Primary Site >> Stomach Cancer
Gene >> CR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207471081:207471081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1487G>A |
| AA Mutation | p.Gly496Asp(p.G496D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207472979:207472979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1778G>A |
| AA Mutation | p.Cys593Tyr(p.C593Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207473011:207473011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1810C>T |
| AA Mutation | p.His604Tyr(p.H604Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207478056:207478056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2897C>T |
| AA Mutation | p.Ala966Val(p.A966V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207475066:207475066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779734792 |
| CDS Mutation | c.2389T>C |
| AA Mutation | p.Tyr797His(p.Y797H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207468824:207468824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147633291 |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Arg220Gln(p.R220Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207466582:207466582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.115A>G |
| AA Mutation | p.Thr39Ala(p.T39A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367058 |
| Start | 207469697:207469697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.820A>T |
| AA Mutation | p.Ile274Phe(p.I274F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207471487:207471487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764276175 |
| CDS Mutation | c.1558C>T |
| AA Mutation | p.Arg520Cys(p.R520C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207473878:207473878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2056C>G |
| AA Mutation | p.Gln686Glu(p.Q686E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207473852:207473852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750302661 |
| CDS Mutation | c.2030G>A |
| AA Mutation | p.Arg677His(p.R677H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207469203:207469203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788T>C |
| AA Mutation | p.Val263Ala(p.V263A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207466627:207466627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.160A>G |
| AA Mutation | p.Thr54Ala(p.T54A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367058 |
| Start | 207476271:207476271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776361702 |
| CDS Mutation | c.2577C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367058 |
| Start | 207472854:207472854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373293174 |
| CDS Mutation | c.1653G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367058 |
| Start | 207473811:207473811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1989G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367058 |
| Start | 207475210:207475210(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2538delA |
| AA Mutation | p.Ala847ProfsTer3(p.A847Pfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367058 |
| Start | 207468699:207468699(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769372920 |
| CDS Mutation | c.624delC |
| AA Mutation | p.Thr209HisfsTer10(p.T209Hfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367058 |
| Start | 207470882:207470882(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1372delG |
| AA Mutation | p.Val458CysfsTer22(p.V458Cfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367058 |
| Start | 207474837:207474837(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2162delC |
| AA Mutation | p.Pro721LeufsTer4(p.P721Lfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |