NM_006579.3(EBP):c.15G>T (p.Ala5=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Mar 29, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000145923.12
Allele description [Variation Report for NM_006579.3(EBP):c.15G>T (p.Ala5=)]
NM_006579.3(EBP):c.15G>T (p.Ala5=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024