T46A (p.Thr46Ala) variant of TNFRSF13B (O14836)
T46A (p.Thr46Ala) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data.
T46A (p.Thr46Ala) variant details
- p.Thr46Ala
- cosmic curated COSV55426
- gnomAD rs1446669063
- Missense
- Variant Prioritization Score for Impact Estimate 0.117
- REVEL 0.14
- CADD 0.93
- Most common in the African/African-American population (allele frequency 0.00041)