S22R (p.Ser22Arg) variant of IL7R (P16871)
S22R (p.Ser22Arg) in IL7R (P16871) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
S22R (p.Ser22Arg) variant details
- p.Ser22Arg
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10028
- gnomAD rs1165388643
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available