Primary Site >> Pancreatic Cancer
Gene >> CUBN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377833 |
| Start | 16835171:16835171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758386041 |
| CDS Mutation | c.10205C>T |
| AA Mutation | p.Ala3402Val(p.A3402V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377833 |
| Start | 16904076:16904076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7952C>A |
| AA Mutation | p.Pro2651His(p.P2651H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377833 |
| Start | 16907517:16907517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199864467 |
| CDS Mutation | c.7696G>A |
| AA Mutation | p.Glu2566Lys(p.E2566K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377833 |
| Start | 16840334:16840334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150358307 |
| CDS Mutation | c.10028C>T |
| AA Mutation | p.Pro3343Leu(p.P3343L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377833 |
| Start | 17127886:17127886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.291G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377833 |
| Start | 16876925:16876925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140524729 |
| CDS Mutation | c.9078C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000377833 |
| Start | 16984280:16984280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4351-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |