W18R (p.Trp18Arg) variant of GRIN2A (Q12879)
W18R (p.Trp18Arg) in GRIN2A (Q12879) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
W18R (p.Trp18Arg) variant details
- p.Trp18Arg
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10040
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.03
- MetaSVM -1.00
- SIFT 0.35
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available