"PreventionGenetics, part of Exact Sciences"[submitter] AND "ATP5F1E"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1316129	NM_006886.4(ATP5F1E):c.86C>A (p.Thr29Lys)	ATP5F1E, SLMO2-ATP5E (T29K)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GLikely benign
Select item 3046491	NM_006886.4(ATP5F1E):c.42A>C (p.Arg14=)	ATP5F1E, SLMO2-ATP5E	Single nucleotide variant (non-coding transcript variant +1 more)	ATP5F1E-related disorder	GLikely benign