Primary Site >> Pancreatic Cancer
Gene >> ROBO2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000461745 |
| Start | 77550915:77550915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199705591 |
| CDS Mutation | c.1157C>T |
| AA Mutation | p.Ala386Val(p.A386V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000461745 |
| Start | 77634993:77634993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762523752 |
| CDS Mutation | c.3884G>A |
| AA Mutation | p.Arg1295Gln(p.R1295Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000487694 |
| Start | 75937558:75937558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.65T>C |
| AA Mutation | p.Met22Thr(p.M22T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000461745 |
| Start | 77596650:77596650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2754T>A |
| AA Mutation | p.Asp918Glu(p.D918E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000461745 |
| Start | 77098114:77098114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.162G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000461745 |
| Start | 77622335:77622335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774727452 |
| CDS Mutation | c.3663C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |