Primary Site >> Stomach Cancer
Gene >> NF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31182616:31182616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.839T>C |
| AA Mutation | p.Ile280Thr(p.I280T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31330360:31330360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5674T>G |
| AA Mutation | p.Leu1892Val(p.L1892V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31360670:31360670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8344A>G |
| AA Mutation | p.Met2782Val(p.M2782V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000358273 |
| Start | 31229974:31229974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2990G>T |
| AA Mutation | p.Arg997Met(p.R997M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31214463:31214463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1405A>C |
| AA Mutation | p.Lys469Gln(p.K469Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31358977:31358977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8122T>G |
| AA Mutation | p.Phe2708Val(p.F2708V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31229200:31229200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2585C>T |
| AA Mutation | p.Thr862Ile(p.T862I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31337476:31337476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6536G>A |
| AA Mutation | p.Arg2179His(p.R2179H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31336461:31336461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6135G>T |
| AA Mutation | p.Leu2045Phe(p.L2045F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31338126:31338126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562367786 |
| CDS Mutation | c.6806G>A |
| AA Mutation | p.Arg2269His(p.R2269H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31229355:31229355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765848298 |
| CDS Mutation | c.2740C>T |
| AA Mutation | p.Arg914Trp(p.R914W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31233156:31233156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3651T>G |
| AA Mutation | p.Asp1217Glu(p.D1217E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31337557:31337557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6617C>G |
| AA Mutation | p.Thr2206Arg(p.T2206R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31206298:31206298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1319G>C |
| AA Mutation | p.Arg440Pro(p.R440P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31260381:31260381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4443T>A |
| AA Mutation | p.Asp1481Glu(p.D1481E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000358273 |
| Start | 31327839:31327839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs786202112 |
| CDS Mutation | c.5609G>A |
| AA Mutation | p.Arg1870Gln(p.R1870Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31223535:31223535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1813A>T |
| AA Mutation | p.Ile605Phe(p.I605F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31201472:31201472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1247G>A |
| AA Mutation | p.Arg416Gln(p.R416Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31350300:31350300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371151718 |
| CDS Mutation | c.7439A>G |
| AA Mutation | p.His2480Arg(p.H2480R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31223496:31223496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1774A>G |
| AA Mutation | p.Ser592Gly(p.S592G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31225225:31225225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151138158 |
| CDS Mutation | c.1976G>A |
| AA Mutation | p.Arg659Gln(p.R659Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31230874:31230874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3146T>C |
| AA Mutation | p.Val1049Ala(p.V1049A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31249057:31249057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4048A>G |
| AA Mutation | p.Ile1350Val(p.I1350V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358273 |
| Start | 31326010:31326010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756450772 |
| CDS Mutation | c.5026G>A |
| AA Mutation | p.Ala1676Thr(p.A1676T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31225133:31225133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555635097 |
| CDS Mutation | c.1884C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31327684:31327684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5454A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31326174:31326174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5190C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31327675:31327675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5445G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31349211:31349211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7281C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31335022:31335022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5997C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31229357:31229357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2742G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358273 |
| Start | 31232856:31232856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3471A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31159039:31159039(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.236delT |
| AA Mutation | p.Leu79TyrfsTer6(p.L79Yfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31350226:31350226(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7368delA |
| AA Mutation | p.Lys2456AsnfsTer33(p.K2456Nfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31357280:31357280(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7884delA |
| AA Mutation | p.Lys2628AsnfsTer16(p.K2628Nfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31350267:31350267(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7409delA |
| AA Mutation | p.Asn2470MetfsTer19(p.N2470Mfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31181474:31181475(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.640_641delAA |
| AA Mutation | p.Asn214Ter(p.N214*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31225126:31225126(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1882delT |
| AA Mutation | p.Tyr628ThrfsTer3(p.Y628Tfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358273 |
| Start | 31206360:31206360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1381C>T |
| AA Mutation | p.Arg461Ter(p.R461*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358273 |
| Start | 31358526:31358526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8017C>T |
| AA Mutation | p.Gln2673Ter(p.Q2673*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358273 |
| Start | 31169985:31169985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397514641 |
| CDS Mutation | c.574C>T |
| AA Mutation | p.Arg192Ter(p.R192*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358273 |
| Start | 31235664:31235664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3762C>A |
| AA Mutation | p.Tyr1254Ter(p.Y1254*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358273 |
| Start | 31374105:31374105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8470C>T |
| AA Mutation | p.Gln2824Ter(p.Q2824*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31226459:31226460(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs780157990 |
| CDS Mutation | c.2033dupC |
| AA Mutation | p.Ile679AspfsTer21(p.I679Dfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358273 |
| Start | 31265317:31265318(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4819dupT |
| AA Mutation | p.Tyr1607LeufsTer15(p.Y1607Lfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000358273 |
| Start | 31260368:31260368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4431-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000358273 |
| Start | 31360518:31360520(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8194_8196delGTT |
| AA Mutation | p.Val2732del(p.V2732del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000358273 |
| Start | 31327757:31327762(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5528_5533delCCAAGA |
| AA Mutation | p.Thr1843_Lys1844del(p.T1843_K1844del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000358273 |
| Start | 31229062:31229067(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2447_2452delGAATGT |
| AA Mutation | p.Arg816_Ser818delinsPro(p.R816_S818delinsP) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |