S47R (p.Ser47Arg) variant of ETV6 (Transcription factor ETV6)
S47R (p.Ser47Arg) in ETV6 (Transcription factor ETV6) 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.
S47R (p.Ser47Arg) variant details
- p.Ser47Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- MetaLR 0.04
- MetaSVM -1.07
- SIFT 1.00
- UniProt: Variant assessed as somatic; high impact.
- Structural context available