Primary Site >> Pancreatic Cancer
Gene >> EML1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262233 |
| Start | 99914659:99914659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1714G>A |
| AA Mutation | p.Ala572Thr(p.A572T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262233 |
| Start | 99901038:99901038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1007C>A |
| AA Mutation | p.Ser336Tyr(p.S336Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262233 |
| Start | 99937849:99937849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2128G>A |
| AA Mutation | p.Val710Met(p.V710M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262233 |
| Start | 99907713:99907713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1084G>C |
| AA Mutation | p.Glu362Gln(p.E362Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262233 |
| Start | 99939216:99939216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553895497 |
| CDS Mutation | c.2211G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262233 |
| Start | 99939276:99939276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542054890 |
| CDS Mutation | c.2271C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |