Primary Site >> Stomach Cancer
Gene >> ASH1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155370637:155370637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6568G>C |
| AA Mutation | p.Glu2190Gln(p.E2190Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155347772:155347772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7702A>G |
| AA Mutation | p.Ser2568Gly(p.S2568G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478316:155478316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754691861 |
| CDS Mutation | c.4554A>C |
| AA Mutation | p.Arg1518Ser(p.R1518S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155357668:155357668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6892A>G |
| AA Mutation | p.Lys2298Glu(p.K2298E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478966:155478966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746450493 |
| CDS Mutation | c.3904C>T |
| AA Mutation | p.Arg1302Trp(p.R1302W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480722:155480722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2148A>C |
| AA Mutation | p.Lys716Asn(p.K716N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155349358:155349358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7538C>T |
| AA Mutation | p.Ala2513Val(p.A2513V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478981:155478981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3889C>T |
| AA Mutation | p.Arg1297Cys(p.R1297C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155343686:155343686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8053C>T |
| AA Mutation | p.Arg2685Cys(p.R2685C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155380066:155380066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6169C>A |
| AA Mutation | p.Leu2057Ile(p.L2057I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479848:155479848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3022T>C |
| AA Mutation | p.Ser1008Pro(p.S1008P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480362:155480362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2508G>A |
| AA Mutation | p.Met836Ile(p.M836I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155521296:155521296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224T>C |
| AA Mutation | p.Val75Ala(p.V75A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480541:155480541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150671158 |
| CDS Mutation | c.2329C>T |
| AA Mutation | p.Arg777Cys(p.R777C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478908:155478908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3962G>A |
| AA Mutation | p.Arg1321Gln(p.R1321Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155349392:155349392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7504A>G |
| AA Mutation | p.Thr2502Ala(p.T2502A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480627:155480627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2243G>A |
| AA Mutation | p.Ser748Asn(p.S748N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478135:155478135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4735T>C |
| AA Mutation | p.Cys1579Arg(p.C1579R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478084:155478084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4786G>C |
| AA Mutation | p.Glu1596Gln(p.E1596Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155354508:155354508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7193A>G |
| AA Mutation | p.Asn2398Ser(p.N2398S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479482:155479482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3388C>T |
| AA Mutation | p.Pro1130Ser(p.P1130S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155342076:155342076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8335G>A |
| AA Mutation | p.Asp2779Asn(p.D2779N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478705:155478705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4165T>G |
| AA Mutation | p.Ser1389Ala(p.S1389A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480697:155480697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765574300 |
| CDS Mutation | c.2173A>G |
| AA Mutation | p.Arg725Gly(p.R725G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479560:155479560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3310C>G |
| AA Mutation | p.Pro1104Ala(p.P1104A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480372:155480372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2498C>G |
| AA Mutation | p.Ser833Cys(p.S833C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155481627:155481627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1243G>T |
| AA Mutation | p.Gly415Cys(p.G415C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155370852:155370852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6479G>A |
| AA Mutation | p.Arg2160Lys(p.R2160K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155521366:155521366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199618784 |
| CDS Mutation | c.154C>T |
| AA Mutation | p.Arg52Trp(p.R52W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478324:155478324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4546C>T |
| AA Mutation | p.Arg1516Cys(p.R1516C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479253:155479253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3617A>T |
| AA Mutation | p.Asp1206Val(p.D1206V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155481182:155481182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1688C>G |
| AA Mutation | p.Ser563Cys(p.S563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155347861:155347861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138122556 |
| CDS Mutation | c.7613G>A |
| AA Mutation | p.Arg2538His(p.R2538H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479721:155479721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3149G>A |
| AA Mutation | p.Arg1050Lys(p.R1050K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155438683:155438683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5472C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155357393:155357393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6993G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155481547:155481547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1323T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155338312:155338312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8595A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155481934:155481934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.936T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155482159:155482159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757122382 |
| CDS Mutation | c.711G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155521424:155521424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.96C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155337711:155337711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8859G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368346 |
| Start | 155352722:155352722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7365T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479205:155479205(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3665delA |
| AA Mutation | p.Lys1222ArgfsTer11(p.K1222Rfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155478228:155478228(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4642delA |
| AA Mutation | p.Ser1548AlafsTer2(p.S1548Afs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155481899:155481899(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.971delA |
| AA Mutation | p.Lys324SerfsTer8(p.K324Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155482001:155482001(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.869delA |
| AA Mutation | p.Lys290SerfsTer8(p.K290Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479962:155479962(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2908delA |
| AA Mutation | p.Ile970LeufsTer9(p.I970Lfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480325:155480325(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2545delA |
| AA Mutation | p.Ile849SerfsTer49(p.I849Sfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155338209:155338209(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761154268 |
| CDS Mutation | c.8698delA |
| AA Mutation | p.Thr2900GlnfsTer44(p.T2900Qfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368346 |
| Start | 155478954:155478954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3916C>T |
| AA Mutation | p.Arg1306Ter(p.R1306*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155480911:155480912(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1958dupA |
| AA Mutation | p.Pro654AlafsTer6(p.P654Afs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155479961:155479962(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2908dupA |
| AA Mutation | p.Ile970AsnfsTer19(p.I970Nfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155482051:155482052(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.818dupA |
| AA Mutation | p.Pro274AlafsTer12(p.P274Afs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368346 |
| Start | 155380123:155380124(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.6111dupT |
| AA Mutation | p.Val2038CysfsTer12(p.V2038Cfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000368346 |
| Start | 155521518:155521518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756914885 |
| CDS Mutation | c.2T>C |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |