Primary Site >> Pancreatic Cancer
Gene >> CNTN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 40929855:40929855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.556C>T |
| AA Mutation | p.Arg186Trp(p.R186W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 41025280:41025280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768554950 |
| CDS Mutation | c.2654A>G |
| AA Mutation | p.Asn885Ser(p.N885S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 40939460:40939460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1354A>G |
| AA Mutation | p.Thr452Ala(p.T452A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 40993239:40993239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2083C>T |
| AA Mutation | p.Pro695Ser(p.P695S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347616 |
| Start | 41020434:41020434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2517C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000347616 |
| Start | 41016793:41016793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2296C>T |
| AA Mutation | p.Arg766Ter(p.R766*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |