NM_000834.5(GRIN2B):c.3117C>T (p.Tyr1039=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003390814.8
Allele description [Variation Report for NM_000834.5(GRIN2B):c.3117C>T (p.Tyr1039=)]
NM_000834.5(GRIN2B):c.3117C>T (p.Tyr1039=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024