Primary Site >> Pancreatic Cancer
Gene >> ROBO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000464233 |
| Start | 78627332:78627332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3864G>T |
| AA Mutation | p.Gln1288His(p.Q1288H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000464233 |
| Start | 78631278:78631278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3509G>T |
| AA Mutation | p.Arg1170Ile(p.R1170I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000464233 |
| Start | 78651874:78651874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2670T>G |
| AA Mutation | p.Ile890Met(p.I890M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000464233 |
| Start | 78662007:78662007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199577218 |
| CDS Mutation | c.2074G>A |
| AA Mutation | p.Glu692Lys(p.E692K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000464233 |
| Start | 78685768:78685768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1320G>T |
| AA Mutation | p.Lys440Asn(p.K440N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000464233 |
| Start | 78617847:78617847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4070C>A |
| AA Mutation | p.Ser1357Tyr(p.S1357Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000464233 |
| Start | 78617846:78617846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4071C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000464233 |
| Start | 78670107:78670107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1537C>T |
| AA Mutation | p.Arg513Ter(p.R513*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |