NM_000368.5(TSC1):c.738-16T>C AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003987981.1
Allele description [Variation Report for NM_000368.5(TSC1):c.738-16T>C]
NM_000368.5(TSC1):c.738-16T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024