Primary Site >> Stomach Cancer
Gene >> SQSTM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179825155:179825155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151191977 |
| CDS Mutation | c.683C>T |
| AA Mutation | p.Pro228Leu(p.P228L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179823884:179823884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139372286 |
| CDS Mutation | c.328C>T |
| AA Mutation | p.Arg110Cys(p.R110C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179824252:179824252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.602G>A |
| AA Mutation | p.Gly201Asp(p.G201D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179833239:179833239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752889531 |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Arg321His(p.R321H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179823039:179823039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569811115 |
| CDS Mutation | c.287G>A |
| AA Mutation | p.Arg96Gln(p.R96Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179833040:179833040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182522590 |
| CDS Mutation | c.763G>A |
| AA Mutation | p.Val255Ile(p.V255I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179823912:179823912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779807674 |
| CDS Mutation | c.356G>A |
| AA Mutation | p.Arg119His(p.R119H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179836532:179836532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1262A>G |
| AA Mutation | p.Asn421Ser(p.N421S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389805 |
| Start | 179823014:179823014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.262T>C |
| AA Mutation | p.Ser88Pro(p.S88P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389805 |
| Start | 179833189:179833189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370970067 |
| CDS Mutation | c.912G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389805 |
| Start | 179836587:179836587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11548636 |
| CDS Mutation | c.1317G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389805 |
| Start | 179823925:179823925(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.372delC |
| AA Mutation | p.Asn125MetfsTer2(p.N125Mfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389805 |
| Start | 179833083:179833083(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.810delC |
| AA Mutation | p.Val271SerfsTer41(p.V271Sfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |