Primary Site >> Stomach Cancer
Gene >> SMAD9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36872726:36872726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200074185 |
| CDS Mutation | c.602C>T |
| AA Mutation | p.Pro201Leu(p.P201L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36853667:36853667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1012T>G |
| AA Mutation | p.Leu338Val(p.L338V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36865711:36865711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777979202 |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Ala277Thr(p.A277T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36872876:36872876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.452A>G |
| AA Mutation | p.Asn151Ser(p.N151S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36872852:36872852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.476A>G |
| AA Mutation | p.Lys159Arg(p.K159R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36872705:36872705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623A>G |
| AA Mutation | p.His208Arg(p.H208R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36879505:36879505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370142437 |
| CDS Mutation | c.185C>T |
| AA Mutation | p.Pro62Leu(p.P62L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36879439:36879439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759141619 |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Arg84His(p.R84H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379826 |
| Start | 36853490:36853490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1189T>A |
| AA Mutation | p.Ser397Thr(p.S397T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379826 |
| Start | 36879393:36879393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559936906 |
| CDS Mutation | c.297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379826 |
| Start | 36865664:36865664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374668463 |
| CDS Mutation | c.876C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379826 |
| Start | 36853509:36853509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772038868 |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379826 |
| Start | 36865715:36865715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374907507 |
| CDS Mutation | c.825G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379826 |
| Start | 36872871:36872871(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.457delC |
| AA Mutation | p.Gln153SerfsTer93(p.Q153Sfs*93) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000379826 |
| Start | 36865690:36865690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553369182 |
| CDS Mutation | c.850C>T |
| AA Mutation | p.Arg284Ter(p.R284*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |