Primary Site >> Stomach Cancer
Gene >> DGKA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331886 |
| Start | 55941575:55941575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241C>T |
| AA Mutation | p.Pro414Leu(p.P414L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331886 |
| Start | 55941521:55941521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1187A>C |
| AA Mutation | p.Lys396Thr(p.K396T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331886 |
| Start | 55953130:55953130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754616028 |
| CDS Mutation | c.2033G>A |
| AA Mutation | p.Arg678Gln(p.R678Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331886 |
| Start | 55953126:55953126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373733309 |
| CDS Mutation | c.2029C>T |
| AA Mutation | p.Arg677Cys(p.R677C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331886 |
| Start | 55940719:55940719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1014C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331886 |
| Start | 55940167:55940167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755946391 |
| CDS Mutation | c.795T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331886 |
| Start | 55939212:55939212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.501T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331886 |
| Start | 55953380:55953380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374495739 |
| CDS Mutation | c.2094C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331886 |
| Start | 55940364:55940364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.849C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331886 |
| Start | 55953730:55953730(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2176delC |
| AA Mutation | p.Arg726AlafsTer9(p.R726Afs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000331886 |
| Start | 55941544:55941544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759785992 |
| CDS Mutation | c.1210C>T |
| AA Mutation | p.Arg404Ter(p.R404*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |