T57T (p.Thr57Thr) variant of PLCG2 (P16885)
T57T (p.Thr57Thr) in PLCG2 (P16885) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
T57T (p.Thr57Thr) variant details
- p.Thr57Thr
- gnomAD 16-81786160-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0881
- CADD 1.05
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available