Primary Site >> Stomach Cancer
Gene >> ACE2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15567792:15567792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1931G>A |
| AA Mutation | p.Arg644Gln(p.R644Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15564210:15564210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769062069 |
| CDS Mutation | c.2123G>A |
| AA Mutation | p.Arg708Gln(p.R708Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15578152:15578152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1234G>A |
| AA Mutation | p.Ala412Thr(p.A412T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15571692:15571692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1769C>T |
| AA Mutation | p.Pro590Leu(p.P590L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15581279:15581279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1012A>G |
| AA Mutation | p.Asn338Asp(p.N338D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15589436:15589436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.604T>C |
| AA Mutation | p.Tyr202His(p.Y202H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15575735:15575735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1373A>C |
| AA Mutation | p.Lys458Thr(p.K458T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252519 |
| Start | 15581303:15581303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988A>C |
| AA Mutation | p.Asn330His(p.N330H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252519 |
| Start | 15561971:15561971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760076142 |
| CDS Mutation | c.2352C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000252519 |
| Start | 15594972:15594972(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.218delT |
| AA Mutation | p.Leu73Ter(p.L73*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000252519 |
| Start | 15567744:15567744(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1979delA |
| AA Mutation | p.Asn660IlefsTer3(p.N660Ifs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |