NM_001110556.2(FLNA):c.5475C>T (p.Asp1825=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000431730.8
Allele description [Variation Report for NM_001110556.2(FLNA):c.5475C>T (p.Asp1825=)]
NM_001110556.2(FLNA):c.5475C>T (p.Asp1825=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 23, 2024