S92T (p.Ser92Thr) variant of TGM1 (P22735)
S92T (p.Ser92Thr) in TGM1 (P22735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
S92T (p.Ser92Thr) variant details
- p.Ser92Thr
- gnomAD rs1270631760
- Missense
- Variant Prioritization Score for Impact Estimate 0.341
- REVEL 0.40
- CADD 16.30
- PolyPhen-2 0.90
- SIFT 0.60
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available