Primary Site >> Pancreatic Cancer
Gene >> RELN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103833561:103833561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752566456 |
| CDS Mutation | c.449C>T |
| AA Mutation | p.Ala150Val(p.A150V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103491980:103491980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9416T>C |
| AA Mutation | p.Val3139Ala(p.V3139A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103498137:103498137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8783A>G |
| AA Mutation | p.Tyr2928Cys(p.Y2928C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103535335:103535335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7330C>T |
| AA Mutation | p.Pro2444Ser(p.P2444S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103551169:103551169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6200C>A |
| AA Mutation | p.Ser2067Tyr(p.S2067Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103636278:103636278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759711654 |
| CDS Mutation | c.2260C>T |
| AA Mutation | p.Arg754Trp(p.R754W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103483741:103483741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115035120 |
| CDS Mutation | c.10093G>A |
| AA Mutation | p.Val3365Ile(p.V3365I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103594389:103594389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3643G>A |
| AA Mutation | p.Asp1215Asn(p.D1215N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428762 |
| Start | 103540273:103540273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116394157 |
| CDS Mutation | c.6854G>A |
| AA Mutation | p.Arg2285His(p.R2285H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428762 |
| Start | 103497844:103497844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8926C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428762 |
| Start | 103557104:103557104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5670C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428762 |
| Start | 103651726:103651726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1827A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000428762 |
| Start | 103540339:103540339(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6788delA |
| AA Mutation | p.Glu2263GlyfsTer20(p.E2263Gfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000428762 |
| Start | 103500781:103500781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8631C>A |
| AA Mutation | p.Tyr2877Ter(p.Y2877*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000428762 |
| Start | 103575546:103575546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4303+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |