CIViC Evidence Items
4766 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 |
|---|---|---|---|---|---|---|---|---|
| D | PDGFRA | D842V | Predictive | Supports | Resistance | Cancer | Imatinib Mesylate | Heinrich et al., 2008 |
| D | PDGFRA | V561D | Predictive | Does Not Support | Resistance | Cancer | Imatinib Mesylate | Heinrich et al., 2008 |
| D | KIT | V560D | Predictive | Supports | Sensitivity/Response | Cancer | Imatinib Mesylate | Heinrich et al., 2008 |
| C | VHL | C162R (c.484T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Kanno et al., 1996 | |
| B | PIK3CA | Exon 21 Mutation AND PIK3CA Exon 10 Mutation | Prognostic | Supports | Poor Outcome | Colorectal Cancer | Liao et al., 2012 | |
| C | VHL | Splice Site (c.464-2A>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | R161G (c.481C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | R167Q (c.500G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | C162W (c.486C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | Splice Site (c.463+2T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | Splice Site (c.464-1G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | Q132* (c.394C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | Q164* (c.490C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | Q195* (c.583C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | E70* (c.208G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | H115Y (c.343C>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | C77_N78insL (c.230_231insTCT) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | L178Q (c.533T>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | L89P (c.266T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | P81S (c.241C>T) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | S80N (c.239G>A) | Predisposing | Supports | Uncertain Significance | Renal Cell Carcinoma | Glavac et al., 1996 | |
| C | VHL | Y98H (c.292T>C) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | Splice Site (c.463+1G>C) | Predisposing | Supports | Uncertain Significance | Renal Cell Carcinoma | Glavac et al., 1996 | |
| C | VHL | V74G (c.221T>G) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | N78S (c.233A>G) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | H115R (c.344A>G) | Predisposing | Supports | Uncertain Significance | Von Hippel-Lindau Disease | Glavac et al., 1996 | |
| C | VHL | V74G (c.221T>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | F76del (c.227_229del) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | S80N (c.239G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | S80I (c.239G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | V84L (c.250G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | L85P (c.254T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | G93R (c.277G>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | R108dup (c.322_324dup) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | L118P (c.353T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | F119L (c.357C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | D121G (c.362A>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | 3'UTR alteration (c.639+10C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Klein et al., 2001 | |
| C | VHL | E70* (c.208G>T) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | V74G (c.221T>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | F76del (c.227_229del) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | S80R (c.240T>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | L89P (c.266T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | G93R (c.277G>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | Y98H (c.292T>C) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | G114S (c.340G>A) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | W117fs (c.349dup) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | F119L (c.357C>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | D121G (c.362A>G) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 | |
| C | VHL | A122I (c.364_365GC>AT) | Predisposing | Supports | Predisposition | Von Hippel-Lindau Disease | Erlic et al., 2010 |