S94N (p.Ser94Asn) variant of SIRT7 (Q9NRC8)
S94N (p.Ser94Asn) in SIRT7 (Q9NRC8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
S94N (p.Ser94Asn) variant details
- p.Ser94Asn
- Ensembl rs2040831324
- Missense
- Variant Prioritization Score for Impact Estimate 0.19
- REVEL 0.05
- ESM-1b 0.00
- AlphaMissense 0.08
- MetaLR 0.02
- MetaSVM -0.99
- CADD 15.77
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available