Primary Site >> Pancreatic Cancer
Gene >> TENM4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278550 |
| Start | 78669045:78669045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201676053 |
| CDS Mutation | c.7300G>A |
| AA Mutation | p.Glu2434Lys(p.E2434K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278550 |
| Start | 78729537:78729537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764922741 |
| CDS Mutation | c.3245C>T |
| AA Mutation | p.Pro1082Leu(p.P1082L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000278550 |
| Start | 78658815:78658815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7553C>A |
| AA Mutation | p.Ser2518Tyr(p.S2518Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278550 |
| Start | 78708453:78708453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539542652 |
| CDS Mutation | c.4117G>A |
| AA Mutation | p.Asp1373Asn(p.D1373N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278550 |
| Start | 78670474:78670474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201865895 |
| CDS Mutation | c.5871G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000278550 |
| Start | 78729440:78729440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3342T>G |
| AA Mutation | p.Tyr1114Ter(p.Y1114*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |