NM_001142800.2(EYS):c.7684C>G (p.Leu2562Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001305221.6
Allele description [Variation Report for NM_001142800.2(EYS):c.7684C>G (p.Leu2562Val)]
NM_001142800.2(EYS):c.7684C>G (p.Leu2562Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024