Primary Site >> Pancreatic Cancer
Gene >> TNC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115048443:115048443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4669G>T |
| AA Mutation | p.Asp1557Tyr(p.D1557Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115064668:115064668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3466C>T |
| AA Mutation | p.Leu1156Phe(p.L1156F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115064816:115064816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3318T>G |
| AA Mutation | p.Ile1106Met(p.I1106M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115082795:115082795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2144C>A |
| AA Mutation | p.Pro715His(p.P715H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115084234:115084234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2106T>G |
| AA Mutation | p.Ile702Met(p.I702M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115084383:115084383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1957C>T |
| AA Mutation | p.Leu653Phe(p.L653F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115086910:115086910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.821T>G |
| AA Mutation | p.Phe274Cys(p.F274C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115087034:115087034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.697A>G |
| AA Mutation | p.Asn233Asp(p.N233D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115084398:115084398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149181557 |
| CDS Mutation | c.1942C>T |
| AA Mutation | p.Arg648Trp(p.R648W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350763 |
| Start | 115064043:115064043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562793021 |
| CDS Mutation | c.3513C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350763 |
| Start | 115086183:115086183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1548C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000350763 |
| Start | 115086123:115086123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1608C>A |
| AA Mutation | p.Cys536Ter(p.C536*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |