S27G (p.Ser27Gly) variant of PTPRC (P08575)
S27G (p.Ser27Gly) in PTPRC (P08575) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data, published literature, and structural context.
S27G (p.Ser27Gly) variant details
- p.Ser27Gly
- gnomAD 1-198692352-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0326
- REVEL 0.01
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.39
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available
- Literature evidence available