NM_006363.6(SEC23B):c.875C>T (p.Thr292Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003136545.3
Allele description [Variation Report for NM_006363.6(SEC23B):c.875C>T (p.Thr292Ile)]
NM_006363.6(SEC23B):c.875C>T (p.Thr292Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024