Primary Site >> Pancreatic Cancer
Gene >> ATG2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96303233:96303233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4865A>G |
| AA Mutation | p.Tyr1622Cys(p.Y1622C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96313424:96313424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3654C>A |
| AA Mutation | p.Phe1218Leu(p.F1218L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96323930:96323930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2506G>A |
| AA Mutation | p.Asp836Asn(p.D836N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96292084:96292084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5441C>T |
| AA Mutation | p.Thr1814Met(p.T1814M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96311214:96311214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757709459 |
| CDS Mutation | c.4064C>T |
| AA Mutation | p.Ala1355Val(p.A1355V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96328694:96328694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1954T>G |
| AA Mutation | p.Ser652Ala(p.S652A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359933 |
| Start | 96347266:96347266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.238T>C |
| AA Mutation | p.Ser80Pro(p.S80P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000359933 |
| Start | 96322736:96322736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2541-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |