Primary Site >> Pancreatic Cancer
Gene >> KMT2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118505068:118505068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782800112 |
| CDS Mutation | c.9167C>T |
| AA Mutation | p.Pro3056Leu(p.P3056L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118502784:118502784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6883G>A |
| AA Mutation | p.Asp2295Asn(p.D2295N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118504578:118504578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8677C>A |
| AA Mutation | p.Leu2893Ile(p.L2893I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118472484:118472484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1325G>A |
| AA Mutation | p.Arg442Gln(p.R442Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118484311:118484311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4215T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118503617:118503617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782809939 |
| CDS Mutation | c.7716A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |