Variant Summary
- Also known as
- C.589DELG,ASP197FS
- HGVS
- ENST00000256474.2:c.589delG,NC_000003.11:g.10191596del,NM_000551.3:c.589del,NP_000542.1:p.Asp197ThrfsTer5
- Variant Type(s)
- frameshift_truncation
- Evidence Items
- 1
Evidence Level Distribution
Level C: 1
Evidence Items
Showing CIViC evidence rows where gene = VHL and variant = D197FS (c.589delG).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | 3 |