A58A (p.Ala58Ala) variant of PLCG2 (P16885)
A58A (p.Ala58Ala) 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, published literature, and structural context.
A58A (p.Ala58Ala) variant details
- p.Ala58Ala
- rs1143685
- gnomAD 16-81786163-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.101
- CADD 2.85
- Most common in the HGDP:NORTHERNHAN population (allele frequency 1)
- Structural context available
- Cited in: A systematic approach to assessing the clinical significance of genetic variants. (PMID 24033266)