R19H (p.Arg19His) variant of AICDA (Q9GZX7)
R19H (p.Arg19His) in AICDA (Q9GZX7) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
R19H (p.Arg19His) variant details
- p.Arg19His
- cosmic curated COSV99984
- TOPMed rs1207955037
- gnomAD rs1207955037
- Missense
- Variant Prioritization Score for Impact Estimate 0.57
- REVEL 0.48
- MetaLR 0.48
- MetaSVM -0.24
- CADD 24.00
- PolyPhen-2 1.00
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available