P38S (p.Pro38Ser) variant of ARID2 (Q68CP9)
P38S (p.Pro38Ser) in ARID2 (Q68CP9) 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 0.73 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- NCI-TCGA Cosmic COSV5759
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.728
- REVEL 0.74
- MetaLR 0.74
- MetaSVM 0.57
- CADD 25.10
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available