P38P (p.Pro38Pro) variant of PLCG2 (P16885)
P38P (p.Pro38Pro) in PLCG2 (P16885) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
P38P (p.Pro38Pro) variant details
- p.Pro38Pro
- rs750924322
- gnomAD 16-81786103-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.102
- CADD 3.04
- Most common in the HGDP:PALESTINIAN population (allele frequency 0.013)
- Structural context available
- PLCG2 SH3 domain domainome 1.0: score -0.803
- Literature evidence available