P56S (p.Pro56Ser) variant of SMARCA2 (P51531)
P56S (p.Pro56Ser) in SMARCA2 (P51531) 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 0.39 / 1. The record also includes structural context.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- rs1448350538
- NCI-TCGA Cosmic COSV6181
- cosmic curated COSV61813
- TOPMed rs1448350538
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.388
- AlphaMissense 0.05
- MetaLR 0.38
- MetaSVM -0.58
- PolyPhen-2 0.00
- SIFT 0.35
- EVE 0.18
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available