Primary Site >> Stomach Cancer
Gene >> SUFU
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102597203:102597203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.820G>A |
| AA Mutation | p.Ala274Thr(p.A274T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102617397:102617397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1265A>G |
| AA Mutation | p.His422Arg(p.H422R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102509177:102509177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.191G>T |
| AA Mutation | p.Gly64Val(p.G64V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102627213:102627213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1335G>T |
| AA Mutation | p.Glu445Asp(p.E445D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102617309:102617309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201326378 |
| CDS Mutation | c.1177C>T |
| AA Mutation | p.Arg393Trp(p.R393W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102509207:102509207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221A>G |
| AA Mutation | p.Tyr74Cys(p.Y74C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369902 |
| Start | 102630145:102630145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765358771 |
| CDS Mutation | c.1445C>T |
| AA Mutation | p.Pro482Leu(p.P482L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369902 |
| Start | 102597229:102597229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762558038 |
| CDS Mutation | c.846C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |