Primary Site >> Stomach Cancer
Gene >> HIST1H1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017726:26017726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7G>A |
| AA Mutation | p.Glu3Lys(p.E3K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017497:26017497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.236A>G |
| AA Mutation | p.Asn79Ser(p.N79S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017264:26017264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.469A>G |
| AA Mutation | p.Lys157Glu(p.K157E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017564:26017564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540194494 |
| CDS Mutation | c.169C>T |
| AA Mutation | p.Arg57Cys(p.R57C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017697:26017697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.36T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017220:26017220(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.513delA |
| AA Mutation | p.Lys171AsnfsTer5(p.K171Nfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017320:26017320(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.413delA |
| AA Mutation | p.Lys138SerfsTer38(p.K138Sfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000244573 |
| Start | 26017533:26017533(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs35510717 |
| CDS Mutation | c.200delA |
| AA Mutation | p.Lys67ArgfsTer25(p.K67Rfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000244573 |
| Start | 26017732:26017732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1A>T |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |