Primary Site >> Stomach Cancer
Gene >> SLC25A22
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320230 |
| Start | 792175:792175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.785A>C |
| AA Mutation | p.Glu262Ala(p.E262A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320230 |
| Start | 794509:794509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116134953 |
| CDS Mutation | c.151G>A |
| AA Mutation | p.Asp51Asn(p.D51N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320230 |
| Start | 792206:792206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.754C>T |
| AA Mutation | p.Arg252Trp(p.R252W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320230 |
| Start | 792014:792014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.873C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320230 |
| Start | 792877:792877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.405G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320230 |
| Start | 791990:791990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs7124179 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000320230 |
| Start | 791923:791923(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.964delC |
| AA Mutation | p.Gln322ArgfsTer52(p.Q322Rfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |