Primary Site >> Stomach Cancer
Gene >> SFRP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436072 |
| Start | 37909641:37909641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.831A>C |
| AA Mutation | p.Arg277Ser(p.R277S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436072 |
| Start | 37916464:37916464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.74A>T |
| AA Mutation | p.Glu25Val(p.E25V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436072 |
| Start | 37916245:37916245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.293A>C |
| AA Mutation | p.Lys98Thr(p.K98T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436072 |
| Start | 37916218:37916218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.320A>G |
| AA Mutation | p.Asp107Gly(p.D107G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436072 |
| Start | 37907621:37907621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899A>G |
| AA Mutation | p.Asp300Gly(p.D300G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436072 |
| Start | 37916388:37916388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436072 |
| Start | 37907497:37907497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1023A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436072 |
| Start | 37907491:37907491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1029G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436072 |
| Start | 37916250:37916250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143563677 |
| CDS Mutation | c.288G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436072 |
| Start | 37907545:37907545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.975A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436072 |
| Start | 37916223:37916223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761497415 |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |