NM_001363541.2(DBN1):c.446G>A (p.Arg149Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004209160.1
Allele description [Variation Report for NM_001363541.2(DBN1):c.446G>A (p.Arg149Gln)]
NM_001363541.2(DBN1):c.446G>A (p.Arg149Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 4, 2024