P53S (p.Pro53Ser) variant of TGFB2 (P61812)
P53S (p.Pro53Ser) in TGFB2 (P61812) 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 0.60 / 1. The record also includes population frequency data and structural context.
P53S (p.Pro53Ser) variant details
- p.Pro53Ser
- NCI-TCGA TCGA novel
- Ensembl rs1656700052
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.597
- REVEL 0.46
- CADD 25.10
- PolyPhen-2 1.00
- SIFT 0.05
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available