Variant Summary
- Also known as
- PRO138THR
- HGVS
- ENST00000234420.5:c.412C>A,NC_000002.11:g.48018217C>A
- Variant Type(s)
- missense_variant
- Evidence Items
- 1
Evidence Level Distribution
Level C: 1
Evidence Items
Showing CIViC evidence rows where gene = MSH6 and variant = P138T.
| Level | Type | Direction | Significance | Disease | Drugs | Rating |
|---|---|---|---|---|---|---|
| C | Oncogenic | Supports | Oncogenicity | Colorectal Cancer | 1 |