W57G (p.Trp57Gly) variant of SLC34A3 (Q8N130)
W57G (p.Trp57Gly) in SLC34A3 (Q8N130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
W57G (p.Trp57Gly) variant details
- p.Trp57Gly
- Ensembl rs1588841231
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available