Primary Site >> Pancreatic Cancer
Gene >> PCNT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359568 |
| Start | 46349815:46349815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1339C>A |
| AA Mutation | p.Leu447Met(p.L447M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359568 |
| Start | 46398041:46398041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764560918 |
| CDS Mutation | c.4474C>T |
| AA Mutation | p.Arg1492Cys(p.R1492C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359568 |
| Start | 46412039:46412039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5966C>A |
| AA Mutation | p.Ala1989Asp(p.A1989D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359568 |
| Start | 46431998:46431998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8534C>T |
| AA Mutation | p.Ser2845Leu(p.S2845L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359568 |
| Start | 46440150:46440150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375486259 |
| CDS Mutation | c.9341C>T |
| AA Mutation | p.Pro3114Leu(p.P3114L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359568 |
| Start | 46437033:46437033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9051C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359568 |
| Start | 46346880:46346880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.858C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359568 |
| Start | 46366893:46366893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2919C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359568 |
| Start | 46431861:46431861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8397C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359568 |
| Start | 46349138:46349138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1159C>T |
| AA Mutation | p.Gln387Ter(p.Q387*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |