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) |
|---|---|---|---|---|
| 595 | SRSF2 | MUTATION | gene_variant | |
| 4304 | SRSF2 | P95H PRO95HIS | NC_000017.11:g.76736877G>T,NC_000017.10:g.74732959G>T,ENST00000359995.10:c.284C>A,ENSP00000353089.5:p.Pro95His,NM_001195427.2:c.284C>A,NP_001182356.1:p.Pro95His | missense_variant |
| 4303 | SRSF2 | P95L PRO95LEU | NC_000017.11:g.76736877G>A,NC_000017.10:g.74732959G>A,ENST00000359995.10:c.284C>T,ENSP00000353089.5:p.Pro95Leu,NM_001195427.2:c.284C>T,NP_001182356.1:p.Pro95Leu | missense_variant |
| 448 | SS18::SSX1 | Fusion T(X;18)(P11.23;Q11),SS18-SSX1,SYT-SSX,SYT-SSX1,SS18-SSX | transcript_fusion | |
| 449 | SS18::SSX2 | Fusion T(X;18)(P11.21;Q11),SS18-SSX2 | transcript_fusion | |
| 450 | SS18::SSX4 | Fusion SS18-SSX4 | transcript_fusion | |
| 2661 | SSBP2::JAK2 | Fusion T(5;9)(Q14.1;P24) | transcript_fusion | |
| 3752 | SSTR5 | expression | ||
| 669 | STAG2 | MUTATION | protein_altering_variant | |
| 422 | STAG2 | Underexpression | ||
| 654 | STAG3 | Underexpression | ||
| 411 | STAT3 | SH2 DOMAIN MUTATION | protein_altering_variant | |
| 634 | STK11 | D194E ASP194GLU,RS786202134 | NC_000019.9:g.1220489C>A,NM_000455.4:c.582C>A,NP_000446.1:p.Asp194Glu,ENST00000326873.7:c.582C>A | missense_variant,loss_of_heterozygosity |
| 303 | STK11 | EXON 1-2 MUTATION | exon_variant | |
| 485 | STK11 | Loss | loss_of_function_variant | |
| 715 | STK11 | Mutation | gene_variant | |
| 304 | STK11 | Underexpression | ||
| 357 | STMN1 | EXPRESSION | ||
| 2849 | STRN3::JAK2 | Fusion STRN3-JAK2 | transcript_fusion | |
| 2218 | STRN::ALK | Fusion STRN-ALK | transcript_fusion | |
| 2287 | STRN::NTRK2 | Fusion STRN-NTRK2 | transcript_fusion | |
| 305 | SYK | OVEREXPRESSION | ||
| 5259 | TAF15::NR4A3 | Fusion TAF15-NR4A3 | transcript_fusion | |
| 483 | TBK1 | Overexpression | ||
| 3359 | TBL1XR1::CSF1R | Fusion TBL1XR1-CSF1R | transcript_fusion | |
| 5052 | TCF3 | TCF3::HLF | ||
| 5083 | TCF3::HLF | Fusion TCF3-HLF | transcript_fusion | |
| 4690 | TCF3::PBX1 | Fusion TCF3-PBX1 | transcript_fusion | |
| 2862 | TERF2::JAK2 | Fusion TERF2-JAK2 | transcript_fusion | |
| 219 | TERT | Amplification | transcript_amplification | |
| 248 | TERT | C228T -124C>T | NC_000005.9:g.1295228G>A | regulatory_region_variant |
| 220 | TERT | Promoter Mutation -124C>T,-146C>T | regulatory_region_variant | |
| 421 | TERT | RS2736100 | NC_000005.9:g.1286516C>A,ENST00000310581.5:c.1574-3777G>T,NM_001193376.1:c.1574-3777G>T,NP_001180305.1:p.= | coding_transcript_intron_variant,polymorphic_sequence_variant |
| 157 | TET2 | Mutation | gene_variant,loss_of_function_variant | |
| 339 | TFF3 | EXPRESSION | ||
| 576 | TFG::ROS1 | Fusion TFG-ROS1 | transcript_fusion | |
| 316 | TGFA | EXPRESSION | ||
| 417 | THBS2 | UNDEREXPRESSION | ||
| 377 | TIMP1 | Overexpression | ||
| 2240 | TLK2 | Amplification | ||
| 5360 | TMB | H-bTMB | ||
| 4943 | TMB | High High Tumor Mutational Burden,TMB-H | ||
| 195 | TMPRSS2::ERG | Fusion TMPRSS2-ERG | transcript_fusion | |
| 774 | TNKS2::PDGFRA | Fusion TNKS2-PDGFRA | transcript_fusion | |
| 371 | TOP1 | Amplification | transcript_amplification | |
| 384 | TOP1 | EXPRESSION | ||
| 383 | TOP2A | EXPRESSION | ||
| 1114 | TP53 | A161T | missense_variant | |
| 1050 | TP53 | A276V ALA276VAL | ENST00000269305.4:c.827C>T | missense_variant |
| 1307 | TP53 | ALTERATION |