Primary Site >> Stomach Cancer
Gene >> FAM83B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54941270:54941270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2299T>G |
| AA Mutation | p.Phe767Val(p.F767V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54940808:54940808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1837A>G |
| AA Mutation | p.Thr613Ala(p.T613A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54941078:54941078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2107T>A |
| AA Mutation | p.Leu703Met(p.L703M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54941930:54941930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768677387 |
| CDS Mutation | c.2959C>T |
| AA Mutation | p.Arg987Cys(p.R987C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54941778:54941778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757361359 |
| CDS Mutation | c.2807G>A |
| AA Mutation | p.Arg936His(p.R936H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54870325:54870325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.79T>C |
| AA Mutation | p.Trp27Arg(p.W27R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54940248:54940248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372267421 |
| CDS Mutation | c.1277C>T |
| AA Mutation | p.Ala426Val(p.A426V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54941771:54941771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2800T>C |
| AA Mutation | p.Tyr934His(p.Y934H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306858 |
| Start | 54941766:54941766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200887888 |
| CDS Mutation | c.2795G>A |
| AA Mutation | p.Arg932His(p.R932H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306858 |
| Start | 54940657:54940657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1686C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306858 |
| Start | 54939876:54939876(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.908delA |
| AA Mutation | p.Asn303MetfsTer11(p.N303Mfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000306858 |
| Start | 54940409:54940409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770940709 |
| CDS Mutation | c.1438C>T |
| AA Mutation | p.Arg480Ter(p.R480*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000306858 |
| Start | 54941960:54941960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367914924 |
| CDS Mutation | c.2989C>T |
| AA Mutation | p.Arg997Ter(p.R997*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |