V41I (p.Val41Ile) variant of GABRA1 (P14867)
V41I (p.Val41Ile) in GABRA1 (P14867) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V41I (p.Val41Ile) variant details
- p.Val41Ile
- NCI-TCGA Cosmic COSV5012
- cosmic curated COSV50122
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available