Primary Site >> Stomach Cancer
Gene >> RERG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256953 |
| Start | 15121071:15121071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.110C>A |
| AA Mutation | p.Pro37His(p.P37H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256953 |
| Start | 15109439:15109439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.271A>C |
| AA Mutation | p.Ser91Arg(p.S91R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256953 |
| Start | 15109346:15109346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.364T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256953 |
| Start | 15111356:15111356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256953 |
| Start | 15111404:15111404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.132A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256953 |
| Start | 15109478:15109478(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.232delG |
| AA Mutation | p.Glu78LysfsTer25(p.E78Kfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000256953 |
| Start | 15109217:15109217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767703721 |
| CDS Mutation | c.493C>T |
| AA Mutation | p.Arg165Ter(p.R165*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |