Primary Site >> Stomach Cancer
Gene >> PRKAB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229328 |
| Start | 119668324:119668324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61748075 |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Gly27Asp(p.G27D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229328 |
| Start | 119672304:119672304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.163C>T |
| AA Mutation | p.Pro55Ser(p.P55S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229328 |
| Start | 119672403:119672403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375579154 |
| CDS Mutation | c.262G>A |
| AA Mutation | p.Gly88Arg(p.G88R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229328 |
| Start | 119668319:119668319(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.80delG |
| AA Mutation | p.Gly27AlafsTer11(p.G27Afs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229328 |
| Start | 119672396:119672396(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.260delG |
| AA Mutation | p.Gly87AlafsTer27(p.G87Afs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229328 |
| Start | 119672395:119672396(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.260dupG |
| AA Mutation | p.Gly88ArgfsTer15(p.G88Rfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229328 |
| Start | 119668318:119668319(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs765766033 |
| CDS Mutation | c.80dupG |
| AA Mutation | p.Thr28HisfsTer39(p.T28Hfs*39) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |