P56Q (p.Pro56Gln) variant of NTRK2 (Q16620)
P56Q (p.Pro56Gln) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.82 / 1. The record also includes population frequency data, published literature, and structural context.
P56Q (p.Pro56Gln) variant details
- p.Pro56Gln
- gnomAD 9-84670915-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.819
- REVEL 0.84
- CADD 26.90
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available