NM_175710.2(CR1L):c.196C>T (p.Arg66Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004374836.1
Allele description [Variation Report for NM_175710.2(CR1L):c.196C>T (p.Arg66Cys)]
NM_175710.2(CR1L):c.196C>T (p.Arg66Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024