NM_000834.5(GRIN2B):c.286G>C (p.Gly96Arg) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002540721.10
Allele description [Variation Report for NM_000834.5(GRIN2B):c.286G>C (p.Gly96Arg)]
NM_000834.5(GRIN2B):c.286G>C (p.Gly96Arg)
Condition(s)
Assertion and evidence details
Last Updated: Nov 10, 2024