NM_001371242.2(CRYBG1):c.2063G>A (p.Arg688Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004255110.1
Allele description [Variation Report for NM_001371242.2(CRYBG1):c.2063G>A (p.Arg688Gln)]
NM_001371242.2(CRYBG1):c.2063G>A (p.Arg688Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024