Primary Site >> Stomach Cancer
Gene >> DMPK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291270 |
| Start | 45771637:45771637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531C>T |
| AA Mutation | p.Arg511Trp(p.R511W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291270 |
| Start | 45779468:45779468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.307A>C |
| AA Mutation | p.Asn103His(p.N103H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291270 |
| Start | 45778577:45778577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760881334 |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166Gln(p.R166Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291270 |
| Start | 45777394:45777394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1079G>A |
| AA Mutation | p.Gly360Asp(p.G360D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291270 |
| Start | 45771658:45771658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745965249 |
| CDS Mutation | c.1510C>T |
| AA Mutation | p.Arg504Cys(p.R504C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291270 |
| Start | 45777709:45777709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375336589 |
| CDS Mutation | c.840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291270 |
| Start | 45777784:45777784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147641100 |
| CDS Mutation | c.765C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291270 |
| Start | 45777447:45777447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769610342 |
| CDS Mutation | c.1026C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000291270 |
| Start | 45779443:45779443(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.332delG |
| AA Mutation | p.Gly111AlafsTer14(p.G111Afs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000291270 |
| Start | 45771364:45771370(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1627_1633delGCCACGG |
| AA Mutation | p.Ala543IlefsTer6(p.A543Ifs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |