Primary Site >> Stomach Cancer
Gene >> NCOR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124430624:124430624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1046G>A |
| AA Mutation | p.Arg349His(p.R349H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124466220:124466220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.658G>A |
| AA Mutation | p.Glu220Lys(p.E220K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124372218:124372218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370196674 |
| CDS Mutation | c.2611G>A |
| AA Mutation | p.Glu871Lys(p.E871K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124342011:124342011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5000C>T |
| AA Mutation | p.Pro1667Leu(p.P1667L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124402458:124402458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376669119 |
| CDS Mutation | c.1586C>A |
| AA Mutation | p.Ala529Glu(p.A529E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124356746:124356746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3137C>T |
| AA Mutation | p.Pro1046Leu(p.P1046L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124437982:124437982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.830G>A |
| AA Mutation | p.Arg277Gln(p.R277Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124430726:124430726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.944G>A |
| AA Mutation | p.Arg315His(p.R315H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124348182:124348182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3977G>A |
| AA Mutation | p.Ser1326Asn(p.S1326N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124398172:124398172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1823A>C |
| AA Mutation | p.Glu608Ala(p.E608A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124400517:124400517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1797G>T |
| AA Mutation | p.Gln599His(p.Q599H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124385782:124385782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1982A>G |
| AA Mutation | p.Asn661Ser(p.N661S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124336963:124336963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747426729 |
| CDS Mutation | c.5905G>A |
| AA Mutation | p.Ala1969Thr(p.A1969T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124402503:124402503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768882087 |
| CDS Mutation | c.1541G>A |
| AA Mutation | p.Arg514His(p.R514H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124327594:124327594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6998C>T |
| AA Mutation | p.Ala2333Val(p.A2333V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124340153:124340153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753590635 |
| CDS Mutation | c.5540G>A |
| AA Mutation | p.Arg1847His(p.R1847H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124483687:124483687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.320G>A |
| AA Mutation | p.Arg107His(p.R107H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124400635:124400635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1679A>G |
| AA Mutation | p.Glu560Gly(p.E560G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124378309:124378309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771023965 |
| CDS Mutation | c.2095G>A |
| AA Mutation | p.Val699Met(p.V699M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124372209:124372209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2620C>G |
| AA Mutation | p.Pro874Ala(p.P874A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124426782:124426782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1168C>T |
| AA Mutation | p.Arg390Cys(p.R390C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124333232:124333232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6653G>A |
| AA Mutation | p.Gly2218Asp(p.G2218D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124336894:124336894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368518568 |
| CDS Mutation | c.5974G>A |
| AA Mutation | p.Ala1992Thr(p.A1992T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124342000:124342000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748517349 |
| CDS Mutation | c.5011C>T |
| AA Mutation | p.Arg1671Cys(p.R1671C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124378258:124378258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2146G>C |
| AA Mutation | p.Glu716Gln(p.E716Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124466258:124466258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776360455 |
| CDS Mutation | c.620C>T |
| AA Mutation | p.Pro207Leu(p.P207L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124378354:124378354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2050A>G |
| AA Mutation | p.Lys684Glu(p.K684E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124426682:124426682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370836867 |
| CDS Mutation | c.1268A>G |
| AA Mutation | p.Tyr423Cys(p.Y423C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124372554:124372554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747451283 |
| CDS Mutation | c.2275G>A |
| AA Mutation | p.Ala759Thr(p.A759T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124340101:124340101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5592C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124362262:124362262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552738969 |
| CDS Mutation | c.2964C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124341833:124341833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375290289 |
| CDS Mutation | c.5178G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124341998:124341998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201769852 |
| CDS Mutation | c.5013C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124343081:124343081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4860C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124340086:124340086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5607G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124350606:124350606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3825C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124430638:124430638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371011372 |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124336841:124336841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757282329 |
| CDS Mutation | c.6027G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124466254:124466254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772776811 |
| CDS Mutation | c.624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124354883:124354883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124348178:124348178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3981C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124372561:124372561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2268T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124340020:124340020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755595126 |
| CDS Mutation | c.5673G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124363682:124363682(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2925delC |
| AA Mutation | p.Ile976SerfsTer87(p.I976Sfs*87) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124400519:124400519(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1795delC |
| AA Mutation | p.Gln599SerfsTer11(p.Q599Sfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124354842:124354842(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3479delA |
| AA Mutation | p.Lys1160SerfsTer8(p.K1160Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124372291:124372291(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2538delC |
| AA Mutation | p.Ala847ArgfsTer117(p.A847Rfs*117) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124348255:124348255(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3904delC |
| AA Mutation | p.His1302MetfsTer12(p.H1302Mfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124348238:124348238(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3921delC |
| AA Mutation | p.Lys1308SerfsTer6(p.K1308Sfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124356743:124356743(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3140delC |
| AA Mutation | p.Pro1047LeufsTer16(p.P1047Lfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124402544:124402544(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1500delG |
| AA Mutation | p.Gln500HisfsTer110(p.Q500Hfs*110) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124402546:124402547(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1497_1498delGC |
| AA Mutation | p.Gln500AlafsTer22(p.Q500Afs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405201 |
| Start | 124362269:124362270(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs746871841 |
| CDS Mutation | c.2956dupC |
| AA Mutation | p.Arg986ProfsTer76(p.R986Pfs*76) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |