V37A (p.Val37Ala) variant of ADH1B (P00325)
V37A (p.Val37Ala) in ADH1B (P00325) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V37A (p.Val37Ala) variant details
- p.Val37Ala
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10052
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available