NM_001393381.1(CRACD):c.2668C>G (p.Arg890Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004374882.1
Allele description [Variation Report for NM_001393381.1(CRACD):c.2668C>G (p.Arg890Gly)]
NM_001393381.1(CRACD):c.2668C>G (p.Arg890Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024