R33S (p.Arg33Ser) variant of ADA (Adenosine deaminase)
R33S (p.Arg33Ser) in ADA (Adenosine deaminase) 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 0.47 / 1. The record also includes population frequency data and structural context.
R33S (p.Arg33Ser) variant details
- p.Arg33Ser
- NCI-TCGA Cosmic COSV6574
- cosmic curated COSV65740
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.47
- REVEL 0.39
- CADD 20.40
- PolyPhen-2 0.04
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available