"Wellcome Centre for Mitochondrial Research, Newcastle University"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 430675	NC_012920.1(MT-TS2):m.6470_15588del	MT-ATP6, MT-ATP8 +18 more	Deletion	Mitochondrial disease	GPathogenic
Select item 430683	NC_012920.1(MT-TS2):m.8839_14895del	MT-ND5, MT-ND6 +12 more	Deletion	Mitochondrial disease	GPathogenic
Select item 430684	NC_012920.1(MT-TS2):m.10106_15067del	MT-ND5, MT-ND6 +9 more	Deletion	Mitochondrial disease	GPathogenic
Select item 430685	NC_012920.1(MT-TS2):m.11263_15374del	MT-TE, MT-CYB +6 more	Deletion	Mitochondrial disease	GPathogenic
Select item 9618	m.14674T>C	MT-TE	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9617	m.14709T>C	MT-TE	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database

ClinVar