Primary Site >> Pancreatic Cancer
Gene >> IL6ST
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55952066:55952066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1562A>G |
| AA Mutation | p.Lys521Arg(p.K521R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55964292:55964292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.512A>G |
| AA Mutation | p.Asp171Gly(p.D171G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000336909 |
| Start | 55968395:55968395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.372G>T |
| AA Mutation | p.Leu124Phe(p.L124F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336909 |
| Start | 55941406:55941406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2433G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336909 |
| Start | 55941508:55941508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2331C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000336909 |
| Start | 55951928:55951928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1699+1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |