Primary Site >> Stomach Cancer
Gene >> HACE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262903 |
| Start | 104777041:104777041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1748C>T |
| AA Mutation | p.Ala583Val(p.A583V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262903 |
| Start | 104791529:104791529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049A>C |
| AA Mutation | p.Lys350Thr(p.K350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262903 |
| Start | 104785156:104785156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1238C>A |
| AA Mutation | p.Pro413His(p.P413H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262903 |
| Start | 104791620:104791620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.958C>A |
| AA Mutation | p.Leu320Ile(p.L320I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262903 |
| Start | 104750375:104750375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2309C>G |
| AA Mutation | p.Pro770Arg(p.P770R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262903 |
| Start | 104796982:104796982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661G>A |
| AA Mutation | p.Ala221Thr(p.A221T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262903 |
| Start | 104750428:104750428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2256C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262903 |
| Start | 104850945:104850945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762497394 |
| CDS Mutation | c.183C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262903 |
| Start | 104795680:104795680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.822G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262903 |
| Start | 104744558:104744558(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2396delA |
| AA Mutation | p.Asn799IlefsTer22(p.N799Ifs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262903 |
| Start | 104750401:104750402(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2282dupT |
| AA Mutation | p.Leu761PhefsTer17(p.L761Ffs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |