Primary Site >> Stomach Cancer
Gene >> CLASP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33584876:33584876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1414G>A |
| AA Mutation | p.Ala472Thr(p.A472T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33577226:33577226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1687G>T |
| AA Mutation | p.Ala563Ser(p.A563S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33501704:33501704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3743C>T |
| AA Mutation | p.Ala1248Val(p.A1248V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399362 |
| Start | 33688308:33688308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534242099 |
| CDS Mutation | c.439G>A |
| AA Mutation | p.Val147Met(p.V147M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33592458:33592458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773840527 |
| CDS Mutation | c.1306A>G |
| AA Mutation | p.Met436Val(p.M436V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33606681:33606681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.905A>G |
| AA Mutation | p.Lys302Arg(p.K302R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33627047:33627047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.277A>C |
| AA Mutation | p.Asn93His(p.N93H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000480013 |
| Start | 33551257:33551257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2509C>T |
| AA Mutation | p.Arg837Trp(p.R837W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000480013 |
| Start | 33517050:33517050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3273T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000480013 |
| Start | 33644815:33644815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760557651 |
| CDS Mutation | c.105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000480013 |
| Start | 33576184:33576184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566880880 |
| CDS Mutation | c.1803G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399362 |
| Start | 33688309:33688309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753918174 |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000480013 |
| Start | 33560869:33560869(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761731080 |
| CDS Mutation | c.2230delA |
| AA Mutation | p.Met744TrpfsTer33(p.M744Wfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |