NM_000503.6(EYA1):c.1278C>T (p.Gly426=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 3, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001668171.2
Allele description
NM_000503.6(EYA1):c.1278C>T (p.Gly426=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 15, 2024