Variant (rsID / SNP)

rs66677059

rs66677059 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTC. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

OTCLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xp11.4
HGVS: NM_000531.6(OTC):c.158T>C (p.Ile53Thr)
Allele change: Missense_I53S

Associated conditions / phenotypes

Ornithine carbamoyltransferase deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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