NM_012162.4(FBXL6):c.1034C>T (p.Pro345Leu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004209288.1
Allele description [Variation Report for NM_012162.4(FBXL6):c.1034C>T (p.Pro345Leu)]
NM_012162.4(FBXL6):c.1034C>T (p.Pro345Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 8, 2024