Primary Site >> Stomach Cancer
Gene >> FUS
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000254108 |
| Start | 31188357:31188357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.832G>A |
| AA Mutation | p.Glu278Lys(p.E278K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000254108 |
| Start | 31186803:31186803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766G>A |
| AA Mutation | p.Gly256Arg(p.G256R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254108 |
| Start | 31185084:31185084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767226101 |
| CDS Mutation | c.669C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254108 |
| Start | 31185102:31185102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781445592 |
| CDS Mutation | c.687T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254108 |
| Start | 31185099:31185099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151073460 |
| CDS Mutation | c.684C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254108 |
| Start | 31185081:31185081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61732969 |
| CDS Mutation | c.666T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |