A63T (p.Ala63Thr) variant of TNFRSF13B (O14836)
A63T (p.Ala63Thr) in TNFRSF13B (O14836) 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 0.21 / 1. The record also includes population frequency data and structural context.
A63T (p.Ala63Thr) variant details
- p.Ala63Thr
- NCI-TCGA Cosmic COSV5542
- cosmic curated COSV55426
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.206
- REVEL 0.26
- CADD 7.75
- PolyPhen-2 0.23
- SIFT 0.47
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available