Primary Site >> Stomach Cancer
Gene >> DOK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276420 |
| Start | 21909901:21909901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649T>G |
| AA Mutation | p.Cys217Gly(p.C217G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276420 |
| Start | 21909766:21909766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539220753 |
| CDS Mutation | c.784G>A |
| AA Mutation | p.Ala262Thr(p.A262T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276420 |
| Start | 21912275:21912275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.299C>T |
| AA Mutation | p.Ala100Val(p.A100V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276420 |
| Start | 21912375:21912375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.199C>T |
| AA Mutation | p.Arg67Trp(p.R67W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276420 |
| Start | 21909723:21909723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.827A>T |
| AA Mutation | p.Asp276Val(p.D276V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276420 |
| Start | 21909628:21909628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750799363 |
| CDS Mutation | c.922C>A |
| AA Mutation | p.Arg308Ser(p.R308S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000276420 |
| Start | 21909566:21909567(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.983dupC |
| AA Mutation | p.Leu329SerfsTer6(p.L329Sfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |