Primary Site >> Stomach Cancer
Gene >> USF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222305 |
| Start | 35270532:35270532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515C>T |
| AA Mutation | p.Ala172Val(p.A172V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222305 |
| Start | 35270787:35270787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.650G>A |
| AA Mutation | p.Arg217Gln(p.R217Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222305 |
| Start | 35270780:35270780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.643G>A |
| AA Mutation | p.Ala215Thr(p.A215T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222305 |
| Start | 35279041:35279041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.918G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222305 |
| Start | 35279190:35279190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373110455 |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222305 |
| Start | 35270780:35270781(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769279094 |
| CDS Mutation | c.649dupC |
| AA Mutation | p.Arg217ProfsTer10(p.R217Pfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |