Primary Site >> Stomach Cancer
Gene >> DOK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69698533:69698533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539C>T |
| AA Mutation | p.Pro180Leu(p.P180L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69698569:69698569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764634905 |
| CDS Mutation | c.575C>T |
| AA Mutation | p.Thr192Met(p.T192M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69757817:69757817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800C>T |
| AA Mutation | p.Ala267Val(p.A267V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69739084:69739084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719A>T |
| AA Mutation | p.Glu240Val(p.E240V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69599430:69599430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221A>G |
| AA Mutation | p.Glu74Gly(p.E74G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69401255:69401255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11A>G |
| AA Mutation | p.Asn4Ser(p.N4S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69757811:69757811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779449377 |
| CDS Mutation | c.794G>A |
| AA Mutation | p.Arg265His(p.R265H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382713 |
| Start | 69677841:69677841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397C>T |
| AA Mutation | p.Arg133Trp(p.R133W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382713 |
| Start | 69757779:69757779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.762A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382713 |
| Start | 69841296:69841296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545055642 |
| CDS Mutation | c.909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |