S38N (p.Ser38Asn) variant of MAOA (P21397)
S38N (p.Ser38Asn) in MAOA (P21397) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
S38N (p.Ser38Asn) variant details
- p.Ser38Asn
- TOPMed rs1270029287
- gnomAD rs1270029287
- Missense
- Variant Prioritization Score for Impact Estimate 0.223
- REVEL 0.15
- MetaLR 0.42
- MetaSVM -0.70
- CADD 0.06
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Latino/Admixed American population (allele frequency 9.5e-05)
- Structural context available