Primary Site >> Stomach Cancer
Gene >> BCS1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359273 |
| Start | 218661205:218661205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758643336 |
| CDS Mutation | c.218G>A |
| AA Mutation | p.Arg73His(p.R73H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359273 |
| Start | 218662909:218662909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.916C>T |
| AA Mutation | p.Arg306Cys(p.R306C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359273 |
| Start | 218661828:218661828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143968821 |
| CDS Mutation | c.530G>A |
| AA Mutation | p.Arg177His(p.R177H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359273 |
| Start | 218663208:218663208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1082T>C |
| AA Mutation | p.Leu361Pro(p.L361P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359273 |
| Start | 218661068:218661068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.81A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359273 |
| Start | 218662583:218662583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.793C>T |
| AA Mutation | p.Arg265Ter(p.R265*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359273 |
| Start | 218661440:218661440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770749420 |
| CDS Mutation | c.355C>T |
| AA Mutation | p.Arg119Ter(p.R119*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |