Primary Site >> Stomach Cancer
Gene >> ITPR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33640497:33640497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.103C>T |
| AA Mutation | p.Arg35Cys(p.R35C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33670458:33670458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2323G>A |
| AA Mutation | p.Ala775Thr(p.A775T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33670774:33670774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200072171 |
| CDS Mutation | c.2545G>A |
| AA Mutation | p.Val849Met(p.V849M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33667156:33667156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139434169 |
| CDS Mutation | c.1579C>T |
| AA Mutation | p.Arg527Cys(p.R527C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33685726:33685726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5566G>A |
| AA Mutation | p.Glu1856Lys(p.E1856K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33682566:33682566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746407544 |
| CDS Mutation | c.4519C>T |
| AA Mutation | p.Arg1507Cys(p.R1507C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33669046:33669046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2079G>C |
| AA Mutation | p.Trp693Cys(p.W693C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33691086:33691086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7202G>T |
| AA Mutation | p.Arg2401Leu(p.R2401L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000374316 |
| Start | 33691109:33691109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7225G>T |
| AA Mutation | p.Ala2409Ser(p.A2409S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33679963:33679963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368822884 |
| CDS Mutation | c.4054G>A |
| AA Mutation | p.Ala1352Thr(p.A1352T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33683299:33683299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4690C>T |
| AA Mutation | p.Arg1564Trp(p.R1564W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33685652:33685652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776342387 |
| CDS Mutation | c.5492C>T |
| AA Mutation | p.Ala1831Val(p.A1831V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33658740:33658740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.440C>T |
| AA Mutation | p.Ala147Val(p.A147V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33668541:33668541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770317269 |
| CDS Mutation | c.1913G>A |
| AA Mutation | p.Cys638Tyr(p.C638Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33684852:33684852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5216A>G |
| AA Mutation | p.Asp1739Gly(p.D1739G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33684924:33684924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5288G>C |
| AA Mutation | p.Gly1763Ala(p.G1763A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33677070:33677070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3503A>C |
| AA Mutation | p.Asn1168Thr(p.N1168T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33684077:33684077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753819461 |
| CDS Mutation | c.4846G>A |
| AA Mutation | p.Val1616Met(p.V1616M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33680398:33680398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4294T>C |
| AA Mutation | p.Tyr1432His(p.Y1432H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33678724:33678724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3857T>G |
| AA Mutation | p.Phe1286Cys(p.F1286C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33670455:33670455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200526442 |
| CDS Mutation | c.2320C>T |
| AA Mutation | p.Arg774Cys(p.R774C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33690939:33690939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7055A>G |
| AA Mutation | p.Glu2352Gly(p.E2352G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33670386:33670386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2251A>C |
| AA Mutation | p.Ile751Leu(p.I751L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33670347:33670347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780991974 |
| CDS Mutation | c.2212C>T |
| AA Mutation | p.Arg738Cys(p.R738C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33695072:33695072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7934A>G |
| AA Mutation | p.Glu2645Gly(p.E2645G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33693698:33693698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7778T>C |
| AA Mutation | p.Met2593Thr(p.M2593T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33663759:33663759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369824854 |
| CDS Mutation | c.1027C>T |
| AA Mutation | p.Arg343Cys(p.R343C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33689297:33689297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6754G>T |
| AA Mutation | p.Ala2252Ser(p.A2252S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33687289:33687289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760282940 |
| CDS Mutation | c.6139C>T |
| AA Mutation | p.Arg2047Cys(p.R2047C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33675729:33675729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3155G>A |
| AA Mutation | p.Gly1052Asp(p.G1052D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33695731:33695731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7967G>A |
| AA Mutation | p.Arg2656His(p.R2656H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33640491:33640491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.97G>C |
| AA Mutation | p.Asp33His(p.D33H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33684875:33684875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5239G>A |
| AA Mutation | p.Glu1747Lys(p.E1747K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33680651:33680651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4447C>A |
| AA Mutation | p.Pro1483Thr(p.P1483T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33674229:33674229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3080G>A |
| AA Mutation | p.Arg1027His(p.R1027H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33689328:33689328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776633313 |
| CDS Mutation | c.6785G>A |
| AA Mutation | p.Arg2262His(p.R2262H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33689382:33689382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6839C>A |
| AA Mutation | p.Pro2280His(p.P2280H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33684800:33684800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756479384 |
| CDS Mutation | c.5164G>A |
| AA Mutation | p.Ala1722Thr(p.A1722T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33692839:33692839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7570C>T |
| AA Mutation | p.Arg2524Cys(p.R2524C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33671178:33671178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2600C>T |
| AA Mutation | p.Ala867Val(p.A867V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33693557:33693557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7637A>G |
| AA Mutation | p.Asp2546Gly(p.D2546G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374316 |
| Start | 33640515:33640515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149697160 |
| CDS Mutation | c.121G>A |
| AA Mutation | p.Ala41Thr(p.A41T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33691700:33691700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113565114 |
| CDS Mutation | c.7311G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33680364:33680364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4260C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33675727:33675727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3153C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33686106:33686106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189648121 |
| CDS Mutation | c.5721G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33664927:33664927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1206T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33670692:33670692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202110116 |
| CDS Mutation | c.2463G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33688726:33688726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750196911 |
| CDS Mutation | c.6639G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33694983:33694983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141751520 |
| CDS Mutation | c.7845C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33663872:33663872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372786080 |
| CDS Mutation | c.1140C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33673710:33673710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146528103 |
| CDS Mutation | c.3048C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33686426:33686426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145776727 |
| CDS Mutation | c.5886C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33665103:33665103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753117025 |
| CDS Mutation | c.1299A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33685689:33685689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772326452 |
| CDS Mutation | c.5529G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33640520:33640520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141205726 |
| CDS Mutation | c.126C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33655830:33655830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.225G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374316 |
| Start | 33688663:33688663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762470840 |
| CDS Mutation | c.6576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374316 |
| Start | 33691619:33691619(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.7234delC |
| AA Mutation | p.Leu2412TrpfsTer48(p.L2412Wfs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374316 |
| Start | 33684659:33684659(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753781307 |
| CDS Mutation | c.5113delG |
| AA Mutation | p.Asp1705ThrfsTer6(p.D1705Tfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |