Primary Site >> Stomach Cancer
Gene >> TRIO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14492717:14492717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369051747 |
| CDS Mutation | c.7783G>A |
| AA Mutation | p.Ala2595Thr(p.A2595T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14498145:14498145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200412299 |
| CDS Mutation | c.8104G>A |
| AA Mutation | p.Val2702Ile(p.V2702I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14291100:14291100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925C>T |
| AA Mutation | p.Pro309Ser(p.P309S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14368774:14368774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774072211 |
| CDS Mutation | c.2941G>A |
| AA Mutation | p.Asp981Asn(p.D981N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14462836:14462836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5578G>T |
| AA Mutation | p.Gly1860Cys(p.G1860C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14378045:14378045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3365G>T |
| AA Mutation | p.Arg1122Met(p.R1122M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14291056:14291056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.881A>T |
| AA Mutation | p.Lys294Ile(p.K294I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14297233:14297233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1338G>A |
| AA Mutation | p.Met446Ile(p.M446I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14488201:14488201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7573C>T |
| AA Mutation | p.Arg2525Cys(p.R2525C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14280366:14280366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767723793 |
| CDS Mutation | c.277C>T |
| AA Mutation | p.Arg93Cys(p.R93C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14471385:14471385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5831C>A |
| AA Mutation | p.Pro1944His(p.P1944H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14485195:14485195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6784T>C |
| AA Mutation | p.Trp2262Arg(p.W2262R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14363784:14363784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2444A>G |
| AA Mutation | p.Asp815Gly(p.D815G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14405912:14405912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4781C>T |
| AA Mutation | p.Thr1594Met(p.T1594M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14507927:14507927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8799A>C |
| AA Mutation | p.Lys2933Asn(p.K2933N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14485136:14485136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55916212 |
| CDS Mutation | c.6725C>T |
| AA Mutation | p.Thr2242Met(p.T2242M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14359436:14359436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2296G>A |
| AA Mutation | p.Glu766Lys(p.E766K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14507135:14507135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755026998 |
| CDS Mutation | c.8626C>T |
| AA Mutation | p.Arg2876Cys(p.R2876C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14358317:14358317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2186A>C |
| AA Mutation | p.Lys729Thr(p.K729T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14291124:14291124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368654118 |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Arg317Trp(p.R317W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000344204 |
| Start | 14498521:14498521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8213A>G |
| AA Mutation | p.Asp2738Gly(p.D2738G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14508346:14508346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9218G>A |
| AA Mutation | p.Arg3073His(p.R3073H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14462857:14462857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774835487 |
| CDS Mutation | c.5599G>A |
| AA Mutation | p.Val1867Met(p.V1867M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14290915:14290915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.740C>T |
| AA Mutation | p.Pro247Leu(p.P247L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14387560:14387560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3693C>A |
| AA Mutation | p.Phe1231Leu(p.F1231L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14369445:14369445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3138G>T |
| AA Mutation | p.Lys1046Asn(p.K1046N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14481572:14481572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6419G>T |
| AA Mutation | p.Arg2140Met(p.R2140M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14485130:14485130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6719C>T |
| AA Mutation | p.Ser2240Leu(p.S2240L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14389316:14389316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3976G>A |
| AA Mutation | p.Val1326Met(p.V1326M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14498599:14498599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8291A>C |
| AA Mutation | p.Asp2764Ala(p.D2764A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14366914:14366914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751285174 |
| CDS Mutation | c.2809G>A |
| AA Mutation | p.Ala937Thr(p.A937T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14400982:14400982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4634C>T |
| AA Mutation | p.Thr1545Ile(p.T1545I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344204 |
| Start | 14316645:14316645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1633C>A |
| AA Mutation | p.Leu545Met(p.L545M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14364786:14364786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2724G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14405943:14405943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4812C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14363746:14363746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141315662 |
| CDS Mutation | c.2406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14462772:14462772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764203841 |
| CDS Mutation | c.5514C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14366880:14366880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370683728 |
| CDS Mutation | c.2775C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14462820:14462820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5562C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14280416:14280416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.327C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14462868:14462868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138509776 |
| CDS Mutation | c.5610G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14387749:14387749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3783A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14461290:14461290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5475G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14504483:14504483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8502C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14461281:14461281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5466G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14359447:14359447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200525310 |
| CDS Mutation | c.2307G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14488176:14488176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7548C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344204 |
| Start | 14504540:14504540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754497690 |
| CDS Mutation | c.8559C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000344204 |
| Start | 14476895:14476895(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752676391 |
| CDS Mutation | c.6092delT |
| AA Mutation | p.Leu2031Ter(p.L2031*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344204 |
| Start | 14487672:14487672(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs746654944 |
| CDS Mutation | c.7050delC |
| AA Mutation | p.Val2351CysfsTer62(p.V2351Cfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344204 |
| Start | 14482585:14482585(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.6472delA |
| AA Mutation | p.Ile2158SerfsTer63(p.I2158Sfs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344204 |
| Start | 14488047:14488047(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774597492 |
| CDS Mutation | c.7425delC |
| AA Mutation | p.Ser2476AlafsTer51(p.S2476Afs*51) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344204 |
| Start | 14387518:14387518(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3657delA |
| AA Mutation | p.Lys1219AsnfsTer43(p.K1219Nfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344204 |
| Start | 14462844:14462844(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5590delG |
| AA Mutation | p.Ala1864ProfsTer32(p.A1864Pfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000344204 |
| Start | 14419850:14419850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749963113 |
| CDS Mutation | c.5032C>T |
| AA Mutation | p.Arg1678Ter(p.R1678*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000344204 |
| Start | 14381199:14381199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3517C>T |
| AA Mutation | p.Gln1173Ter(p.Q1173*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344204 |
| Start | 14488046:14488047(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.7424_7425dupCC |
| AA Mutation | p.Ser2476ProfsTer52(p.S2476Pfs*52) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |