Primary Site >> Stomach Cancer
Gene >> ESAM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278927 |
| Start | 124753953:124753953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.866C>T |
| AA Mutation | p.Ala289Val(p.A289V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278927 |
| Start | 124756658:124756658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371439555 |
| CDS Mutation | c.334C>T |
| AA Mutation | p.Arg112Trp(p.R112W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278927 |
| Start | 124758435:124758435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163A>G |
| AA Mutation | p.Thr55Ala(p.T55A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278927 |
| Start | 124754644:124754644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777566375 |
| CDS Mutation | c.727A>G |
| AA Mutation | p.Thr243Ala(p.T243A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278927 |
| Start | 124756590:124756590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278927 |
| Start | 124754258:124754258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143828847 |
| CDS Mutation | c.813C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |