N26S (p.Asn26Ser) variant of NRAS (GTPase NRas)
N26S (p.Asn26Ser) in NRAS (GTPase NRas) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
N26S (p.Asn26Ser) variant details
- p.Asn26Ser
- ExAC rs773404559
- gnomAD rs773404559
- Missense
- Variant Prioritization Score for Impact Estimate 0.356
- REVEL 0.19
- CADD 22.50
- PolyPhen-2 0.01
- SIFT 0.08
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available