M31I (p.Met31Ile) variant of TNFRSF13B (O14836)
M31I (p.Met31Ile) 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 0.64 / 1. The record also includes population frequency data.
M31I (p.Met31Ile) variant details
- p.Met31Ile
- NCI-TCGA Cosmic COSV5542
- cosmic curated COSV55429
- ExAC rs745349768
- gnomAD rs745349768
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.645
- REVEL 0.56
- CADD 23.10
- PolyPhen-2 0.93
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 0.00048)