Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> WDFY3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84691714:84691714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9121C>A
AA Mutation p.Leu3041Ile(p.L3041I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84702399:84702399(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8550C>A
AA Mutation p.Phe2850Leu(p.F2850L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84713236:84713236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7965T>A
AA Mutation p.Phe2655Leu(p.F2655L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84789854:84789854(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3541C>T
AA Mutation p.Arg1181Cys(p.R1181C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84849955:84849955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.251T>A
AA Mutation p.Val84Asp(p.V84D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84782996:84782996(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4141C>T
AA Mutation p.Arg1381Trp(p.R1381W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84691734:84691734(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773897989
CDS Mutation c.9101C>T
AA Mutation p.Ala3034Val(p.A3034V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84705480:84705480(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8249G>T
AA Mutation p.Arg2750Ile(p.R2750I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84743759:84743759(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6014T>G
AA Mutation p.Phe2005Cys(p.F2005C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000295888
Start 84737364:84737364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6577C>T
AA Mutation p.Arg2193Cys(p.R2193C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84794563:84794563(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762005418
CDS Mutation c.3443G>A
AA Mutation p.Arg1148Gln(p.R1148Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84817465:84817465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1814A>T
AA Mutation p.Asp605Val(p.D605V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84733488:84733488(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7115A>G
AA Mutation p.Glu2372Gly(p.E2372G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84798060:84798060(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2871A>C
AA Mutation p.Lys957Asn(p.K957N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84829047:84829047(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777259178
CDS Mutation c.913C>T
AA Mutation p.Arg305Trp(p.R305W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84766005:84766005(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4993A>G
AA Mutation p.Thr1665Ala(p.T1665A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84724437:84724437(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7430C>A
AA Mutation p.Ala2477Asp(p.A2477D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84740337:84740337(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749960381
CDS Mutation c.6314G>A
AA Mutation p.Arg2105Gln(p.R2105Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000295888
Start 84721409:84721409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7605G>T
AA Mutation p.Lys2535Asn(p.K2535N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84817407:84817407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1872G>C
AA Mutation p.Lys624Asn(p.K624N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84751557:84751557(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5899C>T
AA Mutation p.Arg1967Trp(p.R1967W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84736261:84736261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199971533
CDS Mutation c.6824G>A
AA Mutation p.Arg2275His(p.R2275H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84718506:84718506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7670T>G
AA Mutation p.Phe2557Cys(p.F2557C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84721542:84721542(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7472G>T
AA Mutation p.Arg2491Leu(p.R2491L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84679086:84679086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9980G>T
AA Mutation p.Gly3327Val(p.G3327V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84789847:84789847(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3548G>A
AA Mutation p.Arg1183Gln(p.R1183Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84733459:84733459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7144A>G
AA Mutation p.Lys2382Glu(p.K2382E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84860560:84860560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.32C>T
AA Mutation p.Pro11Leu(p.P11L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84751705:84751705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5751T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84690569:84690569(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376289492
CDS Mutation c.9300G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84836938:84836938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.567T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84679226:84679226(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs530783066
CDS Mutation c.9840C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84860529:84860529(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371936183
CDS Mutation c.63C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84810138:84810138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2094T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84755350:84755350(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5475C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84715357:84715357(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7902A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84789831:84789831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3564C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84817578:84817578(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1701T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84733505:84733505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7098C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84765933:84765933(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5065A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000295888
Start 84794968:84794968(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3179delT
AA Mutation p.Leu1060CysfsTer41(p.L1060Cfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000295888
Start 84755300:84755300(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5525delT
AA Mutation p.Leu1842TyrfsTer10(p.L1842Yfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 43
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000295888
Start 84721410:84721410(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7604delA
AA Mutation p.Lys2535ArgfsTer14(p.K2535Rfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000295888
Start 84826853:84826853(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1085delT
AA Mutation p.Leu362TyrfsTer17(p.L362Yfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000295888
Start 84789775:84789775(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3620delA
AA Mutation p.Asn1207ThrfsTer16(p.N1207Tfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence stop_gained
Transcription ID ENST00000295888
Start 84733489:84733489(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7114G>T
AA Mutation p.Glu2372Ter(p.E2372*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence stop_gained
Transcription ID ENST00000295888
Start 84672972:84672972(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10477G>T
AA Mutation p.Glu3493Ter(p.E3493*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000295888
Start 84692993:84692993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8941C>T
AA Mutation p.Arg2981Ter(p.R2981*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence splice_donor_variant
Transcription ID ENST00000295888
Start 84826813:84826813(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1123+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 50
Mutation Consequence splice_donor_variant
Transcription ID ENST00000295888
Start 84801648:84801648(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2822+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 51
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000295888
Start 84739120:84739120(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6465-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 52
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000295888
Start 84736328:84736328(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6758-1G>T
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> WDFY3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84736210:84736210(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6875G>A
AA Mutation p.Arg2292Gln(p.R2292Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84757146:84757146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5204G>A
AA Mutation p.Arg1735Lys(p.R1735K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84772891:84772891(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753796269
CDS Mutation c.4793C>T
AA Mutation p.Ala1598Val(p.A1598V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84705403:84705403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8326G>A
AA Mutation p.Asp2776Asn(p.D2776N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84772873:84772873(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4811T>C
AA Mutation p.Val1604Ala(p.V1604A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84737235:84737235(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6706G>A
AA Mutation p.Ala2236Thr(p.A2236T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84740395:84740395(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6256T>G
AA Mutation p.Leu2086Val(p.L2086V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84774969:84774969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4605G>T
AA Mutation p.Lys1535Asn(p.K1535N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84740227:84740227(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6424A>T
AA Mutation p.Ser2142Cys(p.S2142C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84696819:84696819(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8601T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84684063:84684063(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs180858713
CDS Mutation c.9606C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000295888
Start 84820099:84820099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1679C>A
AA Mutation p.Ser560Ter(p.S560*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript