A19T (p.Ala19Thr) variant of TIGIT (Q495A1)
A19T (p.Ala19Thr) in TIGIT (Q495A1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
A19T (p.Ala19Thr) variant details
- p.Ala19Thr
- rs377262337
- ClinGen CA2550946
- ClinVar RCV004303227
- ESP rs377262337
- Likely benign
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.0428
- REVEL 0.03
- CADD 0.09
- PolyPhen-2 0.00
- SIFT 0.48
- ClinVar: Likely benign (not specified)
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the HGDP:ORCADIAN population (allele frequency 0.036)
- Structural context available