Primary Site >> Stomach Cancer
Gene >> ERI1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250263 |
| Start | 9020447:9020447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790T>C |
| AA Mutation | p.Tyr264His(p.Y264H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250263 |
| Start | 9011688:9011688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434C>T |
| AA Mutation | p.Pro145Leu(p.P145L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250263 |
| Start | 9011719:9011719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377629544 |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250263 |
| Start | 9008077:9008077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138737787 |
| CDS Mutation | c.216G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250263 |
| Start | 9011737:9011737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371640018 |
| CDS Mutation | c.483G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000250263 |
| Start | 9029898:9029899(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.915_918dupAGCA |
| AA Mutation | p.Val307SerfsTer10(p.V307Sfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000250263 |
| Start | 9029898:9029899(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.917_919dupCAG |
| AA Mutation | p.Ala306dup(p.A306dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |