Primary Site >> Stomach Cancer
Gene >> CCDC174
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383794 |
| Start | 14670967:14670967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1177C>T |
| AA Mutation | p.Pro393Ser(p.P393S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383794 |
| Start | 14667510:14667510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778802009 |
| CDS Mutation | c.811C>T |
| AA Mutation | p.Arg271Cys(p.R271C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383794 |
| Start | 14666851:14666851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.628A>G |
| AA Mutation | p.Arg210Gly(p.R210G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383794 |
| Start | 14670078:14670078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370988051 |
| CDS Mutation | c.1097G>A |
| AA Mutation | p.Arg366His(p.R366H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383794 |
| Start | 14651869:14651869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.33G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000383794 |
| Start | 14668131:14668131(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.908delA |
| AA Mutation | p.Lys303ArgfsTer2(p.K303Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000383794 |
| Start | 14658902:14658903(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs763143298 |
| CDS Mutation | c.286dupA |
| AA Mutation | p.Met96AsnfsTer3(p.M96Nfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |