Primary Site >> Stomach Cancer
Gene >> FUT8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360689 |
| Start | 65733296:65733296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1325A>G |
| AA Mutation | p.Tyr442Cys(p.Y442C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360689 |
| Start | 65721996:65721996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1057C>T |
| AA Mutation | p.Leu353Phe(p.L353F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360689 |
| Start | 65742339:65742339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1657T>C |
| AA Mutation | p.Tyr553His(p.Y553H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360689 |
| Start | 65561573:65561573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10T>C |
| AA Mutation | p.Trp4Arg(p.W4R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360689 |
| Start | 65742305:65742305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1623A>T |
| AA Mutation | p.Lys541Asn(p.K541N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360689 |
| Start | 65669391:65669391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Arg249His(p.R249H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360689 |
| Start | 65616221:65616221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267604027 |
| CDS Mutation | c.330G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360689 |
| Start | 65669267:65669267(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.626delA |
| AA Mutation | p.Lys209SerfsTer24(p.K209Sfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |