NM_001458.5(FLNC):c.795T>C (p.Gly265=) AND not specified
- Germline classification:
- Benign (7 submissions)
- Last evaluated:
- Apr 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000117084.21
Allele description [Variation Report for NM_001458.5(FLNC):c.795T>C (p.Gly265=)]
NM_001458.5(FLNC):c.795T>C (p.Gly265=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024