V78I (p.Val78Ile) variant of AICDA (Q9GZX7)
V78I (p.Val78Ile) in AICDA (Q9GZX7) 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 0.28 / 1. The record also includes population frequency data and structural context.
V78I (p.Val78Ile) variant details
- p.Val78Ile
- NCI-TCGA Cosmic COSV5756
- cosmic curated COSV57563
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.277
- REVEL 0.06
- MetaLR 0.09
- MetaSVM -1.05
- CADD 19.80
- PolyPhen-2 0.00
- SIFT 0.41
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available