Primary Site >> Pancreatic Cancer
Gene >> APOB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21002797:21002797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12625G>A |
| AA Mutation | p.Gly4209Arg(p.G4209R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21001847:21001847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13575T>G |
| AA Mutation | p.Ile4525Met(p.I4525M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21022909:21022909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2738C>A |
| AA Mutation | p.Ala913Asp(p.A913D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21027992:21027992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548108916 |
| CDS Mutation | c.1903C>T |
| AA Mutation | p.Arg635Trp(p.R635W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21028367:21028367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1789A>G |
| AA Mutation | p.Ile597Val(p.I597V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011037:21011037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5831A>G |
| AA Mutation | p.His1944Arg(p.H1944R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21027991:21027991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202001155 |
| CDS Mutation | c.1904G>A |
| AA Mutation | p.Arg635Gln(p.R635Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011675:21011675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775515832 |
| CDS Mutation | c.5193C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010394:21010394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6474T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010976:21010976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5892T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21013248:21013248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4128C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21015446:21015446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3432C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000233242 |
| Start | 21015472:21015472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3406G>T |
| AA Mutation | p.Glu1136Ter(p.E1136*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |