R74H (p.Arg74His) variant of AICDA (Q9GZX7)
R74H (p.Arg74His) 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 0.40 / 1. The record also includes population frequency data and structural context.
R74H (p.Arg74His) variant details
- p.Arg74His
- NCI-TCGA Cosmic COSV5756
- cosmic curated COSV57563
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.396
- REVEL 0.20
- MetaLR 0.23
- MetaSVM -0.70
- CADD 22.20
- PolyPhen-2 0.01
- SIFT 0.55
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available