Primary Site >> Stomach Cancer
Gene >> PRMT8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382622 |
| Start | 3569507:3569507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.655G>A |
| AA Mutation | p.Ala219Thr(p.A219T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000382622 |
| Start | 3583059:3583059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.830A>G |
| AA Mutation | p.Glu277Gly(p.E277G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382622 |
| Start | 3569504:3569504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652C>T |
| AA Mutation | p.Arg218Trp(p.R218W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382622 |
| Start | 3592305:3592305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1054G>A |
| AA Mutation | p.Glu352Lys(p.E352K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382622 |
| Start | 3540664:3540664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134G>A |
| AA Mutation | p.Cys45Tyr(p.C45Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382622 |
| Start | 3592259:3592259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1008G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382622 |
| Start | 3550085:3550085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.411G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382622 |
| Start | 3540665:3540665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756751414 |
| CDS Mutation | c.135C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382622 |
| Start | 3540614:3540614(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.90delC |
| AA Mutation | p.Ser31ProfsTer35(p.S31Pfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382622 |
| Start | 3540627:3540627(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761127642 |
| CDS Mutation | c.103delC |
| AA Mutation | p.Gln35SerfsTer31(p.Q35Sfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382622 |
| Start | 3576967:3576968(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.809_810insATGG |
| AA Mutation | p.Asn271TrpfsTer43(p.N271Wfs*43) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382622 |
| Start | 3576968:3576969(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.812_813insAACCCCGTCTCTACAAAGCATACAAAAA |
| AA Mutation | p.Asn271LysfsTer51(p.N271Kfs*51) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |