Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNRC6B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000301923
Start 40156169:40156169(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.100G>A
AA Mutation p.Glu34Lys(p.E34K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40285735:40285735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3673C>T
AA Mutation p.Arg1225Trp(p.R1225W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40261873:40261873(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157G>A
AA Mutation p.Ala53Thr(p.A53T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40273482:40273482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3023G>A
AA Mutation p.Arg1008His(p.R1008H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40310829:40310829(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4271C>T
AA Mutation p.Ala1424Val(p.A1424V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40265740:40265740(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1510T>C
AA Mutation p.Ser504Pro(p.S504P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40264891:40264891(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.661G>A
AA Mutation p.Ala221Thr(p.A221T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40265746:40265746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1516G>T
AA Mutation p.Val506Phe(p.V506F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40308603:40308603(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4212G>T
AA Mutation p.Glu1404Asp(p.E1404D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40246080:40246080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.71A>G
AA Mutation p.Lys24Arg(p.K24R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40266883:40266883(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61743871
CDS Mutation c.2653C>T
AA Mutation p.Arg885Trp(p.R885W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40312591:40312591(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4522G>A
AA Mutation p.Gly1508Ser(p.G1508S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40265861:40265861(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1631A>G
AA Mutation p.His544Arg(p.H544R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40265227:40265227(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.997A>G
AA Mutation p.Ser333Gly(p.S333G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40266213:40266213(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1983G>T
AA Mutation p.Lys661Asn(p.K661N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40308574:40308574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4183C>T
AA Mutation p.Arg1395Cys(p.R1395C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40266659:40266659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2429G>A
AA Mutation p.Gly810Asp(p.G810D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40280073:40280073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3341A>G
AA Mutation p.Asp1114Gly(p.D1114G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40266613:40266613(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2383G>A
AA Mutation p.Gly795Ser(p.G795S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40265691:40265691(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1461C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40265382:40265382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1152T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40310959:40310959(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761947050
CDS Mutation c.4401C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40264893:40264893(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.663C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40308525:40308525(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4134C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40323073:40323073(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766288864
CDS Mutation c.5334C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40323151:40323151(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5412A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40246084:40246084(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40321170:40321170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5055T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40261947:40261947(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766891086
CDS Mutation c.231C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40315970:40315970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4932T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40312927:40312927(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373209801
CDS Mutation c.4608G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000454349
Start 40273462:40273462(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370055398
CDS Mutation c.3003C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40312587:40312587(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4523delG
AA Mutation p.Gly1508ValfsTer8(p.G1508Vfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40266498:40266498(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2273delA
AA Mutation p.Asn758ThrfsTer34(p.N758Tfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40266006:40266006(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1776delG
AA Mutation p.Tyr593ThrfsTer16(p.Y593Tfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40273449:40273449(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2995delG
AA Mutation p.Glu999ArgfsTer48(p.E999Rfs*48)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40266476:40266476(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2251delG
AA Mutation p.Glu751ArgfsTer41(p.E751Rfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40262044:40262044(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.332delC
AA Mutation p.Pro111LeufsTer29(p.P111Lfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40265862:40265862(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1636delC
AA Mutation p.Leu546SerfsTer63(p.L546Sfs*63)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 40
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40301156:40301156(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3943C>T
AA Mutation p.Arg1315Ter(p.R1315*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40300931:40300931(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3862C>T
AA Mutation p.Gln1288Ter(p.Q1288*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40266356:40266356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2126G>A
AA Mutation p.Trp709Ter(p.W709*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40261984:40261984(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268G>T
AA Mutation p.Glu90Ter(p.E90*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40266661:40266661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2431C>T
AA Mutation p.Arg811Ter(p.R811*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40266367:40266367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2137C>T
AA Mutation p.Arg713Ter(p.R713*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40323221:40323221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5482G>T
AA Mutation p.Gly1828Ter(p.G1828*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40301234:40301235(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4023dupT
AA Mutation p.Gly1342TrpfsTer56(p.G1342Wfs*56)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000454349
Start 40301265:40301266(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4053_4059dupACCCAAC
AA Mutation p.Ala1354ThrfsTer46(p.A1354Tfs*46)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TNRC6B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40265998:40265998(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1768C>T
AA Mutation p.Arg590Cys(p.R590C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40266746:40266746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2516C>T
AA Mutation p.Ser839Leu(p.S839L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000454349
Start 40262167:40262167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451G>A
AA Mutation p.Ala151Thr(p.A151T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000301923
Start 40125843:40125843(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753937261
CDS Mutation c.26C>T
AA Mutation p.Ser9Leu(p.S9L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40265479:40265479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1249C>T
AA Mutation p.Arg417Ter(p.R417*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40277105:40277105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3170C>A
AA Mutation p.Ser1057Ter(p.S1057*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40280030:40280030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3298C>T
AA Mutation p.Arg1100Ter(p.R1100*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40266784:40266784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2554C>T
AA Mutation p.Arg852Ter(p.R852*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000454349
Start 40266367:40266367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2137C>T
AA Mutation p.Arg713Ter(p.R713*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript