Primary Site >> Stomach Cancer
Gene >> CPA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011292 |
| Start | 130381811:130381811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537076438 |
| CDS Mutation | c.329G>A |
| AA Mutation | p.Arg110Gln(p.R110Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011292 |
| Start | 130385187:130385187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782790983 |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Gly277Ser(p.G277S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011292 |
| Start | 130383418:130383418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.511G>T |
| AA Mutation | p.Ala171Ser(p.A171S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011292 |
| Start | 130382190:130382190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464G>A |
| AA Mutation | p.Arg155His(p.R155H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011292 |
| Start | 130385903:130385903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1052G>A |
| AA Mutation | p.Gly351Asp(p.G351D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011292 |
| Start | 130384620:130384620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.781T>C |
| AA Mutation | p.Phe261Leu(p.F261L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000011292 |
| Start | 130383734:130383734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.636C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000011292 |
| Start | 130381839:130381839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782032191 |
| CDS Mutation | c.357C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |