NM_001278356.2(FRS2):c.1084C>T (p.Arg362Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004220798.1
Allele description [Variation Report for NM_001278356.2(FRS2):c.1084C>T (p.Arg362Cys)]
NM_001278356.2(FRS2):c.1084C>T (p.Arg362Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024