MT-TR[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 690111	NC_012920.1(MT-CYB):m.10405T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690112	NC_012920.1(MT-CYB):m.10406G>A	MT-TR	Single nucleotide variant	Mitochondrial disease +1 more	GPathogenic/Likely pathogenic
Select item 690113	NC_012920.1(MT-CYB):m.10408T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely pathogenic
Select item 690115	NC_012920.1(MT-CYB):m.10410T>A	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690114	NC_012920.1(MT-CYB):m.10410T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690116	NC_012920.1(MT-CYB):m.10411A>G	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690117	NC_012920.1(MT-CYB):m.10420A>G	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690118	NC_012920.1(MT-CYB):m.10427G>A	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 1684922	NC_012920.1(MT-TR):m.10437G>A	MT-TR	Single nucleotide variant	not specified	GUncertain significance
Select item 9623	m.10438A>G	MT-TR	Single nucleotide variant	Mitochondrial disease	GPathogenic
Select item 690119	NC_012920.1(MT-CYB):m.10440T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690120	NC_012920.1(MT-CYB):m.10446A>G	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690121	NC_012920.1(MT-CYB):m.10448T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 30000	m.10450A>G	MT-TR	Single nucleotide variant	Mitochondrial disease	GPathogenic
Select item 690122	NC_012920.1(MT-CYB):m.10454T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690123	NC_012920.1(MT-CYB):m.10455A>G	MT-TR	Single nucleotide variant	Mitochondrial disease	GUncertain significance FDA Recognized database
Select item 690124	NC_012920.1(MT-CYB):m.10456A>G	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690125	NC_012920.1(MT-CYB):m.10457T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690126	NC_012920.1(MT-CYB):m.10460T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely pathogenic
Select item 690127	NC_012920.1(MT-CYB):m.10462T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690128	NC_012920.1(MT-CYB):m.10463T>C	MT-TR	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign

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Items: 21