Primary Site >> Stomach Cancer
Gene >> MPO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58279550:58279550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.521G>A |
| AA Mutation | p.Arg174His(p.R174H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58270838:58270838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2056T>C |
| AA Mutation | p.Phe686Leu(p.F686L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58271848:58271848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1837A>C |
| AA Mutation | p.Thr613Pro(p.T613P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58272901:58272901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1639C>T |
| AA Mutation | p.Leu547Phe(p.L547F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58275568:58275568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761949874 |
| CDS Mutation | c.1339C>T |
| AA Mutation | p.Arg447Trp(p.R447W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58277887:58277887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1144C>A |
| AA Mutation | p.Leu382Met(p.L382M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000225275 |
| Start | 58279525:58279525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.546C>G |
| AA Mutation | p.Asn182Lys(p.N182K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225275 |
| Start | 58275646:58275646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138620426 |
| CDS Mutation | c.1261C>T |
| AA Mutation | p.Arg421Trp(p.R421W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225275 |
| Start | 58277996:58277996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142018618 |
| CDS Mutation | c.1035C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225275 |
| Start | 58273436:58273436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779934310 |
| CDS Mutation | c.1599C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |