Primary Site >> Stomach Cancer
Gene >> FZD7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035266:202035266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.619C>A |
| AA Mutation | p.Pro207Thr(p.P207T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035582:202035582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.935G>A |
| AA Mutation | p.Arg312His(p.R312H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035315:202035315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668G>A |
| AA Mutation | p.Arg223His(p.R223H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202034720:202034720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.73G>A |
| AA Mutation | p.Ala25Thr(p.A25T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035398:202035398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751C>T |
| AA Mutation | p.Arg251Cys(p.R251C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035359:202035359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752131418 |
| CDS Mutation | c.712C>T |
| AA Mutation | p.Arg238Cys(p.R238C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202034764:202034764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.117G>T |
| AA Mutation | p.Lys39Asn(p.K39N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202036271:202036271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1624A>G |
| AA Mutation | p.Ile542Val(p.I542V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286201 |
| Start | 202036194:202036194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1547C>T |
| AA Mutation | p.Pro516Leu(p.P516L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035802:202035802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1155G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035610:202035610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376375888 |
| CDS Mutation | c.963C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286201 |
| Start | 202035046:202035046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779481471 |
| CDS Mutation | c.399G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |