V69I (p.Val69Ile) variant of CD79A (P11912)
V69I (p.Val69Ile) in CD79A (P11912) 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 0.04 / 1. The record also includes population frequency data and structural context.
V69I (p.Val69Ile) variant details
- p.Val69Ile
- rs782563209
- NCI-TCGA Cosmic COSV5573
- cosmic curated COSV55738
- ExAC rs782563209
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0396
- REVEL 0.01
- CADD 0.00
- PolyPhen-2 0.01
- SIFT 0.95
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available