I119N (p.Ile119Asn) variant of MAOA (P21397)
I119N (p.Ile119Asn) in MAOA (P21397) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes variant effect predictions and structural context.
I119N (p.Ile119Asn) variant details
- p.Ile119Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- MetaLR 0.07
- MetaSVM -1.14
- SIFT 0.00
- UniProt: Variant assessed as somatic; high impact.
- Structural context available