NM_001458.5(FLNC):c.7990+9C>T AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000439956.4
Allele description [Variation Report for NM_001458.5(FLNC):c.7990+9C>T]
NM_001458.5(FLNC):c.7990+9C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024