NM_033378.2(CGB2):c.43G>A (p.Gly15Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004208645.1
Allele description [Variation Report for NM_033378.2(CGB2):c.43G>A (p.Gly15Arg)]
NM_033378.2(CGB2):c.43G>A (p.Gly15Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 29, 2024