N17M (p.Asn17Met) variant of AICDA (Q9GZX7)
N17M (p.Asn17Met) in AICDA (Q9GZX7) 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.
N17M (p.Asn17Met) variant details
- p.Asn17Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- MetaLR 0.76
- MetaSVM 0.74
- SIFT 0.00
- UniProt: Variant assessed as somatic; high impact.
- Structural context available