Primary Site >> Stomach Cancer
Gene >> AURKB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000585124 |
| Start | 8205373:8205373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Gly235Asp(p.G235D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000585124 |
| Start | 8206872:8206872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761178783 |
| CDS Mutation | c.415C>T |
| AA Mutation | p.Arg139Cys(p.R139C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000585124 |
| Start | 8207602:8207602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.175G>A |
| AA Mutation | p.Glu59Lys(p.E59K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000585124 |
| Start | 8204968:8204968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144169786 |
| CDS Mutation | c.938C>T |
| AA Mutation | p.Ser313Leu(p.S313L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000585124 |
| Start | 8205007:8205007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899C>T |
| AA Mutation | p.Ala300Val(p.A300V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000585124 |
| Start | 8205226:8205226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851G>A |
| AA Mutation | p.Arg284His(p.R284H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000585124 |
| Start | 8207196:8207196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141915374 |
| CDS Mutation | c.378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |