB3):c.64T>C (p.Trp22Arg)	NDUFB3 (W22R)	Single nucleotide variant (missense variant)	Mitochondrial complex 1 deficiency, nuclear type 25 +3 more	GPathogenic/Likely pathogenic
Select item 809137	NM_002491.3(NDUFB3):c.201del (p.Phe68fs)	NDUFB3 (F68fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 1879516	NM_002491.3(NDUFB3):c.288G>A (p.Lys96=)	NDUFB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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