NM_001017995.3(SH3PXD2B):c.1616G>A (p.Arg539Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001859009.3
Allele description
NM_001017995.3(SH3PXD2B):c.1616G>A (p.Arg539Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024