Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CUL9

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43188678:43188678(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571511276
CDS Mutation c.2143C>T
AA Mutation p.Arg715Trp(p.R715W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43198746:43198746(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374241248
CDS Mutation c.2941G>A
AA Mutation p.Val981Met(p.V981M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43187039:43187039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1331A>C
AA Mutation p.Glu444Ala(p.E444A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43204467:43204467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368858642
CDS Mutation c.4267C>T
AA Mutation p.Arg1423Cys(p.R1423C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43206366:43206366(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5068G>A
AA Mutation p.Asp1690Asn(p.D1690N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43220822:43220822(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756946015
CDS Mutation c.6499G>A
AA Mutation p.Asp2167Asn(p.D2167N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43224157:43224157(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755209921
CDS Mutation c.7347G>A
AA Mutation p.Met2449Ile(p.M2449I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43198846:43198846(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3041C>A
AA Mutation p.Ser1014Tyr(p.S1014Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43204768:43204768(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557163267
CDS Mutation c.4360C>T
AA Mutation p.Arg1454Trp(p.R1454W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43216252:43216252(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6031C>T
AA Mutation p.Arg2011Cys(p.R2011C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43213856:43213856(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759125679
CDS Mutation c.5632C>T
AA Mutation p.Arg1878Cys(p.R1878C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43206147:43206147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368997213
CDS Mutation c.4934G>A
AA Mutation p.Arg1645His(p.R1645H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43193089:43193089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2269C>A
AA Mutation p.Leu757Met(p.L757M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43203547:43203547(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751503492
CDS Mutation c.3980G>A
AA Mutation p.Arg1327Gln(p.R1327Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43213886:43213886(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5662C>A
AA Mutation p.Leu1888Ile(p.L1888I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43193072:43193072(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2252C>T
AA Mutation p.Ala751Val(p.A751V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43187807:43187807(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1676C>T
AA Mutation p.Thr559Ile(p.T559I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43193113:43193113(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755755698
CDS Mutation c.2293C>T
AA Mutation p.Arg765Trp(p.R765W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43200020:43200020(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3248T>C
AA Mutation p.Ile1083Thr(p.I1083T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43213256:43213256(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769189873
CDS Mutation c.5320G>A
AA Mutation p.Val1774Met(p.V1774M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43213872:43213872(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5648A>G
AA Mutation p.His1883Arg(p.H1883R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43206012:43206012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4799A>G
AA Mutation p.Tyr1600Cys(p.Y1600C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000252050
Start 43204857:43204857(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4449G>T
AA Mutation p.Gln1483His(p.Q1483H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43186147:43186147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765124435
CDS Mutation c.943C>T
AA Mutation p.Arg315Trp(p.R315W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43205402:43205402(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4772C>T
AA Mutation p.Thr1591Ile(p.T1591I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43184860:43184860(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.550C>T
AA Mutation p.Arg184Trp(p.R184W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43196096:43196096(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2416T>C
AA Mutation p.Ser806Pro(p.S806P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43188555:43188555(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368734594
CDS Mutation c.2020C>T
AA Mutation p.Arg674Cys(p.R674C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43184728:43184728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.418G>A
AA Mutation p.Ala140Thr(p.A140T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43184617:43184617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.307G>T
AA Mutation p.Asp103Tyr(p.D103Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43206042:43206042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376817499
CDS Mutation c.4829C>T
AA Mutation p.Ser1610Leu(p.S1610L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43186423:43186423(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs535350840
CDS Mutation c.1219C>T
AA Mutation p.Arg407Trp(p.R407W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43221273:43221273(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6704G>A
AA Mutation p.Arg2235His(p.R2235H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43221285:43221285(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6716G>C
AA Mutation p.Cys2239Ser(p.C2239S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43187742:43187742(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1611C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43203464:43203464(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3897G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43222584:43222584(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150159860
CDS Mutation c.6975G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43216248:43216248(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150965930
CDS Mutation c.6027G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43184766:43184766(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115556089
CDS Mutation c.456C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43223295:43223295(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7182C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43220866:43220866(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761300039
CDS Mutation c.6543C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43220581:43220581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771839457
CDS Mutation c.6405G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43186416:43186416(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781457405
CDS Mutation c.1212C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000252050
Start 43186268:43186268(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1068delC
AA Mutation p.Arg357GlufsTer138(p.R357Efs*138)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence stop_gained
Transcription ID ENST00000252050
Start 43198662:43198662(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2857C>T
AA Mutation p.Arg953Ter(p.R953*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000252050
Start 43196643:43196643(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2586-2A>G
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> CUL9

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43187071:43187071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1363G>A
AA Mutation p.Ala455Thr(p.A455T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43206146:43206146(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs568298914
CDS Mutation c.4933C>T
AA Mutation p.Arg1645Cys(p.R1645C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43216414:43216414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6193G>A
AA Mutation p.Val2065Ile(p.V2065I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43213212:43213212(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531967221
CDS Mutation c.5276G>A
AA Mutation p.Arg1759Gln(p.R1759Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43188588:43188588(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760068503
CDS Mutation c.2053G>A
AA Mutation p.Val685Met(p.V685M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43196776:43196776(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2717G>T
AA Mutation p.Arg906Ile(p.R906I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43185599:43185599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.739C>A
AA Mutation p.His247Asn(p.H247N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000252050
Start 43187888:43187888(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377731849
CDS Mutation c.1757G>A
AA Mutation p.Arg586Gln(p.R586Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43184448:43184448(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.138G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43199308:43199308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3093C>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000252050
Start 43199976:43199976(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3204T>C
Mutation Classification Silent
Feature Type Transcript