NM_001122955.4(BSCL2):c.409G>A (p.Asp137Asn) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jan 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000727086.5
Allele description [Variation Report for NM_001122955.4(BSCL2):c.409G>A (p.Asp137Asn)]
NM_001122955.4(BSCL2):c.409G>A (p.Asp137Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024