I69V (p.Ile69Val) variant of AGTRAP (Q6RW13)
I69V (p.Ile69Val) in AGTRAP (Q6RW13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
I69V (p.Ile69Val) variant details
- p.Ile69Val
- TOPMed rs1295068400
- gnomAD rs1295068400
- Missense
- Variant Prioritization Score for Impact Estimate 0.182
- REVEL 0.09
- ESM-1b 0.00
- AlphaMissense 0.10
- MetaLR 0.09
- MetaSVM -1.05
- CADD 20.90
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available