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Variant (rsID / SNP)

rs118161496

NUBPL

rs118161496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUBPL. Location: chromosome 14, position 32,319,298. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NUBPLConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
14:32319298
Cytoband
14q12
HGVS
NM_025152.3(NUBPL):c.815-27T>C
Allele change
Silent

Associated conditions / phenotypes

Inborn genetic diseases|Mitochondrial complex I deficiency|Mitochondrial complex 1 deficiency, nuclear type 21

Public references

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