Primary Site >> Stomach Cancer
Gene >> CCDC125
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396496 |
| Start | 69294821:69294821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770049283 |
| CDS Mutation | c.896G>A |
| AA Mutation | p.Arg299Gln(p.R299Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396496 |
| Start | 69282844:69282844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1421G>C |
| AA Mutation | p.Ser474Thr(p.S474T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396496 |
| Start | 69300059:69300059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.769A>T |
| AA Mutation | p.Asn257Tyr(p.N257Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396496 |
| Start | 69294889:69294889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374738926 |
| CDS Mutation | c.828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396496 |
| Start | 69282946:69282946(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1319delA |
| AA Mutation | p.Asn440ThrfsTer9(p.N440Tfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000396496 |
| Start | 69285384:69285384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1183G>T |
| AA Mutation | p.Glu395Ter(p.E395*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |