P56S (p.Pro56Ser) variant of ID3 (Q02535)
P56S (p.Pro56Ser) in ID3 (Q02535) 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 0.89 / 1. The record also includes population frequency data and structural context.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- NCI-TCGA Cosmic COSV6580
- Ensembl rs2124330296
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.893
- REVEL 0.94
- MetaLR 0.99
- MetaSVM 1.04
- CADD 31.00
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available