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Overview
Mutation
Expression
Methylation
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Colon Cancer: Gene >> FOXK2
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000335255
Start
82563518:82563518(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.584G>A
AA Mutation
p.Ser195Asn(p.S195N)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000335255
Start
82582922:82582922(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1091C>T
AA Mutation
p.Pro364Leu(p.P364L)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000335255
Start
82582771:82582771(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.940C>T
AA Mutation
p.Arg314Cys(p.R314C)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000335255
Start
82585935:82585935(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1311C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000335255
Start
82563435:82563435(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs148118470
CDS Mutation
c.501G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000335255
Start
82582821:82582821(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs762735443
CDS Mutation
c.990G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000335255
Start
82587250:82587250(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs145491566
CDS Mutation
c.1764G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000335255
Start
82563501:82563501(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.567C>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
9
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000335255
Start
82586097:82586097(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs748655226
CDS Mutation
c.1473G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
10
Mutation Consequence
splice_acceptor_variant
Transcription ID
ENST00000335255
Start
82582740:82582740(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.910-1G>T
Mutation Classification
Splice_Site
Feature Type
Transcript
Rectum Cancer: Gene >> FOXK2
No Mutation Annotation!