Primary Site >> Stomach Cancer
Gene >> EAF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273668 |
| Start | 121857039:121857039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777157009 |
| CDS Mutation | c.367C>T |
| AA Mutation | p.Arg123Cys(p.R123C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273668 |
| Start | 121872739:121872739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273668 |
| Start | 121835333:121835333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.48T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273668 |
| Start | 121854735:121854735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.250T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273668 |
| Start | 121835303:121835303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273668 |
| Start | 121872559:121872559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.507A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000273668 |
| Start | 121854722:121854722(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.243delA |
| AA Mutation | p.Lys81AsnfsTer4(p.K81Nfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000273668 |
| Start | 121854787:121854787(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.306delA |
| AA Mutation | p.Lys102AsnfsTer8(p.K102Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000273668 |
| Start | 121854812:121854812(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768770510 |
| CDS Mutation | c.334delA |
| AA Mutation | p.Thr112GlnfsTer30(p.T112Qfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000273668 |
| Start | 121854811:121854812(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs746509911 |
| CDS Mutation | c.334dupA |
| AA Mutation | p.Thr112AsnfsTer4(p.T112Nfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |