NM_005236.3(ERCC4):c.1727G>C (p.Arg576Thr) AND not specified
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Sep 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000120831.5
Allele description [Variation Report for NM_005236.3(ERCC4):c.1727G>C (p.Arg576Thr)]
NM_005236.3(ERCC4):c.1727G>C (p.Arg576Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 5, 2024