NM_001355436.2(SPTB):c.4482G>A (p.Val1494=) AND not provided
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001640503.25
Allele description [Variation Report for NM_001355436.2(SPTB):c.4482G>A (p.Val1494=)]
NM_001355436.2(SPTB):c.4482G>A (p.Val1494=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024