NM_024007.5(EBF1):c.1712C>A (p.Thr571Asn) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004117691.1
Allele description [Variation Report for NM_024007.5(EBF1):c.1712C>A (p.Thr571Asn)]
NM_024007.5(EBF1):c.1712C>A (p.Thr571Asn)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024