NM_001134363.3(RBM20):c.954A>G (p.Gln318=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 20, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000218706.4
Allele description [Variation Report for NM_001134363.3(RBM20):c.954A>G (p.Gln318=)]
NM_001134363.3(RBM20):c.954A>G (p.Gln318=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024