NM_000660.7(TGFB1):c.635-14C>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002680704.3
Allele description [Variation Report for NM_000660.7(TGFB1):c.635-14C>G]
NM_000660.7(TGFB1):c.635-14C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024