Variant Summary
- Also known as
- C.413C>G,PRO138ARG
- HGVS
- ENST00000256474.2:c.413C>G,NC_000003.11:g.10188270C>G,NM_000551.3:c.413C>G,NP_000542.1:p.Pro138Arg
- 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 = P138R (c.413C>G).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Oncogenic | Supports | Oncogenicity | Clear Cell Renal Cell Carcinoma | 1 |