CIViC Variants
1951 variants indexed
Variant Types
Sequence Ontology (SO) terms describing the molecular consequence of each variant, as curated in CIViC. Hover a bar for the definition.
| CIViC ID | Gene | Variant | HGVS | Type(s) |
|---|---|---|---|---|
| 341 | CD44 | CD44s Expression | ||
| 3373 | CD44 | CD44v6 | alternatively_spliced_transcript | |
| 5012 | CD72::ROS1 | Fusion CD72-ROS1 | transcript_fusion | |
| 4908 | CD74::ROS1 | Fusion CD74-ROS1 | transcript_fusion | |
| 664 | CDH1 | MUTATION | transcription_variant | |
| 236 | CDK12 | Loss-of-function | loss_of_function_variant | |
| 2764 | CDK12 | Mutation | ||
| 553 | CDK4 | Amplification | transcript_amplification | |
| 25 | CDK4 | EXPRESSION | ||
| 556 | CDK4 | R24C ARG24CYS,RS11547328 | NM_000075.3:c.70C>T,NP_000066.1:p.Arg24Cys,ENST00000257904.6:c.70C>T,NC_000012.11:g.58145431G>A | missense_variant |
| 3042 | CDK6 | EXPRESSION | ||
| 602 | CDK6 | Overexpression | ||
| 355 | CDKN1A | EXPRESSION | ||
| 3313 | CDKN1A | rs1059234 | ||
| 2671 | CDKN1A | rs1801270 | ||
| 360 | CDKN1B | CYTOPLASMIC MISLOCALIZATION | ||
| 372 | CDKN1B | EXPRESSION | ||
| 2654 | CDKN2A | Deletion | ||
| 554 | CDKN2A | Loss | loss_of_function_variant | |
| 2704 | CDKN2A | Mutation | ||
| 27 | CDKN2A | Promoter Hypermethylation | ||
| 641 | CDKN2A | RS3814960 | NC_000009.11:g.21975017C>T,NM_000077.4:c.-191G>A | 5_prime_UTR_exon_variant |
| 2884 | CDKN2A | c.151-1G>C | ||
| 272 | CDKN2A | p16 Expression | ||
| 555 | CDKN2B | Loss | transcript_ablation | |
| 784 | CDKN2B | METHYLATION | ||
| 410 | CDX2 | EXPRESSION | ||
| 594 | CEBPA | BIALLELIC INACTIVATION | loss_of_function_variant | |
| 29 | CEBPA | Mutation | loss_of_function_variant,transcript_variant | |
| 28 | CEBPA | N-TERMINAL FRAME SHIFT | frameshift_truncation,dominant_negative_variant | |
| 3270 | CENPC::ABL1 | Fusion CENPC-ABL1 | transcript_fusion | |
| 4498 | CEP43::FGFR1 | Fusion FGFR1OP-FGFR1,FGFR1OP::FGFR1,CEP43-FGFR1 | transcript_fusion | |
| 392 | CFLAR | EXPRESSION | ||
| 4337 | CHD7::BEND2 | Fusion CHD7-BEND2,Translocation (t(8;X)(q12.2;p22.13)) | transcript_fusion | |
| 4441 | CHEK1 | Mutation | ||
| 1693 | CHEK1 | Overexpression | ||
| 785 | CHEK2 | 1100DELC THR367METFS,RS555607708 | NC_000022.10:g.29091857delG,NM_007194.3:c.1100delC,NP_009125.1:p.Thr367Metfs,ENST00000328354.6:c.1100delC,NC_000022.10:g.29091857del | frameshift_truncation |
| 787 | CHEK2 | I157T ILE157THR,I200T,RS17879961 | NM_007194.3:c.470T>C,NP_009125.1:p.Ile157Thr,ENST00000328354.6:c.470T>C,NC_000022.10:g.29121087A>G | missense_variant |
| 788 | CHEK2 | IVS2+1G>A | ||
| 230 | CHEK2 | Loss-of-function | loss_of_function_variant | |
| 2959 | CHEK2 | R474C c.1420C>T | missense_variant | |
| 4436 | CHEK2 | mutation | ||
| 3252 | CIC::DUX4 | Fusion CIC-DUX4 | transcript_fusion | |
| 474 | CIP2A | EXPRESSION | ||
| 475 | CIP2A | Underexpression | ||
| 4946 | CK | High | ||
| 520 | CLTC::ALK | Fusion T(2;17)(P23;Q23),CLTC-ALK | transcript_fusion | |
| 2972 | COL1A1::PDGFB | Fusion COL1A1-PDGFB | transcript_fusion | |
| 713 | CRBN | Mutation | ||
| 560 | CSF3R | Mutation | protein_altering_variant |