Primary Site >> Stomach Cancer
Gene >> BCAS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028528:54028528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587A>G |
| AA Mutation | p.Lys196Arg(p.K196R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028796:54028796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570638388 |
| CDS Mutation | c.319A>G |
| AA Mutation | p.Thr107Ala(p.T107A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 53995912:53995912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.862A>G |
| AA Mutation | p.Met288Val(p.M288V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028897:54028897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757394101 |
| CDS Mutation | c.218C>A |
| AA Mutation | p.Ala73Glu(p.A73E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028897:54028897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218C>T |
| AA Mutation | p.Ala73Val(p.A73V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 53953603:53953603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1509G>T |
| AA Mutation | p.Lys503Asn(p.K503N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 53957449:53957449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1399A>G |
| AA Mutation | p.Lys467Glu(p.K467E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028864:54028864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.251C>T |
| AA Mutation | p.Ala84Val(p.A84V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395961 |
| Start | 54058130:54058130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.97G>T |
| AA Mutation | p.Val33Phe(p.V33F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395961 |
| Start | 53967029:53967029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1227A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395961 |
| Start | 54058113:54058113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.114G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028485:54028485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395961 |
| Start | 53957435:53957435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758117005 |
| CDS Mutation | c.1413C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028782:54028782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761415105 |
| CDS Mutation | c.333C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395961 |
| Start | 53953671:53953672(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1440dupT |
| AA Mutation | p.Ile481TyrfsTer7(p.I481Yfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395961 |
| Start | 54028827:54028828(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.287dupT |
| AA Mutation | p.Met98AspfsTer25(p.M98Dfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |