Variant Summary
- Also known as
- C.193T>G,SER65ALA,RS869025616
- HGVS
- NM_000551.3:c.193T>G,NP_000542.1:p.Ser65Ala,NC_000003.11:g.10183724T>G,ENST00000256474.2:c.193T>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 = S65A (c.193T>G).
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | 3 |