Primary Site >> Stomach Cancer
Gene >> OSMR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38924442:38924442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377012343 |
| CDS Mutation | c.1891G>A |
| AA Mutation | p.Val631Met(p.V631M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38876261:38876261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147223683 |
| CDS Mutation | c.134G>A |
| AA Mutation | p.Arg45His(p.R45H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38924589:38924589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2038C>A |
| AA Mutation | p.Leu680Ile(p.L680I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38885456:38885456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811C>A |
| AA Mutation | p.Pro271Thr(p.P271T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38881672:38881672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.326C>T |
| AA Mutation | p.Thr109Ile(p.T109I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38917556:38917556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1296G>T |
| AA Mutation | p.Glu432Asp(p.E432D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38876258:38876258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372089425 |
| CDS Mutation | c.131C>T |
| AA Mutation | p.Thr44Met(p.T44M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274276 |
| Start | 38933423:38933423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2919T>A |
| AA Mutation | p.Asp973Glu(p.D973E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274276 |
| Start | 38884017:38884017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.609G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274276 |
| Start | 38876358:38876358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.231C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274276 |
| Start | 38931887:38931887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549104124 |
| CDS Mutation | c.2217G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274276 |
| Start | 38869107:38869107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.63C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274276 |
| Start | 38881757:38881757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.411A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000274276 |
| Start | 38923227:38923227(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1849delA |
| AA Mutation | p.Thr617GlnfsTer20(p.T617Qfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000274276 |
| Start | 38886137:38886137(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.941delA |
| AA Mutation | p.Asn314IlefsTer3(p.N314Ifs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000274276 |
| Start | 38904425:38904425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147586955 |
| CDS Mutation | c.1207C>T |
| AA Mutation | p.Arg403Ter(p.R403*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |