Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FMN2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240123326:240123326(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773346283
CDS Mutation c.1763C>T
AA Mutation p.Thr588Met(p.T588M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240334181:240334181(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4717T>G
AA Mutation p.Phe1573Val(p.F1573V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240093510:240093510(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1401G>C
AA Mutation p.Lys467Asn(p.K467N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092674:240092674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.565G>A
AA Mutation p.Ala189Thr(p.A189T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207530:240207530(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2718A>C
AA Mutation p.Glu906Asp(p.E906D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240093404:240093404(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1295C>T
AA Mutation p.Ser432Phe(p.S432F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092143:240092143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.34G>A
AA Mutation p.Ala12Thr(p.A12T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240334113:240334113(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4649C>T
AA Mutation p.Ala1550Val(p.A1550V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240188242:240188242(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199730080
CDS Mutation c.1966C>T
AA Mutation p.Arg656Cys(p.R656C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207298:240207298(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771047438
CDS Mutation c.2486C>T
AA Mutation p.Pro829Leu(p.P829L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207058:240207058(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371967368
CDS Mutation c.2246C>T
AA Mutation p.Thr749Met(p.T749M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092483:240092483(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.374C>T
AA Mutation p.Ala125Val(p.A125V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092582:240092582(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.473C>T
AA Mutation p.Pro158Leu(p.P158L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092332:240092332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.223T>C
AA Mutation p.Phe75Leu(p.F75L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240093551:240093551(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1442G>A
AA Mutation p.Arg481His(p.R481H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092167:240092167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.58G>A
AA Mutation p.Gly20Ser(p.G20S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092327:240092327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.218C>T
AA Mutation p.Ser73Leu(p.S73L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240329436:240329436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4405C>A
AA Mutation p.Arg1469Ser(p.R1469S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000319653
Start 240329340:240329340(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4309T>C
AA Mutation p.Phe1437Leu(p.F1437L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240092558:240092558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.449C>A
AA Mutation p.Ala150Asp(p.A150D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207148:240207148(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2336C>A
AA Mutation p.Thr779Lys(p.T779K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207012:240207012(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145706266
CDS Mutation c.2200C>T
AA Mutation p.Arg734Trp(p.R734W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207811:240207811(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772595784
CDS Mutation c.2999C>T
AA Mutation p.Pro1000Leu(p.P1000L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208356:240208356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3544G>A
AA Mutation p.Val1182Met(p.V1182M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208711:240208711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3899G>T
AA Mutation p.Arg1300Met(p.R1300M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240329079:240329079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4219G>A
AA Mutation p.Ala1407Thr(p.A1407T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207156:240207156(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2344T>C
AA Mutation p.Cys782Arg(p.C782R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208374:240208374(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3562C>T
AA Mutation p.Pro1188Ser(p.P1188S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240472415:240472415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5104T>C
AA Mutation p.Ser1702Pro(p.S1702P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240178035:240178035(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772498975
CDS Mutation c.1897G>A
AA Mutation p.Asp633Asn(p.D633N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208653:240208653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3841G>T
AA Mutation p.Gly1281Trp(p.G1281W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207059:240207059(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2247G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240211097:240211097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3927C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207758:240207758(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764580443
CDS Mutation c.2946C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240208103:240208103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3291C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207626:240207626(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2814C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240092925:240092925(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.816G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207593:240207593(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2781C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240206969:240206969(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754303422
CDS Mutation c.2157C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207035:240207035(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144753167
CDS Mutation c.2223G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240123327:240123327(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762987742
CDS Mutation c.1764G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207068:240207068(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140392779
CDS Mutation c.2256C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207692:240207692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2880C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000319653
Start 240208101:240208101(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3293delC
AA Mutation p.Pro1098LeufsTer177(p.P1098Lfs*177)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000319653
Start 240207540:240207540(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2732delC
AA Mutation p.Pro911LeufsTer364(p.P911Lfs*364)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000319653
Start 240208167:240208167(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3359delC
AA Mutation p.Pro1120LeufsTer155(p.P1120Lfs*155)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000319653
Start 240093500:240093500(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1394delC
AA Mutation p.Pro465ArgfsTer15(p.P465Rfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000319653
Start 240207371:240207371(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2559T>A
AA Mutation p.Cys853Ter(p.C853*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> FMN2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208536:240208536(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774306832
CDS Mutation c.3724G>T
AA Mutation p.Gly1242Cys(p.G1242C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240329361:240329361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4330A>G
AA Mutation p.Ile1444Val(p.I1444V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208711:240208711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3899G>T
AA Mutation p.Arg1300Met(p.R1300M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240211213:240211213(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4043T>C
AA Mutation p.Ile1348Thr(p.I1348T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240208630:240208630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3818G>T
AA Mutation p.Gly1273Val(p.G1273V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240329091:240329091(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779310703
CDS Mutation c.4231G>A
AA Mutation p.Glu1411Lys(p.E1411K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240333939:240333939(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4637T>G
AA Mutation p.Phe1546Cys(p.F1546C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240392516:240392516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4864A>C
AA Mutation p.Ile1622Leu(p.I1622L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240333922:240333922(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369715134
CDS Mutation c.4620G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240123240:240123240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1677G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000319653
Start 240330687:240330687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4522C>T
AA Mutation p.Arg1508Ter(p.R1508*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000319653
Start 240207118:240207119(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2312dupC
AA Mutation p.Gly772TrpfsTer3(p.G772Wfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript