Primary Site >> Stomach Cancer
Gene >> MMP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102842164:102842164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.615G>T |
| AA Mutation | p.Lys205Asn(p.K205N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102842724:102842724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298T>G |
| AA Mutation | p.Phe100Val(p.F100V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102840546:102840546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673G>T |
| AA Mutation | p.Gly225Cys(p.G225C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102842214:102842214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.565C>T |
| AA Mutation | p.Pro189Ser(p.P189S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102842795:102842795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554987933 |
| CDS Mutation | c.227C>T |
| AA Mutation | p.Thr76Met(p.T76M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102842760:102842760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377547395 |
| CDS Mutation | c.262C>T |
| AA Mutation | p.Arg88Cys(p.R88C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102843450:102843450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.97C>T |
| AA Mutation | p.Leu33Phe(p.L33F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299855 |
| Start | 102839233:102839233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147533686 |
| CDS Mutation | c.946C>T |
| AA Mutation | p.Arg316Cys(p.R316C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299855 |
| Start | 102843529:102843529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200221002 |
| CDS Mutation | c.18C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |