G9A (p.Gly9Ala) variant of NTRK2 (Q16620)
G9A (p.Gly9Ala) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
G9A (p.Gly9Ala) variant details
- p.Gly9Ala
- gnomAD 9-84670774-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.432
- REVEL 0.41
- CADD 23.50
- PolyPhen-2 0.90
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available