Primary Site >> Stomach Cancer
Gene >> XDH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31350165:31350165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2690G>A |
| AA Mutation | p.Gly897Asp(p.G897D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31375397:31375397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769088676 |
| CDS Mutation | c.1585C>A |
| AA Mutation | p.Gln529Lys(p.Q529K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31349779:31349779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2876A>C |
| AA Mutation | p.Lys959Thr(p.K959T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31403066:31403066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751261129 |
| CDS Mutation | c.179G>A |
| AA Mutation | p.Arg60His(p.R60H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31366000:31366000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372844459 |
| CDS Mutation | c.2432C>T |
| AA Mutation | p.Thr811Met(p.T811M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31370434:31370434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1901G>A |
| AA Mutation | p.Cys634Tyr(p.C634Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31368046:31368046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2112G>T |
| AA Mutation | p.Lys704Asn(p.K704N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31339596:31339596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116290580 |
| CDS Mutation | c.3667C>T |
| AA Mutation | p.Arg1223Cys(p.R1223C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31339620:31339620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3643T>C |
| AA Mutation | p.Ser1215Pro(p.S1215P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31366022:31366022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2410A>G |
| AA Mutation | p.Thr804Ala(p.T804A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31373928:31373928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1631C>T |
| AA Mutation | p.Ala544Val(p.A544V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31337760:31337760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3832G>A |
| AA Mutation | p.Ala1278Thr(p.A1278T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31337802:31337802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3790C>T |
| AA Mutation | p.Pro1264Ser(p.P1264S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31366072:31366072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149717617 |
| CDS Mutation | c.2360G>A |
| AA Mutation | p.Arg787Gln(p.R787Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31381723:31381723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192453952 |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Val348Ile(p.V348I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31403054:31403054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.191A>G |
| AA Mutation | p.Lys64Arg(p.K64R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31344699:31344699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3389C>T |
| AA Mutation | p.Ala1130Val(p.A1130V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31349792:31349792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762858102 |
| CDS Mutation | c.2863C>T |
| AA Mutation | p.His955Tyr(p.H955Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31375429:31375429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1553A>C |
| AA Mutation | p.Lys518Thr(p.K518T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31349714:31349714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775019798 |
| CDS Mutation | c.2941C>T |
| AA Mutation | p.Arg981Trp(p.R981W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31337661:31337661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3931G>A |
| AA Mutation | p.Val1311Met(p.V1311M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31337654:31337654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3938A>C |
| AA Mutation | p.Lys1313Thr(p.K1313T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379416 |
| Start | 31344717:31344717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3371A>G |
| AA Mutation | p.Asp1124Gly(p.D1124G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379416 |
| Start | 31405916:31405916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.91A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379416 |
| Start | 31370424:31370424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142197675 |
| CDS Mutation | c.1911C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379416 |
| Start | 31372239:31372239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756999209 |
| CDS Mutation | c.1845C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379416 |
| Start | 31347549:31347549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs45562835 |
| CDS Mutation | c.3249C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379416 |
| Start | 31366924:31366924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2268C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379416 |
| Start | 31366035:31366035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2397T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379416 |
| Start | 31350104:31350104(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772878388 |
| CDS Mutation | c.2751delG |
| AA Mutation | p.Gln919ArgfsTer10(p.Q919Rfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |