A41T (p.Ala41Thr) variant of F10 (Coagulation factor X)
A41T (p.Ala41Thr) in F10 (Coagulation factor X) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
A41T (p.Ala41Thr) variant details
- p.Ala41Thr
- NCI-TCGA Cosmic COSV6502
- cosmic curated COSV65023
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.603
- REVEL 0.66
- CADD 23.30
- PolyPhen-2 0.69
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available