Variant Summary
- Also known as
- C.346C>G,LEU116VAL
- HGVS
- ENST00000256474.2:c.346C>G,NC_000003.11:g.10188203C>G,NM_000551.3:c.346C>G,NP_000542.1:p.Leu116Val
- 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 = L116V (c.346C>G).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | 4 |