Primary Site >> Stomach Cancer
Gene >> CREBBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731861:3731861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4805G>A |
| AA Mutation | p.Arg1602His(p.R1602H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3850560:3850560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758740001 |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Ala179Thr(p.A179T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3729643:3729643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5404G>A |
| AA Mutation | p.Val1802Met(p.V1802M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3729496:3729496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5551C>A |
| AA Mutation | p.Arg1851Ser(p.R1851S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3740493:3740493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4039C>T |
| AA Mutation | p.Arg1347Trp(p.R1347W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3773776:3773776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150767375 |
| CDS Mutation | c.2438C>T |
| AA Mutation | p.Pro813Leu(p.P813L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731464:3731464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4900G>A |
| AA Mutation | p.Val1634Met(p.V1634M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3738616:3738616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4337G>A |
| AA Mutation | p.Arg1446His(p.R1446H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728386:3728386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6661A>G |
| AA Mutation | p.Met2221Val(p.M2221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3770835:3770835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747877878 |
| CDS Mutation | c.2615C>T |
| AA Mutation | p.Thr872Met(p.T872M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3757912:3757912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3506G>A |
| AA Mutation | p.Arg1169His(p.R1169H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728007:3728007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182347573 |
| CDS Mutation | c.7040C>T |
| AA Mutation | p.Ala2347Val(p.A2347V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728616:3728616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6431C>T |
| AA Mutation | p.Ala2144Val(p.A2144V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731416:3731416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776549587 |
| CDS Mutation | c.4948G>A |
| AA Mutation | p.Val1650Ile(p.V1650I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728017:3728017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7030C>T |
| AA Mutation | p.Arg2344Trp(p.R2344W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731301:3731301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781364836 |
| CDS Mutation | c.5063C>T |
| AA Mutation | p.Thr1688Met(p.T1688M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3736654:3736654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4556A>G |
| AA Mutation | p.Tyr1519Cys(p.Y1519C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3758952:3758952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3271C>T |
| AA Mutation | p.Arg1091Cys(p.R1091C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3736798:3736798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4412T>A |
| AA Mutation | p.Ile1471Asn(p.I1471N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728833:3728833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6214C>T |
| AA Mutation | p.Arg2072Trp(p.R2072W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731862:3731862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4804C>T |
| AA Mutation | p.Arg1602Cys(p.R1602C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3770607:3770607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2843A>G |
| AA Mutation | p.Gln948Arg(p.Q948R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3745298:3745298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3893A>G |
| AA Mutation | p.Tyr1298Cys(p.Y1298C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262367 |
| Start | 3749627:3749627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749189606 |
| CDS Mutation | c.3836C>T |
| AA Mutation | p.Pro1279Leu(p.P1279L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3770944:3770944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2506C>A |
| AA Mutation | p.Leu836Met(p.L836M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3774573:3774573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2279C>A |
| AA Mutation | p.Pro760Gln(p.P760Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3727762:3727762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7285G>A |
| AA Mutation | p.Asp2429Asn(p.D2429N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3736140:3736140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4624G>A |
| AA Mutation | p.Gly1542Ser(p.G1542S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3793415:3793415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1187C>T |
| AA Mutation | p.Thr396Met(p.T396M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728451:3728451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765821935 |
| CDS Mutation | c.6596A>T |
| AA Mutation | p.Gln2199Leu(p.Q2199L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262367 |
| Start | 3729496:3729496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763253161 |
| CDS Mutation | c.5551C>T |
| AA Mutation | p.Arg1851Cys(p.R1851C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728852:3728852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374150949 |
| CDS Mutation | c.6195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3778748:3778748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1893C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731198:3731198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5166G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728765:3728765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772950054 |
| CDS Mutation | c.6282G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3736096:3736096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749565984 |
| CDS Mutation | c.4668A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3729596:3729596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373848722 |
| CDS Mutation | c.5451G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3793432:3793432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3850609:3850609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753948670 |
| CDS Mutation | c.486G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3736680:3736680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372936553 |
| CDS Mutation | c.4530G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3770834:3770834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781112420 |
| CDS Mutation | c.2616G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3727886:3727886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3850420:3850420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140708841 |
| CDS Mutation | c.675G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731926:3731926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563033919 |
| CDS Mutation | c.4740C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3778787:3778787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61754522 |
| CDS Mutation | c.1854C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728705:3728705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731372:3731372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756979739 |
| CDS Mutation | c.4992C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262367 |
| Start | 3793433:3793433(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1169delA |
| AA Mutation | p.Asn390ThrfsTer3(p.N390Tfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262367 |
| Start | 3727897:3727897(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.7150delC |
| AA Mutation | p.His2384ThrfsTer12(p.H2384Tfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000262367 |
| Start | 3767720:3767720(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3250delA |
| AA Mutation | p.Ile1084SerfsTer15(p.I1084Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262367 |
| Start | 3731889:3731889(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4777delA |
| AA Mutation | p.Thr1593ProfsTer42(p.T1593Pfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262367 |
| Start | 3728281:3728281(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6766delC |
| AA Mutation | p.Leu2256SerfsTer46(p.L2256Sfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262367 |
| Start | 3739628:3739628(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4230delT |
| AA Mutation | p.Phe1410LeufsTer49(p.F1410Lfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262367 |
| Start | 3736718:3736718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4492C>T |
| AA Mutation | p.Arg1498Ter(p.R1498*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262367 |
| Start | 3740454:3740454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587783490 |
| CDS Mutation | c.4078C>T |
| AA Mutation | p.Arg1360Ter(p.R1360*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |