A13V (p.Ala13Val) variant of NTRK2 (Q16620)
A13V (p.Ala13Val) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
A13V (p.Ala13Val) variant details
- p.Ala13Val
- cosmic curated COSV52853
- Missense
- Variant Prioritization Score for Impact Estimate 0.257
- REVEL 0.04
- CADD 21.80
- PolyPhen-2 0.00
- SIFT 0.15
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available