S3T (p.Ser3Thr) variant of NTRK2 (Q16620)
S3T (p.Ser3Thr) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and published literature.
S3T (p.Ser3Thr) variant details
- p.Ser3Thr
- gnomAD 9-84670755-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.158
- REVEL 0.07
- CADD 19.00
- PolyPhen-2 0.05
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Literature evidence available