S14N (p.Ser14Asn) variant of NTRK1 (P04629)
S14N (p.Ser14Asn) in NTRK1 (P04629) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
S14N (p.Ser14Asn) variant details
- p.Ser14Asn
- Ensembl rs2102879012
- Missense
- Variant Prioritization Score for Impact Estimate 0.232
- REVEL 0.13
- MetaLR 0.16
- MetaSVM -0.96
- CADD 10.90
- PolyPhen-2 0.00
- SIFT 0.35
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available