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Variant (rsID / SNP)

rs140776586

NDUFA10

rs140776586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA10. Location: chromosome 2, position 240,960,670. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NDUFA10Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:240960670
Cytoband
2q37.3
HGVS
NM_004544.4(NDUFA10):c.404T>C (p.Leu135Ser)
Allele change
Silent

Associated conditions / phenotypes

Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.