Primary Site >> Stomach Cancer
Gene >> ACE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290866 |
| Start | 63497166:63497166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367916721 |
| CDS Mutation | c.3721G>A |
| AA Mutation | p.Gly1241Ser(p.G1241S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000290866 |
| Start | 63491380:63491380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769406157 |
| CDS Mutation | c.2911C>T |
| AA Mutation | p.Arg971Trp(p.R971W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290866 |
| Start | 63479862:63479862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148460287 |
| CDS Mutation | c.605C>T |
| AA Mutation | p.Pro202Leu(p.P202L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290866 |
| Start | 63493934:63493934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3149A>C |
| AA Mutation | p.Asn1050Thr(p.N1050T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290866 |
| Start | 63482672:63482672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35865660 |
| CDS Mutation | c.1325G>A |
| AA Mutation | p.Arg442His(p.R442H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290866 |
| Start | 63482614:63482614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148018765 |
| CDS Mutation | c.1267G>A |
| AA Mutation | p.Val423Met(p.V423M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63496505:63496505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755556171 |
| CDS Mutation | c.3492G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63496828:63496828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759423545 |
| CDS Mutation | c.3534G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63496855:63496855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141429845 |
| CDS Mutation | c.3561G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63480395:63480395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556856171 |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63491343:63491343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148024347 |
| CDS Mutation | c.2874C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63481655:63481655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1035G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63480350:63480350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767910089 |
| CDS Mutation | c.669G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63482589:63482589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138521921 |
| CDS Mutation | c.1242C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290866 |
| Start | 63493992:63493992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371996217 |
| CDS Mutation | c.3207C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000290866 |
| Start | 63494393:63494393(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3308delC |
| AA Mutation | p.Pro1103GlnfsTer69(p.P1103Qfs*69) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000290866 |
| Start | 63483065:63483065(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1384delA |
| AA Mutation | p.Ile462LeufsTer63(p.I462Lfs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000290866 |
| Start | 63493435:63493435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2913-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000290866 |
| Start | 63496517:63496517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779188587 |
| CDS Mutation | c.3503+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |