S28R (p.Ser28Arg) variant of BRCA2 (P51587)
S28R (p.Ser28Arg) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as likely benign.
S28R (p.Ser28Arg) variant details
- p.Ser28Arg
- Ensembl rs2138703678
- NCI-TCGA Cosmic COSV1012
- cosmic curated COSV10120
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign