Primary Site >> Stomach Cancer
Gene >> MMP14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311852 |
| Start | 22842618:22842618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.589G>A |
| AA Mutation | p.Gly197Ser(p.G197S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311852 |
| Start | 22842576:22842576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757252435 |
| CDS Mutation | c.547G>A |
| AA Mutation | p.Glu183Lys(p.E183K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311852 |
| Start | 22843794:22843794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.935C>A |
| AA Mutation | p.Pro312His(p.P312H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000311852 |
| Start | 22843416:22843416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848A>G |
| AA Mutation | p.Tyr283Cys(p.Y283C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311852 |
| Start | 22843728:22843728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.869C>T |
| AA Mutation | p.Pro290Leu(p.P290L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311852 |
| Start | 22842574:22842574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.545C>T |
| AA Mutation | p.Ala182Val(p.A182V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311852 |
| Start | 22845889:22845889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754278637 |
| CDS Mutation | c.1599C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311852 |
| Start | 22844703:22844703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1224A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311852 |
| Start | 22843819:22843819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371131343 |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311852 |
| Start | 22845359:22845359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565268793 |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000311852 |
| Start | 22841913:22841923(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.259_269delGCCATGAGGCG |
| AA Mutation | p.Ala87ProfsTer12(p.A87Pfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |