K19N (p.Lys19Asn) variant of PRRT2 (Q7Z6L0)
K19N (p.Lys19Asn) in PRRT2 (Q7Z6L0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
K19N (p.Lys19Asn) variant details
- p.Lys19Asn
- ExAC rs759681485
- TOPMed rs759681485
- gnomAD rs759681485
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- REVEL 0.03
- CADD 15.40
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available