G13G (p.Gly13Gly) variant of PRRT2 (Q7Z6L0)
G13G (p.Gly13Gly) in PRRT2 (Q7Z6L0) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
G13G (p.Gly13Gly) variant details
- p.Gly13Gly
- rs2142422128
- gnomAD 16-29813093-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.332
- CADD 7.46
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available