NM_002467.6(MYC):c.909C>G (p.Ser303Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004258900.1
Allele description [Variation Report for NM_002467.6(MYC):c.909C>G (p.Ser303Arg)]
NM_002467.6(MYC):c.909C>G (p.Ser303Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 18, 2024