"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ATP5MF-PTC - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2657720	NM_015545.4(PTCD1):c.2091T>C (p.Leu697=)	ATP5MF-PTCD1, PTCD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657721	NM_015545.4(PTCD1):c.1282G>A (p.Ala428Thr)	ATP5MF-PTCD1, PTCD1 (A428T +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 810139	NM_015545.4(PTCD1):c.1087C>G (p.Pro363Ala)	ATP5MF-PTCD1, PTCD1 (P363A +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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