Primary Site >> Stomach Cancer
Gene >> WNT9A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272164 |
| Start | 227921855:227921855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.761G>A |
| AA Mutation | p.Gly254Asp(p.G254D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272164 |
| Start | 227921585:227921585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552502207 |
| CDS Mutation | c.1031G>A |
| AA Mutation | p.Arg344His(p.R344H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272164 |
| Start | 227921618:227921618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998G>T |
| AA Mutation | p.Arg333Leu(p.R333L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272164 |
| Start | 227924352:227924352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750699209 |
| CDS Mutation | c.401C>T |
| AA Mutation | p.Thr134Met(p.T134M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272164 |
| Start | 227921832:227921832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369422293 |
| CDS Mutation | c.784G>A |
| AA Mutation | p.Gly262Ser(p.G262S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272164 |
| Start | 227924226:227924226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.527G>T |
| AA Mutation | p.Ser176Ile(p.S176I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272164 |
| Start | 227921896:227921896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.720C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000272164 |
| Start | 227924253:227924253(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.500delG |
| AA Mutation | p.Gly167AlafsTer38(p.G167Afs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000272164 |
| Start | 227924252:227924253(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs779992922 |
| CDS Mutation | c.500dupG |
| AA Mutation | p.Cys168LeufsTer6(p.C168Lfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |