Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NCOR1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16064938:16064938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5033T>A
AA Mutation p.Ile1678Asn(p.I1678N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16121061:16121061(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1843C>G
AA Mutation p.Pro615Ala(p.P615A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16070181:16070181(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4497G>T
AA Mutation p.Met1499Ile(p.M1499I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16070354:16070354(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4324G>A
AA Mutation p.Glu1442Lys(p.E1442K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16034878:16034878(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7022G>T
AA Mutation p.Gly2341Val(p.G2341V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16101667:16101667(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2273A>G
AA Mutation p.Glu758Gly(p.E758G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000268712
Start 16108912:16108912(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2056A>T
AA Mutation p.Thr686Ser(p.T686S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000268712
Start 16046952:16046952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6678G>T
AA Mutation p.Met2226Ile(p.M2226I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16032375:16032375(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7244A>G
AA Mutation p.Gln2415Arg(p.Q2415R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16062126:16062126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5366C>A
AA Mutation p.Pro1789Gln(p.P1789Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16071626:16071626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3935T>C
AA Mutation p.Leu1312Pro(p.L1312P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16121166:16121166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1738C>T
AA Mutation p.Arg580Cys(p.R580C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16146529:16146529(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.929G>A
AA Mutation p.Arg310His(p.R310H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16034815:16034815(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7085A>G
AA Mutation p.Tyr2362Cys(p.Y2362C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16057953:16057953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6122A>G
AA Mutation p.Gln2041Arg(p.Q2041R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16057628:16057628(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6278T>C
AA Mutation p.Val2093Ala(p.V2093A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16171816:16171816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.422C>T
AA Mutation p.Ala141Val(p.A141V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16080025:16080025(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3440G>A
AA Mutation p.Gly1147Glu(p.G1147E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16065553:16065553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772605440
CDS Mutation c.4883G>A
AA Mutation p.Arg1628His(p.R1628H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16032447:16032447(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7172G>A
AA Mutation p.Arg2391Gln(p.R2391Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16048935:16048935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6446C>A
AA Mutation p.Pro2149His(p.P2149H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16108851:16108851(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2117T>C
AA Mutation p.Val706Ala(p.V706A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16080707:16080707(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3198G>T
AA Mutation p.Leu1066Phe(p.L1066F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16070483:16070483(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4195A>G
AA Mutation p.Ile1399Val(p.I1399V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16047082:16047082(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201721277
CDS Mutation c.6548G>A
AA Mutation p.Arg2183His(p.R2183H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16086361:16086361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776976570
CDS Mutation c.3098C>T
AA Mutation p.Pro1033Leu(p.P1033L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16091919:16091919(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2960G>A
AA Mutation p.Cys987Tyr(p.C987Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16194470:16194470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.100C>A
AA Mutation p.His34Asn(p.H34N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16065690:16065690(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780188590
CDS Mutation c.4746G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16070421:16070421(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143182424
CDS Mutation c.4257G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16068006:16068006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4629C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16101669:16101669(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781757424
CDS Mutation c.2271G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16071436:16071436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4125G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16064964:16064964(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5007A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16108889:16108889(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2079G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16121065:16121065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145739289
CDS Mutation c.1839G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16139094:16139094(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761867754
CDS Mutation c.1266G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16139166:16139166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1194G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16057696:16057696(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6210G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16101570:16101570(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2370T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000268712
Start 16065526:16065526(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4910delC
AA Mutation p.Pro1637GlnfsTer19(p.P1637Qfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000268712
Start 16121191:16121191(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1713delG
AA Mutation p.Arg572GlufsTer18(p.R572Efs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000268712
Start 16146495:16146495(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.963delA
AA Mutation p.Val322TrpfsTer4(p.V322Wfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000268712
Start 16121226:16121226(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1678G>T
AA Mutation p.Glu560Ter(p.E560*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence stop_gained
Transcription ID ENST00000268712
Start 16039466:16039466(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6922C>T
AA Mutation p.Arg2308Ter(p.R2308*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence stop_gained
Transcription ID ENST00000268712
Start 16098390:16098390(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2797C>T
AA Mutation p.Arg933Ter(p.R933*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000268712
Start 16065020:16065020(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4952-1G>T
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> NCOR1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16061710:16061710(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5572G>T
AA Mutation p.Ala1858Ser(p.A1858S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16062111:16062111(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5381G>A
AA Mutation p.Arg1794Gln(p.R1794Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16080470:16080470(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150513105
CDS Mutation c.3338G>A
AA Mutation p.Arg1113Gln(p.R1113Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16080620:16080620(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3285A>C
AA Mutation p.Glu1095Asp(p.E1095D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16139178:16139178(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1182G>T
AA Mutation p.Glu394Asp(p.E394D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16108861:16108861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2107G>A
AA Mutation p.Ala703Thr(p.A703T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16153367:16153367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.761T>G
AA Mutation p.Phe254Cys(p.F254C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000268712
Start 16101623:16101623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2317A>T
AA Mutation p.Lys773Ter(p.K773*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000268712
Start 16101524:16101524(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2416G>T
AA Mutation p.Glu806Ter(p.E806*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript