Primary Site >> Stomach Cancer
Gene >> OAS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000202917 |
| Start | 112919431:112919431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1081A>T |
| AA Mutation | p.Arg361Trp(p.R361W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000202917 |
| Start | 112911191:112911191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610A>G |
| AA Mutation | p.Lys204Glu(p.K204E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000202917 |
| Start | 112911113:112911113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532A>G |
| AA Mutation | p.Thr178Ala(p.T178A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000202917 |
| Start | 112916666:112916666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812A>G |
| AA Mutation | p.Tyr271Cys(p.Y271C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112916548:112916548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.694C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112916730:112916730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144257676 |
| CDS Mutation | c.876G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112916658:112916658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.804C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112911133:112911133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773579176 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112908796:112908796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112908637:112908637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.282C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000202917 |
| Start | 112908748:112908748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147639145 |
| CDS Mutation | c.393G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |