ClinVar (all) for Orgtrack (Select 505198) - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 143927	NC_012920.1(MT-CYB):m.15670T>C	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GLikely benign
Select item 143926	NC_012920.1(MT-CYB):m.15607A>G	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GBenign
Select item 143925	NC_012920.1(MT-CYB):m.15452C>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143924	NC_012920.1(MT-CYB):m.15431G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143923	NC_012920.1(MT-CYB):m.15259C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143922	NC_012920.1(MT-CYB):m.15148G>A	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GLikely benign
Select item 143921	NC_012920.1(MT-CYB):m.15061A>G	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GLikely benign
Select item 143920	NC_012920.1(MT-CYB):m.14935T>C	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143919	NC_012920.1(MT-CYB):m.14905G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GBenign
Select item 143918	NC_012920.1(MT-TE):m.14732A>G	MT-TE	Single nucleotide variant	Familial cancer of breast	GUncertain significance
Select item 143905	NC_012920.1(MT-TT):m.15943T>C	MT-TT	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 143904	NC_012920.1(MT-TT):m.15932T>G	MT-TT	Single nucleotide variant	Ovarian neoplasm	GUncertain significance
Select item 143903	NC_012920.1(MT-TT):m.15928G>A	MT-TT	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 143902	NC_012920.1(MT-TT):m.15927G>A	MT-TT	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 143901	NC_012920.1(MT-TT):m.15890C>A	MT-TT	Single nucleotide variant	Ovarian neoplasm	GUncertain significance
Select item 143900	NC_012920.1(MT-CYB):m.15884G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143899	NC_012920.1(MT-CYB):m.15784T>C	MT-CYB	Single nucleotide variant	Familial cancer of breast	GBenign
Select item 143898	NC_012920.1(MT-CYB):m.15758A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143897	NC_012920.1(MT-CYB):m.15682A>G	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143896	NC_012920.1(MT-CYB):m.15649A>G	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143895	NC_012920.1(MT-CYB):m.15637C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143894	NC_012920.1(MT-CYB):m.15553G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143893	NC_012920.1(MT-CYB):m.15511T>C	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 143892	NC_012920.1(MT-CYB):m.15470T>C	MT-CYB	Single nucleotide variant	not provided	GBenign
Select item 143891	NC_012920.1(MT-CYB):m.15459C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 143890	NC_012920.1(MT-CYB):m.15458T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143889	NC_012920.1(MT-CYB):m.15453T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 143888	NC_012920.1(MT-CYB):m.15385C>T	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143887	NC_012920.1(MT-CYB):m.15363A>G	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143886	NC_012920.1(MT-CYB):m.15355G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143885	NC_012920.1(MT-CYB):m.15349C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143884	NC_012920.1(MT-CYB):m.15349C>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GUncertain significance
Select item 143883	NC_012920.1(MT-CYB):m.15346G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143882	NC_012920.1(MT-CYB):m.15334C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143881	NC_012920.1(MT-CYB):m.15328A>G	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143880	NC_012920.1(MT-CYB):m.15323G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143879	NC_012920.1(MT-CYB):m.15314G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143878	NC_012920.1(MT-CYB):m.15289T>C	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143877	NC_012920.1(MT-CYB):m.15226A>G	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143876	NC_012920.1(MT-CYB):m.15214T>C	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143875	NC_012920.1(MT-CYB):m.15098A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 143874	NC_012920.1(MT-CYB):m.15058C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143873	NC_012920.1(MT-CYB):m.15049C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143872	NC_012920.1(MT-CYB):m.15001T>C	MT-CYB	Single nucleotide variant	Familial cancer of breast	GLikely benign
Select item 143871	NC_012920.1(MT-CYB):m.14974C>G	MT-CYB	Single nucleotide variant	Familial cancer of breast	GUncertain significance
Select item 143870	NC_012920.1(MT-CYB):m.14968T>C	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143869	NC_012920.1(MT-CYB):m.14950C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143868	NC_012920.1(MT-CYB):m.14891C>G	MT-CYB	Single nucleotide variant	Familial cancer of breast	GUncertain significance
Select item 143867	NC_012920.1(MT-CYB):m.14800C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143866	NC_012920.1(MT-CYB):m.14784T>C	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143865	NC_012920.1(MT-CYB):m.14753C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143864	NC_012920.1(MT-CYB):m.14743A>G		Single nucleotide variant	Ovarian neoplasm	GUncertain significance
Select item 140592	NC_012920.1(MT-CYB):m.15326A>G	MT-CYB	Single nucleotide variant	Mitochondrial disease	GBenign FDA Recognized database
Select item 140591	NC_012920.1(MT-CYB):m.15301G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GBenign
Select item 140590	NC_012920.1(MT-CYB):m.15287T>C	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 140589	NC_012920.1(MT-CYB):m.15043G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GBenign
Select item 140588	NC_012920.1(MT-CYB):m.14783T>C	MT-CYB	Single nucleotide variant	Familial cancer of breast	GBenign
Select item 140587	NC_012920.1(MT-CYB):m.14766C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign

ClinVar

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Links from Orgtrack

Items: 58