NM_144605.5(SEPTIN12):c.698A>G (p.Asn233Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004452983.1
Allele description [Variation Report for NM_144605.5(SEPTIN12):c.698A>G (p.Asn233Ser)]
NM_144605.5(SEPTIN12):c.698A>G (p.Asn233Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024