Primary Site >> Pancreatic Cancer
Gene >> ROBO3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397801 |
| Start | 124873322:124873322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1549G>A |
| AA Mutation | p.Gly517Ser(p.G517S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397801 |
| Start | 124870266:124870266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768314789 |
| CDS Mutation | c.868C>T |
| AA Mutation | p.Arg290Cys(p.R290C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397801 |
| Start | 124869050:124869050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.409G>A |
| AA Mutation | p.Asp137Asn(p.D137N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397801 |
| Start | 124879912:124879912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752717878 |
| CDS Mutation | c.3922G>A |
| AA Mutation | p.Val1308Met(p.V1308M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397801 |
| Start | 124870273:124870273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199762736 |
| CDS Mutation | c.875G>A |
| AA Mutation | p.Arg292His(p.R292H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397801 |
| Start | 124870223:124870223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.825G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |