Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NLRC5

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026955:57026955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2012G>T
AA Mutation p.Gly671Val(p.G671V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57054818:57054818(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370896719
CDS Mutation c.3574C>T
AA Mutation p.Arg1192Trp(p.R1192W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026867:57026867(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1924C>G
AA Mutation p.His642Asp(p.H642D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57082492:57082492(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5565C>A
AA Mutation p.Phe1855Leu(p.F1855L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026929:57026929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1986G>T
AA Mutation p.Glu662Asp(p.E662D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57059482:57059482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3936G>T
AA Mutation p.Gln1312His(p.Q1312H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026508:57026508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1565C>T
AA Mutation p.Ala522Val(p.A522V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026648:57026648(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1705G>C
AA Mutation p.Ala569Pro(p.A569P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026001:57026001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1058C>T
AA Mutation p.Ala353Val(p.A353V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57042056:57042056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3104A>G
AA Mutation p.Gln1035Arg(p.Q1035R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57025983:57025983(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1040G>A
AA Mutation p.Arg347His(p.R347H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57055084:57055084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151217415
CDS Mutation c.3649G>A
AA Mutation p.Val1217Met(p.V1217M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57037223:57037223(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751227747
CDS Mutation c.2740G>A
AA Mutation p.Gly914Arg(p.G914R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262510
Start 57067470:57067470(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4406G>T
AA Mutation p.Ser1469Ile(p.S1469I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262510
Start 57077800:57077800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5001G>T
AA Mutation p.Leu1667Phe(p.L1667F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57081536:57081536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5415G>T
AA Mutation p.Lys1805Asn(p.K1805N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57058118:57058118(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3800T>G
AA Mutation p.Leu1267Arg(p.L1267R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57069870:57069870(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758530512
CDS Mutation c.4534G>A
AA Mutation p.Ala1512Thr(p.A1512T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57025781:57025781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.838C>G
AA Mutation p.Leu280Val(p.L280V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262510
Start 57047547:57047547(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3341T>A
AA Mutation p.Leu1114His(p.L1114H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57028361:57028361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2219T>C
AA Mutation p.Leu740Pro(p.L740P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57023794:57023794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778759493
CDS Mutation c.365G>A
AA Mutation p.Arg122His(p.R122H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57029777:57029777(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2248C>T
AA Mutation p.Arg750Trp(p.R750W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262510
Start 57067827:57067827(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772554645
CDS Mutation c.4498C>T
AA Mutation p.Arg1500Trp(p.R1500W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57026228:57026228(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770877382
CDS Mutation c.1285G>A
AA Mutation p.Val429Met(p.V429M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57067786:57067786(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4457T>C
AA Mutation p.Leu1486Pro(p.L1486P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57082470:57082470(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5543A>G
AA Mutation p.Glu1848Gly(p.E1848G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57036107:57036107(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2635G>T
AA Mutation p.Gly879Trp(p.G879W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57077966:57077966(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5027A>G
AA Mutation p.Asp1676Gly(p.D1676G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57033649:57033649(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2523G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57047611:57047611(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140783117
CDS Mutation c.3405G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57025762:57025762(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145752799
CDS Mutation c.819G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57076846:57076846(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113401504
CDS Mutation c.4779C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57026347:57026347(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1404G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57061639:57061639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4092C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57066567:57066567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4275G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57026758:57026758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1815C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57041500:57041500(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2955C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57026086:57026086(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141391037
CDS Mutation c.1143C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57078012:57078012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5073G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57070574:57070574(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746507291
CDS Mutation c.4623G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57082510:57082510(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5583G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000262510
Start 57028129:57028129(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149479147
CDS Mutation c.2133G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000262510
Start 57026773:57026773(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1832delA
AA Mutation p.Lys611ArgfsTer3(p.K611Rfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000262510
Start 57026401:57026401(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1461delT
AA Mutation p.Phe487LeufsTer8(p.F487Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000262510
Start 57079112:57079112(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5149delC
AA Mutation p.His1717IlefsTer29(p.H1717Ifs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000262510
Start 57031430:57031430(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2447delC
AA Mutation p.Pro816ArgfsTer30(p.P816Rfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000262510
Start 57026284:57026284(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1346delC
AA Mutation p.Pro449LeufsTer17(p.P449Lfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence stop_gained
Transcription ID ENST00000262510
Start 57028378:57028378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2236G>T
AA Mutation p.Glu746Ter(p.E746*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence stop_gained
Transcription ID ENST00000262510
Start 57054758:57054758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3514C>T
AA Mutation p.Gln1172Ter(p.Q1172*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000262510
Start 57074673:57074673(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4741C>T
AA Mutation p.Gln1581Ter(p.Q1581*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000262510
Start 57036113:57036113(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2641C>T
AA Mutation p.Gln881Ter(p.Q881*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000262510
Start 57025730:57025730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.787C>T
AA Mutation p.Gln263Ter(p.Q263*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000262510
Start 57051620:57051620(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3505C>T
AA Mutation p.Gln1169Ter(p.Q1169*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000262510
Start 57026283:57026284(version: GRCh38)
Mutation Type INS
dbSNP_RS rs772651939
CDS Mutation c.1346dupC
AA Mutation p.Gly450TrpfsTer105(p.G450Wfs*105)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 56
Mutation Consequence splice_donor_variant
Transcription ID ENST00000262510
Start 57039851:57039851(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2870+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 57
Mutation Consequence splice_donor_variant
Transcription ID ENST00000262510
Start 57061532:57061532(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4070+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 58
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000262510
Start 57067386:57067386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4323-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 59
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000262510
Start 57043514:57043514(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3114-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 60
Mutation Consequence splice_donor_variant
Transcription ID ENST00000262510
Start 57042066:57042066(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3113+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> NLRC5

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262510
Start 57081607:57081607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5486T>C
AA Mutation p.Ile1829Thr(p.I1829T)
Mutation Classification Missense_Mutation
Feature Type Transcript