Primary Site >> Stomach Cancer
Gene >> DCX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338081 |
| Start | 111410095:111410095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587783541 |
| CDS Mutation | c.547C>T |
| AA Mutation | p.Arg183Cys(p.R183C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338081 |
| Start | 111333087:111333087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1015C>A |
| AA Mutation | p.Arg339Ser(p.R339S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338081 |
| Start | 111401169:111401169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.769T>G |
| AA Mutation | p.Phe257Val(p.F257V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338081 |
| Start | 111410087:111410087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.555T>G |
| AA Mutation | p.Ile185Met(p.I185M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338081 |
| Start | 111312653:111312653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1258C>T |
| AA Mutation | p.Arg420Trp(p.R420W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338081 |
| Start | 111330945:111330945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758499194 |
| CDS Mutation | c.1148G>A |
| AA Mutation | p.Arg383His(p.R383H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338081 |
| Start | 111401185:111401185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.753C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338081 |
| Start | 111410093:111410093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772189954 |
| CDS Mutation | c.549T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338081 |
| Start | 111401158:111401158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.780C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338081 |
| Start | 111331001:111331001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1092C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338081 |
| Start | 111401217:111401217(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.721delC |
| AA Mutation | p.Gln241SerfsTer30(p.Q241Sfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338081 |
| Start | 111410866:111410866(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.109delT |
| AA Mutation | p.Cys37ValfsTer40(p.C37Vfs*40) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338081 |
| Start | 111312702:111312702(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1209delC |
| AA Mutation | p.Lys404SerfsTer82(p.K404Sfs*82) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000338081 |
| Start | 111330943:111330943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587783592 |
| CDS Mutation | c.1150C>T |
| AA Mutation | p.Arg384Ter(p.R384*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |