S13F (p.Ser13Phe) variant of IL7R (P16871)
S13F (p.Ser13Phe) in IL7R (P16871) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S13F (p.Ser13Phe) variant details
- p.Ser13Phe
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10028
- NCI-TCGA Cosmic COSV5741
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available