Primary Site >> Stomach Cancer
Gene >> PDLIM7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355841 |
| Start | 177490891:177490891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.551A>C |
| AA Mutation | p.Glu184Ala(p.E184A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355841 |
| Start | 177492647:177492647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753547502 |
| CDS Mutation | c.127G>A |
| AA Mutation | p.Gly43Arg(p.G43R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355841 |
| Start | 177492611:177492611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.163G>A |
| AA Mutation | p.Gly55Ser(p.G55S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355841 |
| Start | 177492638:177492638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.136G>A |
| AA Mutation | p.Val46Met(p.V46M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355841 |
| Start | 177488117:177488117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1001A>G |
| AA Mutation | p.Asp334Gly(p.D334G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355841 |
| Start | 177484089:177484089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371472586 |
| CDS Mutation | c.1152C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355841 |
| Start | 177489470:177489470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.792A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |