Primary Site >> Stomach Cancer
Gene >> FGL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381840 |
| Start | 17864715:17864715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771078136 |
| CDS Mutation | c.816C>A |
| AA Mutation | p.Ser272Arg(p.S272R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381840 |
| Start | 17868606:17868606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.721C>A |
| AA Mutation | p.His241Asn(p.H241N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381840 |
| Start | 17874057:17874057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.464G>C |
| AA Mutation | p.Trp155Ser(p.W155S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381840 |
| Start | 17868620:17868620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146098986 |
| CDS Mutation | c.707C>T |
| AA Mutation | p.Thr236Met(p.T236M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381840 |
| Start | 17874395:17874395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.371A>G |
| AA Mutation | p.Gln124Arg(p.Q124R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381840 |
| Start | 17882174:17882174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146639128 |
| CDS Mutation | c.69C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000381840 |
| Start | 17874071:17874071(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.450delA |
| AA Mutation | p.Lys150AsnfsTer15(p.K150Nfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |