P71S (p.Pro71Ser) variant of CASP9 (Caspase-9)
P71S (p.Pro71Ser) in CASP9 (Caspase-9) 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 0.24 / 1. The record also includes population frequency data and structural context.
P71S (p.Pro71Ser) variant details
- p.Pro71Ser
- NCI-TCGA Cosmic COSV6160
- cosmic curated COSV61601
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.238
- REVEL 0.08
- CADD 23.60
- PolyPhen-2 0.52
- SIFT 0.11
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available