NM_001142800.2(EYS):c.5629C>T (p.Arg1877Trp) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 30, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000898699.11
Allele description [Variation Report for NM_001142800.2(EYS):c.5629C>T (p.Arg1877Trp)]
NM_001142800.2(EYS):c.5629C>T (p.Arg1877Trp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024