Primary Site >> Stomach Cancer
Gene >> FZD3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240093 |
| Start | 28520728:28520728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748470823 |
| CDS Mutation | c.280C>T |
| AA Mutation | p.Arg94Cys(p.R94C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240093 |
| Start | 28503153:28503153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.140C>A |
| AA Mutation | p.Pro47His(p.P47H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240093 |
| Start | 28503070:28503070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.57T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240093 |
| Start | 28527495:28527495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.735C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000240093 |
| Start | 28555877:28555877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1693C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240093 |
| Start | 28551725:28551725(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1533delT |
| AA Mutation | p.His512MetfsTer8(p.H512Mfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240093 |
| Start | 28527642:28527642(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.888delT |
| AA Mutation | p.Phe296LeufsTer10(p.F296Lfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000240093 |
| Start | 28527598:28527598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838G>T |
| AA Mutation | p.Gly280Ter(p.G280*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240093 |
| Start | 28527641:28527642(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs765036679 |
| CDS Mutation | c.888dupT |
| AA Mutation | p.Thr297TyrfsTer25(p.T297Yfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |