Primary Site >> Stomach Cancer
Gene >> TGFBI
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136055747:136055747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763560027 |
| CDS Mutation | c.1478C>T |
| AA Mutation | p.Thr493Met(p.T493M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136047310:136047310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533509858 |
| CDS Mutation | c.661G>A |
| AA Mutation | p.Asp221Asn(p.D221N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136046370:136046370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766343295 |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Val112Ile(p.V112I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136060855:136060855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1825A>C |
| AA Mutation | p.Asn609His(p.N609H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136046401:136046401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780759366 |
| CDS Mutation | c.365C>T |
| AA Mutation | p.Thr122Met(p.T122M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136049562:136049562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202239395 |
| CDS Mutation | c.895G>A |
| AA Mutation | p.Asp299Asn(p.D299N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136053042:136053042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769820632 |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Ala350Val(p.A350V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000442011 |
| Start | 136047418:136047418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771481298 |
| CDS Mutation | c.769C>T |
| AA Mutation | p.Arg257Trp(p.R257W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136047401:136047401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.752A>G |
| AA Mutation | p.Asp251Gly(p.D251G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442011 |
| Start | 136063213:136063213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2039G>T |
| AA Mutation | p.Arg680Met(p.R680M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442011 |
| Start | 136055748:136055748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1479G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442011 |
| Start | 136047288:136047288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442011 |
| Start | 136046459:136046459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779817855 |
| CDS Mutation | c.423C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000442011 |
| Start | 136055735:136055750(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1471_1486delCTGTTCACGATGGACC |
| AA Mutation | p.Leu491GlyfsTer3(p.L491Gfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |