Primary Site >> Stomach Cancer
Gene >> OAS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112967981:112967981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2911G>A |
| AA Mutation | p.Gly971Arg(p.G971R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112965798:112965798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2458G>A |
| AA Mutation | p.Val820Met(p.V820M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112967966:112967966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2896C>A |
| AA Mutation | p.Leu966Ile(p.L966I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112946864:112946864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764044255 |
| CDS Mutation | c.758G>A |
| AA Mutation | p.Arg253Gln(p.R253Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112950859:112950859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1541G>A |
| AA Mutation | p.Ser514Asn(p.S514N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112941763:112941763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.371G>A |
| AA Mutation | p.Ser124Asn(p.S124N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112967487:112967487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539747098 |
| CDS Mutation | c.2759C>T |
| AA Mutation | p.Ala920Val(p.A920V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112941753:112941753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.361C>T |
| AA Mutation | p.Pro121Ser(p.P121S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112948019:112948019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949G>C |
| AA Mutation | p.Ala317Pro(p.A317P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228928 |
| Start | 112941667:112941667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369476665 |
| CDS Mutation | c.275C>T |
| AA Mutation | p.Ala92Val(p.A92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228928 |
| Start | 112949022:112949022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267603314 |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228928 |
| Start | 112944628:112944628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.613C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000228928 |
| Start | 112941719:112941719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755611962 |
| CDS Mutation | c.327G>A |
| AA Mutation | p.Trp109Ter(p.W109*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000228928 |
| Start | 112948853:112948862(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1030-1_1038delGGGCCTTCCA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |