Primary Site >> Stomach Cancer
Gene >> TACC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1728365:1728365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.963A>T |
| AA Mutation | p.Glu321Asp(p.E321D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1740973:1740973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2210A>T |
| AA Mutation | p.Glu737Val(p.E737V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1728618:1728618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142494551 |
| CDS Mutation | c.1216G>A |
| AA Mutation | p.Asp406Asn(p.D406N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1728426:1728426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1024G>A |
| AA Mutation | p.Val342Ile(p.V342I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1727727:1727727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Val109Met(p.V109M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1723798:1723798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.233T>G |
| AA Mutation | p.Leu78Arg(p.L78R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313288 |
| Start | 1723551:1723551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.130G>T |
| AA Mutation | p.Val44Leu(p.V44L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313288 |
| Start | 1737317:1737317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1825C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313288 |
| Start | 1728377:1728377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313288 |
| Start | 1728581:1728581(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs778789226 |
| CDS Mutation | c.1185delC |
| AA Mutation | p.Met396CysfsTer65(p.M396Cfs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313288 |
| Start | 1728580:1728581(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs757553939 |
| CDS Mutation | c.1185dupC |
| AA Mutation | p.Met396HisfsTer17(p.M396Hfs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |