V29M (p.Val29Met) variant of TNFRSF13B (O14836)
V29M (p.Val29Met) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
V29M (p.Val29Met) variant details
- p.Val29Met
- cosmic curated COSV55428
- TOPMed rs1409789148
- gnomAD rs1409789148
- Missense
- Variant Prioritization Score for Impact Estimate 0.147
- REVEL 0.20
- CADD 2.53
- PolyPhen-2 0.01
- SIFT 0.14
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available