Primary Site >> Stomach Cancer
Gene >> HOXA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222718 |
| Start | 27101319:27101319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.538C>A |
| AA Mutation | p.Leu180Met(p.L180M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222718 |
| Start | 27102296:27102296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.205G>A |
| AA Mutation | p.Ala69Thr(p.A69T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222718 |
| Start | 27102286:27102286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215G>A |
| AA Mutation | p.Arg72His(p.R72H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222718 |
| Start | 27102149:27102149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750882072 |
| CDS Mutation | c.352A>G |
| AA Mutation | p.Thr118Ala(p.T118A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222718 |
| Start | 27100915:27100915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.942T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222718 |
| Start | 27101209:27101209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.648C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222718 |
| Start | 27101437:27101437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748975641 |
| CDS Mutation | c.420C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222718 |
| Start | 27101056:27101056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140022054 |
| CDS Mutation | c.801C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222718 |
| Start | 27102141:27102141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762714236 |
| CDS Mutation | c.360A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222718 |
| Start | 27100771:27100771(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1086delT |
| AA Mutation | p.Phe362LeufsTer13(p.F362Lfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222718 |
| Start | 27100874:27100874(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.983delT |
| AA Mutation | p.Phe328SerfsTer25(p.F328Sfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222718 |
| Start | 27102426:27102426(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.75delT |
| AA Mutation | p.Pro27LeufsTer21(p.P27Lfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |