S40N (p.Ser40Asn) variant of TIGIT (Q495A1)
S40N (p.Ser40Asn) in TIGIT (Q495A1) is a missense 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.
S40N (p.Ser40Asn) variant details
- p.Ser40Asn
- rs933863885
- gnomAD 3-114293979-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.333
- CADD 9.95
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available