Primary Site >> Stomach Cancer
Gene >> TOPBP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133661103:133661103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.25T>G |
| AA Mutation | p.Phe9Val(p.F9V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133608557:133608557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4403A>G |
| AA Mutation | p.Tyr1468Cys(p.Y1468C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133620245:133620245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3281T>C |
| AA Mutation | p.Leu1094Pro(p.L1094P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133623141:133623141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3128A>G |
| AA Mutation | p.Asn1043Ser(p.N1043S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133640111:133640111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2081A>G |
| AA Mutation | p.His694Arg(p.H694R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133618344:133618344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3461G>C |
| AA Mutation | p.Arg1154Thr(p.R1154T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133655431:133655431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.601C>G |
| AA Mutation | p.Leu201Val(p.L201V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133620189:133620189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751699737 |
| CDS Mutation | c.3337C>T |
| AA Mutation | p.Arg1113Cys(p.R1113C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133653517:133653517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.750G>C |
| AA Mutation | p.Lys250Asn(p.K250N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133628672:133628672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201984734 |
| CDS Mutation | c.2582C>T |
| AA Mutation | p.Thr861Met(p.T861M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260810 |
| Start | 133640048:133640048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2144C>T |
| AA Mutation | p.Ala715Val(p.A715V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260810 |
| Start | 133652580:133652580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748945735 |
| CDS Mutation | c.972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260810 |
| Start | 133659040:133659040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61747713 |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260810 |
| Start | 133656825:133656825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.396C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260810 |
| Start | 133637990:133637990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260810 |
| Start | 133640089:133640089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2103T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260810 |
| Start | 133611036:133611036(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4141delA |
| AA Mutation | p.Ile1381SerfsTer61(p.I1381Sfs*61) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260810 |
| Start | 133616887:133616887(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3798delA |
| AA Mutation | p.Lys1266AsnfsTer10(p.K1266Nfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260810 |
| Start | 133640059:133640059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770032653 |
| CDS Mutation | c.2133G>A |
| AA Mutation | p.Trp711Ter(p.W711*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |