NM_000110.4(DPYD):c.1472A>T (p.Glu491Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003995190.1
Allele description [Variation Report for NM_000110.4(DPYD):c.1472A>T (p.Glu491Val)]
NM_000110.4(DPYD):c.1472A>T (p.Glu491Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024