ClinVar for Gene (Select 4512) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 232

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3337313	NC_012920.1(MT-CO1):m.7375A>G	MT-CO1	Single nucleotide variant	not provided	GUncertain significance
Select item 3337312	NC_012920.1(MT-CO1):m.7348T>C	MT-CO1	Single nucleotide variant	not provided	GUncertain significance
Select item 3337311	NC_012920.1(MT-CO1):m.6423C>T	MT-CO1	Single nucleotide variant	not provided	GUncertain significance
Select item 3337310	NC_012920.1(MT-CO1):m.6217T>C	MT-CO1	Single nucleotide variant	not provided	GUncertain significance
Select item 2412795	NC_012920.1(MT-CO1):m.6243G>A	MT-CO1	Single nucleotide variant	not provided	Gnot provided
Select item 1684904	NC_012920.1(MT-CO1):m.7023G>A	MT-CO1	Single nucleotide variant	not specified	GUncertain significance
Select item 1676315	NC_012920.1(MT-CO1):m.7028C>T	MT-CO1	Single nucleotide variant	Mitochondrial disease	GBenignFDA Recognized database
Select item 1328511	NC_012920.1(MT-CO1):m.7092T>C	MT-CO1	Single nucleotide variant	Mitochondrial disease	GUncertain significanceFDA Recognized database
Select item 994645	NC_012920.1(MT-CO1):m.6497T>C	MT-CO1	Single nucleotide variant	not specified	GBenign
Select item 994644	NC_012920.1(MT-CO1):m.6254A>G	MT-CO1	Single nucleotide variant	not provided	GLikely benign
Select item 994643	NC_012920.1(MT-CO1):m.6047A>G	MT-CO1	Single nucleotide variant	not specified	GBenign
Select item 994642	NC_012920.1(MT-CO1):m.5999T>C	MT-CO1	Single nucleotide variant	not specified	GBenign
Select item 805036	NC_012920.1(MT-CO1):m.7274C>T	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805035	NC_012920.1(MT-CO1):m.7196C>A	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805034	NC_012920.1(MT-CO1):m.7013G>A	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805033	NC_012920.1(MT-CO1):m.6911T>C	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805032	NC_012920.1(MT-CO1):m.6899G>C	MT-CO1	Single nucleotide variant	not provided	GUncertain significance
Select item 805031	NC_012920.1(MT-CO1):m.6896T>C	MT-CO1	Single nucleotide variant	not provided	GLikely benign
Select item 805030	NC_012920.1(MT-CO1):m.6776T>C	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805029	NC_012920.1(MT-CO1):m.6713C>T	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805028	NC_012920.1(MT-CO1):m.6671T>C	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805027	NC_012920.1(MT-CO1):m.6626T>C	MT-CO1	Single nucleotide variant	not provided	GLikely benign
Select item 805026	NC_012920.1(MT-CO1):m.6446G>A	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805025	NC_012920.1(MT-CO1):m.6353A>G	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805024	NC_012920.1(MT-CO1):m.6026G>A	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 805023	NC_012920.1(MT-CO1):m.5918T>C	MT-CO1	Single nucleotide variant	not provided	GBenign
Select item 692747	NC_012920.1(MT-CO1):m.7440T>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692746	NC_012920.1(MT-CO1):m.7440T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692745	NC_012920.1(MT-CO1):m.7432A>T	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692744	NC_012920.1(MT-CO1):m.7431T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692743	NC_012920.1(MT-CO1):m.7419G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692742	NC_012920.1(MT-CO1):m.7408A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692741	NC_012920.1(MT-CO1):m.7389T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692740	NC_012920.1(MT-CO1):m.7374A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692739	NC_012920.1(MT-CO1):m.7365C>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692738	NC_012920.1(MT-CO1):m.7363A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692737	NC_012920.1(MT-CO1):m.7362G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692736	NC_012920.1(MT-CO1):m.7357T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692735	NC_012920.1(MT-CO1):m.7356G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692734	NC_012920.1(MT-CO1):m.7347G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692733	NC_012920.1(MT-CO1):m.7332G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692732	NC_012920.1(MT-CO1):m.7309T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692731	NC_012920.1(MT-CO1):m.7300T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692730	NC_012920.1(MT-CO1):m.7299A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692729	NC_012920.1(MT-CO1):m.7290A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692728	NC_012920.1(MT-CO1):m.7284T>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692727	NC_012920.1(MT-CO1):m.7279T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692726	NC_012920.1(MT-CO1):m.7278T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692725	NC_012920.1(MT-CO1):m.7272G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692724	NC_012920.1(MT-CO1):m.7270T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692723	NC_012920.1(MT-CO1):m.7269G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692722	NC_012920.1(MT-CO1):m.7258T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692721	NC_012920.1(MT-CO1):m.7257A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692720	NC_012920.1(MT-CO1):m.7249C>T	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692719	NC_012920.1(MT-CO1):m.7245A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692718	NC_012920.1(MT-CO1):m.7233C>T	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692717	NC_012920.1(MT-CO1):m.7222A>G	MT-CO1	Single nucleotide variant	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency	GLikely pathogenic
Select item 692716	NC_012920.1(MT-CO1):m.7191T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692715	NC_012920.1(MT-CO1):m.7187A>T	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692714	NC_012920.1(MT-CO1):m.7168A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692713	NC_012920.1(MT-CO1):m.7159T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692712	NC_012920.1(MT-CO1):m.7158A>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692711	NC_012920.1(MT-CO1):m.7158A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692710	NC_012920.1(MT-CO1):m.7155T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692709	NC_012920.1(MT-CO1):m.7153T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692708	NC_012920.1(MT-CO1):m.7150T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692707	NC_012920.1(MT-CO1):m.7149A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692706	NC_012920.1(MT-CO1):m.7147C>T	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692705	NC_012920.1(MT-CO1):m.7146_7147inv	MT-CO1	Inversion	Leigh syndrome	GUncertain significance
Select item 692704	NC_012920.1(MT-CO1):m.7146A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692703	NC_012920.1(MT-CO1):m.7138T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692702	NC_012920.1(MT-CO1):m.7129A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692701	NC_012920.1(MT-CO1):m.7125A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692700	NC_012920.1(MT-CO1):m.7119G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692699	NC_012920.1(MT-CO1):m.7084T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692698	NC_012920.1(MT-CO1):m.7083A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692697	NC_012920.1(MT-CO1):m.7080T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692696	NC_012920.1(MT-CO1):m.7077G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692695	NC_012920.1(MT-CO1):m.7053G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692694	NC_012920.1(MT-CO1):m.7051T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692693	NC_012920.1(MT-CO1):m.7032T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692692	NC_012920.1(MT-CO1):m.7020G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692691	NC_012920.1(MT-CO1):m.7015A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692690	NC_012920.1(MT-CO1):m.6987T>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692689	NC_012920.1(MT-CO1):m.6978G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692688	NC_012920.1(MT-CO1):m.6972G>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692687	NC_012920.1(MT-CO1):m.6951G>A	MT-CO1	Single nucleotide variant	Mitochondrial disease	GLikely benignFDA Recognized database
Select item 692686	NC_012920.1(MT-CO1):m.6924G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692685	NC_012920.1(MT-CO1):m.6916T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692684	NC_012920.1(MT-CO1):m.6915G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692683	NC_012920.1(MT-CO1):m.6912G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692682	NC_012920.1(MT-CO1):m.6909G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692681	NC_012920.1(MT-CO1):m.6897A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692680	NC_012920.1(MT-CO1):m.6891A>G	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692679	NC_012920.1(MT-CO1):m.6876G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692678	NC_012920.1(MT-CO1):m.6868G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692677	NC_012920.1(MT-CO1):m.6856T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692676	NC_012920.1(MT-CO1):m.6855G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692675	NC_012920.1(MT-CO1):m.6852G>A	MT-CO1	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692674	NC_012920.1(MT-CO1):m.6844T>C	MT-CO1	Single nucleotide variant	Leigh syndrome	GUncertain significance

<< First< Prev

Page of 3