Primary Site >> Pancreatic Cancer
Gene >> PCDH18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344876 |
| Start | 137530344:137530344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200753356 |
| CDS Mutation | c.1745G>A |
| AA Mutation | p.Arg582His(p.R582H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344876 |
| Start | 137528486:137528486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2732T>A |
| AA Mutation | p.Ile911Asn(p.I911N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344876 |
| Start | 137521441:137521441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766154132 |
| CDS Mutation | c.2996C>T |
| AA Mutation | p.Thr999Ile(p.T999I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344876 |
| Start | 137530188:137530188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202041043 |
| CDS Mutation | c.1901G>A |
| AA Mutation | p.Arg634Gln(p.R634Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344876 |
| Start | 137530897:137530897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1192A>G |
| AA Mutation | p.Lys398Glu(p.K398E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344876 |
| Start | 137531170:137531170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.919A>C |
| AA Mutation | p.Thr307Pro(p.T307P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344876 |
| Start | 137530073:137530073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2016G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |