Primary Site >> Stomach Cancer
Gene >> SENP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448372 |
| Start | 48047018:48047018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1736T>C |
| AA Mutation | p.Phe579Ser(p.F579S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448372 |
| Start | 48049085:48049085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1455G>T |
| AA Mutation | p.Lys485Asn(p.K485N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000448372 |
| Start | 48047021:48047021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1733A>C |
| AA Mutation | p.Glu578Ala(p.E578A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000448372 |
| Start | 48048974:48048974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1566C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000448372 |
| Start | 48048045:48048045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35097848 |
| CDS Mutation | c.1647C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000448372 |
| Start | 48065113:48065113(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758434980 |
| CDS Mutation | c.1227delA |
| AA Mutation | p.Gly410ValfsTer4(p.G410Vfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000448372 |
| Start | 48083614:48083614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760121910 |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Arg177Ter(p.R177*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |