Primary Site >> Stomach Cancer
Gene >> BIN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316724 |
| Start | 127070595:127070595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.273G>T |
| AA Mutation | p.Glu91Asp(p.E91D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316724 |
| Start | 127076648:127076648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.143T>C |
| AA Mutation | p.Val48Ala(p.V48A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316724 |
| Start | 127070576:127070576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292G>T |
| AA Mutation | p.Asp98Tyr(p.D98Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316724 |
| Start | 127070592:127070592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.276C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316724 |
| Start | 127106911:127106911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.33G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000316724 |
| Start | 127063939:127063939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.692G>A |
| AA Mutation | p.Trp231Ter(p.W231*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000316724 |
| Start | 127051153:127051153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764951306 |
| CDS Mutation | c.1461+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |