Variant Summary
- Also known as
- C.449A>G,ASN150SER,RS760184234
- HGVS
- NM_000551.3:c.449A>G,NP_000542.1:p.Asn150Ser,NC_000003.11:g.10188306A>G,ENST00000256474.2:c.449A>G
- 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 = N150S (c.449A>G).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | 2 |