N98K (p.Asn98Lys) variant of SIRT7 (Q9NRC8)
N98K (p.Asn98Lys) in SIRT7 (Q9NRC8) 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.
N98K (p.Asn98Lys) variant details
- p.Asn98Lys
- ExAC rs746011931
- TOPMed rs746011931
- gnomAD rs746011931
- Missense
- Variant Prioritization Score for Impact Estimate 0.14
- REVEL 0.01
- ESM-1b 0.00
- AlphaMissense 0.12
- MetaLR 0.01
- MetaSVM -0.94
- CADD 15.26
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Structural context available