NM_018677.4(ACSS2):c.501G>A (p.Met167Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004233782.1
Allele description [Variation Report for NM_018677.4(ACSS2):c.501G>A (p.Met167Ile)]
NM_018677.4(ACSS2):c.501G>A (p.Met167Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 15, 2024