Primary Site >> Stomach Cancer
Gene >> MARS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262027 |
| Start | 57511715:57511715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1386G>T |
| AA Mutation | p.Glu462Asp(p.E462D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262027 |
| Start | 57515025:57515025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2171C>T |
| AA Mutation | p.Pro724Leu(p.P724L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262027 |
| Start | 57512849:57512849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587777718 |
| CDS Mutation | c.1852C>T |
| AA Mutation | p.Arg618Cys(p.R618C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262027 |
| Start | 57512856:57512856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777332933 |
| CDS Mutation | c.1859A>G |
| AA Mutation | p.Tyr620Cys(p.Y620C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262027 |
| Start | 57512946:57512946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1949T>C |
| AA Mutation | p.Leu650Pro(p.L650P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262027 |
| Start | 57512827:57512827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149742633 |
| CDS Mutation | c.1830G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262027 |
| Start | 57504246:57504246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753577413 |
| CDS Mutation | c.1315C>T |
| AA Mutation | p.Arg439Ter(p.R439*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |