Primary Site >> Stomach Cancer
Gene >> CACNA2D1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81950414:81950414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138331326 |
| CDS Mutation | c.3290G>A |
| AA Mutation | p.Gly1097Asp(p.G1097D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82066474:82066474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.709G>T |
| AA Mutation | p.Asp237Tyr(p.D237Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81984679:81984679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1886A>G |
| AA Mutation | p.Tyr629Cys(p.Y629C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81969952:81969952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779277828 |
| CDS Mutation | c.2273C>T |
| AA Mutation | p.Thr758Ile(p.T758I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000356253 |
| Start | 82335137:82335137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292G>A |
| AA Mutation | p.Val98Met(p.V98M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82117082:82117082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.488A>G |
| AA Mutation | p.His163Arg(p.H163R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82170584:82170584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.320T>G |
| AA Mutation | p.Val107Gly(p.V107G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82007746:82007746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1373T>C |
| AA Mutation | p.Leu458Pro(p.L458P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81974490:81974490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2054A>G |
| AA Mutation | p.Glu685Gly(p.E685G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000356253 |
| Start | 82038079:82038079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1036A>C |
| AA Mutation | p.Asn346His(p.N346H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82038178:82038178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.937A>G |
| AA Mutation | p.Arg313Gly(p.R313G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 82117050:82117050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.520G>A |
| AA Mutation | p.Glu174Lys(p.E174K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356253 |
| Start | 81982583:81982583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1975A>G |
| AA Mutation | p.Thr659Ala(p.T659A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 82443397:82443397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746712870 |
| CDS Mutation | c.63C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 81971860:81971860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147499376 |
| CDS Mutation | c.2094C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 82032854:82032854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148592476 |
| CDS Mutation | c.1086G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 81961998:81961998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749722010 |
| CDS Mutation | c.2898G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 82032857:82032857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542878600 |
| CDS Mutation | c.1083C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 81968966:81968966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2352A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 82014411:82014411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1212T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356253 |
| Start | 81959329:81959329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3141T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356253 |
| Start | 82038203:82038203(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.912delT |
| AA Mutation | p.Gln305SerfsTer8(p.Q305Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356253 |
| Start | 82038167:82038167(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.948delA |
| AA Mutation | p.Val317CysfsTer2(p.V317Cfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000356253 |
| Start | 81959313:81959313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752471498 |
| CDS Mutation | c.3157C>T |
| AA Mutation | p.Arg1053Ter(p.R1053*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |