Primary Site >> Pancreatic Cancer
Gene >> ANK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357077 |
| Start | 113356320:113356320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7702T>G |
| AA Mutation | p.Cys2568Gly(p.C2568G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357077 |
| Start | 113353969:113353969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777085522 |
| CDS Mutation | c.5351G>A |
| AA Mutation | p.Arg1784Gln(p.R1784Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357077 |
| Start | 113336037:113336037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771751897 |
| CDS Mutation | c.3571C>T |
| AA Mutation | p.Arg1191Trp(p.R1191W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357077 |
| Start | 113049758:113049758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.30C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357077 |
| Start | 113242206:113242206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.888T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357077 |
| Start | 113343131:113343131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357077 |
| Start | 113357987:113357987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |