NM_175710.2(CR1L):c.804C>T (p.Ser268=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003414749.8
Allele description [Variation Report for NM_175710.2(CR1L):c.804C>T (p.Ser268=)]
NM_175710.2(CR1L):c.804C>T (p.Ser268=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024