Primary Site >> Stomach Cancer
Gene >> THBS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169248658:169248658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766329088 |
| CDS Mutation | c.368C>T |
| AA Mutation | p.Thr123Met(p.T123M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169223358:169223358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2891T>A |
| AA Mutation | p.Met964Lys(p.M964K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169248563:169248563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.463C>A |
| AA Mutation | p.Gln155Lys(p.Q155K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169239664:169239664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1064G>A |
| AA Mutation | p.Cys355Tyr(p.C355Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169240501:169240501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748832623 |
| CDS Mutation | c.983C>T |
| AA Mutation | p.Ala328Val(p.A328V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169225205:169225205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184952882 |
| CDS Mutation | c.2713G>A |
| AA Mutation | p.Val905Ile(p.V905I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169223466:169223466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566007634 |
| CDS Mutation | c.2783G>A |
| AA Mutation | p.Arg928Gln(p.R928Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169229589:169229589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201813061 |
| CDS Mutation | c.2242G>A |
| AA Mutation | p.Gly748Ser(p.G748S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169237684:169237684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241C>G |
| AA Mutation | p.Thr414Ser(p.T414S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169237208:169237208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1439G>A |
| AA Mutation | p.Gly480Asp(p.G480D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169237262:169237262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746512177 |
| CDS Mutation | c.1385G>A |
| AA Mutation | p.Arg462His(p.R462H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169221437:169221437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3364T>C |
| AA Mutation | p.Tyr1122His(p.Y1122H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169248746:169248746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.280G>A |
| AA Mutation | p.Gly94Ser(p.G94S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366787 |
| Start | 169248730:169248730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369355659 |
| CDS Mutation | c.296C>T |
| AA Mutation | p.Thr99Met(p.T99M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169237243:169237243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1404G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169248453:169248453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.573C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169222203:169222203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770863471 |
| CDS Mutation | c.3267G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169229662:169229662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2169G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169241864:169241864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.789C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169248882:169248882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769151177 |
| CDS Mutation | c.144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169232694:169232694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1902C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169241855:169241855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148909888 |
| CDS Mutation | c.798C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366787 |
| Start | 169232010:169232010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200328575 |
| CDS Mutation | c.2121C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366787 |
| Start | 169237229:169237229(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1418delG |
| AA Mutation | p.Gly473AlafsTer277(p.G473Afs*277) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000366787 |
| Start | 169226284:169226284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757104686 |
| CDS Mutation | c.2434C>T |
| AA Mutation | p.Arg812Ter(p.R812*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |