Primary Site >> Stomach Cancer
Gene >> SPOCK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 136988466:136988466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.884A>C |
| AA Mutation | p.Lys295Thr(p.K295T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 136988502:136988502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.848C>A |
| AA Mutation | p.Pro283His(p.P283H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 137498417:137498417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.142G>A |
| AA Mutation | p.Val48Ile(p.V48I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 136992564:136992564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750490230 |
| CDS Mutation | c.626G>A |
| AA Mutation | p.Arg209Gln(p.R209Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 137067777:137067777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.527G>A |
| AA Mutation | p.Cys176Tyr(p.C176Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 137498474:137498474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760728894 |
| CDS Mutation | c.85G>A |
| AA Mutation | p.Gly29Arg(p.G29R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 136988523:136988523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.827A>T |
| AA Mutation | p.Lys276Met(p.K276M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 136988559:136988559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.791T>G |
| AA Mutation | p.Leu264Arg(p.L264R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 137067787:137067787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139465331 |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Ala173Thr(p.A173T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 137498482:137498482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.77C>T |
| AA Mutation | p.Ala26Val(p.A26V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 137498404:137498404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.155A>G |
| AA Mutation | p.Asp52Gly(p.D52G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394945 |
| Start | 136988523:136988523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.827A>C |
| AA Mutation | p.Lys276Thr(p.K276T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394945 |
| Start | 137498484:137498484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.75C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394945 |
| Start | 137112516:137112516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144155642 |
| CDS Mutation | c.393G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394945 |
| Start | 137140632:137140633(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.293_294dupTG |
| AA Mutation | p.Thr99Ter(p.T99*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |