V17A (p.Val17Ala) variant of ERCC5 (P28715)
V17A (p.Val17Ala) in ERCC5 (P28715) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V17A (p.Val17Ala) variant details
- p.Val17Ala
- NCI-TCGA Cosmic COSV9995
- Ensembl rs1595373084
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available