S94G (p.Ser94Gly) variant of SIRT7 (Q9NRC8)
S94G (p.Ser94Gly) 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.
S94G (p.Ser94Gly) variant details
- p.Ser94Gly
- ExAC rs756369194
- gnomAD rs756369194
- Missense
- Variant Prioritization Score for Impact Estimate 0.14
- REVEL 0.04
- ESM-1b 0.00
- AlphaMissense 0.06
- MetaLR 0.01
- MetaSVM -0.95
- CADD 14.84
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available