P38S (p.Pro38Ser) variant of SYNGAP1 (Q96PV0)
P38S (p.Pro38Ser) in SYNGAP1 (Q96PV0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- NCI-TCGA Cosmic COSV9953
- cosmic curated COSV99538
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.71
- CADD 19.10
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available