Related gene-specific medical variations for Gene (Select 4579) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 690025	NC_012920.1(MT-CYB):m.5889A>G	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690024	NC_012920.1(MT-CYB):m.5885T>C	MT-TY	Single nucleotide variant	See cases +1 more	GUncertain significance
Select item 690023	NC_012920.1(MT-CYB):m.5876A>G	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690022	NC_012920.1(MT-CYB):m.5875C>T	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690021	NC_012920.1(MT-CYB):m.5867C>T	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690020	NC_012920.1(MT-CYB):m.5865T>C	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690019	NC_012920.1(MT-CYB):m.5864G>A	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690018	NC_012920.1(MT-CYB):m.5858T>C	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690017	NC_012920.1(MT-CYB):m.5855A>G	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690016	NC_012920.1(MT-CYB):m.5852T>C	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690015	NC_012920.1(MT-CYB):m.5846C>T	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690014	NC_012920.1(MT-CYB):m.5841T>C	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690013	NC_012920.1(MT-CYB):m.5840C>T	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GLikely benign
Select item 690012	NC_012920.1(MT-CYB):m.5840C>A	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690011	NC_012920.1(MT-CYB):m.5839C>T	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 690010	NC_012920.1(MT-CYB):m.5837G>A	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 690009	NC_012920.1(MT-CYB):m.5836A>G	MT-TY	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign