Primary Site >> Stomach Cancer
Gene >> ACSS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25030900:25030900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112767555 |
| CDS Mutation | c.490C>T |
| AA Mutation | p.Arg164Cys(p.R164C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25014053:25014053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775016558 |
| CDS Mutation | c.1360G>A |
| AA Mutation | p.Ala454Thr(p.A454T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25007895:25007895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761291852 |
| CDS Mutation | c.1937G>A |
| AA Mutation | p.Arg646Gln(p.R646Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25057876:25057876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.227T>C |
| AA Mutation | p.Leu76Pro(p.L76P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25030765:25030765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625A>G |
| AA Mutation | p.Asn209Asp(p.N209D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25009322:25009322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1838A>T |
| AA Mutation | p.Lys613Met(p.K613M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25007826:25007826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201279440 |
| CDS Mutation | c.2006G>C |
| AA Mutation | p.Ser669Thr(p.S669T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25030762:25030762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.628G>A |
| AA Mutation | p.Asp210Asn(p.D210N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25012915:25012915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756942221 |
| CDS Mutation | c.1604C>T |
| AA Mutation | p.Ala535Val(p.A535V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25007818:25007818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143890712 |
| CDS Mutation | c.2014G>A |
| AA Mutation | p.Ala672Thr(p.A672T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25012817:25012817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780332877 |
| CDS Mutation | c.1702G>A |
| AA Mutation | p.Ala568Thr(p.A568T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25022969:25022969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.931T>C |
| AA Mutation | p.Tyr311His(p.Y311H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323482 |
| Start | 25023570:25023570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.703G>A |
| AA Mutation | p.Val235Met(p.V235M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323482 |
| Start | 25012920:25012920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1599C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323482 |
| Start | 25023526:25023526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.747G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323482 |
| Start | 25057956:25057956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323482 |
| Start | 25023535:25023535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323482 |
| Start | 25023541:25023541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769037015 |
| CDS Mutation | c.732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323482 |
| Start | 25015219:25015220(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1257dupC |
| AA Mutation | p.Ile420HisfsTer4(p.I420Hfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323482 |
| Start | 25021416:25021417(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1080dupT |
| AA Mutation | p.Glu361Ter(p.E361*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |