NM_001387889.1(SFMBT2):c.877G>A (p.Ala293Thr) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 28, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000883892.3
Allele description
NM_001387889.1(SFMBT2):c.877G>A (p.Ala293Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023