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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> HPX
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000265983
Start
6431739:6431739(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs142045379
CDS Mutation
c.1031G>A
AA Mutation
p.Arg344Gln(p.R344Q)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000265983
Start
6440197:6440197(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs764988248
CDS Mutation
c.304C>T
AA Mutation
p.Arg102Cys(p.R102C)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000265983
Start
6438471:6438471(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.375G>T
AA Mutation
p.Glu125Asp(p.E125D)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000265983
Start
6437455:6437455(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.688C>T
AA Mutation
p.Pro230Ser(p.P230S)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000265983
Start
6437453:6437453(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.690C>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000265983
Start
6440895:6440895(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.69C>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000265983
Start
6431370:6431370(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1230A>G
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000265983
Start
6440471:6440471(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
null
CDS Mutation
c.210delT
AA Mutation
p.Phe70LeufsTer16(p.F70Lfs*16)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Rectum Cancer: Gene >> HPX
No Mutation Annotation!