D59D (p.Asp59Asp) variant of PLCG2 (P16885)
D59D (p.Asp59Asp) in PLCG2 (P16885) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
D59D (p.Asp59Asp) variant details
- p.Asp59Asp
- gnomAD 16-81786166-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.399
- CADD 11.30
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available