Primary Site >> Stomach Cancer
Gene >> DCN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91158337:91158337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779618769 |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166Gln(p.R166Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91146072:91146072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775666283 |
| CDS Mutation | c.1066G>A |
| AA Mutation | p.Gly356Arg(p.G356R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91178383:91178383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.170G>A |
| AA Mutation | p.Arg57His(p.R57H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91146089:91146089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766286927 |
| CDS Mutation | c.1049G>A |
| AA Mutation | p.Arg350His(p.R350H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91157111:91157111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778750338 |
| CDS Mutation | c.616C>T |
| AA Mutation | p.Arg206Cys(p.R206C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91158404:91158404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.430T>A |
| AA Mutation | p.Leu144Met(p.L144M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91178377:91178377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.176A>G |
| AA Mutation | p.Gln59Arg(p.Q59R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000052754 |
| Start | 91153171:91153171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144174426 |
| CDS Mutation | c.671C>T |
| AA Mutation | p.Thr224Met(p.T224M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000052754 |
| Start | 91157115:91157115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771673142 |
| CDS Mutation | c.612C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |