Primary Site >> Stomach Cancer
Gene >> MMP17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131845324:131845324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1079A>G |
| AA Mutation | p.Asp360Gly(p.D360G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131841735:131841735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.818C>T |
| AA Mutation | p.Pro273Leu(p.P273L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131840619:131840619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146831311 |
| CDS Mutation | c.469C>T |
| AA Mutation | p.Arg157Cys(p.R157C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131840652:131840652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502A>G |
| AA Mutation | p.Ser168Gly(p.S168G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131840614:131840614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376422502 |
| CDS Mutation | c.464C>T |
| AA Mutation | p.Thr155Met(p.T155M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131849987:131849987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779153151 |
| CDS Mutation | c.1390G>A |
| AA Mutation | p.Gly464Ser(p.G464S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131845320:131845320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754540566 |
| CDS Mutation | c.1075C>T |
| AA Mutation | p.Arg359Trp(p.R359W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131849954:131849954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374439053 |
| CDS Mutation | c.1357C>T |
| AA Mutation | p.Arg453Cys(p.R453C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360564 |
| Start | 131841711:131841711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794T>C |
| AA Mutation | p.Ile265Thr(p.I265T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360564 |
| Start | 131840807:131840807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201315531 |
| CDS Mutation | c.657C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360564 |
| Start | 131845130:131845130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756840716 |
| CDS Mutation | c.981C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360564 |
| Start | 131845406:131845406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745522975 |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360564 |
| Start | 131849971:131849971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750337417 |
| CDS Mutation | c.1374G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000360564 |
| Start | 131849800:131849800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199551747 |
| CDS Mutation | c.1205-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |