NM_005236.3(ERCC4):c.33C>T (p.Ala11=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 12, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000251617.5
Allele description [Variation Report for NM_005236.3(ERCC4):c.33C>T (p.Ala11=)]
NM_005236.3(ERCC4):c.33C>T (p.Ala11=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024