P51H (p.Pro51His) variant of PTPRC (P08575)
P51H (p.Pro51His) in PTPRC (P08575) 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 0.29 / 1. The record also includes population frequency data and structural context.
P51H (p.Pro51His) variant details
- p.Pro51His
- NCI-TCGA Cosmic COSV9904
- TOPMed rs1279852502
- gnomAD rs1279852502
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- REVEL 0.14
- CADD 23.60
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available