Primary Site >> Stomach Cancer
Gene >> OSR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272223 |
| Start | 19353639:19353639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.167C>T |
| AA Mutation | p.Thr56Met(p.T56M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272223 |
| Start | 19353287:19353287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.519G>T |
| AA Mutation | p.Lys173Asn(p.K173N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272223 |
| Start | 19353169:19353169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.637C>T |
| AA Mutation | p.Arg213Trp(p.R213W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272223 |
| Start | 19353580:19353580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Val76Met(p.V76M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272223 |
| Start | 19353218:19353218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759056843 |
| CDS Mutation | c.588G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000272223 |
| Start | 19353394:19353394(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.412delG |
| AA Mutation | p.Glu138ArgfsTer16(p.E138Rfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |