G39G (p.Gly39Gly) variant of PTPN11 (Q06124)
G39G (p.Gly39Gly) in PTPN11 (Q06124) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
G39G (p.Gly39Gly) variant details
- p.Gly39Gly
- rs779813529
- gnomAD 12-112446378-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.554
- CADD 12.90
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available