NM_000435.3(NOTCH3):c.4974C>T (p.Leu1658=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 1, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001663866.1
Allele description
NM_000435.3(NOTCH3):c.4974C>T (p.Leu1658=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023