Primary Site >> Stomach Cancer
Gene >> SEMA3B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616701 |
| Start | 50273626:50273626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.902A>G |
| AA Mutation | p.Asp301Gly(p.D301G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616701 |
| Start | 50275795:50275795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1796C>T |
| AA Mutation | p.Ala599Val(p.A599V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616701 |
| Start | 50275396:50275396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1586C>T |
| AA Mutation | p.Ala529Val(p.A529V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616701 |
| Start | 50276686:50276686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2230C>T |
| AA Mutation | p.Arg744Cys(p.R744C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616701 |
| Start | 50276648:50276648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2192G>A |
| AA Mutation | p.Arg731Lys(p.R731K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616701 |
| Start | 50275820:50275820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1821C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616701 |
| Start | 50274471:50274471(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1251delG |
| AA Mutation | p.Arg418AlafsTer41(p.R418Afs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |