N35T (p.Asn35Thr) variant of GRIN2A (Q12879)
N35T (p.Asn35Thr) in GRIN2A (Q12879) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
N35T (p.Asn35Thr) variant details
- p.Asn35Thr
- rs2544032516
- ClinGen CA394715725
- ClinVar RCV002280008
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available