Primary Site >> Stomach Cancer
Gene >> SIGLEC8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321424 |
| Start | 51457200:51457200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.765C>A |
| AA Mutation | p.Phe255Leu(p.F255L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321424 |
| Start | 51457979:51457979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.409T>C |
| AA Mutation | p.Ser137Pro(p.S137P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321424 |
| Start | 51457487:51457487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779904630 |
| CDS Mutation | c.707C>T |
| AA Mutation | p.Thr236Ile(p.T236I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321424 |
| Start | 51452480:51452480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1399G>C |
| AA Mutation | p.Asp467His(p.D467H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321424 |
| Start | 51454231:51454231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1233C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321424 |
| Start | 51452388:51452388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1491C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321424 |
| Start | 51455473:51455473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771076418 |
| CDS Mutation | c.996C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321424 |
| Start | 51455524:51455524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321424 |
| Start | 51457732:51457732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.462C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321424 |
| Start | 51452581:51452581(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1298delC |
| AA Mutation | p.Pro433GlnfsTer23(p.P433Qfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000321424 |
| Start | 51455484:51455484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141833256 |
| CDS Mutation | c.985C>T |
| AA Mutation | p.Arg329Ter(p.R329*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |