Related gene-specific medical variations for Gene (Select 4519) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062051	NC_012920.1(MT-CYB):m.15261G>C	MT-CYB	Single nucleotide variant	Mitochondrial disease	GUncertain significance
Select item 2583106	NC_012920.1(MT-CYB):m.14864T>C	MT-CYB	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	Gnot provided
Select item 693973	NC_012920.1(MT-CYB):m.15885C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693972	NC_012920.1(MT-CYB):m.15882G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693971	NC_012920.1(MT-CYB):m.15873T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693970	NC_012920.1(MT-CYB):m.15860A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693969	NC_012920.1(MT-CYB):m.15860A>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693968	NC_012920.1(MT-CYB):m.15852T>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693967	NC_012920.1(MT-CYB):m.15852T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693966	NC_012920.1(MT-CYB):m.15851A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693965	NC_012920.1(MT-CYB):m.15849C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693964	NC_012920.1(MT-CYB):m.15843T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693963	NC_012920.1(MT-CYB):m.15834T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693962	NC_012920.1(MT-CYB):m.15831T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693961	NC_012920.1(MT-CYB):m.15828C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693960	NC_012920.1(MT-CYB):m.15824A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693959	NC_012920.1(MT-CYB):m.15813T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693958	NC_012920.1(MT-CYB):m.15813T>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693957	NC_012920.1(MT-CYB):m.15804T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693956	NC_012920.1(MT-CYB):m.15803G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693955	NC_012920.1(MT-CYB):m.15793C>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693954	NC_012920.1(MT-CYB):m.15791A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693953	NC_012920.1(MT-CYB):m.15789C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693952	NC_012920.1(MT-CYB):m.15785T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693951	NC_012920.1(MT-CYB):m.15779T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693950	NC_012920.1(MT-CYB):m.15777G>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693949	NC_012920.1(MT-CYB):m.15776A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693948	NC_012920.1(MT-CYB):m.15774T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693947	NC_012920.1(MT-CYB):m.15773G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693946	NC_012920.1(MT-CYB):m.15770C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693945	NC_012920.1(MT-CYB):m.15747T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693944	NC_012920.1(MT-CYB):m.15743C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693943	NC_012920.1(MT-CYB):m.15740C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693942	NC_012920.1(MT-CYB):m.15737G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693941	NC_012920.1(MT-CYB):m.15735C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693940	NC_012920.1(MT-CYB):m.15734G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693939	NC_012920.1(MT-CYB):m.15732C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693938	NC_012920.1(MT-CYB):m.15731G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693937	NC_012920.1(MT-CYB):m.15725C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693936	NC_012920.1(MT-CYB):m.15708G>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693935	NC_012920.1(MT-CYB):m.15693T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693934	NC_012920.1(MT-CYB):m.15692A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693933	NC_012920.1(MT-CYB):m.15690T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693932	NC_012920.1(MT-CYB):m.15686A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693931	NC_012920.1(MT-CYB):m.15674T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693930	NC_012920.1(MT-CYB):m.15672T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693929	NC_012920.1(MT-CYB):m.15664C>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693928	NC_012920.1(MT-CYB):m.15663T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693927	NC_012920.1(MT-CYB):m.15662A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693926	NC_012920.1(MT-CYB):m.15657T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693925	NC_012920.1(MT-CYB):m.15654T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693924	NC_012920.1(MT-CYB):m.15653A>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693923	NC_012920.1(MT-CYB):m.15653A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693922	NC_012920.1(MT-CYB):m.15651C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693921	NC_012920.1(MT-CYB):m.15650G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693920	NC_012920.1(MT-CYB):m.15644A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693919	NC_012920.1(MT-CYB):m.15642T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693918	NC_012920.1(MT-CYB):m.15639T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693917	NC_012920.1(MT-CYB):m.15638A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693916	NC_012920.1(MT-CYB):m.15623G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693915	NC_012920.1(MT-CYB):m.15617G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693914	NC_012920.1(MT-CYB):m.15617G>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693913	NC_012920.1(MT-CYB):m.15614G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693912	NC_012920.1(MT-CYB):m.15612G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693911	NC_012920.1(MT-CYB):m.15596G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693910	NC_012920.1(MT-CYB):m.15584A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693909	NC_012920.1(MT-CYB):m.15581A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693908	NC_012920.1(MT-CYB):m.15575G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693907	NC_012920.1(MT-CYB):m.15567T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693906	NC_012920.1(MT-CYB):m.15557G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693905	NC_012920.1(MT-CYB):m.15542C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693904	NC_012920.1(MT-CYB):m.15534A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693903	NC_012920.1(MT-CYB):m.15533A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693902	NC_012920.1(MT-CYB):m.15531T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693901	NC_012920.1(MT-CYB):m.15525A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693900	NC_012920.1(MT-CYB):m.15524A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693899	NC_012920.1(MT-CYB):m.15522C>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693898	NC_012920.1(MT-CYB):m.15521G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693897	NC_012920.1(MT-CYB):m.15519T>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693896	NC_012920.1(MT-CYB):m.15519T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693895	NC_012920.1(MT-CYB):m.15512T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693894	NC_012920.1(MT-CYB):m.15501A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693893	NC_012920.1(MT-CYB):m.15500G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693892	NC_012920.1(MT-CYB):m.15488G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693891	NC_012920.1(MT-CYB):m.15483C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693890	NC_012920.1(MT-CYB):m.15479T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693889	NC_012920.1(MT-CYB):m.15468C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693888	NC_012920.1(MT-CYB):m.15465T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693887	NC_012920.1(MT-CYB):m.15462T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693886	NC_012920.1(MT-CYB):m.15452_15453delinsAC	MT-CYB	Indel	Leigh syndrome	GUncertain significance
Select item 693885	NC_012920.1(MT-CYB):m.15450T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693884	NC_012920.1(MT-CYB):m.15449T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693883	NC_012920.1(MT-CYB):m.15434C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693882	NC_012920.1(MT-CYB):m.15428G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693881	NC_012920.1(MT-CYB):m.15414A>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693880	NC_012920.1(MT-CYB):m.15413T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693879	NC_012920.1(MT-CYB):m.15404T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693878	NC_012920.1(MT-CYB):m.15402C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693877	NC_012920.1(MT-CYB):m.15401A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693876	NC_012920.1(MT-CYB):m.15386C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign

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