S29F (p.Ser29Phe) variant of AGTRAP (Q6RW13)
S29F (p.Ser29Phe) in AGTRAP (Q6RW13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
S29F (p.Ser29Phe) variant details
- p.Ser29Phe
- TOPMed rs1421005786
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.31
- ESM-1b 1.00
- AlphaMissense 0.49
- MetaLR 0.29
- MetaSVM -0.47
- CADD 23.50
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available