R27G (p.Arg27Gly) variant of NTRK2 (Q16620)
R27G (p.Arg27Gly) 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.
R27G (p.Arg27Gly) variant details
- p.Arg27Gly
- gnomAD rs1181332313
- Missense
- Variant Prioritization Score for Impact Estimate 0.483
- REVEL 0.44
- CADD 24.50
- PolyPhen-2 0.86
- SIFT 0.65
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available