Primary Site >> Stomach Cancer
Gene >> MME
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155148593:155148593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1541A>C |
| AA Mutation | p.Asn514Thr(p.N514T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155138225:155138225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Glu282Lys(p.E282K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155143482:155143482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369531733 |
| CDS Mutation | c.1228C>T |
| AA Mutation | p.Arg410Cys(p.R410C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155116921:155116921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746423553 |
| CDS Mutation | c.589A>G |
| AA Mutation | p.Lys197Glu(p.K197E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155168515:155168515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1804G>C |
| AA Mutation | p.Asp602His(p.D602H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155115077:155115077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.280C>T |
| AA Mutation | p.Arg94Cys(p.R94C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155143546:155143546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1292C>T |
| AA Mutation | p.Ala431Val(p.A431V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360490 |
| Start | 155148593:155148593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1541A>T |
| AA Mutation | p.Asn514Ile(p.N514I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360490 |
| Start | 155144379:155144379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1338G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360490 |
| Start | 155084293:155084293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760249373 |
| CDS Mutation | c.126T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |