A2V (p.Ala2Val) variant of FANCC (Fanconi anemia group C protein)
A2V (p.Ala2Val) in FANCC (Fanconi anemia group C protein) is a missense change. Clinical records from ClinVar and UniProt describe it as benign/likely benign in the context of Hereditary cancer-predisposing syndrome; not specified; not provided. The record also includes structural context.
A2V (p.Ala2Val) variant details
- p.Ala2Val
- Ensembl rs587780940
- Benign/Likely benign
- Hereditary cancer-predisposing syndrome; not specified; not provided
- Missense
- ClinVar: Benign/Likely benign (Hereditary cancer-predisposing syndrome; not specified; not prov)
- UniProt: Likely benign
- Structural context available