A17V (p.Ala17Val) variant of NTRK1 (P04629)
A17V (p.Ala17Val) in NTRK1 (P04629) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
A17V (p.Ala17Val) variant details
- p.Ala17Val
- Ensembl rs2102879031
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.12
- MetaLR 0.12
- MetaSVM -1.00
- CADD 15.50
- PolyPhen-2 0.01
- SIFT 0.15
- Most common in the Non-Finnish European population (allele frequency 1.6e-05)
- Structural context available