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) |
|---|---|---|---|---|
| 2416 | H3-3A | K28M K27M | ENST00000366813.1:c.83A>T,ENSP00000355778.1:p.Lys28Met | non_conservative_missense_variant |
| 2652 | H3-3A | MUTATION | ||
| 2420 | H3-3B | K36M | ||
| 2815 | H3C2 | K27M | ||
| 486 | HAVCR2 | Overexpression | ||
| 2581 | HEY1::NCOA2 | Fusion HEY1-NCOA2 | transcript_fusion | |
| 671 | HGF | EXPRESSION | ||
| 433 | HIF1A | 3' UTR Polymorphism | NC_000014.8:g.62213848T>C | 3_prime_UTR_variant,SNP |
| 660 | HIF1A | EXPRESSION | ||
| 434 | HIF1A | OVEREXPRESSION | ||
| 4405 | HIP1::ALK | Fusion HIP1-ALK | transcript_fusion | |
| 821 | HLA-C | COPY-NEUTRAL LOSS OF HETEROZYGOSITY | loss_of_heterozygosity | |
| 423 | HLA-DRA | EXPRESSION | ||
| 2969 | HMGA2::LPP | Fusion HMGA2-LPP | transcript_fusion | |
| 344 | HMOX1 | EXPRESSION | ||
| 772 | HOXB13 | G84E RS138213197,GLY84GLU | NC_000017.10:g.46805705C>T,NM_006361.5:c.251G>A,NP_006352.2:p.Gly84Glu,ENST00000290295.7:c.251G>A | missense_variant |
| 274 | HRAS | G13D GLY13ASP,RS104894226 | NC_000011.9:g.534285C>T,NP_005334.1:p.Gly13Asp,NM_005343.3:c.38G>A,ENST00000451590.1:c.38G>A | missense_variant |
| 275 | HRAS | Mutation | coding_transcript_variant | |
| 2570 | HRAS | Q61 | ||
| 386 | HSPA5 | EXPRESSION | ||
| 400 | HSPB1 | EXPRESSION | ||
| 490 | HSPH1 | NUCLEAR EXPRESSION | ||
| 491 | HSPH1 | T17 DELETION | short_tandem_repeat_variation | |
| 645 | IDH1 | Mutation | transcript_variant | |
| 58 | IDH1 | R132 ARG132 | NC_000002.11:g.209113113G>A,NC_000002.11:g.209113112C>T,NC_000002.11:g.209113113G>C,NC_000002.11:g.209113112C>A,NC_000002.11:g.209113113G>T,NC_000002.11:g.209113112C>G | protein_altering_variant |
| 59 | IDH1 | R132C RS121913499,ARG132CYS | NM_005896.3:c.394C>T,NP_005887.2:p.Arg132Cys,NC_000002.11:g.209113113G>A,ENST00000415913.1:c.394C>T | missense_variant |
| 927 | IDH1 | R132G RS121913499,ARG132GLY | NM_001282386.1:c.394C>G,NP_001269315.1:p.Arg132Gly,NC_000002.11:g.209113113G>C,ENST00000415913.1:c.394C>G | missense_variant |
| 420 | IDH1 | R132H ARG132HIS,RS121913500 | NM_001282386.1:c.395G>A,NP_005887.2:p.Arg132His,NC_000002.11:g.209113112C>T,ENST00000415913.1:c.395G>A | missense_variant |
| 880 | IDH1 | R132L RS121913500,ARG132LEU | NM_001282386.1:c.395G>T,NP_001269315.1:p.Arg132Leu,NC_000002.11:g.209113112C>A,ENST00000415913.1:c.395G>T | missense_variant |
| 928 | IDH1 | R132S RS121913499,ARG132SER | NM_001282386.1:c.394C>A,NP_001269315.1:p.Arg132Ser,NC_000002.11:g.209113113G>T,ENST00000415913.1:c.394C>A | missense_variant |
| 570 | IDH2 | Mutation | protein_altering_variant | |
| 62 | IDH2 | R140 ARG140 | protein_altering_variant | |
| 199 | IDH2 | R172 ARG172 | protein_altering_variant | |
| 4459 | IDH2 | R172G | ||
| 63 | IDH2 | R172K ARG172LYS,R120K,RS121913503 | NC_000015.9:g.90631838C>T,NM_002168.3:c.515G>A,NP_002159.2:p.Arg172Lys,ENST00000330062.3:c.515G>A | missense_variant |
| 4462 | IDH2 | R172W | ||
| 5020 | IFNGR1 | Loss | ||
| 380 | IGF1R | EXPRESSION | ||
| 391 | IGF1R | NUCLEAR EXPRESSION | ||
| 3259 | IGF1R | Overexpression | ||
| 156 | IGF2 | Overexpression | ||
| 2663 | IGH::CRLF2 | Fusion IGH-CRLF2 | transcript_fusion | |
| 5106 | IGH::DUX4 | Fusion IGH-DUX4 | transcript_fusion | |
| 3954 | IGH::EPOR | Fusion IGH-EPOR | transcript_fusion | |
| 5084 | IGH::IL3 | Fusion IGH-IL3 | transcript_fusion | |
| 5148 | IGH::MYC | Fusion IGH-MYC | transcript_fusion | |
| 200 | IKZF1 | Deletion | transcript_ablation | |
| 2744 | IKZF1 | Loss-of-function | ||
| 5073 | IL3 | IGH::IL3 | ||
| 2911 | IL6 | Overexpression |