Primary Site >> Pancreatic Cancer
Gene >> CELSR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109266155:109266155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375830885 |
| CDS Mutation | c.5962C>T |
| AA Mutation | p.Arg1988Cys(p.R1988C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109265837:109265837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5830C>T |
| AA Mutation | p.Pro1944Ser(p.P1944S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109268626:109268626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374375242 |
| CDS Mutation | c.6364C>T |
| AA Mutation | p.Arg2122Trp(p.R2122W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109272893:109272893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8204C>T |
| AA Mutation | p.Ala2735Val(p.A2735V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109269502:109269502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6891C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250517:109250517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.438G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252188:109252188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199976988 |
| CDS Mutation | c.2109C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |