NM_001308142.2(MRTFB):c.2078G>A (p.Ser693Asn) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004500633.1
Allele description [Variation Report for NM_001308142.2(MRTFB):c.2078G>A (p.Ser693Asn)]
NM_001308142.2(MRTFB):c.2078G>A (p.Ser693Asn)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024