NM_001770.6(CD19):c.488G>A (p.Arg163His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001882387.7
Allele description [Variation Report for NM_001770.6(CD19):c.488G>A (p.Arg163His)]
NM_001770.6(CD19):c.488G>A (p.Arg163His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024