S49F (p.Ser49Phe) variant of DAP3 (P51398)
S49F (p.Ser49Phe) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
S49F (p.Ser49Phe) variant details
- p.Ser49Phe
- gnomAD rs1385496823
- Missense
- Variant Prioritization Score for Impact Estimate 0.163
- REVEL 0.04
- ESM-1b 0.00
- AlphaMissense 0.09
- CADD 9.70
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available