"OMIM"[submitter] AND "MT-TP"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9571	m.15965A>G	MT-TP	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 9572	m.15967G>A	MT-TP	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GPathogenic
Select item 9570	NC_012920.1(MT-TP):m.15990C>T	MT-TP	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database

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