Primary Site >> Stomach Cancer
Gene >> SMOX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4187307:4187307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768438474 |
| CDS Mutation | c.1568G>A |
| AA Mutation | p.Arg523His(p.R523H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4182225:4182225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Gly249Asp(p.G249D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000305958 |
| Start | 4183653:4183653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760395151 |
| CDS Mutation | c.1529C>T |
| AA Mutation | p.Ala510Val(p.A510V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4183517:4183517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393C>T |
| AA Mutation | p.Arg465Trp(p.R465W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4182450:4182450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138153642 |
| CDS Mutation | c.971C>T |
| AA Mutation | p.Pro324Leu(p.P324L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4183578:4183578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764313286 |
| CDS Mutation | c.1454C>T |
| AA Mutation | p.Thr485Met(p.T485M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4182735:4182735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762061401 |
| CDS Mutation | c.1256G>A |
| AA Mutation | p.Arg419His(p.R419H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305958 |
| Start | 4177467:4177467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186455590 |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Val109Met(p.V109M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305958 |
| Start | 4182826:4182826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79238665 |
| CDS Mutation | c.1347G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305958 |
| Start | 4182381:4182381(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.908delG |
| AA Mutation | p.Gly303AlafsTer20(p.G303Afs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305958 |
| Start | 4182380:4182381(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs746816975 |
| CDS Mutation | c.908dupG |
| AA Mutation | p.Arg304GlnfsTer4(p.R304Qfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |