Primary Site >> Stomach Cancer
Gene >> GCDH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222214 |
| Start | 12897356:12897356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1010C>T |
| AA Mutation | p.Ala337Val(p.A337V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222214 |
| Start | 12896308:12896308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.739G>A |
| AA Mutation | p.Ala247Thr(p.A247T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222214 |
| Start | 12896076:12896076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.590A>G |
| AA Mutation | p.Tyr197Cys(p.Y197C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222214 |
| Start | 12896938:12896938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775606471 |
| CDS Mutation | c.881G>A |
| AA Mutation | p.Arg294Gln(p.R294Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222214 |
| Start | 12897847:12897847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368251933 |
| CDS Mutation | c.1227C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222214 |
| Start | 12893589:12893589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222214 |
| Start | 12896309:12896309(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.744delC |
| AA Mutation | p.Arg249GlyfsTer15(p.R249Gfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222214 |
| Start | 12897787:12897787(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs755038561 |
| CDS Mutation | c.1173delG |
| AA Mutation | p.Asn392MetfsTer9(p.N392Mfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |