P17T (p.Pro17Thr) variant of TIGIT (Q495A1)
P17T (p.Pro17Thr) in TIGIT (Q495A1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data, published literature, and structural context.
P17T (p.Pro17Thr) variant details
- p.Pro17Thr
- gnomAD 3-114293882-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0418
- CADD 0.19
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 3.2e-05)
- Structural context available
- Literature evidence available