ClinVar Miner

List of variants in gene NDUFS1 reported as likely benign for Leigh syndrome

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_001199981.1(NDUFS1):c.1143A>G (p.Arg381=) rs1801318
NM_001199981.1(NDUFS1):c.858G>T (p.Ala286=) rs1127566
NM_005006.6(NDUFS1):c.*256C>T rs10198830
NM_005006.6(NDUFS1):c.*336G>T rs1044120
NM_005006.6(NDUFS1):c.*457T>A rs4147728
NM_005006.6(NDUFS1):c.*733A>G rs6707707
NM_005006.6(NDUFS1):c.*846delT rs58253838
NM_005006.6(NDUFS1):c.-47C>G rs4147707
NM_005006.6(NDUFS1):c.123C>T (p.Val41=) rs2230888
NM_005006.6(NDUFS1):c.414T>C (p.Asp138=) rs11548670
NM_005006.6(NDUFS1):c.551+14C>A rs10206644
NM_005006.6(NDUFS1):c.975C>T (p.Arg325=) rs2230890

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