V30V (p.Val30Val) variant of PLCG2 (P16885)
V30V (p.Val30Val) in PLCG2 (P16885) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
V30V (p.Val30Val) variant details
- p.Val30Val
- gnomAD 16-81786079-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.256
- CADD 8.91
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- PLCG2 SH3 domain domainome 1.0: score 0.0387
- Literature evidence available