Primary Site >> Stomach Cancer
Gene >> MTRF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41260747:41260747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.161G>A |
| AA Mutation | p.Ser54Asn(p.S54N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41226463:41226463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1094A>C |
| AA Mutation | p.Lys365Thr(p.K365T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41233909:41233909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.969A>C |
| AA Mutation | p.Arg323Ser(p.R323S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41226509:41226509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376093788 |
| CDS Mutation | c.1048C>T |
| AA Mutation | p.Arg350Cys(p.R350C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41253018:41253018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.520C>A |
| AA Mutation | p.Leu174Ile(p.L174I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41252695:41252695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.647G>A |
| AA Mutation | p.Cys216Tyr(p.C216Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379477 |
| Start | 41260691:41260691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217A>G |
| AA Mutation | p.Lys73Glu(p.K73E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379477 |
| Start | 41260629:41260629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.279G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379477 |
| Start | 41240396:41240396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202087808 |
| CDS Mutation | c.735C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |