T49T (p.Thr49Thr) variant of PLCG2 (P16885)
T49T (p.Thr49Thr) 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.
T49T (p.Thr49Thr) variant details
- p.Thr49Thr
- rs969768555
- gnomAD 16-81786136-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0857
- CADD 0.71
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available