Variant Summary
- Also known as
- C.275A>G,ASP92GLY
- HGVS
- ENST00000256474.2:c.275A>G,NC_000003.11:g.10183806A>G,NM_000551.3:c.275A>G,NP_000542.1:p.Asp92Gly
- 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 = D92G (c.275A>G).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | 2 |