Variant Summary
- Also known as
- C.278G>A,GLY93ASP,RS1553619440
- HGVS
- ENST00000256474.2:c.278G>A,NC_000003.11:g.10183809G>A,NM_000551.3:c.278G>A,NP_000542.1:p.Gly93Asp
- Variant Type(s)
- missense_variant
- Evidence Items
- 1
Evidence Level Distribution
Level C: 1
Evidence Items
Showing CIViC evidence rows where gene = VHL and variant = G93D (c.278G>A).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | 3 |