Primary Site >> Pancreatic Cancer
Gene >> DUOX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45135937:45135937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.853G>A |
| AA Mutation | p.Ala285Thr(p.A285T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000321429 |
| Start | 45139598:45139598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1388C>T |
| AA Mutation | p.Thr463Ile(p.T463I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45144995:45144995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762543874 |
| CDS Mutation | c.2237G>A |
| AA Mutation | p.Arg746Gln(p.R746Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45151987:45151987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773920813 |
| CDS Mutation | c.3128G>A |
| AA Mutation | p.Arg1043His(p.R1043H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45160919:45160919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3785G>T |
| AA Mutation | p.Gly1262Val(p.G1262V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45163551:45163551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140681354 |
| CDS Mutation | c.4268C>T |
| AA Mutation | p.Thr1423Met(p.T1423M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000321429 |
| Start | 45163685:45163685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4402C>A |
| AA Mutation | p.Leu1468Met(p.L1468M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000321429 |
| Start | 45141323:45141323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564683577 |
| CDS Mutation | c.1597C>T |
| AA Mutation | p.Arg533Ter(p.R533*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |