A26T (p.Ala26Thr) variant of SHMT2 (P34897)
A26T (p.Ala26Thr) in SHMT2 (P34897) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
A26T (p.Ala26Thr) variant details
- p.Ala26Thr
- rs112251410
- gnomAD rs112251410
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.267
- REVEL 0.03
- AlphaMissense 0.09
- MetaLR 0.03
- MetaSVM -1.06
- CADD 20.10
- PolyPhen-2 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 0.00013)
- Structural context available