F31L (p.Phe31Leu) variant of RET (P07949)
F31L (p.Phe31Leu) in RET (P07949) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
F31L (p.Phe31Leu) variant details
- p.Phe31Leu
- Ensembl rs2132656948
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available