P16R (p.Pro16Arg) variant of KCNA1 (Q09470)
P16R (p.Pro16Arg) in KCNA1 (Q09470) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data and structural context.
P16R (p.Pro16Arg) variant details
- p.Pro16Arg
- rs1565432905
- NCI-TCGA Cosmic COSV6683
- Variant assessed as somatic; high impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.541
- REVEL 0.40
- CADD 23.40
- PolyPhen-2 0.01
- SIFT 0.03
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available