Primary Site >> Stomach Cancer
Gene >> DKC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369550 |
| Start | 154764937:154764937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782010351 |
| CDS Mutation | c.55C>T |
| AA Mutation | p.Arg19Trp(p.R19W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369550 |
| Start | 154767364:154767364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374771308 |
| CDS Mutation | c.622G>A |
| AA Mutation | p.Asp208Asn(p.D208N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369550 |
| Start | 154774690:154774690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1244A>G |
| AA Mutation | p.Glu415Gly(p.E415G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369550 |
| Start | 154768397:154768397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.736C>A |
| AA Mutation | p.Leu246Ile(p.L246I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369550 |
| Start | 154767342:154767342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781789313 |
| CDS Mutation | c.600C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369550 |
| Start | 154767041:154767041(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.498delG |
| AA Mutation | p.Thr167ProfsTer7(p.T167Pfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000369550 |
| Start | 154776859:154776860(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1537_1538insAAATG |
| AA Mutation | p.Ser513Ter(p.S513*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |