Primary Site >> Stomach Cancer
Gene >> TCF19
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376255 |
| Start | 31159495:31159495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.26G>A |
| AA Mutation | p.Arg9His(p.R9H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376255 |
| Start | 31162614:31162614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.935G>A |
| AA Mutation | p.Gly312Asp(p.G312D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376255 |
| Start | 31162544:31162544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536786193 |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Gly289Arg(p.G289R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376255 |
| Start | 31161732:31161732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.524T>A |
| AA Mutation | p.Ile175Asn(p.I175N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376255 |
| Start | 31159604:31159604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.135G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376255 |
| Start | 31162543:31162543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369152415 |
| CDS Mutation | c.864C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000376255 |
| Start | 31159535:31159535(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751224053 |
| CDS Mutation | c.72delC |
| AA Mutation | p.Ala25ProfsTer72(p.A25Pfs*72) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |