Primary Site >> Stomach Cancer
Gene >> SMAD3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67181330:67181330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.748G>A |
| AA Mutation | p.Ala250Thr(p.A250T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67187446:67187446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091A>G |
| AA Mutation | p.Tyr364Cys(p.Y364C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67165352:67165352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.500C>A |
| AA Mutation | p.Pro167His(p.P167H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67190511:67190511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1253G>A |
| AA Mutation | p.Ser418Asn(p.S418N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67181384:67181384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs794727798 |
| CDS Mutation | c.802C>T |
| AA Mutation | p.Arg268Cys(p.R268C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67181305:67181305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.723C>G |
| AA Mutation | p.Asn241Lys(p.N241K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67184798:67184798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Val315Ile(p.V315I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327367 |
| Start | 67164960:67164960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.272T>C |
| AA Mutation | p.Leu91Pro(p.L91P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327367 |
| Start | 67184839:67184839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150994304 |
| CDS Mutation | c.984G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327367 |
| Start | 67165051:67165051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760286714 |
| CDS Mutation | c.363C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000327367 |
| Start | 67184841:67184842(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.986_987insTATCACATTAATCTCAAAGAGATTCGAATGA |
| AA Mutation | p.Thr330IlefsTer10(p.T330Ifs*10) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |