"Center for Pediatric Genomic Medicine, Children's Mercy Hospital and - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 235655	NC_012920.1:m.14911C>T	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 445709	NC_012920.1(MT-CYB):m.15071T>C	MT-CYB	Single nucleotide variant	Leigh syndrome +1 more	GBenign/Likely benign
Select item 445359	NC_012920.1:m.15191T>C	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 235375	NC_012920.1:m.15217G>A	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 377041	NC_012920.1:m.15235A>G	MT-CYB	Single nucleotide variant	not provided	GBenign
Select item 376959	NC_012920.1:m.15262T>C	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 235525	NC_012920.1(MT-CYB):m.15437G>A	MT-CYB	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke +3 more	GUncertain significance
Select item 143892	NC_012920.1(MT-CYB):m.15470T>C	MT-CYB	Single nucleotide variant	not provided	GBenign
Select item 377154	NC_012920.1:m.15487A>G	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 9687	NC_012920.1(MT-CYB):m.15497G>A	MT-CYB	Single nucleotide variant	Leigh syndrome +1 more	GBenign/Likely benign
Select item 143893	NC_012920.1:m.15511T>C	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 235650	NC_012920.1:m.15514T>C	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 235623	NC_012920.1(MT-CYB):m.15746A>G	MT-CYB	Single nucleotide variant	not provided +1 more	GBenign
Select item 377195	NC_012920.1(MT-CYB):m.15777G>A	MT-CYB	Single nucleotide variant	Leigh syndrome +1 more	GBenign/Likely benign
Select item 235581	NC_012920.1:m.15833C>T	MT-CYB	Single nucleotide variant	not provided	GLikely benign
Select item 377369	NC_012920.1(MT-CYB):m.15848A>G	MT-CYB	Single nucleotide variant	Mitochondrial disease	GUncertain significance FDA Recognized database