A34T (p.Ala34Thr) variant of NTRK1 (P04629)
A34T (p.Ala34Thr) in NTRK1 (P04629) 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 0.18 / 1. The record also includes population frequency data and structural context.
A34T (p.Ala34Thr) variant details
- p.Ala34Thr
- NCI-TCGA TCGA novel
- gnomAD rs1436042701
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.05
- MetaLR 0.10
- MetaSVM -1.02
- CADD 13.60
- PolyPhen-2 0.00
- SIFT 0.16
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the 1KG:IBS population (allele frequency 0.017)
- Structural context available