Primary Site >> Stomach Cancer
Gene >> ACSS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81231133:81231133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1591T>G |
| AA Mutation | p.Phe531Val(p.F531V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81253328:81253328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182895257 |
| CDS Mutation | c.1741G>A |
| AA Mutation | p.Val581Met(p.V581M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81216922:81216922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772788931 |
| CDS Mutation | c.1376C>T |
| AA Mutation | p.Ala459Val(p.A459V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81078359:81078359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.239C>A |
| AA Mutation | p.Ala80Asp(p.A80D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81139177:81139177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.692G>T |
| AA Mutation | p.Arg231Met(p.R231M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81078357:81078357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.237A>C |
| AA Mutation | p.Lys79Asn(p.K79N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81139186:81139186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701A>G |
| AA Mutation | p.Tyr234Cys(p.Y234C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000548058 |
| Start | 81134970:81134970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.611C>A |
| AA Mutation | p.Ser204Tyr(p.S204Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000548058 |
| Start | 81151906:81151906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.984C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000548058 |
| Start | 81231096:81231096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768212741 |
| CDS Mutation | c.1554G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000548058 |
| Start | 81109596:81109596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770447768 |
| CDS Mutation | c.348C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |