NM_003343.6(UBE2G2):c.392A>G (p.Asn131Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004677775.1
Allele description [Variation Report for NM_003343.6(UBE2G2):c.392A>G (p.Asn131Ser)]
NM_003343.6(UBE2G2):c.392A>G (p.Asn131Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024