N9S (p.Asn9Ser) variant of ABCC9 (O60706)
N9S (p.Asn9Ser) in ABCC9 (O60706) 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.
N9S (p.Asn9Ser) variant details
- p.Asn9Ser
- ExAC rs776881654
- TOPMed rs776881654
- gnomAD rs776881654
- Missense
- Variant Prioritization Score for Impact Estimate 0.364
- REVEL 0.32
- CADD 19.90
- PolyPhen-2 0.08
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 3.2e-06)
- Structural context available