NM_017617.5(NOTCH1):c.52G>A (p.Ala18Thr) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 7, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001648232.2
Allele description [Variation Report for NM_017617.5(NOTCH1):c.52G>A (p.Ala18Thr)]
NM_017617.5(NOTCH1):c.52G>A (p.Ala18Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024