Primary Site >> Stomach Cancer
Gene >> MEF2C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437473 |
| Start | 88752004:88752004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.442C>A |
| AA Mutation | p.Pro148Thr(p.P148T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437473 |
| Start | 88761270:88761270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.317C>T |
| AA Mutation | p.Ser106Phe(p.S106F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000437473 |
| Start | 88729218:88729218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.964G>A |
| AA Mutation | p.Glu322Lys(p.E322K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000437473 |
| Start | 88722779:88722779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768570497 |
| CDS Mutation | c.1247C>T |
| AA Mutation | p.Ala416Val(p.A416V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000437473 |
| Start | 88722790:88722790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1236G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000437473 |
| Start | 88722730:88722730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756839313 |
| CDS Mutation | c.1296C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000437473 |
| Start | 88804604:88804604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780952466 |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |