C0919267[trait identifier] AND "Department of Zoology Govt. MVM Colleg - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 143864	NC_012920.1(MT-CYB):m.14743A>G		Single nucleotide variant	Ovarian neoplasm	GUncertain significance
Select item 143865	NC_012920.1(MT-CYB):m.14753C>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 143874	NC_012920.1(MT-CYB):m.15058C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143921	NC_012920.1(MT-CYB):m.15061A>G	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GLikely benign
Select item 143875	NC_012920.1(MT-CYB):m.15098A>G	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 143922	NC_012920.1(MT-CYB):m.15148G>A	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GLikely benign
Select item 143923	NC_012920.1(MT-CYB):m.15259C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143879	NC_012920.1(MT-CYB):m.15314G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143881	NC_012920.1(MT-CYB):m.15328A>G	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143882	NC_012920.1(MT-CYB):m.15334C>T	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143887	NC_012920.1(MT-CYB):m.15363A>G	MT-CYB	Single nucleotide variant	not specified	GBenign
Select item 143924	NC_012920.1(MT-CYB):m.15431G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143925	NC_012920.1(MT-CYB):m.15452C>A	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 143891	NC_012920.1(MT-CYB):m.15459C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 143893	NC_012920.1(MT-CYB):m.15511T>C	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 143926	NC_012920.1(MT-CYB):m.15607A>G	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GBenign
Select item 143927	NC_012920.1(MT-CYB):m.15670T>C	MT-CYB	Single nucleotide variant	Ovarian neoplasm	GLikely benign
Select item 143900	NC_012920.1(MT-CYB):m.15884G>A	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign
Select item 143901	NC_012920.1(MT-TT):m.15890C>A	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 143904	NC_012920.1(MT-TT):m.15932T>G	MT-TT	Single nucleotide variant	Ovarian neoplasm	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

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Items: 24