P26A (p.Pro26Ala) variant of RB1 (P06400)
P26A (p.Pro26Ala) in RB1 (P06400) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Retinoblastoma. The record also includes structural context.
P26A (p.Pro26Ala) variant details
- p.Pro26Ala
- Ensembl rs2138027626
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Retinoblastoma
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Retinoblastoma)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available