NM_024408.4(NOTCH2):c.3789A>C (p.Gly1263=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 3, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000591481.5
Allele description [Variation Report for NM_024408.4(NOTCH2):c.3789A>C (p.Gly1263=)]
NM_024408.4(NOTCH2):c.3789A>C (p.Gly1263=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024