Primary Site >> Stomach Cancer
Gene >> MKRN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255977 |
| Start | 140455134:140455134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1197G>T |
| AA Mutation | p.Glu399Asp(p.E399D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255977 |
| Start | 140471973:140471973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224G>C |
| AA Mutation | p.Cys75Ser(p.C75S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255977 |
| Start | 140459229:140459229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759635628 |
| CDS Mutation | c.549G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255977 |
| Start | 140456741:140456741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772862496 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255977 |
| Start | 140459106:140459106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1062761 |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255977 |
| Start | 140459184:140459184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.594A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255977 |
| Start | 140455224:140455224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1062775 |
| CDS Mutation | c.1107G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |