"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 136323	NM_004208.4(AIFM1):c.1329C>T (p.Tyr443=)	RAB33A, AIFM1	Single nucleotide variant (synonymous variant +2 more)	Inborn genetic diseases +6 more	GBenign/Likely benign
Select item 367894	NM_004208.4(AIFM1):c.72C>T (p.Cys24=)	LOC130068679, RAB33A +1 more	Single nucleotide variant (synonymous variant +1 more)	Severe X-linked mitochondrial encephalomyopathy +4 more	GBenign/Likely benign