Primary Site >> Pancreatic Cancer
Gene >> MECOM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169089026:169089026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2995C>A |
| AA Mutation | p.Pro999Thr(p.P999T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169090034:169090034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2803G>A |
| AA Mutation | p.Ala935Thr(p.A935T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169102115:169102115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2152C>T |
| AA Mutation | p.Pro718Ser(p.P718S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169115524:169115524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1784C>A |
| AA Mutation | p.Ala595Asp(p.A595D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169116221:169116221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780293564 |
| CDS Mutation | c.1087G>A |
| AA Mutation | p.Val363Ile(p.V363I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000494292 |
| Start | 169663356:169663356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17G>A |
| AA Mutation | p.Arg6Lys(p.R6K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000468789 |
| Start | 169127891:169127891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150481592 |
| CDS Mutation | c.219G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000468789 |
| Start | 169115968:169115974(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1334_1340delATAATAA |
| AA Mutation | p.Asn445ArgfsTer14(p.N445Rfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |