Primary Site >> Stomach Cancer
Gene >> KRT17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311208 |
| Start | 41621745:41621745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759193608 |
| CDS Mutation | c.682G>A |
| AA Mutation | p.Ala228Thr(p.A228T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311208 |
| Start | 41621657:41621657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200256057 |
| CDS Mutation | c.770G>A |
| AA Mutation | p.Arg257His(p.R257H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311208 |
| Start | 41623014:41623014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.451G>A |
| AA Mutation | p.Asp151Asn(p.D151N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311208 |
| Start | 41620684:41620684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752588997 |
| CDS Mutation | c.1156C>T |
| AA Mutation | p.Arg386Cys(p.R386C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311208 |
| Start | 41624124:41624124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564768263 |
| CDS Mutation | c.386G>A |
| AA Mutation | p.Arg129His(p.R129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311208 |
| Start | 41624353:41624353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748631498 |
| CDS Mutation | c.157G>A |
| AA Mutation | p.Gly53Arg(p.G53R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311208 |
| Start | 41624222:41624222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.288C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000311208 |
| Start | 41620535:41620535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753628412 |
| CDS Mutation | c.1204+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |