Primary Site >> Stomach Cancer
Gene >> WISP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230529 |
| Start | 112069492:112069492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.937A>G |
| AA Mutation | p.Ile313Val(p.I313V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230529 |
| Start | 112061010:112061010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.68G>A |
| AA Mutation | p.Gly23Asp(p.G23D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230529 |
| Start | 112068349:112068349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Arg245Lys(p.R245K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230529 |
| Start | 112064768:112064768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.360T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230529 |
| Start | 112068231:112068231(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs781790231 |
| CDS Mutation | c.624delA |
| AA Mutation | p.Lys208AsnfsTer24(p.K208Nfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230529 |
| Start | 112068231:112068232(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.623_624delAA |
| AA Mutation | p.Lys208MetfsTer21(p.K208Mfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000230529 |
| Start | 112069512:112069512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.957C>A |
| AA Mutation | p.Cys319Ter(p.C319*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |