Primary Site >> Pancreatic Cancer
Gene >> PDZRN3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263666 |
| Start | 73384627:73384627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1939C>T |
| AA Mutation | p.Arg647Cys(p.R647C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263666 |
| Start | 73389845:73389845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375528245 |
| CDS Mutation | c.1387C>T |
| AA Mutation | p.Arg463Cys(p.R463C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263666 |
| Start | 73383777:73383777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745814121 |
| CDS Mutation | c.2789C>T |
| AA Mutation | p.Thr930Met(p.T930M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263666 |
| Start | 73384048:73384048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2518C>T |
| AA Mutation | p.Arg840Trp(p.R840W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263666 |
| Start | 73384488:73384488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773653572 |
| CDS Mutation | c.2078G>A |
| AA Mutation | p.Arg693His(p.R693H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263666 |
| Start | 73385727:73385727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1577A>G |
| AA Mutation | p.Asp526Gly(p.D526G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263666 |
| Start | 73383785:73383785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762491376 |
| CDS Mutation | c.2781C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263666 |
| Start | 73385681:73385681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1623C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263666 |
| Start | 73391051:73391051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538722275 |
| CDS Mutation | c.1320C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263666 |
| Start | 73384364:73384364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2202C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |