S40G (p.Ser40Gly) variant of TIGIT (Q495A1)
S40G (p.Ser40Gly) in TIGIT (Q495A1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data, published literature, and structural context.
S40G (p.Ser40Gly) variant details
- p.Ser40Gly
- gnomAD 3-114293978-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0513
- CADD 0.39
- SIFT 0.20
- Most common in the REMAINING population (allele frequency 4.7e-05)
- Structural context available
- Literature evidence available