Primary Site >> Stomach Cancer
Gene >> MMP21
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125773942:125773942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.586C>T |
| AA Mutation | p.Arg196Cys(p.R196C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125773932:125773932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.596C>T |
| AA Mutation | p.Ala199Val(p.A199V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125772334:125772334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.863T>G |
| AA Mutation | p.Val288Gly(p.V288G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125775698:125775698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124C>A |
| AA Mutation | p.Arg42Ser(p.R42S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125773855:125773855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673G>A |
| AA Mutation | p.Asp225Asn(p.D225N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125772730:125772730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766839501 |
| CDS Mutation | c.718C>T |
| AA Mutation | p.Arg240Trp(p.R240W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368808 |
| Start | 125770564:125770564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767318046 |
| CDS Mutation | c.1007C>T |
| AA Mutation | p.Ala336Val(p.A336V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368808 |
| Start | 125773859:125773859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150959910 |
| CDS Mutation | c.669G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368808 |
| Start | 125772725:125772725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.723C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368808 |
| Start | 125773958:125773958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368808 |
| Start | 125772662:125772662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146537734 |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |