Primary Site >> Pancreatic Cancer
Gene >> UTRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144438863:144438863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1360A>C |
| AA Mutation | p.Lys454Gln(p.K454Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144437619:144437619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1114G>A |
| AA Mutation | p.Ala372Thr(p.A372T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144459299:144459299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2652C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144458930:144458930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2445G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144754794:144754794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8430C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367545 |
| Start | 144447307:144447307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764291295 |
| CDS Mutation | c.1711C>T |
| AA Mutation | p.Arg571Ter(p.R571*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |