S94R (p.Ser94Arg) variant of SIRT7 (Q9NRC8)
S94R (p.Ser94Arg) in SIRT7 (Q9NRC8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
S94R (p.Ser94Arg) variant details
- p.Ser94Arg
- ESP rs138673054
- TOPMed rs138673054
- gnomAD rs138673054
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- REVEL 0.03
- ESM-1b 0.00
- AlphaMissense 0.12
- MetaLR 0.01
- MetaSVM -0.96
- CADD 15.55
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available