Primary Site >> Stomach Cancer
Gene >> TGFBR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000212355 |
| Start | 91729811:91729811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.731C>T |
| AA Mutation | p.Pro244Leu(p.P244L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000212355 |
| Start | 91716264:91716264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1838T>C |
| AA Mutation | p.Val613Ala(p.V613A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000212355 |
| Start | 91720182:91720182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748447003 |
| CDS Mutation | c.1124G>A |
| AA Mutation | p.Arg375Gln(p.R375Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000212355 |
| Start | 91719409:91719409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469A>C |
| AA Mutation | p.Lys490Thr(p.K490T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000212355 |
| Start | 91712253:91712253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2156A>G |
| AA Mutation | p.Lys719Arg(p.K719R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000212355 |
| Start | 91719451:91719451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542785122 |
| CDS Mutation | c.1427C>T |
| AA Mutation | p.Ser476Leu(p.S476L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000212355 |
| Start | 91712471:91712471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1938C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000212355 |
| Start | 91695763:91695763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2346G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000212355 |
| Start | 91708769:91708769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376382556 |
| CDS Mutation | c.2181C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000212355 |
| Start | 91712257:91712257(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2152delC |
| AA Mutation | p.Gln718ArgfsTer20(p.Q718Rfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000212355 |
| Start | 91758669:91758669(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.328delC |
| AA Mutation | p.Leu110TrpfsTer5(p.L110Wfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000212355 |
| Start | 91716654:91716654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1621G>T |
| AA Mutation | p.Glu541Ter(p.E541*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000212355 |
| Start | 91734928:91734928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.416C>A |
| AA Mutation | p.Ser139Ter(p.S139*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |