Primary Site >> Stomach Cancer
Gene >> ME1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369705 |
| Start | 83212045:83212045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757421355 |
| CDS Mutation | c.1598C>T |
| AA Mutation | p.Pro533Leu(p.P533L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369705 |
| Start | 83223929:83223929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770124490 |
| CDS Mutation | c.1280G>A |
| AA Mutation | p.Arg427His(p.R427H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369705 |
| Start | 83237746:83237746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.997C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369705 |
| Start | 83237720:83237720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1023T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369705 |
| Start | 83212044:83212044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749327529 |
| CDS Mutation | c.1599G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369705 |
| Start | 83346233:83346233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754174776 |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |