Primary Site >> Stomach Cancer
Gene >> WWOX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000566780 |
| Start | 78109825:78109825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.220T>G |
| AA Mutation | p.Phe74Val(p.F74V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000566780 |
| Start | 78424997:78424997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.733G>T |
| AA Mutation | p.Asp245Tyr(p.D245Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000566780 |
| Start | 78432705:78432705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1009G>A |
| AA Mutation | p.Val337Met(p.V337M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000566780 |
| Start | 78386871:78386871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.528G>T |
| AA Mutation | p.Lys176Asn(p.K176N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000566780 |
| Start | 78164273:78164273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377356629 |
| CDS Mutation | c.500G>A |
| AA Mutation | p.Arg167His(p.R167H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000566780 |
| Start | 78432646:78432646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772959465 |
| CDS Mutation | c.950C>T |
| AA Mutation | p.Thr317Met(p.T317M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000566780 |
| Start | 79211658:79211658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369673368 |
| CDS Mutation | c.1107G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |