S136P (p.Ser136Pro) variant of CHM (P24386)
S136P (p.Ser136Pro) in CHM (P24386) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
S136P (p.Ser136Pro) variant details
- p.Ser136Pro
- gnomAD rs1158967997
- Missense
- Variant Prioritization Score for Impact Estimate 0.102
- REVEL 0.04
- MetaLR 0.09
- MetaSVM -1.02
- CADD 8.84
- PolyPhen-2 0.00
- SIFT 0.13
- Population evidence available
- Structural context available