Primary Site >> Stomach Cancer
Gene >> RALGDS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372050 |
| Start | 133102885:133102885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748828691 |
| CDS Mutation | c.1807G>A |
| AA Mutation | p.Ala603Thr(p.A603T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372050 |
| Start | 133101567:133101567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2407C>T |
| AA Mutation | p.Arg803Cys(p.R803C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372050 |
| Start | 133101674:133101674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143871051 |
| CDS Mutation | c.2300C>T |
| AA Mutation | p.Thr767Met(p.T767M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372050 |
| Start | 133098684:133098684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776063928 |
| CDS Mutation | c.2648G>A |
| AA Mutation | p.Arg883Gln(p.R883Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372050 |
| Start | 133110425:133110425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374734282 |
| CDS Mutation | c.359C>T |
| AA Mutation | p.Thr120Met(p.T120M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372050 |
| Start | 133102862:133102862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1830G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372050 |
| Start | 133098737:133098737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745773402 |
| CDS Mutation | c.2595C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000372050 |
| Start | 133110297:133110297(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.487delA |
| AA Mutation | p.Arg163GlyfsTer105(p.R163Gfs*105) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000372050 |
| Start | 133103229:133103229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1791+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000372050 |
| Start | 133108717:133108719(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs781367443 |
| CDS Mutation | c.732_734delCCT |
| AA Mutation | p.Leu245del(p.L245del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |