Primary Site >> Stomach Cancer
Gene >> ERP29
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261735 |
| Start | 112022353:112022353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752987002 |
| CDS Mutation | c.487G>A |
| AA Mutation | p.Ala163Thr(p.A163T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261735 |
| Start | 112022284:112022284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418G>A |
| AA Mutation | p.Ala140Thr(p.A140T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261735 |
| Start | 112022494:112022494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.628T>G |
| AA Mutation | p.Leu210Val(p.L210V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261735 |
| Start | 112022443:112022443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Glu193Lys(p.E193K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261735 |
| Start | 112022628:112022628(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.766delG |
| AA Mutation | p.Ala256ProfsTer38(p.A256Pfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261735 |
| Start | 112019884:112019884(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.276delG |
| AA Mutation | p.Ile93SerfsTer8(p.I93Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261735 |
| Start | 112022483:112022484(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs754819048 |
| CDS Mutation | c.621dupG |
| AA Mutation | p.Lys208GlufsTer22(p.K208Efs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |