Primary Site >> Stomach Cancer
Gene >> ACSBG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78173686:78173686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146939982 |
| CDS Mutation | c.1996C>T |
| AA Mutation | p.Arg666Trp(p.R666W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78193998:78193998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.476G>A |
| AA Mutation | p.Ser159Asn(p.S159N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78193944:78193944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749048599 |
| CDS Mutation | c.530C>T |
| AA Mutation | p.Thr177Ile(p.T177I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78234474:78234474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201367266 |
| CDS Mutation | c.28G>A |
| AA Mutation | p.Gly10Ser(p.G10S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78179628:78179628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1406G>C |
| AA Mutation | p.Arg469Pro(p.R469P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78234443:78234443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.59A>T |
| AA Mutation | p.Asp20Val(p.D20V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258873 |
| Start | 78193571:78193571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774511900 |
| CDS Mutation | c.598G>A |
| AA Mutation | p.Ala200Thr(p.A200T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258873 |
| Start | 78174478:78174478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556850320 |
| CDS Mutation | c.1749C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258873 |
| Start | 78234463:78234463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767615515 |
| CDS Mutation | c.39C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258873 |
| Start | 78173714:78173714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149258367 |
| CDS Mutation | c.1968C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |