Primary Site >> Stomach Cancer
Gene >> CELSR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109268631:109268631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6369C>A |
| AA Mutation | p.His2123Gln(p.H2123Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109258471:109258471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3350T>C |
| AA Mutation | p.Val1117Ala(p.V1117A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109264213:109264213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752581225 |
| CDS Mutation | c.5137G>A |
| AA Mutation | p.Gly1713Ser(p.G1713S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251836:109251836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1757G>A |
| AA Mutation | p.Gly586Asp(p.G586D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109253354:109253354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3275G>T |
| AA Mutation | p.Arg1092Leu(p.R1092L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109272332:109272332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7981G>A |
| AA Mutation | p.Asp2661Asn(p.D2661N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109270074:109270074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7249G>A |
| AA Mutation | p.Ala2417Thr(p.A2417T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109267926:109267926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766391495 |
| CDS Mutation | c.6184G>A |
| AA Mutation | p.Ala2062Thr(p.A2062T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109264566:109264566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5402C>T |
| AA Mutation | p.Pro1801Leu(p.P1801L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250423:109250423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566938988 |
| CDS Mutation | c.344G>A |
| AA Mutation | p.Arg115His(p.R115H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251707:109251707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780774580 |
| CDS Mutation | c.1628G>A |
| AA Mutation | p.Arg543His(p.R543H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109261074:109261074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369058742 |
| CDS Mutation | c.3991C>T |
| AA Mutation | p.Arg1331Cys(p.R1331C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252942:109252942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2863C>A |
| AA Mutation | p.Gln955Lys(p.Q955K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109258510:109258510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3389C>T |
| AA Mutation | p.Thr1130Met(p.T1130M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252880:109252880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2801G>A |
| AA Mutation | p.Ser934Asn(p.S934N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109261843:109261843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753290065 |
| CDS Mutation | c.4333G>A |
| AA Mutation | p.Gly1445Arg(p.G1445R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109268934:109268934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141644848 |
| CDS Mutation | c.6557G>A |
| AA Mutation | p.Arg2186His(p.R2186H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252154:109252154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762541244 |
| CDS Mutation | c.2075G>A |
| AA Mutation | p.Arg692Gln(p.R692Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109264330:109264330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5254G>A |
| AA Mutation | p.Gly1752Ser(p.G1752S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109253113:109253113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372546163 |
| CDS Mutation | c.3034C>T |
| AA Mutation | p.Arg1012Cys(p.R1012C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109267614:109267614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6080C>T |
| AA Mutation | p.Ser2027Phe(p.S2027F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251961:109251961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1882A>G |
| AA Mutation | p.Ser628Gly(p.S628G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252663:109252663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370447679 |
| CDS Mutation | c.2584G>A |
| AA Mutation | p.Gly862Ser(p.G862S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251086:109251086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1007C>T |
| AA Mutation | p.Pro336Leu(p.P336L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252760:109252760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2681T>C |
| AA Mutation | p.Val894Ala(p.V894A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109269148:109269148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6670G>A |
| AA Mutation | p.Ala2224Thr(p.A2224T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109274044:109274044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8767C>T |
| AA Mutation | p.His2923Tyr(p.H2923Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109258926:109258926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749003003 |
| CDS Mutation | c.3805G>A |
| AA Mutation | p.Val1269Ile(p.V1269I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250222:109250222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762922547 |
| CDS Mutation | c.143C>T |
| AA Mutation | p.Ser48Leu(p.S48L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109267930:109267930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753241841 |
| CDS Mutation | c.6188C>T |
| AA Mutation | p.Thr2063Met(p.T2063M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109258722:109258722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3601C>T |
| AA Mutation | p.Pro1201Ser(p.P1201S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251788:109251788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780159848 |
| CDS Mutation | c.1709G>A |
| AA Mutation | p.Arg570Gln(p.R570Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000271332 |
| Start | 109261626:109261626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4295C>T |
| AA Mutation | p.Ala1432Val(p.A1432V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251261:109251261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1182T>A |
| AA Mutation | p.Asp394Glu(p.D394E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251706:109251706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1627C>T |
| AA Mutation | p.Arg543Cys(p.R543C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109262874:109262874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148197539 |
| CDS Mutation | c.4613G>A |
| AA Mutation | p.Arg1538Gln(p.R1538Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250432:109250432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534540588 |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Gly118Asp(p.G118D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109270958:109270958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746343874 |
| CDS Mutation | c.7515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250940:109250940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.861T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109264089:109264089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5013C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109266166:109266166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778661369 |
| CDS Mutation | c.5973C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250811:109250811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147986274 |
| CDS Mutation | c.732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109251957:109251957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1878C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109258625:109258625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252695:109252695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779256212 |
| CDS Mutation | c.2616C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109258460:109258460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3339C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109250382:109250382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.303T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109270967:109270967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7524T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109272951:109272951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8262C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271332 |
| Start | 109252497:109252497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142987028 |
| CDS Mutation | c.2418C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |