Primary Site >> Stomach Cancer
Gene >> GSN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121302098:121302098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.280G>A |
| AA Mutation | p.Ala94Thr(p.A94T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121302001:121302001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.183G>T |
| AA Mutation | p.Lys61Asn(p.K61N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121328987:121328987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2012C>T |
| AA Mutation | p.Ala671Val(p.A671V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121318747:121318747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211G>A |
| AA Mutation | p.Gly404Asp(p.G404D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121317155:121317155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.976C>A |
| AA Mutation | p.Leu326Met(p.L326M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121329007:121329007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371328761 |
| CDS Mutation | c.2032C>T |
| AA Mutation | p.Arg678Cys(p.R678C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000373818 |
| Start | 121329315:121329315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2118G>T |
| AA Mutation | p.Gln706His(p.Q706H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121317089:121317089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.910T>C |
| AA Mutation | p.Ser304Pro(p.S304P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121332439:121332439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755630687 |
| CDS Mutation | c.2185C>T |
| AA Mutation | p.Arg729Trp(p.R729W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121317135:121317135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956A>G |
| AA Mutation | p.Asn319Ser(p.N319S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373818 |
| Start | 121310713:121310713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs180689280 |
| CDS Mutation | c.534C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373818 |
| Start | 121302094:121302094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774617795 |
| CDS Mutation | c.276C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000373818 |
| Start | 121327307:121327307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1741-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000373818 |
| Start | 121318881:121318881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113048496 |
| CDS Mutation | c.1344+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |