A38V (p.Ala38Val) variant of ERCC5 (P28715)
A38V (p.Ala38Val) in ERCC5 (P28715) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
A38V (p.Ala38Val) variant details
- p.Ala38Val
- NCI-TCGA TCGA novel
- Ensembl rs2140517228
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.