T37A (p.Thr37Ala) variant of PTPRC (P08575)
T37A (p.Thr37Ala) 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 0.04 / 1. The record also includes population frequency data and structural context.
T37A (p.Thr37Ala) variant details
- p.Thr37Ala
- NCI-TCGA Cosmic COSV6142
- gnomAD rs1666220314
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0445
- REVEL 0.03
- CADD 0.03
- PolyPhen-2 0.00
- SIFT 0.41
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available