Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DCX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410232:111410232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.410G>A
AA Mutation p.Arg137His(p.R137H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111401075:111401075(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.863T>G
AA Mutation p.Phe288Cys(p.F288C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111312676:111312676(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780314121
CDS Mutation c.1235C>T
AA Mutation p.Thr412Met(p.T412M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410832:111410832(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.143A>G
AA Mutation p.His48Arg(p.H48R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410158:111410158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.484G>A
AA Mutation p.Asp162Asn(p.D162N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410133:111410133(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.509G>A
AA Mutation p.Arg170Gln(p.R170Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111330960:111330960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1133G>T
AA Mutation p.Ser378Ile(p.S378I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410155:111410155(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.487G>A
AA Mutation p.Ala163Thr(p.A163T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410211:111410211(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.431G>A
AA Mutation p.Arg144His(p.R144H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000338081
Start 111312711:111312711(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1200C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000338081
Start 111410300:111410300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000338081
Start 111410189:111410189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.453C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000338081
Start 111312675:111312675(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775046398
CDS Mutation c.1236G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000338081
Start 111401014:111401014(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs587783579;rs797045517
CDS Mutation c.924delA
AA Mutation p.Lys308AsnfsTer10(p.K308Nfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000338081
Start 111401291:111401291(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.647delA
AA Mutation p.Lys216ArgfsTer16(p.K216Rfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000338081
Start 111312702:111312702(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1209delC
AA Mutation p.Lys404SerfsTer82(p.K404Sfs*82)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000338081
Start 111401241:111401241(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.697delA
AA Mutation p.Thr233HisfsTer5(p.T233Hfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000338081
Start 111410284:111410284(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587783519
CDS Mutation c.358C>T
AA Mutation p.Arg120Ter(p.R120*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> DCX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410283:111410283(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.359G>A
AA Mutation p.Arg120Gln(p.R120Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410392:111410392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.250C>T
AA Mutation p.Leu84Phe(p.L84F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410130:111410130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.512C>A
AA Mutation p.Ser171Tyr(p.S171Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111410223:111410223(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs122457137
CDS Mutation c.419G>A
AA Mutation p.Arg140His(p.R140H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000338081
Start 111401299:111401299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.639C>A
AA Mutation p.Phe213Leu(p.F213L)
Mutation Classification Missense_Mutation
Feature Type Transcript