Primary Site >> Stomach Cancer
Gene >> SENP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7564685:7564685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781493025 |
| CDS Mutation | c.776G>A |
| AA Mutation | p.Arg259His(p.R259H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7570479:7570479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377210008 |
| CDS Mutation | c.1465C>T |
| AA Mutation | p.Arg489Cys(p.R489C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7564991:7564991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988A>C |
| AA Mutation | p.Ser330Arg(p.S330R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7571385:7571385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1627C>G |
| AA Mutation | p.Leu543Val(p.L543V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7565498:7565498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1126G>A |
| AA Mutation | p.Val376Met(p.V376M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7570482:7570482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1468C>T |
| AA Mutation | p.Arg490Cys(p.R490C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321337 |
| Start | 7570432:7570432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1418T>C |
| AA Mutation | p.Val473Ala(p.V473A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321337 |
| Start | 7570481:7570481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1467C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321337 |
| Start | 7564969:7564969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546618207 |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321337 |
| Start | 7563639:7563639(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.568delC |
| AA Mutation | p.Arg190GlyfsTer11(p.R190Gfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321337 |
| Start | 7563731:7563731(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.660delC |
| AA Mutation | p.Met221TrpfsTer94(p.M221Wfs*94) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |