Primary Site >> Stomach Cancer
Gene >> DKK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 107035455:107035455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.137C>T |
| AA Mutation | p.Thr46Met(p.T46M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 106924081:106924081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653G>A |
| AA Mutation | p.Arg218His(p.R218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 106925810:106925810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201662083 |
| CDS Mutation | c.362G>A |
| AA Mutation | p.Arg121His(p.R121H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 107035563:107035563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.29C>T |
| AA Mutation | p.Ser10Leu(p.S10L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 106924082:106924082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753265155 |
| CDS Mutation | c.652C>T |
| AA Mutation | p.Arg218Cys(p.R218C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 106924189:106924189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.545C>T |
| AA Mutation | p.Pro182Leu(p.P182L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285311 |
| Start | 106925862:106925862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.310C>T |
| AA Mutation | p.Arg104Trp(p.R104W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285311 |
| Start | 106925818:106925818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.354C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285311 |
| Start | 106925836:106925836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774248896 |
| CDS Mutation | c.336A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |