MT-ND2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376834	NC_012920.1:m.4472T>C	MT-ND2	Single nucleotide variant	not provided	GUncertain significance
Select item 692445	NC_012920.1(MT-ND2):m.4480T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692446	NC_012920.1(MT-ND2):m.4482G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692447	NC_012920.1(MT-ND2):m.4488C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692448	NC_012920.1(MT-ND2):m.4491G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692449	NC_012920.1(MT-ND2):m.4494A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692450	NC_012920.1(MT-ND2):m.4495T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692451	NC_012920.1(MT-ND2):m.4497T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692452	NC_012920.1(MT-ND2):m.4500T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692453	NC_012920.1(MT-ND2):m.4501C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692454	NC_012920.1(MT-ND2):m.4503A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692455	NC_012920.1(MT-ND2):m.4506A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692456	NC_012920.1(MT-ND2):m.4509T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692457	NC_012920.1(MT-ND2):m.4512G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692458	NC_012920.1(MT-ND2):m.4513C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692459	NC_012920.1(MT-ND2):m.4531C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692460	NC_012920.1(MT-ND2):m.4548T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692461	NC_012920.1(MT-ND2):m.4554A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692462	NC_012920.1(MT-ND2):m.4560G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692463	NC_012920.1(MT-ND2):m.4561T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692464	NC_012920.1(MT-ND2):m.4579T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692465	NC_012920.1(MT-ND2):m.4596G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 618727	NC_012920.1:m.4597T>C	MT-ND2	Single nucleotide variant	not provided	GUncertain significance
Select item 692466	NC_012920.1(MT-ND2):m.4611del	MT-ND2	Deletion	Leigh syndrome	GLikely pathogenic
Select item 692467	NC_012920.1(MT-ND2):m.4612T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692468	NC_012920.1(MT-ND2):m.4615A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692469	NC_012920.1(MT-ND2):m.4632G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692470	NC_012920.1(MT-ND2):m.4638A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692471	NC_012920.1(MT-ND2):m.4639T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 9718	m.4640C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692472	NC_012920.1(MT-ND2):m.4654C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692474	NC_012920.1(MT-ND2):m.4659G>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692473	NC_012920.1(MT-ND2):m.4659G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 370047	NC_012920.1:m.4664C>T	MT-ND2	Single nucleotide variant	Developmental delay +1 more	GUncertain significance
Select item 692475	NC_012920.1(MT-ND2):m.4665G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692476	NC_012920.1(MT-ND2):m.4674A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692477	NC_012920.1(MT-ND2):m.4676C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692478	NC_012920.1(MT-ND2):m.4680C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 9721	m.4681T>C	MT-ND2	Single nucleotide variant	Leigh syndrome due to mitochondrial complex I deficiency	GPathogenic
Select item 235516	NC_012920.1:m.4688T>C	MT-ND2	Single nucleotide variant	not provided	GLikely benign
Select item 692479	NC_012920.1(MT-ND2):m.4689A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692480	NC_012920.1(MT-ND2):m.4690T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692481	NC_012920.1(MT-ND2):m.4695T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692482	NC_012920.1(MT-ND2):m.4696T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692483	NC_012920.1(MT-ND2):m.4702A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692484	NC_012920.1(MT-ND2):m.4705T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692485	NC_012920.1(MT-ND2):m.4707C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692486	NC_012920.1(MT-ND2):m.4717A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692487	NC_012920.1(MT-ND2):m.4722A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692489	NC_012920.1(MT-ND2):m.4725A>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692488	NC_012920.1(MT-ND2):m.4725A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692490	NC_012920.1(MT-ND2):m.4728A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692491	NC_012920.1(MT-ND2):m.4732A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 235579	NC_012920.1:m.4733T>C	MT-ND2	Single nucleotide variant	not provided	GLikely benign
Select item 692492	NC_012920.1(MT-ND2):m.4734A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 1328512	NC_012920.1(MT-ND2):m.4735C>G	MT-ND2	Single nucleotide variant	Mitochondrial disease	GUncertain significance FDA Recognized database
Select item 692493	NC_012920.1(MT-ND2):m.4735C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692494	NC_012920.1(MT-ND2):m.4745A>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692495	NC_012920.1(MT-ND2):m.4746T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692496	NC_012920.1(MT-ND2):m.4749T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692497	NC_012920.1(MT-ND2):m.4759T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692498	NC_012920.1(MT-ND2):m.4762T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692499	NC_012920.1(MT-ND2):m.4763C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692500	NC_012920.1(MT-ND2):m.4764A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692501	NC_012920.1(MT-ND2):m.4765T>C	MT-ND2	Single nucleotide variant	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 692503	NC_012920.1(MT-ND2):m.4768_4769delinsCG	MT-ND2	Indel	Leigh syndrome	GUncertain significance
Select item 235413	NC_012920.1:m.4768T>C	MT-ND2	Single nucleotide variant	not provided	GUncertain significance
Select item 441150	NC_012920.1:m.4769A>G	MT-ND2	Single nucleotide variant	Mitochondrial disease	GBenign FDA Recognized database
Select item 692504	NC_012920.1(MT-ND2):m.4770G>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 692506	NC_012920.1(MT-ND2):m.4788G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692507	NC_012920.1(MT-ND2):m.4789G>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 9720	m.4810G>A	MT-ND2	Single nucleotide variant	Mitochondrial complex I deficiency	GPathogenic
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 235544	NC_012920.1:m.4823T>C	MT-ND2	Single nucleotide variant	not provided	GLikely benign
Select item 692510	NC_012920.1(MT-ND2):m.4824A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692511	NC_012920.1(MT-ND2):m.4833A>G	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 692513	NC_012920.1(MT-ND2):m.4843C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692514	NC_012920.1(MT-ND2):m.4894T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692515	NC_012920.1(MT-ND2):m.4902A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692516	NC_012920.1(MT-ND2):m.4908C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692517	NC_012920.1(MT-ND2):m.4911T>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 9716	m.4917A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692518	NC_012920.1(MT-ND2):m.4923A>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 692521	NC_012920.1(MT-ND2):m.4929C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
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 692524	NC_012920.1(MT-ND2):m.4936C>T	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 692525	NC_012920.1(MT-ND2):m.4944A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 692526	NC_012920.1(MT-ND2):m.4948T>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 692528	NC_012920.1(MT-ND2):m.4954T>C	MT-ND2	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 692529	NC_012920.1(MT-ND2):m.4959G>A	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 692531	NC_012920.1(MT-ND2):m.4965A>G	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign

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