P21S (p.Pro21Ser) variant of GRIN2A (Q12879)
P21S (p.Pro21Ser) in GRIN2A (Q12879) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes variant effect predictions and structural context.
P21S (p.Pro21Ser) variant details
- p.Pro21Ser
- cosmic curated COSV10463
- TOPMed rs1285592726
- gnomAD rs1285592726
- Likely benign
- Missense
- MetaLR 0.04
- MetaSVM -1.11
- SIFT 0.32
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available