NM_001134363.3(RBM20):c.2862C>T (p.Asp954=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 5, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000183835.1
Allele description [Variation Report for NM_001134363.3(RBM20):c.2862C>T (p.Asp954=)]
NM_001134363.3(RBM20):c.2862C>T (p.Asp954=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024