I9M (p.Ile9Met) variant of MAOA (P21397)
I9M (p.Ile9Met) in MAOA (P21397) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
I9M (p.Ile9Met) variant details
- p.Ile9Met
- TOPMed rs1439692807
- gnomAD rs1439692807
- Missense
- Variant Prioritization Score for Impact Estimate 0.061
- REVEL 0.01
- MetaLR 0.01
- MetaSVM -1.01
- CADD 0.03
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Latino/Admixed American population (allele frequency 2.8e-05)
- Structural context available