Primary Site >> Stomach Cancer
Gene >> ADGRG4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136371409:136371409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7478T>C |
| AA Mutation | p.Ile2493Thr(p.I2493T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136323213:136323213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780690525 |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Ser169Asn(p.S169N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136345769:136345769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2063A>G |
| AA Mutation | p.Glu688Gly(p.E688G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136345658:136345658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764341510 |
| CDS Mutation | c.1952G>A |
| AA Mutation | p.Ser651Asn(p.S651N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136346609:136346609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2903C>G |
| AA Mutation | p.Ala968Gly(p.A968G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136346624:136346624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2918T>C |
| AA Mutation | p.Ile973Thr(p.I973T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136308803:136308803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.26A>C |
| AA Mutation | p.Lys9Thr(p.K9T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349507:136349507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5801T>A |
| AA Mutation | p.Val1934Asp(p.V1934D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136344625:136344625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919G>A |
| AA Mutation | p.Val307Ile(p.V307I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349351:136349351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5645C>T |
| AA Mutation | p.Ser1882Phe(p.S1882F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136414172:136414172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201992547 |
| CDS Mutation | c.9050G>A |
| AA Mutation | p.Arg3017Gln(p.R3017Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136348643:136348643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4937T>C |
| AA Mutation | p.Leu1646Pro(p.L1646P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136350404:136350404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567340291 |
| CDS Mutation | c.6698C>T |
| AA Mutation | p.Ser2233Leu(p.S2233L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136361484:136361484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7174G>A |
| AA Mutation | p.Ala2392Thr(p.A2392T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136323233:136323233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526C>T |
| AA Mutation | p.Arg176Cys(p.R176C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136346941:136346941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746420720 |
| CDS Mutation | c.3235C>T |
| AA Mutation | p.Pro1079Ser(p.P1079S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347851:136347851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4145G>T |
| AA Mutation | p.Ser1382Ile(p.S1382I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347692:136347692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3986C>T |
| AA Mutation | p.Ala1329Val(p.A1329V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136405936:136405936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8899T>G |
| AA Mutation | p.Phe2967Val(p.F2967V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136346458:136346458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2752A>C |
| AA Mutation | p.Thr918Pro(p.T918P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349311:136349311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5605A>G |
| AA Mutation | p.Arg1869Gly(p.R1869G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136345456:136345456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1750T>G |
| AA Mutation | p.Leu584Val(p.L584V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136412309:136412309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144761853 |
| CDS Mutation | c.8980C>T |
| AA Mutation | p.Arg2994Trp(p.R2994W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136400033:136400033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8492C>T |
| AA Mutation | p.Ala2831Val(p.A2831V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136403258:136403258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8590A>G |
| AA Mutation | p.Met2864Val(p.M2864V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347426:136347426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3720C>A |
| AA Mutation | p.His1240Gln(p.H1240Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349281:136349281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773478883 |
| CDS Mutation | c.5575C>G |
| AA Mutation | p.Gln1859Glu(p.Q1859E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136323198:136323198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491T>C |
| AA Mutation | p.Leu164Pro(p.L164P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347287:136347287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3581G>A |
| AA Mutation | p.Gly1194Asp(p.G1194D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136350258:136350258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6552T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136414233:136414233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9111G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136345035:136345035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749064564 |
| CDS Mutation | c.1329C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349491:136349491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5785C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347915:136347915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4209G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136345797:136345797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748146182 |
| CDS Mutation | c.2091C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136348614:136348614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4908A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136348344:136348344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4638T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136363501:136363501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7302A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136344819:136344819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1113T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347945:136347945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4239T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136345803:136345803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2097T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136347177:136347177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3471C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349121:136349121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5415T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370652 |
| Start | 136349364:136349364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5658C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370652 |
| Start | 136344727:136344727(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs765131609 |
| CDS Mutation | c.1027delA |
| AA Mutation | p.Thr343ArgfsTer138(p.T343Rfs*138) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370652 |
| Start | 136322809:136322809(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.108delT |
| AA Mutation | p.Phe36LeufsTer8(p.F36Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370652 |
| Start | 136405906:136405906(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771931957 |
| CDS Mutation | c.8874delT |
| AA Mutation | p.Phe2958LeufsTer6(p.F2958Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |