Primary Site >> Stomach Cancer
Gene >> CPS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210677897:210677897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4415T>G |
| AA Mutation | p.Leu1472Arg(p.L1472R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210576392:210576392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.283A>G |
| AA Mutation | p.Thr95Ala(p.T95A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210599504:210599504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1492G>A |
| AA Mutation | p.Ala498Thr(p.A498T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000233072 |
| Start | 210599559:210599559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1547G>T |
| AA Mutation | p.Cys516Phe(p.C516F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210600648:210600648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1643A>C |
| AA Mutation | p.Gln548Pro(p.Q548P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210637776:210637776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2762T>G |
| AA Mutation | p.Leu921Arg(p.L921R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210606764:210606764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2015T>C |
| AA Mutation | p.Leu672Pro(p.L672P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210602254:210602254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1760G>A |
| AA Mutation | p.Arg587His(p.R587H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210647930:210647930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3209A>G |
| AA Mutation | p.Lys1070Arg(p.K1070R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210602217:210602217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1723A>C |
| AA Mutation | p.Lys575Gln(p.K575Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210606815:210606815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201256385 |
| CDS Mutation | c.2066G>A |
| AA Mutation | p.Arg689His(p.R689H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210642541:210642541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3017T>G |
| AA Mutation | p.Leu1006Arg(p.L1006R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210674912:210674912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765106604 |
| CDS Mutation | c.4112G>A |
| AA Mutation | p.Arg1371Gln(p.R1371Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210605155:210605155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1890A>C |
| AA Mutation | p.Lys630Asn(p.K630N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210608492:210608492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766970243 |
| CDS Mutation | c.2324G>A |
| AA Mutation | p.Arg775His(p.R775H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210642513:210642513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2989G>T |
| AA Mutation | p.Val997Phe(p.V997F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210606814:210606814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147443001 |
| CDS Mutation | c.2065C>T |
| AA Mutation | p.Arg689Cys(p.R689C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210608426:210608426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2258T>C |
| AA Mutation | p.Val753Ala(p.V753A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210637748:210637748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2734T>A |
| AA Mutation | p.Phe912Ile(p.F912I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233072 |
| Start | 210647907:210647907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3186C>A |
| AA Mutation | p.Asn1062Lys(p.N1062K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233072 |
| Start | 210675763:210675763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548201746 |
| CDS Mutation | c.4197C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233072 |
| Start | 210577439:210577439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.400C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233072 |
| Start | 210599455:210599455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1443T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233072 |
| Start | 210600673:210600673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1668G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233072 |
| Start | 210675805:210675805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4239A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233072 |
| Start | 210647970:210647970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751008875 |
| CDS Mutation | c.3249C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000233072 |
| Start | 210600587:210600587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1582G>T |
| AA Mutation | p.Glu528Ter(p.E528*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |