NM_001099271.2(POC5):c.1692T>G (p.Ser564=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002621954.2
Allele description
NM_001099271.2(POC5):c.1692T>G (p.Ser564=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024