Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FN1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215381052:215381052(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4920C>A
AA Mutation p.Phe1640Leu(p.F1640L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215394606:215394606(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767515823
CDS Mutation c.3718G>A
AA Mutation p.Gly1240Ser(p.G1240S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215372025:215372025(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6325G>T
AA Mutation p.Ala2109Ser(p.A2109S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215407314:215407314(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2526A>C
AA Mutation p.Arg842Ser(p.R842S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215424304:215424304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1058G>A
AA Mutation p.Gly353Asp(p.G353D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215386857:215386857(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs116558455
CDS Mutation c.4171C>T
AA Mutation p.Arg1391Cys(p.R1391C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215424308:215424308(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs13306372
CDS Mutation c.1054G>A
AA Mutation p.Gly352Ser(p.G352S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215422223:215422223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1414A>G
AA Mutation p.Thr472Ala(p.T472A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215384071:215384071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4570C>T
AA Mutation p.Arg1524Cys(p.R1524C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359671
Start 215372373:215372373(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775650652
CDS Mutation c.5977G>A
AA Mutation p.Glu1993Lys(p.E1993K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215408423:215408423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2303T>C
AA Mutation p.Leu768Pro(p.L768P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215364934:215364934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6923G>T
AA Mutation p.Trp2308Leu(p.W2308L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215391760:215391760(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3851G>A
AA Mutation p.Arg1284His(p.R1284H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215383451:215383451(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140153061
CDS Mutation c.4654G>A
AA Mutation p.Asp1552Asn(p.D1552N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359671
Start 215373411:215373411(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5885G>T
AA Mutation p.Gly1962Val(p.G1962V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215404577:215404577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3065C>T
AA Mutation p.Ala1022Val(p.A1022V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215364898:215364898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6959C>T
AA Mutation p.Thr2320Ile(p.T2320I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215391706:215391706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3905A>G
AA Mutation p.Tyr1302Cys(p.Y1302C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215430736:215430736(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748170344
CDS Mutation c.664C>T
AA Mutation p.Arg222Cys(p.R222C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215406243:215406243(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2981C>A
AA Mutation p.Thr994Lys(p.T994K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215375243:215375243(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770932448
CDS Mutation c.5855G>A
AA Mutation p.Arg1952His(p.R1952H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215425250:215425250(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.880T>C
AA Mutation p.Tyr294His(p.Y294H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215408375:215408375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772449186
CDS Mutation c.2351G>A
AA Mutation p.Arg784Gln(p.R784Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215423521:215423521(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1222G>A
AA Mutation p.Val408Ile(p.V408I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215367940:215367940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6668G>A
AA Mutation p.Arg2223Gln(p.R2223Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215372249:215372249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6101T>G
AA Mutation p.Ile2034Ser(p.I2034S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215420783:215420783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1565A>G
AA Mutation p.Asp522Gly(p.D522G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215406267:215406267(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2957G>A
AA Mutation p.Ser986Asn(p.S986N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215375638:215375638(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs573992192
CDS Mutation c.5695G>A
AA Mutation p.Ala1899Thr(p.A1899T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215375306:215375306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5792C>T
AA Mutation p.Thr1931Ile(p.T1931I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215419278:215419278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1783G>C
AA Mutation p.Gly595Arg(p.G595R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215428325:215428325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.699T>A
AA Mutation p.Asp233Glu(p.D233E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215365559:215365559(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6817A>G
AA Mutation p.Met2273Val(p.M2273V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215386856:215386856(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369288293
CDS Mutation c.4172G>A
AA Mutation p.Arg1391His(p.R1391H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215397827:215397827(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3370G>A
AA Mutation p.Gly1124Arg(p.G1124R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215375324:215375324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139452116
CDS Mutation c.5774C>T
AA Mutation p.Pro1925Leu(p.P1925L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215425242:215425242(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201079072
CDS Mutation c.888G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215433349:215433349(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.390A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215384123:215384123(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374970848
CDS Mutation c.4518C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215379235:215379235(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5244G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215384939:215384939(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144486467
CDS Mutation c.4377G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215386800:215386800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4228C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215409675:215409675(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147004347
CDS Mutation c.2187C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215370391:215370391(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6483C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215379262:215379262(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376598003
CDS Mutation c.5217C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215406437:215406437(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375777163
CDS Mutation c.2787G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215407302:215407302(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145300210
CDS Mutation c.2538G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215365533:215365533(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs568449322
CDS Mutation c.6843C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215397798:215397798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3399A>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215407308:215407308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2532C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215424192:215424192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745915615
CDS Mutation c.1170G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence frameshift_variant
Transcription ID ENST00000359671
Start 215433404:215433407(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.332_335delCTTA
AA Mutation p.Thr111MetfsTer8(p.T111Mfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000359671
Start 215380832:215380832(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5140delC
AA Mutation p.Leu1714Ter(p.L1714*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000359671
Start 215378239:215378239(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5373delT
AA Mutation p.Ser1791ArgfsTer9(p.S1791Rfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 55
Mutation Consequence stop_gained
Transcription ID ENST00000359671
Start 215409725:215409725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2137G>T
AA Mutation p.Gly713Ter(p.G713*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence stop_gained
Transcription ID ENST00000359671
Start 215362031:215362031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7027G>T
AA Mutation p.Glu2343Ter(p.E2343*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 57
Mutation Consequence stop_gained
Transcription ID ENST00000359671
Start 215409985:215409985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2071G>T
AA Mutation p.Glu691Ter(p.E691*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000359671
Start 215430838:215430839(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.561dupT
AA Mutation p.Asp188Ter(p.D188*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000359671
Start 215391738:215391739(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3872dupC
AA Mutation p.Ser1292IlefsTer3(p.S1292Ifs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FN1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215361583:215361583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7133A>G
AA Mutation p.Gln2378Arg(p.Q2378R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215433398:215433398(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.341G>A
AA Mutation p.Arg114His(p.R114H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215383451:215383451(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140153061
CDS Mutation c.4654G>A
AA Mutation p.Asp1552Asn(p.D1552N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215414843:215414843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1935G>T
AA Mutation p.Trp645Cys(p.W645C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215375324:215375324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139452116
CDS Mutation c.5774C>T
AA Mutation p.Pro1925Leu(p.P1925L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215424175:215424175(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1187A>G
AA Mutation p.Gln396Arg(p.Q396R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215373394:215373394(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767081660
CDS Mutation c.5902G>A
AA Mutation p.Glu1968Lys(p.E1968K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215361565:215361565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7151C>A
AA Mutation p.Ser2384Tyr(p.S2384Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359671
Start 215375671:215375671(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5662G>T
AA Mutation p.Asp1888Tyr(p.D1888Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215386846:215386846(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764031352
CDS Mutation c.4182C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215404468:215404468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3174T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215394709:215394709(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3615T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000359671
Start 215375323:215375323(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752013950
CDS Mutation c.5775G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000359671
Start 215407178:215407178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2662G>T
AA Mutation p.Glu888Ter(p.E888*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript