T141N (p.Thr141Asn) variant of TNXB (Tenascin-X)
T141N (p.Thr141Asn) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
T141N (p.Thr141Asn) variant details
- p.Thr141Asn
- cosmic curated COSV10092
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- REVEL 0.03
- ESM-1b 0.49
- AlphaMissense 0.07
- MetaLR 0.17
- MetaSVM -0.92
- CADD 17.90
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.2e-05)
- Structural context available