Primary Site >> Stomach Cancer
Gene >> EGR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467173:138467173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.724G>A |
| AA Mutation | p.Ala242Thr(p.A242T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467971:138467971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1522G>A |
| AA Mutation | p.Ala508Thr(p.A508T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467068:138467068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.619C>T |
| AA Mutation | p.Pro207Ser(p.P207S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467413:138467413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.964C>T |
| AA Mutation | p.Arg322Cys(p.R322C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467638:138467638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1189G>A |
| AA Mutation | p.Ala397Thr(p.A397T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467051:138467051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.602C>A |
| AA Mutation | p.Pro201His(p.P201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467832:138467832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200476410 |
| CDS Mutation | c.1383G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239938 |
| Start | 138465863:138465863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368477832 |
| CDS Mutation | c.102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239938 |
| Start | 138466998:138466998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202122132 |
| CDS Mutation | c.549C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000239938 |
| Start | 138467442:138467443(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs746692720 |
| CDS Mutation | c.1000dupC |
| AA Mutation | p.His334ProfsTer13(p.H334Pfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |