Primary Site >> Pancreatic Cancer
Gene >> CR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207466762:207466762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.295G>A |
| AA Mutation | p.Gly99Arg(p.G99R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207469707:207469707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201791442 |
| CDS Mutation | c.830C>T |
| AA Mutation | p.Pro277Leu(p.P277L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207468887:207468887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.722T>A |
| AA Mutation | p.Phe241Tyr(p.F241Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207469724:207469724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.847C>T |
| AA Mutation | p.Leu283Phe(p.L283F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367058 |
| Start | 207474309:207474309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2132T>A |
| AA Mutation | p.Ile711Asn(p.I711N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367058 |
| Start | 207474996:207474996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139322251 |
| CDS Mutation | c.2319C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |