NM_033127.4(SEC16B):c.1838G>C (p.Cys613Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004105767.1
Allele description [Variation Report for NM_033127.4(SEC16B):c.1838G>C (p.Cys613Ser)]
NM_033127.4(SEC16B):c.1838G>C (p.Cys613Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 15, 2024