NM_001080449.3(DNA2):c.2430C>G (p.Phe810Leu) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Aug 2, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000246790.6
Allele description [Variation Report for NM_001080449.3(DNA2):c.2430C>G (p.Phe810Leu)]
NM_001080449.3(DNA2):c.2430C>G (p.Phe810Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024