CIViC Evidence Items
660 evidence items indexed
Evidence Level Distribution
CIViC evidence levels reflect study design quality, from A (strongest) to E (weakest).
AValidated — meta-analysis, systematic review, or major guideline
BClinical — prospective trial or retrospective cohort study
CCase study — single case report or small case series
DPreclinical — in vitro or animal model data
EInferential — computational prediction or biological rationale
Gene × Evidence Type
Count of CIViC evidence items per gene and evidence type category. Hover a column header for the type definition.
| Predictive | Diagnostic | Prognostic | Functional | Predispos. | Oncogenic | |
|---|---|---|---|---|---|---|
| BCR::ABL1 | 323 | 11 | ||||
| BRAF | 186 | 4 | 26 | 2 | 1 | |
| EGFR | 248 | 12 | 3 | 2 | ||
| EML4::ALK | 64 | |||||
| ERBB2 | 142 | 2 | ||||
| FLT3 | 55 | 2 | 21 | |||
| KIT | 102 | 3 | 7 | |||
| KRAS | 159 | 4 | 24 | 4 | ||
| PIK3CA | 156 | 16 | 4 | |||
| PTEN | 53 | 1 | 3 | 1 | 2 | 1 |
| TP53 | 52 | 40 | 100 | 2 | ||
| VHL | 5 | 2 | 3 | 635 | 15 |
Predictive:Links a variant to treatment response or resistance
Diagnostic:Supports or refutes a specific disease diagnosis
Prognostic:Informs disease progression or clinical outcome
Functional:Characterises the biological effect of a variant
Predisposing:Germline variant associated with cancer predisposition
Oncogenic:Characterises the variant's role in oncogenesis
| Level | Gene | Variant | Type | Direction | Significance | Disease | Drugs | Source |
|---|---|---|---|---|---|---|---|---|
| C | VHL | Y175* (c.525C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Olschwang et al., 1998 | |
| C | VHL | V166F (c.496G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Olschwang et al., 1998 | |
| C | VHL | V170G (c.509T>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Olschwang et al., 1998 | |
| C | VHL | G114R (c.340G>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Ciotti et al., 2009 | |
| C | VHL | S65W (c.194C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Zhou et al., 2010 | |
| C | VHL | R177* (c.529A>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Zhou et al., 2010 | |
| C | VHL | Splice Site (c.340+1G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Zhou et al., 2010 | |
| C | VHL | R113* (c.337C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | L129fs (c.384delT) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | S183* (c.548C>A) | Predisposing | Supports | Uncertain Significance | Renal Cell Carcinoma | Glavac et al., 1996 | |
| C | VHL | R161* (c.481C>T) | Predisposing | Supports | Uncertain Significance | Renal Cell Carcinoma | Glavac et al., 1996 | |
| C | VHL | R113* (c.337C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Yoshida et al., 2000 | |
| C | VHL | N131S (c.392A>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Yoshida et al., 2000 | |
| C | VHL | R167Q (c.500G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Yoshida et al., 2000 | |
| C | VHL | R167W (c.499C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Yoshida et al., 2000 | |
| C | VHL | C162Y (c.485G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Yoshida et al., 2000 | |
| C | VHL | F76del (c.227_229del) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Yoshida et al., 2000 | |
| C | VHL | R107G (c.319C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | R161Q (c.482G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | R161P (c.482G>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | R167Q (c.500G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | Q164* (c.490C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | Q195* (c.583C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | E94* (c.280G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | G93C (c.277G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | G93S (c.277G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | G93V (c.278G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | L188V (c.562C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | L198Q (c.593T>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | F119L (c.357C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | F136C (c.407T>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | S65A (c.193T>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | S68W (c.203C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | S80N (c.239G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | Y156N (c.466T>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | Y156C (c.467A>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | Y98H (c.292T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Neumann et al., 2002 | |
| C | VHL | P61fs (c.183insC) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | S65* (c.194C>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | E94* (c.280G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | Y175* (c.525C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | V194fs (c.581_582del) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | A149fs (c.449del14-nt) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | R167W (c.499C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | R161* (c.481C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Cybulski et al., 2002 | |
| C | VHL | Null (Partial deletion of Exons 2 & 3) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Benhammou et al., 2010 | |
| C | VHL | F136S (c.407T>C) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Rocha et al., 2003 | |
| C | VHL | P146fs (c.437del) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Rocha et al., 2003 | |
| C | VHL | R167W (c.499C>T) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Rocha et al., 2003 | |
| C | VHL | R167Q (c.500G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Rocha et al., 2003 |