NM_001458.5(FLNC):c.4812G>A (p.Pro1604=) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001700969.2
Allele description [Variation Report for NM_001458.5(FLNC):c.4812G>A (p.Pro1604=)]
NM_001458.5(FLNC):c.4812G>A (p.Pro1604=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024