Y18V (p.Tyr18Val) variant of ZRSR2 (Q15696)
Y18V (p.Tyr18Val) in ZRSR2 (Q15696) 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.
Y18V (p.Tyr18Val) variant details
- p.Tyr18Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- MetaLR 0.01
- MetaSVM -1.04
- SIFT 0.08
- UniProt: Variant assessed as somatic; high impact.
- Structural context available