Primary Site >> Stomach Cancer
Gene >> PDLIM4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253754 |
| Start | 132272159:132272159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.923C>A |
| AA Mutation | p.Ala308Glu(p.A308E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253754 |
| Start | 132271850:132271850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.730G>C |
| AA Mutation | p.Ala244Pro(p.A244P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253754 |
| Start | 132270963:132270963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.376C>T |
| AA Mutation | p.Pro126Ser(p.P126S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253754 |
| Start | 132271012:132271012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755408398 |
| CDS Mutation | c.425G>A |
| AA Mutation | p.Arg142His(p.R142H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253754 |
| Start | 132271041:132271041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368514608 |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Glu152Lys(p.E152K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253754 |
| Start | 132271849:132271849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768047246 |
| CDS Mutation | c.729C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |