Primary Site >> Pancreatic Cancer
Gene >> CDH11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947916:64947916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751908119 |
| CDS Mutation | c.2078G>A |
| AA Mutation | p.Arg693His(p.R693H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64950995:64950995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1666C>T |
| AA Mutation | p.Arg556Trp(p.R556W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947883:64947883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2111C>A |
| AA Mutation | p.Pro704His(p.P704H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64972032:64972032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1423G>A |
| AA Mutation | p.Ala475Thr(p.A475T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 65004791:65004791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547313548 |
| CDS Mutation | c.79C>T |
| AA Mutation | p.Arg27Trp(p.R27W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 64972009:64972009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146549125 |
| CDS Mutation | c.1446C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 64998656:64998656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574599418 |
| CDS Mutation | c.429G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |