NM_000368.5(TSC1):c.3373T>C (p.Leu1125=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000762583.21
Allele description [Variation Report for NM_000368.5(TSC1):c.3373T>C (p.Leu1125=)]
NM_000368.5(TSC1):c.3373T>C (p.Leu1125=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024