ClinVar for Gene (Select 4536) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3337324	NC_012920.1(MT-ND2):m.4929C>A	MT-ND2	Single nucleotide variant	not provided	GUncertain significance
Select item 1328512	NC_012920.1(MT-ND2):m.4735C>G	MT-ND2	Single nucleotide variant	Mitochondrial disease	GUncertain significanceFDA Recognized database
Select item 692597	NC_012920.1(MT-ND2):m.5496A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692596	NC_012920.1(MT-ND2):m.5494T>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692595	NC_012920.1(MT-ND2):m.5493T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692594	NC_012920.1(MT-ND2):m.5484A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692593	NC_012920.1(MT-ND2):m.5466A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692592	NC_012920.1(MT-ND2):m.5463C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692591	NC_012920.1(MT-ND2):m.5460G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692590	NC_012920.1(MT-ND2):m.5452C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692589	NC_012920.1(MT-ND2):m.5451A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692588	NC_012920.1(MT-ND2):m.5444C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692587	NC_012920.1(MT-ND2):m.5442T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692586	NC_012920.1(MT-ND2):m.5437C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692585	NC_012920.1(MT-ND2):m.5367_5385del	MT-ND2	Deletion	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency	GLikely pathogenic
Select item 692584	NC_012920.1(MT-ND2):m.5331C>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692583	NC_012920.1(MT-ND2):m.5331C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692582	NC_012920.1(MT-ND2):m.5325A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692581	NC_012920.1(MT-ND2):m.5325A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692580	NC_012920.1(MT-ND2):m.5320C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692579	NC_012920.1(MT-ND2):m.5320C>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692578	NC_012920.1(MT-ND2):m.5319A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692577	NC_012920.1(MT-ND2):m.5319A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692576	NC_012920.1(MT-ND2):m.5316G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692575	NC_012920.1(MT-ND2):m.5311T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692574	NC_012920.1(MT-ND2):m.5310A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692573	NC_012920.1(MT-ND2):m.5301A>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692572	NC_012920.1(MT-ND2):m.5301A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692571	NC_012920.1(MT-ND2):m.5298A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692570	NC_012920.1(MT-ND2):m.5296T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692569	NC_012920.1(MT-ND2):m.5295C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692568	NC_012920.1(MT-ND2):m.5295C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692567	NC_012920.1(MT-ND2):m.5293G>A	MT-ND2	Single nucleotide variant	Mitochondrial disease	GLikely benignFDA Recognized database
Select item 692566	NC_012920.1(MT-ND2):m.5289A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692565	NC_012920.1(MT-ND2):m.5277T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692564	NC_012920.1(MT-ND2):m.5273A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692563	NC_012920.1(MT-ND2):m.5268A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692562	NC_012920.1(MT-ND2):m.5266T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692561	NC_012920.1(MT-ND2):m.5265A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692560	NC_012920.1(MT-ND2):m.5263C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692559	NC_012920.1(MT-ND2):m.5262G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692558	NC_012920.1(MT-ND2):m.5211C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692557	NC_012920.1(MT-ND2):m.5206C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692556	NC_012920.1(MT-ND2):m.5205T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692555	NC_012920.1(MT-ND2):m.5194C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692554	NC_012920.1(MT-ND2):m.5191C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692553	NC_012920.1(MT-ND2):m.5190A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692552	NC_012920.1(MT-ND2):m.5186A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692551	NC_012920.1(MT-ND2):m.5178C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692550	NC_012920.1(MT-ND2):m.5166A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692549	NC_012920.1(MT-ND2):m.5149C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692548	NC_012920.1(MT-ND2):m.5128A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692547	NC_012920.1(MT-ND2):m.5127A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692546	NC_012920.1(MT-ND2):m.5095T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692545	NC_012920.1(MT-ND2):m.5094A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692544	NC_012920.1(MT-ND2):m.5086C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692543	NC_012920.1(MT-ND2):m.5080A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692542	NC_012920.1(MT-ND2):m.5076C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692541	NC_012920.1(MT-ND2):m.5074T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692540	NC_012920.1(MT-ND2):m.5073A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692539	NC_012920.1(MT-ND2):m.5069A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692538	NC_012920.1(MT-ND2):m.5067A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692537	NC_012920.1(MT-ND2):m.5047T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692536	NC_012920.1(MT-ND2):m.5046G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692535	NC_012920.1(MT-ND2):m.5038T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692534	NC_012920.1(MT-ND2):m.5010T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692533	NC_012920.1(MT-ND2):m.5001dup	MT-ND2	Duplication	Mitochondrial disease	GUncertain significanceFDA Recognized database
Select item 692532	NC_012920.1(MT-ND2):m.4974G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692531	NC_012920.1(MT-ND2):m.4965A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692530	NC_012920.1(MT-ND2):m.4960C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692529	NC_012920.1(MT-ND2):m.4959G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692528	NC_012920.1(MT-ND2):m.4954T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692527	NC_012920.1(MT-ND2):m.4953A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692526	NC_012920.1(MT-ND2):m.4948T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692525	NC_012920.1(MT-ND2):m.4944A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692524	NC_012920.1(MT-ND2):m.4936C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692523	NC_012920.1(MT-ND2):m.4935A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692522	NC_012920.1(MT-ND2):m.4935A>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692521	NC_012920.1(MT-ND2):m.4929C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692520	NC_012920.1(MT-ND2):m.4924G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692519	NC_012920.1(MT-ND2):m.4924G>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692518	NC_012920.1(MT-ND2):m.4923A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692517	NC_012920.1(MT-ND2):m.4911T>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692516	NC_012920.1(MT-ND2):m.4908C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692515	NC_012920.1(MT-ND2):m.4902A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692514	NC_012920.1(MT-ND2):m.4894T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692513	NC_012920.1(MT-ND2):m.4843C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692512	NC_012920.1(MT-ND2):m.4842A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692511	NC_012920.1(MT-ND2):m.4833A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692510	NC_012920.1(MT-ND2):m.4824A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692509	NC_012920.1(MT-ND2):m.4812G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692508	NC_012920.1(MT-ND2):m.4812G>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692507	NC_012920.1(MT-ND2):m.4789G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692506	NC_012920.1(MT-ND2):m.4788G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692505	NC_012920.1(MT-ND2):m.4776G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692504	NC_012920.1(MT-ND2):m.4770G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692503	NC_012920.1(MT-ND2):m.4768_4769delinsCG	MT-ND2	Indel	Leigh syndrome	GUncertain significance
Select item 692502	NC_012920.1(MT-ND2):m.4767A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692501	NC_012920.1(MT-ND2):m.4765T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692500	NC_012920.1(MT-ND2):m.4764A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance

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