NM_015630.4(EPC2):c.1082A>G (p.Asn361Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004162101.1
Allele description [Variation Report for NM_015630.4(EPC2):c.1082A>G (p.Asn361Ser)]
NM_015630.4(EPC2):c.1082A>G (p.Asn361Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024