Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NCOR2

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000405201
Start 124354839:124354839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3482T>C
AA Mutation p.Leu1161Pro(p.L1161P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124326194:124326194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7360G>A
AA Mutation p.Ala2454Thr(p.A2454T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124344728:124344728(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4583T>C
AA Mutation p.Val1528Ala(p.V1528A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124333259:124333259(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749006415
CDS Mutation c.6626C>T
AA Mutation p.Thr2209Met(p.T2209M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124344702:124344702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4609C>T
AA Mutation p.Arg1537Trp(p.R1537W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124362138:124362138(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs536539471
CDS Mutation c.3088G>A
AA Mutation p.Ala1030Thr(p.A1030T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124347899:124347899(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs562298385
CDS Mutation c.3998G>A
AA Mutation p.Arg1333His(p.R1333H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124336761:124336761(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775458405
CDS Mutation c.6107G>A
AA Mutation p.Arg2036His(p.R2036H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000405201
Start 124473131:124473131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.412G>T
AA Mutation p.Asp138Tyr(p.D138Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124372440:124372440(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2389A>G
AA Mutation p.Thr797Ala(p.T797A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124486558:124486558(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.116T>G
AA Mutation p.Leu39Arg(p.L39R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124342053:124342053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774193502
CDS Mutation c.4958G>A
AA Mutation p.Arg1653Gln(p.R1653Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124378369:124378369(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367654646
CDS Mutation c.2035G>A
AA Mutation p.Ala679Thr(p.A679T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124466207:124466207(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760665839
CDS Mutation c.671G>A
AA Mutation p.Arg224His(p.R224H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124327435:124327435(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552340226
CDS Mutation c.7157G>A
AA Mutation p.Arg2386Gln(p.R2386Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124347890:124347890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4007C>T
AA Mutation p.Pro1336Leu(p.P1336L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124362207:124362207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3019C>T
AA Mutation p.Pro1007Ser(p.P1007S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124419991:124419991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1448T>C
AA Mutation p.Val483Ala(p.V483A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
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
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124343115:124343115(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767880178
CDS Mutation c.4826C>T
AA Mutation p.Ser1609Leu(p.S1609L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124378359:124378359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2045A>G
AA Mutation p.Lys682Arg(p.K682R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124327544:124327544(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7048A>G
AA Mutation p.Lys2350Glu(p.K2350E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124495247:124495247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200569241
CDS Mutation c.5C>T
AA Mutation p.Ser2Leu(p.S2L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124335166:124335166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6380A>G
AA Mutation p.Gln2127Arg(p.Q2127R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124483717:124483717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.290A>C
AA Mutation p.Lys97Thr(p.K97T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124430727:124430727(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.943C>T
AA Mutation p.Arg315Cys(p.R315C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124344810:124344810(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4501C>T
AA Mutation p.Arg1501Cys(p.R1501C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124420037:124420037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1402C>A
AA Mutation p.Leu468Ile(p.L468I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124335529:124335529(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6219G>T
AA Mutation p.Glu2073Asp(p.E2073D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124346593:124346593(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766376384
CDS Mutation c.4330C>T
AA Mutation p.Arg1444Trp(p.R1444W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124355442:124355442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3371C>T
AA Mutation p.Ala1124Val(p.A1124V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124355520:124355520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375804883
CDS Mutation c.3293G>A
AA Mutation p.Arg1098His(p.R1098H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124372291:124372291(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532518067
CDS Mutation c.2538C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124326219:124326219(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766761610
CDS Mutation c.7335C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124327440:124327440(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375299131
CDS Mutation c.7152C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124348235:124348235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3924G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124336838:124336838(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371641181
CDS Mutation c.6030G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124402424:124402424(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765176410
CDS Mutation c.1620C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124344853:124344853(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs560814961
CDS Mutation c.4458C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124326363:124326363(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs536482449
CDS Mutation c.7191C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124378310:124378310(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776612196
CDS Mutation c.2094C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124372159:124372159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780909563
CDS Mutation c.2670G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124325435:124325435(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7512C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124346741:124346741(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771028465
CDS Mutation c.4182C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124344934:124344934(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370364401
CDS Mutation c.4377C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124372135:124372135(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200016013
CDS Mutation c.2694C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124350675:124350675(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748022862
CDS Mutation c.3756G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124346807:124346807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4116T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124466215:124466215(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755095650
CDS Mutation c.663G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124340119:124340119(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200208502
CDS Mutation c.5574G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124356705:124356705(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs771862790
CDS Mutation c.3178delC
AA Mutation p.Arg1060ValfsTer3(p.R1060Vfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 52
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124473090:124473090(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.453delC
AA Mutation p.Ser152AlafsTer21(p.S152Afs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124346710:124346710(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4213delC
AA Mutation p.Leu1405Ter(p.L1405*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124372308:124372308(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2521delG
AA Mutation p.Glu841ArgfsTer123(p.E841Rfs*123)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124362270:124362270(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2956delC
AA Mutation p.Arg986GlyfsTer77(p.R986Gfs*77)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124457117:124457117(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.751delC
AA Mutation p.Gln251ArgfsTer22(p.Q251Rfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 57
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
Mutation ID 58
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
Mutation ID 59
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
Mutation ID 60
Mutation Consequence inframe_deletion
Transcription ID ENST00000405201
Start 124340362:124340367(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5415_5420delCCGGGA
AA Mutation p.Asp1807_Arg1808del(p.D1807_R1808del)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> NCOR2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124337136:124337136(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5732C>T
AA Mutation p.Pro1911Leu(p.P1911L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124354112:124354112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3674A>G
AA Mutation p.Tyr1225Cys(p.Y1225C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000405201
Start 124336827:124336827(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762352790
CDS Mutation c.6041C>T
AA Mutation p.Ser2014Leu(p.S2014L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000405201
Start 124343009:124343009(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760461669
CDS Mutation c.4932C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
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
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000405201
Start 124400518:124400519(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1795dupC
AA Mutation p.Gln599ProfsTer13(p.Q599Pfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript