NM_006946.4(SPTBN2):c.2771C>A (p.Pro924Gln) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000932384.6
Allele description [Variation Report for NM_006946.4(SPTBN2):c.2771C>A (p.Pro924Gln)]
NM_006946.4(SPTBN2):c.2771C>A (p.Pro924Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 26, 2024