Primary Site >> Stomach Cancer
Gene >> ADRB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827333:148827333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502C>T |
| AA Mutation | p.Pro168Ser(p.P168S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827129:148827129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.298A>G |
| AA Mutation | p.Thr100Ala(p.T100A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827019:148827019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.188G>A |
| AA Mutation | p.Arg63His(p.R63H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827576:148827576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.745G>A |
| AA Mutation | p.Glu249Lys(p.E249K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827085:148827085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.254C>A |
| AA Mutation | p.Ala85Glu(p.A85E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827718:148827718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369459230 |
| CDS Mutation | c.887A>G |
| AA Mutation | p.His296Arg(p.H296R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827150:148827150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.319G>A |
| AA Mutation | p.Glu107Lys(p.E107K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827776:148827776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827185:148827185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.354G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305988 |
| Start | 148827902:148827902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761680537 |
| CDS Mutation | c.1071C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305988 |
| Start | 148826835:148826838(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4_7delGGGC |
| AA Mutation | p.Gly2AsnfsTer94(p.G2Nfs*94) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |