S41T (p.Ser41Thr) variant of NTRK2 (Q16620)
S41T (p.Ser41Thr) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
S41T (p.Ser41Thr) variant details
- p.Ser41Thr
- gnomAD rs1454412423
- Missense
- Variant Prioritization Score for Impact Estimate 0.293
- REVEL 0.31
- CADD 16.40
- PolyPhen-2 0.00
- SIFT 0.82
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available