Primary Site >> Pancreatic Cancer
Gene >> TNR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175396708:175396708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1076A>T |
| AA Mutation | p.Tyr359Phe(p.Y359F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175362729:175362729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531733667 |
| CDS Mutation | c.2788G>A |
| AA Mutation | p.Glu930Lys(p.E930K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175330104:175330104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3763C>A |
| AA Mutation | p.Leu1255Ile(p.L1255I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175363726:175363726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2689T>G |
| AA Mutation | p.Ser897Ala(p.S897A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175365950:175365950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2242G>A |
| AA Mutation | p.Ala748Thr(p.A748T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175396799:175396799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.985C>A |
| AA Mutation | p.Pro329Thr(p.P329T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263525 |
| Start | 175323377:175323377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4057C>T |
| AA Mutation | p.Arg1353Trp(p.R1353W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263525 |
| Start | 175335742:175335742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3600C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263525 |
| Start | 175406667:175406667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142523357 |
| CDS Mutation | c.48C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |