Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FLNA

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000369850
Start 154358568:154358568(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782787267
CDS Mutation c.4475G>A
AA Mutation p.Gly1492Asp(p.G1492D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364651:154364651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1897G>A
AA Mutation p.Val633Met(p.V633M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154351023:154351023(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7042A>G
AA Mutation p.Asn2348Asp(p.N2348D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154359566:154359566(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377390031;rs786205192
CDS Mutation c.4060G>A
AA Mutation p.Asp1354Asn(p.D1354N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154360580:154360580(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3215C>T
AA Mutation p.Ala1072Val(p.A1072V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364666:154364666(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782534475
CDS Mutation c.1882G>A
AA Mutation p.Asp628Asn(p.D628N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154348994:154348994(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7799C>T
AA Mutation p.Pro2600Leu(p.P2600L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154350977:154350977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7088C>T
AA Mutation p.Ala2363Val(p.A2363V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364617:154364617(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1931C>T
AA Mutation p.Ala644Val(p.A644V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154366144:154366144(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1309C>T
AA Mutation p.Arg437Trp(p.R437W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154359353:154359353(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4196A>G
AA Mutation p.Lys1399Arg(p.K1399R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154362495:154362495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2488G>T
AA Mutation p.Asp830Tyr(p.D830Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154354973:154354973(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782352193
CDS Mutation c.5069C>T
AA Mutation p.Thr1690Met(p.T1690M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154360442:154360442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3353G>T
AA Mutation p.Gly1118Val(p.G1118V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154360458:154360458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3337G>A
AA Mutation p.Glu1113Lys(p.E1113K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154352348:154352348(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368547421
CDS Mutation c.6602G>A
AA Mutation p.Arg2201His(p.R2201H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154350162:154350162(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7202T>C
AA Mutation p.Leu2401Pro(p.L2401P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364362:154364362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2033G>A
AA Mutation p.Arg678His(p.R678H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154353401:154353401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5917A>T
AA Mutation p.Ile1973Phe(p.I1973F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364050:154364050(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2252G>A
AA Mutation p.Gly751Asp(p.G751D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154359564:154359564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4062C>G
AA Mutation p.Asp1354Glu(p.D1354E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154367898:154367898(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.566G>A
AA Mutation p.Ser189Asn(p.S189N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154349847:154349847(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782450850
CDS Mutation c.7354G>A
AA Mutation p.Val2452Met(p.V2452M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154348968:154348968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7825G>A
AA Mutation p.Val2609Met(p.V2609M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154357476:154357476(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4903C>T
AA Mutation p.Arg1635Cys(p.R1635C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154352342:154352342(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6608T>C
AA Mutation p.Val2203Ala(p.V2203A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154360418:154360418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3377A>G
AA Mutation p.Tyr1126Cys(p.Y1126C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154366143:154366143(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782320818
CDS Mutation c.1310G>A
AA Mutation p.Arg437Gln(p.R437Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154351928:154351928(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782275601
CDS Mutation c.6863G>A
AA Mutation p.Arg2288His(p.R2288H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154366603:154366603(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1024T>G
AA Mutation p.Phe342Val(p.F342V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154366844:154366844(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.875A>G
AA Mutation p.Glu292Gly(p.E292G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154361775:154361775(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782239678
CDS Mutation c.2839G>A
AA Mutation p.Val947Ile(p.V947I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154353584:154353584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5830C>A
AA Mutation p.Pro1944Thr(p.P1944T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364675:154364675(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1873G>A
AA Mutation p.Asp625Asn(p.D625N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154350156:154350156(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7208A>G
AA Mutation p.Asp2403Gly(p.D2403G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154361421:154361421(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782546714
CDS Mutation c.3094C>T
AA Mutation p.Arg1032Cys(p.R1032C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154358548:154358548(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782701954
CDS Mutation c.4495G>A
AA Mutation p.Val1499Met(p.V1499M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154359114:154359114(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782529594
CDS Mutation c.4344G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154366211:154366211(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782598234
CDS Mutation c.1242C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154360573:154360573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3222G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154361755:154361755(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2859G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154351921:154351921(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782651736
CDS Mutation c.6870C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154365246:154365246(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782684339
CDS Mutation c.1581C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154353008:154353008(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782365685
CDS Mutation c.6219C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154362081:154362081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2724C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154349014:154349014(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7779G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154359606:154359606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4020G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154350143:154350143(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782129907
CDS Mutation c.7221C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154371176:154371176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.70C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154364712:154364712(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1836G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154360477:154360477(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3318C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154349830:154349830(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782747934
CDS Mutation c.7371G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154364100:154364100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2202C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154353119:154353119(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782221205
CDS Mutation c.6108G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154354688:154354688(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782091683
CDS Mutation c.5241G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154359265:154359265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4284T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154358537:154358537(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200857989
CDS Mutation c.4506C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154357546:154357546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4833C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000369850
Start 154354896:154354896(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5146delC
AA Mutation p.Gln1716SerfsTer23(p.Q1716Sfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 60
Mutation Consequence frameshift_variant
Transcription ID ENST00000369850
Start 154365224:154365224(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1603delG
AA Mutation p.Asp535MetfsTer34(p.D535Mfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 61
Mutation Consequence frameshift_variant
Transcription ID ENST00000369850
Start 154349560:154349560(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7558delC
AA Mutation p.Arg2520ValfsTer16(p.R2520Vfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 62
Mutation Consequence frameshift_variant
Transcription ID ENST00000369850
Start 154361439:154361439(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3076delG
AA Mutation p.Ala1026LeufsTer20(p.A1026Lfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000369850
Start 154352240:154352240(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6710delG
AA Mutation p.Gly2237GlufsTer109(p.G2237Efs*109)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 64
Mutation Consequence stop_gained
Transcription ID ENST00000369850
Start 154350921:154350921(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7144G>T
AA Mutation p.Glu2382Ter(p.E2382*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 65
Mutation Consequence stop_gained
Transcription ID ENST00000369850
Start 154350109:154350109(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7255C>T
AA Mutation p.Arg2419Ter(p.R2419*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 66
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000369850
Start 154360589:154360589(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3208-2A>G
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 67
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000369850
Start 154358356:154358356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4599-1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> FLNA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154353615:154353615(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5799C>G
AA Mutation p.Ser1933Arg(p.S1933R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154360096:154360096(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3699C>G
AA Mutation p.Ile1233Met(p.I1233M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154364878:154364878(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200673062
CDS Mutation c.1771G>A
AA Mutation p.Val591Ile(p.V591I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154371040:154371040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.206C>T
AA Mutation p.Thr69Met(p.T69M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369850
Start 154362247:154362247(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2651G>A
AA Mutation p.Arg884His(p.R884H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000369850
Start 154359096:154359096(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4362T>G
Mutation Classification Silent
Feature Type Transcript