Primary Site >> Stomach Cancer
Gene >> CBFA2T3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88879392:88879392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760316068 |
| CDS Mutation | c.1540C>T |
| AA Mutation | p.Arg514Cys(p.R514C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88879301:88879301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751448990 |
| CDS Mutation | c.1631C>T |
| AA Mutation | p.Thr544Met(p.T544M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88885082:88885082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1081G>A |
| AA Mutation | p.Asp361Asn(p.D361N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88891953:88891953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376580768 |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Glu214Lys(p.E214K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88892273:88892273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779831852 |
| CDS Mutation | c.592C>T |
| AA Mutation | p.Arg198Cys(p.R198C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88891908:88891908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774579712 |
| CDS Mutation | c.685C>T |
| AA Mutation | p.Arg229Trp(p.R229W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88892357:88892357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745883820 |
| CDS Mutation | c.508G>A |
| AA Mutation | p.Gly170Arg(p.G170R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88885061:88885061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147184929 |
| CDS Mutation | c.1102C>T |
| AA Mutation | p.Arg368Cys(p.R368C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268679 |
| Start | 88885195:88885195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Pro323Leu(p.P323L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268679 |
| Start | 88879381:88879381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1551C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268679 |
| Start | 88901523:88901523(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758778776 |
| CDS Mutation | c.285delC |
| AA Mutation | p.Ser96ProfsTer24(p.S96Pfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |