Primary Site >> Pancreatic Cancer
Gene >> ZEB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144389572:144389572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3524A>G |
| AA Mutation | p.Asp1175Gly(p.D1175G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144429973:144429973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.127A>G |
| AA Mutation | p.Lys43Glu(p.K43E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144404923:144404923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769433211 |
| CDS Mutation | c.505C>T |
| AA Mutation | p.Arg169Cys(p.R169C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144399352:144399352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835C>T |
| AA Mutation | p.Ala612Val(p.A612V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409487 |
| Start | 144404000:144404000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.723T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409487 |
| Start | 144389889:144389889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3207G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000409487 |
| Start | 144398426:144398426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587784566 |
| CDS Mutation | c.2761C>T |
| AA Mutation | p.Arg921Ter(p.R921*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |