Primary Site >> Stomach Cancer
Gene >> RUNX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308873 |
| Start | 24902516:24902516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202187723 |
| CDS Mutation | c.854C>T |
| AA Mutation | p.Ser285Leu(p.S285L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308873 |
| Start | 24919252:24919252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532C>T |
| AA Mutation | p.Arg178Trp(p.R178W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308873 |
| Start | 24927712:24927712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301G>A |
| AA Mutation | p.Val101Met(p.V101M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308873 |
| Start | 24927668:24927668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.345G>T |
| AA Mutation | p.Glu115Asp(p.E115D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308873 |
| Start | 24902407:24902407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.963G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308873 |
| Start | 24919259:24919259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779977917 |
| CDS Mutation | c.525C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308873 |
| Start | 24902641:24902641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144597350 |
| CDS Mutation | c.729C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |