NM_000548.5(TSC2):c.3768G>A (p.Pro1256=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000334320.3
Allele description
NM_000548.5(TSC2):c.3768G>A (p.Pro1256=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 14, 2021