NM_001142800.2(EYS):c.5510G>C (p.Trp1837Ser) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jul 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000963176.21
Allele description [Variation Report for NM_001142800.2(EYS):c.5510G>C (p.Trp1837Ser)]
NM_001142800.2(EYS):c.5510G>C (p.Trp1837Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024