Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FCGBP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39902642:39902642(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782628037
CDS Mutation c.4186G>A
AA Mutation p.Asp1396Asn(p.D1396N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39872185:39872185(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201350567
CDS Mutation c.11642C>T
AA Mutation p.Ala3881Val(p.A3881V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39872591:39872591(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368867080
CDS Mutation c.11236G>A
AA Mutation p.Ala3746Thr(p.A3746T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875537:39875537(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10454C>T
AA Mutation p.Pro3485Leu(p.P3485L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875831:39875831(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369849185
CDS Mutation c.10160C>T
AA Mutation p.Ser3387Leu(p.S3387L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39918188:39918188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2108A>C
AA Mutation p.Asp703Ala(p.D703A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875402:39875402(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10589G>A
AA Mutation p.Arg3530Gln(p.R3530Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39915439:39915439(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2575G>A
AA Mutation p.Asp859Asn(p.D859N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39902112:39902112(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4598C>T
AA Mutation p.Pro1533Leu(p.P1533L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39892021:39892021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6622T>C
AA Mutation p.Cys2208Arg(p.C2208R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39893474:39893474(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5893G>A
AA Mutation p.Ala1965Thr(p.A1965T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39902273:39902273(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4555G>A
AA Mutation p.Val1519Met(p.V1519M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39873375:39873375(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11024G>A
AA Mutation p.Gly3675Asp(p.G3675D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39915567:39915567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2447C>T
AA Mutation p.Ala816Val(p.A816V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39879830:39879830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8593G>A
AA Mutation p.Val2865Met(p.V2865M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39892048:39892048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6595G>A
AA Mutation p.Val2199Met(p.V2199M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927613:39927613(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.749C>T
AA Mutation p.Thr250Ile(p.T250I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875445:39875445(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10546G>A
AA Mutation p.Ala3516Thr(p.A3516T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39918585:39918585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1711T>A
AA Mutation p.Tyr571Asn(p.Y571N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39872120:39872120(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11707G>A
AA Mutation p.Ala3903Thr(p.A3903T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927083:39927083(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1279G>A
AA Mutation p.Ala427Thr(p.A427T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39886438:39886438(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7741G>A
AA Mutation p.Gly2581Arg(p.G2581R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39872384:39872384(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750656477
CDS Mutation c.11443C>T
AA Mutation p.Arg3815Trp(p.R3815W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39891988:39891988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6655G>A
AA Mutation p.Ala2219Thr(p.A2219T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927461:39927461(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.901C>T
AA Mutation p.Pro301Ser(p.P301S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39893107:39893107(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6260G>A
AA Mutation p.Arg2087Gln(p.R2087Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39883332:39883332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747177556
CDS Mutation c.8503G>A
AA Mutation p.Gly2835Arg(p.G2835R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927293:39927293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139397827
CDS Mutation c.1069G>A
AA Mutation p.Val357Met(p.V357M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39894369:39894369(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5392C>T
AA Mutation p.Arg1798Trp(p.R1798W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927628:39927628(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.734C>T
AA Mutation p.Thr245Met(p.T245M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39913825:39913825(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs34041323
CDS Mutation c.3262G>A
AA Mutation p.Val1088Met(p.V1088M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39872549:39872549(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753209481
CDS Mutation c.11278C>T
AA Mutation p.Arg3760Trp(p.R3760W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39915322:39915322(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2692G>A
AA Mutation p.Ala898Thr(p.A898T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39928042:39928042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201635572
CDS Mutation c.320C>T
AA Mutation p.Ala107Val(p.A107V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39928298:39928298(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.64C>A
AA Mutation p.Gln22Lys(p.Q22K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39891952:39891952(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750153640
CDS Mutation c.6691G>A
AA Mutation p.Gly2231Arg(p.G2231R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39893464:39893464(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5903C>T
AA Mutation p.Pro1968Leu(p.P1968L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39902566:39902566(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782042524
CDS Mutation c.4262A>C
AA Mutation p.Glu1421Ala(p.E1421A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39924469:39924469(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1567C>T
AA Mutation p.Arg523Cys(p.R523C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39891841:39891841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6802G>A
AA Mutation p.Val2268Met(p.V2268M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39892044:39892044(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370331745
CDS Mutation c.6599C>T
AA Mutation p.Pro2200Leu(p.P2200L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875820:39875820(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748128460
CDS Mutation c.10171G>A
AA Mutation p.Asp3391Asn(p.D3391N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39902372:39902372(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4456G>A
AA Mutation p.Asp1486Asn(p.D1486N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39886405:39886405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7774G>A
AA Mutation p.Gly2592Arg(p.G2592R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39866991:39866991(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12079T>C
AA Mutation p.Cys4027Arg(p.C4027R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39913875:39913875(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3212C>T
AA Mutation p.Pro1071Leu(p.P1071L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39918580:39918580(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1716G>C
AA Mutation p.Gln572His(p.Q572H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39899606:39899606(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782167689
CDS Mutation c.4877C>T
AA Mutation p.Pro1626Leu(p.P1626L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927145:39927145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377164847
CDS Mutation c.1217C>T
AA Mutation p.Thr406Met(p.T406M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875576:39875576(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10415C>T
AA Mutation p.Ala3472Val(p.A3472V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927290:39927290(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1072G>A
AA Mutation p.Ala358Thr(p.A358T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39924639:39924639(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1397C>T
AA Mutation p.Ala466Val(p.A466V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39918409:39918409(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1887G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39894172:39894172(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5589G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39863656:39863656(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12570G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39891728:39891728(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6915C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39879882:39879882(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8541C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39875785:39875785(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10206G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39875503:39875503(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771508776
CDS Mutation c.10488C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39891758:39891758(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773651497
CDS Mutation c.6885C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39875728:39875728(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151261300
CDS Mutation c.10263C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39875917:39875917(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767337737
CDS Mutation c.10074C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39893313:39893313(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6054G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 64
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39892037:39892037(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6606G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 65
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39915386:39915386(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2628C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 66
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39877183:39877183(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774328891
CDS Mutation c.9534C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 67
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39927186:39927186(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148301068
CDS Mutation c.1176G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 68
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39902598:39902598(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4230C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 69
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39915509:39915509(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2505C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 70
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39893219:39893219(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6148C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 71
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39915710:39915710(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772034554
CDS Mutation c.2304G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 72
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39873716:39873716(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139763150
CDS Mutation c.10683C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 73
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39892178:39892178(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6465C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 74
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39878096:39878096(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771414365
CDS Mutation c.9009G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 75
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39892031:39892031(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772696382
CDS Mutation c.6612G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 76
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39924434:39924434(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777358795
CDS Mutation c.1602C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 77
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39927294:39927294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1068C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 78
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39918286:39918286(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752581812
CDS Mutation c.2010C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 79
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39918513:39918513(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1783C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 80
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39886052:39886052(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749443396
CDS Mutation c.8127C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 81
Mutation Consequence frameshift_variant
Transcription ID ENST00000616721
Start 39927915:39927915(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.447delC
AA Mutation p.Gly150AlafsTer25(p.G150Afs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 82
Mutation Consequence stop_gained
Transcription ID ENST00000616721
Start 39877741:39877741(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9364A>T
AA Mutation p.Lys3122Ter(p.K3122*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 83
Mutation Consequence stop_gained
Transcription ID ENST00000616721
Start 39899664:39899664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4819C>T
AA Mutation p.Gln1607Ter(p.Q1607*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 84
Mutation Consequence stop_gained
Transcription ID ENST00000616721
Start 39894085:39894085(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5676C>A
AA Mutation p.Cys1892Ter(p.C1892*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> FCGBP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39927905:39927905(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.457G>T
AA Mutation p.Ala153Ser(p.A153S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39875810:39875810(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10181G>A
AA Mutation p.Ser3394Asn(p.S3394N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39902118:39902118(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4592A>C
AA Mutation p.Glu1531Ala(p.E1531A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000616721
Start 39866893:39866893(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12177G>T
AA Mutation p.Glu4059Asp(p.E4059D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000616721
Start 39877273:39877273(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9444G>T
AA Mutation p.Glu3148Asp(p.E3148D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39891791:39891791(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6852G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39894334:39894334(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5427C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39906289:39906289(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773478477
CDS Mutation c.3432G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39892031:39892031(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772696382
CDS Mutation c.6612G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39877913:39877913(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554943335
CDS Mutation c.9192G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000616721
Start 39927585:39927585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.777C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000616721
Start 39913699:39913699(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3388G>T
AA Mutation p.Glu1130Ter(p.E1130*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript