Primary Site >> Stomach Cancer
Gene >> MMP25
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336577 |
| Start | 3050340:3050340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.455A>C |
| AA Mutation | p.Glu152Ala(p.E152A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336577 |
| Start | 3050441:3050441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757540476 |
| CDS Mutation | c.556G>A |
| AA Mutation | p.Asp186Asn(p.D186N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336577 |
| Start | 3050408:3050408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523G>C |
| AA Mutation | p.Ala175Pro(p.A175P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336577 |
| Start | 3047521:3047521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377224522 |
| CDS Mutation | c.206C>T |
| AA Mutation | p.Ala69Val(p.A69V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336577 |
| Start | 3050095:3050095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752362899 |
| CDS Mutation | c.319C>T |
| AA Mutation | p.Arg107Trp(p.R107W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336577 |
| Start | 3050296:3050296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376257566 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336577 |
| Start | 3050527:3050527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.642C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336577 |
| Start | 3058633:3058633(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1386delC |
| AA Mutation | p.Ser463ProfsTer97(p.S463Pfs*97) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |