NM_001387889.1(SFMBT2):c.1415A>G (p.Tyr472Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004666171.1
Allele description [Variation Report for NM_001387889.1(SFMBT2):c.1415A>G (p.Tyr472Cys)]
NM_001387889.1(SFMBT2):c.1415A>G (p.Tyr472Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024