Primary Site >> Stomach Cancer
Gene >> SDCBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58575964:58575964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305G>A |
| AA Mutation | p.Gly102Glu(p.G102E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58575996:58575996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753892979 |
| CDS Mutation | c.337C>T |
| AA Mutation | p.Arg113Cys(p.R113C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58578151:58578151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755236342 |
| CDS Mutation | c.521C>T |
| AA Mutation | p.Ala174Val(p.A174V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58579634:58579634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756701491 |
| CDS Mutation | c.590G>A |
| AA Mutation | p.Arg197Gln(p.R197Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58579776:58579776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.732G>T |
| AA Mutation | p.Gln244His(p.Q244H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58581724:58581724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.881C>T |
| AA Mutation | p.Thr294Ile(p.T294I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58580530:58580530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764C>T |
| AA Mutation | p.Ala255Val(p.A255V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58572273:58572273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144425100 |
| CDS Mutation | c.199C>T |
| AA Mutation | p.Arg67Cys(p.R67C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260130 |
| Start | 58572274:58572274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148588308 |
| CDS Mutation | c.200G>A |
| AA Mutation | p.Arg67His(p.R67H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260130 |
| Start | 58572287:58572287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146620229 |
| CDS Mutation | c.213C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |