Primary Site >> Stomach Cancer
Gene >> MST1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449682 |
| Start | 49686116:49686116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755308635 |
| CDS Mutation | c.1093C>T |
| AA Mutation | p.Arg365Cys(p.R365C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449682 |
| Start | 49684352:49684352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1978T>C |
| AA Mutation | p.Cys660Arg(p.C660R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449682 |
| Start | 49684637:49684637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750408728 |
| CDS Mutation | c.1789C>T |
| AA Mutation | p.Arg597Cys(p.R597C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449682 |
| Start | 49684850:49684850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1657G>A |
| AA Mutation | p.Gly553Ser(p.G553S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449682 |
| Start | 49687592:49687592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769228908 |
| CDS Mutation | c.319C>T |
| AA Mutation | p.Arg107Trp(p.R107W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000449682 |
| Start | 49687065:49687065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610G>A |
| AA Mutation | p.Ala204Thr(p.A204T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449682 |
| Start | 49686111:49686111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1098G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449682 |
| Start | 49687216:49687216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.540T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449682 |
| Start | 49684112:49684112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2094A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449682 |
| Start | 49685315:49685315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377097129 |
| CDS Mutation | c.1491C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449682 |
| Start | 49686078:49686078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770411107 |
| CDS Mutation | c.1131C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000449682 |
| Start | 49685473:49685473(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs747477010 |
| CDS Mutation | c.1421delC |
| AA Mutation | p.Pro474GlnfsTer52(p.P474Qfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |