Variant Summary
- Also known as
- C.466T>A,TYR156ASN
- HGVS
- ENST00000256474.2:c.466T>A,NC_000003.11:g.10191473T>A,NM_000551.3:c.466T>A,NP_000542.1:p.Tyr156Asn
- 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 = Y156N (c.466T>A).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | 3 |