G9V (p.Gly9Val) variant of NTRK2 (Q16620)
G9V (p.Gly9Val) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
G9V (p.Gly9Val) variant details
- p.Gly9Val
- cosmic curated COSV99457
- TOPMed rs1421322179
- gnomAD rs1421322179
- Missense
- Variant Prioritization Score for Impact Estimate 0.484
- REVEL 0.50
- CADD 25.50
- PolyPhen-2 0.97
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available