Primary Site >> Stomach Cancer
Gene >> KDM1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356634 |
| Start | 23050466:23050466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.597T>G |
| AA Mutation | p.Ile199Met(p.I199M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356634 |
| Start | 23079130:23079130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1936T>C |
| AA Mutation | p.Trp646Arg(p.W646R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356634 |
| Start | 23072138:23072138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1491A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356634 |
| Start | 23079018:23079018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377276193 |
| CDS Mutation | c.1824C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356634 |
| Start | 23055991:23055991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.883C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356634 |
| Start | 23073310:23073310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1569A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000356634 |
| Start | 23083188:23083188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746295431 |
| CDS Mutation | c.2383C>T |
| AA Mutation | p.Arg795Ter(p.R795*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |