Primary Site >> Stomach Cancer
Gene >> COLQ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383788 |
| Start | 15456527:15456527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1007C>T |
| AA Mutation | p.Ala336Val(p.A336V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383788 |
| Start | 15488213:15488213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314G>A |
| AA Mutation | p.Gly105Asp(p.G105D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383788 |
| Start | 15458204:15458204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.936T>G |
| AA Mutation | p.Ser312Arg(p.S312R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383788 |
| Start | 15466376:15466376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.779C>A |
| AA Mutation | p.Pro260His(p.P260H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383788 |
| Start | 15455929:15455929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774638847 |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Gly389Ser(p.G389S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000383788 |
| Start | 15474926:15474926(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.554delA |
| AA Mutation | p.Lys185ArgfsTer39(p.K185Rfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000383788 |
| Start | 15474233:15474233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.595G>T |
| AA Mutation | p.Glu199Ter(p.E199*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |