NM_020964.3(EPG5):c.6516C>T (p.Tyr2172=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Nov 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001613420.5
Allele description [Variation Report for NM_020964.3(EPG5):c.6516C>T (p.Tyr2172=)]
NM_020964.3(EPG5):c.6516C>T (p.Tyr2172=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024