Primary Site >> Stomach Cancer
Gene >> MAGEC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141881571:141881571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.684A>C |
| AA Mutation | p.Lys228Asn(p.K228N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141865600:141865600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.253T>G |
| AA Mutation | p.Phe85Val(p.F85V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141897785:141897785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1885G>A |
| AA Mutation | p.Ala629Thr(p.A629T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141895275:141895275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.916T>A |
| AA Mutation | p.Ser306Thr(p.S306T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141879253:141879253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.337T>G |
| AA Mutation | p.Ser113Ala(p.S113A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141881482:141881482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.595T>C |
| AA Mutation | p.Tyr199His(p.Y199H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141897365:141897365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1607G>T |
| AA Mutation | p.Ser536Ile(p.S536I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141865565:141865565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218A>T |
| AA Mutation | p.Gln73Leu(p.Q73L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141897127:141897127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1369G>T |
| AA Mutation | p.Asp457Tyr(p.D457Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141881662:141881662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751683228 |
| CDS Mutation | c.775A>G |
| AA Mutation | p.Thr259Ala(p.T259A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141897116:141897116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1358G>T |
| AA Mutation | p.Arg453Met(p.R453M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141865553:141865553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206G>C |
| AA Mutation | p.Gly69Ala(p.G69A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141897313:141897313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752119740 |
| CDS Mutation | c.1555G>T |
| AA Mutation | p.Asp519Tyr(p.D519Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298296 |
| Start | 141865497:141865497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150C>A |
| AA Mutation | p.Asp50Glu(p.D50E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298296 |
| Start | 141895382:141895382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750027584 |
| CDS Mutation | c.1023C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298296 |
| Start | 141865482:141865482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.135G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298296 |
| Start | 141895531:141895531(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1096delG |
| AA Mutation | p.Ala366ArgfsTer51(p.A366Rfs*51) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000298296 |
| Start | 141865567:141865567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781575911 |
| CDS Mutation | c.220C>T |
| AA Mutation | p.Arg74Ter(p.R74*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |