NM_001159773.2(CANT1):c.667C>T (p.Arg223Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002903809.1
Allele description [Variation Report for NM_001159773.2(CANT1):c.667C>T (p.Arg223Cys)]
NM_001159773.2(CANT1):c.667C>T (p.Arg223Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 13, 2023