R82H (p.Arg82His) variant of KCNA2 (P16389)
R82H (p.Arg82His) in KCNA2 (P16389) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Developmental and epileptic encephalopathy, 32. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data and structural context.
R82H (p.Arg82His) variant details
- p.Arg82His
- rs1386301058
- ClinGen CA341606246
- NCI-TCGA Cosmic COSV6036
- cosmic curated COSV60369
- Uncertain significance
- Developmental and epileptic encephalopathy, 32
- Missense
- Variant Prioritization Score for Impact Estimate 0.784
- REVEL 0.78
- CADD 26.80
- PolyPhen-2 1.00
- SIFT 0.04
- ClinVar: Uncertain significance (Developmental and epileptic encephalopathy, 32)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available