Primary Site >> Stomach Cancer
Gene >> ADAMTS18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77322422:77322422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2077T>A |
| AA Mutation | p.Phe693Ile(p.F693I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77363868:77363868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.990A>C |
| AA Mutation | p.Lys330Asn(p.K330N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293200:77293200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3065C>T |
| AA Mutation | p.Ala1022Val(p.A1022V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293198:77293198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370743740 |
| CDS Mutation | c.3067G>A |
| AA Mutation | p.Ala1023Thr(p.A1023T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77320063:77320063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2318G>A |
| AA Mutation | p.Gly773Asp(p.G773D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77359417:77359417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1223C>T |
| AA Mutation | p.Ala408Val(p.A408V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293197:77293197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3068C>T |
| AA Mutation | p.Ala1023Val(p.A1023V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293077:77293077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3188A>G |
| AA Mutation | p.Glu1063Gly(p.E1063G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77322430:77322430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2069A>G |
| AA Mutation | p.Asn690Ser(p.N690S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282849 |
| Start | 77335902:77335902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1713G>C |
| AA Mutation | p.Trp571Cys(p.W571C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77356009:77356009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1391C>G |
| AA Mutation | p.Thr464Arg(p.T464R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77335865:77335865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149189203 |
| CDS Mutation | c.1750G>A |
| AA Mutation | p.Gly584Arg(p.G584R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77300386:77300386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2551A>G |
| AA Mutation | p.Asn851Asp(p.N851D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77362176:77362176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145G>T |
| AA Mutation | p.Arg382Ile(p.R382I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77367512:77367512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.707C>A |
| AA Mutation | p.Ser236Tyr(p.S236Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77335780:77335780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835A>G |
| AA Mutation | p.Gln612Arg(p.Q612R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77367693:77367693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526T>A |
| AA Mutation | p.Phe176Ile(p.F176I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77319934:77319934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2447G>T |
| AA Mutation | p.Gly816Val(p.G816V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77291378:77291378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150975249 |
| CDS Mutation | c.3290G>A |
| AA Mutation | p.Arg1097His(p.R1097H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77289294:77289294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3520A>G |
| AA Mutation | p.Thr1174Ala(p.T1174A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77319906:77319906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756053041 |
| CDS Mutation | c.2475C>A |
| AA Mutation | p.Phe825Leu(p.F825L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282849 |
| Start | 77359421:77359421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1219T>G |
| AA Mutation | p.Phe407Val(p.F407V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77431521:77431521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758362638 |
| CDS Mutation | c.269C>T |
| AA Mutation | p.Ala90Val(p.A90V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77356034:77356034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1366G>A |
| AA Mutation | p.Ala456Thr(p.A456T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77367668:77367668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.551T>C |
| AA Mutation | p.Leu184Pro(p.L184P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77297341:77297341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2749A>C |
| AA Mutation | p.Thr917Pro(p.T917P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77325885:77325885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2013A>C |
| AA Mutation | p.Lys671Asn(p.K671N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77364219:77364219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941T>A |
| AA Mutation | p.Val314Asp(p.V314D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293230:77293230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3035G>T |
| AA Mutation | p.Arg1012Met(p.R1012M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293225:77293225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200775058 |
| CDS Mutation | c.3040C>T |
| AA Mutation | p.Arg1014Cys(p.R1014C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77284040:77284040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3582G>T |
| AA Mutation | p.Trp1194Cys(p.W1194C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77335836:77335836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559246837 |
| CDS Mutation | c.1779C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77322348:77322348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762433658 |
| CDS Mutation | c.2151C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77300312:77300312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2625C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77289331:77289331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3483G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77431574:77431574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80153679 |
| CDS Mutation | c.216C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77300372:77300372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770824755 |
| CDS Mutation | c.2565T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77353784:77353784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1563T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77295022:77295022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140716153 |
| CDS Mutation | c.2907A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282849 |
| Start | 77322414:77322414(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772504358 |
| CDS Mutation | c.2085delT |
| AA Mutation | p.Phe695LeufsTer7(p.F695Lfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000282849 |
| Start | 77431528:77431528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191773926 |
| CDS Mutation | c.262C>T |
| AA Mutation | p.Arg88Ter(p.R88*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282849 |
| Start | 77294976:77294977(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2952dupA |
| AA Mutation | p.Ala985SerfsTer31(p.A985Sfs*31) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000282849 |
| Start | 77362201:77362212(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1109_1120delAATGGCAGTCTG |
| AA Mutation | p.Gln370_Ala374delinsPro(p.Q370_A374delinsP) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | inframe_insertion;splice_region_variant |
| Transcription ID | ENST00000282849 |
| Start | 77363883:77363884(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.973-1_974dupGGT |
| AA Mutation | p.Val325dup(p.V325dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |