Primary Site >> Stomach Cancer
Gene >> WNT2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112509374:112509374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112C>T |
| AA Mutation | p.Arg38Cys(p.R38C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516275:112516275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35058556 |
| CDS Mutation | c.539G>A |
| AA Mutation | p.Arg180His(p.R180H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112509428:112509428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166G>A |
| AA Mutation | p.Val56Ile(p.V56I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516374:112516374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.638C>T |
| AA Mutation | p.Ala213Val(p.A213V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112517242:112517242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803G>A |
| AA Mutation | p.Arg268His(p.R268H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516239:112516239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.503G>A |
| AA Mutation | p.Cys168Tyr(p.C168Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516142:112516142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.406A>G |
| AA Mutation | p.Ser136Gly(p.S136G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112515014:112515014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.323A>G |
| AA Mutation | p.Gln108Arg(p.Q108R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516409:112516409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673G>T |
| AA Mutation | p.Gly225Cys(p.G225C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516245:112516245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.509C>T |
| AA Mutation | p.Pro170Leu(p.P170L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369684 |
| Start | 112517254:112517254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815C>A |
| AA Mutation | p.Ala272Asp(p.A272D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369686 |
| Start | 112491061:112491061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369684 |
| Start | 112514982:112514982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535167553 |
| CDS Mutation | c.291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369684 |
| Start | 112516240:112516240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.504T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369684 |
| Start | 112514889:112514889(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.202delG |
| AA Mutation | p.Ala68HisfsTer3(p.A68Hfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |