Primary Site >> Stomach Cancer
Gene >> CPB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282957 |
| Start | 148845516:148845516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142211299 |
| CDS Mutation | c.871C>T |
| AA Mutation | p.Arg291Cys(p.R291C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282957 |
| Start | 148827870:148827870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.47A>G |
| AA Mutation | p.His16Arg(p.H16R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282957 |
| Start | 148857488:148857488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1013T>G |
| AA Mutation | p.Leu338Arg(p.L338R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282957 |
| Start | 148828064:148828064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134C>A |
| AA Mutation | p.Ala45Asp(p.A45D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282957 |
| Start | 148840687:148840687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.274G>C |
| AA Mutation | p.Val92Leu(p.V92L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282957 |
| Start | 148840955:148840955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766816862 |
| CDS Mutation | c.454C>T |
| AA Mutation | p.Arg152Cys(p.R152C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282957 |
| Start | 148841903:148841903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282957 |
| Start | 148857507:148857507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1032C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282957 |
| Start | 148859826:148859826(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1082delG |
| AA Mutation | p.Gly361AlafsTer59(p.G361Afs*59) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |