Primary Site >> Stomach Cancer
Gene >> KRT81
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327741 |
| Start | 52287624:52287624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34187924 |
| CDS Mutation | c.998C>T |
| AA Mutation | p.Thr333Met(p.T333M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327741 |
| Start | 52288033:52288033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369316032 |
| CDS Mutation | c.851A>G |
| AA Mutation | p.Asp284Gly(p.D284G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327741 |
| Start | 52288374:52288374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148570041 |
| CDS Mutation | c.722G>A |
| AA Mutation | p.Arg241Gln(p.R241Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327741 |
| Start | 52288109:52288109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758856533 |
| CDS Mutation | c.775G>A |
| AA Mutation | p.Val259Met(p.V259M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327741 |
| Start | 52291412:52291412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770430502 |
| CDS Mutation | c.54C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327741 |
| Start | 52287701:52287701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.921G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000327741 |
| Start | 52291373:52291373(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.93delC |
| AA Mutation | p.Tyr32ThrfsTer71(p.Y32Tfs*71) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |