R14M (p.Arg14Met) variant of TIGIT (Q495A1)
R14M (p.Arg14Met) in TIGIT (Q495A1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
R14M (p.Arg14Met) variant details
- p.Arg14Met
- rs1431949855
- gnomAD 3-114293973-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.203
- CADD 8.26
- SIFT 0.13
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available
- Literature evidence available