Primary Site >> Pancreatic Cancer
Gene >> MST1R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898631:49898631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1606T>C |
| AA Mutation | p.Cys536Arg(p.C536R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49903267:49903267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.343C>T |
| AA Mutation | p.Pro115Ser(p.P115S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898584:49898584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1653G>A |
| AA Mutation | p.Met551Ile(p.M551I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296474 |
| Start | 49887547:49887547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3963G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296474 |
| Start | 49897338:49897338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2125C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296474 |
| Start | 49902866:49902866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.744A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000296474 |
| Start | 49891788:49891788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150876558 |
| CDS Mutation | c.3322C>T |
| AA Mutation | p.Arg1108Ter(p.R1108*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |