Related gene-specific medical variations for Gene (Select 4540) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 693677	NC_012920.1(MT-ND5):m.14144C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693676	NC_012920.1(MT-ND5):m.14143A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693675	NC_012920.1(MT-ND5):m.14142C>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693674	NC_012920.1(MT-ND5):m.14142C>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693673	NC_012920.1(MT-ND5):m.14140A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693672	NC_012920.1(MT-ND5):m.14138T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693671	NC_012920.1(MT-ND5):m.14129C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693670	NC_012920.1(MT-ND5):m.14128A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693669	NC_012920.1(MT-ND5):m.14122A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693668	NC_012920.1(MT-ND5):m.14113T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693667	NC_012920.1(MT-ND5):m.14112C>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693666	NC_012920.1(MT-ND5):m.14110T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693665	NC_012920.1(MT-ND5):m.14091A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693664	NC_012920.1(MT-ND5):m.14071A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693663	NC_012920.1(MT-ND5):m.14063T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693662	NC_012920.1(MT-ND5):m.14062A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693661	NC_012920.1(MT-ND5):m.14060T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693660	NC_012920.1(MT-ND5):m.14059A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693659	NC_012920.1(MT-ND5):m.14053A>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693658	NC_012920.1(MT-ND5):m.14053A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693657	NC_012920.1(MT-ND5):m.14051C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693656	NC_012920.1(MT-ND5):m.14050T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693655	NC_012920.1(MT-ND5):m.14047A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693654	NC_012920.1(MT-ND5):m.14042A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693653	NC_012920.1(MT-ND5):m.14041C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693652	NC_012920.1(MT-ND5):m.14040G>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693651	NC_012920.1(MT-ND5):m.14035T>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693650	NC_012920.1(MT-ND5):m.14029A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693649	NC_012920.1(MT-ND5):m.14020T>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693648	NC_012920.1(MT-ND5):m.14003C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693647	NC_012920.1(MT-ND5):m.13981C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693646	NC_012920.1(MT-ND5):m.13974A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693645	NC_012920.1(MT-ND5):m.13973A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693644	NC_012920.1(MT-ND5):m.13967C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693643	NC_012920.1(MT-ND5):m.13966A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693642	NC_012920.1(MT-ND5):m.13958G>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693641	NC_012920.1(MT-ND5):m.13948C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693640	NC_012920.1(MT-ND5):m.13946T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693639	NC_012920.1(MT-ND5):m.13943C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693638	NC_012920.1(MT-ND5):m.13934C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693637	NC_012920.1(MT-ND5):m.13933A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693636	NC_012920.1(MT-ND5):m.13928G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693635	NC_012920.1(MT-ND5):m.13928G>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693634	NC_012920.1(MT-ND5):m.13924C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693633	NC_012920.1(MT-ND5):m.13919T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693632	NC_012920.1(MT-ND5):m.13919T>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693631	NC_012920.1(MT-ND5):m.13913T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693630	NC_012920.1(MT-ND5):m.13907A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693629	NC_012920.1(MT-ND5):m.13889G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693628	NC_012920.1(MT-ND5):m.13888T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693627	NC_012920.1(MT-ND5):m.13886T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693626	NC_012920.1(MT-ND5):m.13885C>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693625	NC_012920.1(MT-ND5):m.13880C>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693624	NC_012920.1(MT-ND5):m.13879T>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693623	NC_012920.1(MT-ND5):m.13879T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693622	NC_012920.1(MT-ND5):m.13874T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693621	NC_012920.1(MT-ND5):m.13862A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693620	NC_012920.1(MT-ND5):m.13835C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693619	NC_012920.1(MT-ND5):m.13834A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693618	NC_012920.1(MT-ND5):m.13820T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693617	NC_012920.1(MT-ND5):m.13819T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693616	NC_012920.1(MT-ND5):m.13816A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693615	NC_012920.1(MT-ND5):m.13813G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693614	NC_012920.1(MT-ND5):m.13810G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693613	NC_012920.1(MT-ND5):m.13802C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693612	NC_012920.1(MT-ND5):m.13801A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693611	NC_012920.1(MT-ND5):m.13790A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693610	NC_012920.1(MT-ND5):m.13789T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693609	NC_012920.1(MT-ND5):m.13781T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693608	NC_012920.1(MT-ND5):m.13780A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693607	NC_012920.1(MT-ND5):m.13770C>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693606	NC_012920.1(MT-ND5):m.13768T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693605	NC_012920.1(MT-ND5):m.13768T>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693603	NC_012920.1(MT-ND5):m.13762T>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693602	NC_012920.1(MT-ND5):m.13762T>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693601	NC_012920.1(MT-ND5):m.13760C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693600	NC_012920.1(MT-ND5):m.13759G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693599	NC_012920.1(MT-ND5):m.13754C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693598	NC_012920.1(MT-ND5):m.13753T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693597	NC_012920.1(MT-ND5):m.13748A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693596	NC_012920.1(MT-ND5):m.13741A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693595	NC_012920.1(MT-ND5):m.13726G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693594	NC_012920.1(MT-ND5):m.13712C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693593	NC_012920.1(MT-ND5):m.13711G>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693592	NC_012920.1(MT-ND5):m.13681A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693591	NC_012920.1(MT-ND5):m.13681A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693590	NC_012920.1(MT-ND5):m.13676A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693589	NC_012920.1(MT-ND5):m.13664T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693588	NC_012920.1(MT-ND5):m.13661A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693587	NC_012920.1(MT-ND5):m.13651A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693586	NC_012920.1(MT-ND5):m.13651A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693585	NC_012920.1(MT-ND5):m.13651A>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693584	NC_012920.1(MT-ND5):m.13649C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693583	NC_012920.1(MT-ND5):m.13645T>A	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693582	NC_012920.1(MT-ND5):m.13630A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693581	NC_012920.1(MT-ND5):m.13616T>C	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693580	NC_012920.1(MT-ND5):m.13615A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693579	NC_012920.1(MT-ND5):m.13612A>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693578	NC_012920.1(MT-ND5):m.13606A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693577	NC_012920.1(MT-ND5):m.13594A>G	MT-ND5	Single nucleotide variant	Leigh syndrome	GBenign

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