Primary Site >> Stomach Cancer
Gene >> PDZD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32069599:32069599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2482G>A |
| AA Mutation | p.Ala828Thr(p.A828T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32088729:32088729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5281A>G |
| AA Mutation | p.Ser1761Gly(p.S1761G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983390:31983390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712G>A |
| AA Mutation | p.Ala238Thr(p.A238T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32061118:32061118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372658069 |
| CDS Mutation | c.2435G>A |
| AA Mutation | p.Arg812Gln(p.R812Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32057974:32057974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771417889 |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Ala691Thr(p.A691T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32069606:32069606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2489G>A |
| AA Mutation | p.Ser830Asn(p.S830N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074113:32074113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771893787 |
| CDS Mutation | c.3007C>T |
| AA Mutation | p.Arg1003Cys(p.R1003C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32058011:32058011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542284593 |
| CDS Mutation | c.2108C>T |
| AA Mutation | p.Ala703Val(p.A703V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983600:31983600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368272828 |
| CDS Mutation | c.922C>T |
| AA Mutation | p.Arg308Cys(p.R308C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32090670:32090670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142528798 |
| CDS Mutation | c.7222G>A |
| AA Mutation | p.Gly2408Ser(p.G2408S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32089258:32089258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5810T>C |
| AA Mutation | p.Val1937Ala(p.V1937A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32088900:32088900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5452A>G |
| AA Mutation | p.Thr1818Ala(p.T1818A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074170:32074170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371935614 |
| CDS Mutation | c.3064C>T |
| AA Mutation | p.Arg1022Trp(p.R1022W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31799382:31799382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134A>G |
| AA Mutation | p.Tyr45Cys(p.Y45C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32087598:32087598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4150T>G |
| AA Mutation | p.Ser1384Ala(p.S1384A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32093008:32093008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372031921 |
| CDS Mutation | c.7829C>T |
| AA Mutation | p.Ala2610Val(p.A2610V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32090595:32090595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7147G>T |
| AA Mutation | p.Gly2383Cys(p.G2383C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983307:31983307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749035781 |
| CDS Mutation | c.629C>T |
| AA Mutation | p.Ala210Val(p.A210V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32107986:32107986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8371G>T |
| AA Mutation | p.Ala2791Ser(p.A2791S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31799393:31799393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145A>G |
| AA Mutation | p.Asn49Asp(p.N49D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32048583:32048583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1564A>C |
| AA Mutation | p.Met522Leu(p.M522L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32077474:32077474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3550A>C |
| AA Mutation | p.Lys1184Gln(p.K1184Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983583:31983583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.905C>A |
| AA Mutation | p.Thr302Asn(p.T302N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32072207:32072207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2615A>G |
| AA Mutation | p.Asp872Gly(p.D872G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32087925:32087925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745438758 |
| CDS Mutation | c.4477G>A |
| AA Mutation | p.Ala1493Thr(p.A1493T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32089965:32089965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6517T>C |
| AA Mutation | p.Ser2173Pro(p.S2173P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32087974:32087974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4526C>A |
| AA Mutation | p.Pro1509His(p.P1509H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32057948:32057948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368227764 |
| CDS Mutation | c.2045C>T |
| AA Mutation | p.Ser682Leu(p.S682L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32090166:32090166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6718C>A |
| AA Mutation | p.Pro2240Thr(p.P2240T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32037334:32037334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753954633 |
| CDS Mutation | c.1511G>A |
| AA Mutation | p.Arg504His(p.R504H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32088981:32088981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748596911 |
| CDS Mutation | c.5533G>A |
| AA Mutation | p.Val1845Ile(p.V1845I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983361:31983361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683A>G |
| AA Mutation | p.Asn228Ser(p.N228S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31995711:31995711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1114G>A |
| AA Mutation | p.Ala372Thr(p.A372T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32090586:32090586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7138G>T |
| AA Mutation | p.Gly2380Trp(p.G2380W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074542:32074542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3436A>G |
| AA Mutation | p.Thr1146Ala(p.T1146A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32061043:32061043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2360G>A |
| AA Mutation | p.Arg787His(p.R787H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983468:31983468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790T>G |
| AA Mutation | p.Phe264Val(p.F264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32088212:32088212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4764G>T |
| AA Mutation | p.Lys1588Asn(p.K1588N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983340:31983340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662T>C |
| AA Mutation | p.Val221Ala(p.V221A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31799418:31799418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.170T>C |
| AA Mutation | p.Val57Ala(p.V57A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32089616:32089616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6168C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32088107:32088107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79008030 |
| CDS Mutation | c.4659C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32073884:32073884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2778C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32090633:32090633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779360450 |
| CDS Mutation | c.7185C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32091038:32091038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761253819 |
| CDS Mutation | c.7590G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32087339:32087339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762003118 |
| CDS Mutation | c.3891G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32058090:32058090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2187A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32098468:32098468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747709270 |
| CDS Mutation | c.8052C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32098594:32098594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8178T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438447 |
| Start | 31799434:31799434(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.192delC |
| AA Mutation | p.Glu65LysfsTer21(p.E65Kfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074423:32074423(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3322delC |
| AA Mutation | p.Gln1108SerfsTer17(p.Q1108Sfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438447 |
| Start | 32087786:32087786(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4342delG |
| AA Mutation | p.Asp1448ThrfsTer57(p.D1448Tfs*57) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000438447 |
| Start | 32048628:32048628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766389561 |
| CDS Mutation | c.1609C>T |
| AA Mutation | p.Arg537Ter(p.R537*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074422:32074423(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3322dupC |
| AA Mutation | p.Gln1108ProfsTer5(p.Q1108Pfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438447 |
| Start | 32071411:32071412(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2567dupA |
| AA Mutation | p.Asp857GlyfsTer6(p.D857Gfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438447 |
| Start | 31799549:31799550(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs763648903 |
| CDS Mutation | c.308dupG |
| AA Mutation | p.Lys104GlnfsTer38(p.K104Qfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |