NM_000548.5(TSC2):c.5199C>T (p.Thr1733=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000242377.5
Allele description [Variation Report for NM_000548.5(TSC2):c.5199C>T (p.Thr1733=)]
NM_000548.5(TSC2):c.5199C>T (p.Thr1733=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024