E68D (p.Glu68Asp) variant of TNXB (Tenascin-X)
E68D (p.Glu68Asp) in TNXB (Tenascin-X) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes structural context.
E68D (p.Glu68Asp) variant details
- p.Glu68Asp
- cosmic curated COSV64484
- NCI-TCGA Cosmic COSV6448
- cosmic curated COSV64482
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.232
- ESM-1b 0.00
- AlphaMissense 0.46
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Structural context available