V7L (p.Val7Leu) variant of PLCG2 (P16885)
V7L (p.Val7Leu) in PLCG2 (P16885) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
V7L (p.Val7Leu) variant details
- p.Val7Leu
- gnomAD 16-81786008-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.25
- CADD 9.54
- PolyPhen-2 0.00
- SIFT 0.44
- Population evidence available
- Structural context available
- PLCG2 SH3 domain domainome 1.0: score -0.0794
- Literature evidence available