Primary Site >> Stomach Cancer
Gene >> MMP16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88118837:88118837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734T>G |
| AA Mutation | p.Val245Gly(p.V245G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327140:88327140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.67T>G |
| AA Mutation | p.Leu23Val(p.L23V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88074671:88074671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1156C>T |
| AA Mutation | p.Arg386Trp(p.R386W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88041751:88041751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1534A>C |
| AA Mutation | p.Asn512His(p.N512H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88197191:88197191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.248A>C |
| AA Mutation | p.Asn83Thr(p.N83T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88056207:88056207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1294A>G |
| AA Mutation | p.Ser432Gly(p.S432G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88046680:88046680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1478A>G |
| AA Mutation | p.His493Arg(p.H493R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327154:88327154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.53C>T |
| AA Mutation | p.Ser18Leu(p.S18L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88074719:88074719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1108A>G |
| AA Mutation | p.Asn370Asp(p.N370D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88197252:88197252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.187C>A |
| AA Mutation | p.Leu63Met(p.L63M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327097:88327097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.110C>T |
| AA Mutation | p.Thr37Met(p.T37M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88041601:88041601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200606225 |
| CDS Mutation | c.1684G>T |
| AA Mutation | p.Val562Leu(p.V562L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88041519:88041519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1766G>A |
| AA Mutation | p.Arg589Lys(p.R589K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88116581:88116581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141858403 |
| CDS Mutation | c.1009G>A |
| AA Mutation | p.Gly337Arg(p.G337R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88327184:88327184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199761222 |
| CDS Mutation | c.23C>T |
| AA Mutation | p.Thr8Ile(p.T8I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88041730:88041730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1555C>A |
| AA Mutation | p.Pro519Thr(p.P519T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88116530:88116530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060C>T |
| AA Mutation | p.Arg354Cys(p.R354C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88046676:88046676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1482A>T |
| AA Mutation | p.Lys494Asn(p.K494N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88074718:88074718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1109A>T |
| AA Mutation | p.Asn370Ile(p.N370I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286614 |
| Start | 88041505:88041505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749473846 |
| CDS Mutation | c.1780C>T |
| AA Mutation | p.Arg594Cys(p.R594C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286614 |
| Start | 88074630:88074630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143304974 |
| CDS Mutation | c.1197C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286614 |
| Start | 88041647:88041647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1638A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286614 |
| Start | 88056160:88056160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200751407 |
| CDS Mutation | c.1341C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |