Primary Site >> Stomach Cancer
Gene >> THBS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39589075:39589075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1762G>T |
| AA Mutation | p.Asp588Tyr(p.D588Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39593526:39593526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3125A>G |
| AA Mutation | p.Gln1042Arg(p.Q1042R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39594102:39594102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762068138 |
| CDS Mutation | c.3271C>T |
| AA Mutation | p.Arg1091Cys(p.R1091C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582631:39582631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506T>C |
| AA Mutation | p.Ile169Thr(p.I169T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39593502:39593502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777901728 |
| CDS Mutation | c.3101G>A |
| AA Mutation | p.Arg1034His(p.R1034H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582681:39582681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367736106 |
| CDS Mutation | c.556G>A |
| AA Mutation | p.Val186Ile(p.V186I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39593636:39593636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376857586 |
| CDS Mutation | c.3235G>A |
| AA Mutation | p.Ala1079Thr(p.A1079T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39593423:39593423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3022T>G |
| AA Mutation | p.Phe1008Val(p.F1008V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39583633:39583633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.644T>C |
| AA Mutation | p.Val215Ala(p.V215A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39585546:39585546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1103G>A |
| AA Mutation | p.Cys368Tyr(p.C368Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39587431:39587431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369659280 |
| CDS Mutation | c.1205G>A |
| AA Mutation | p.Arg402His(p.R402H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582262:39582262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774720607 |
| CDS Mutation | c.137G>A |
| AA Mutation | p.Arg46His(p.R46H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260356 |
| Start | 39589921:39589921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2043C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582665:39582665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582500:39582500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752307452 |
| CDS Mutation | c.375G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260356 |
| Start | 39588963:39588963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1650A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260356 |
| Start | 39593458:39593458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754843401 |
| CDS Mutation | c.3057C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582728:39582728(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.608delG |
| AA Mutation | p.Gly203AlafsTer13(p.G203Afs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260356 |
| Start | 39582237:39582237(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.115delG |
| AA Mutation | p.Ala39ProfsTer11(p.A39Pfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000260356 |
| Start | 39583615:39583616(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.631dupG |
| AA Mutation | p.Val211GlyfsTer33(p.X211_splice) |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000260356 |
| Start | 39585564:39585564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539874413 |
| CDS Mutation | c.1120+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |