Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KLF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733159:130733159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875G>A
AA Mutation	p.Arg292Gln(p.R292Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733156:130733156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878C>T
AA Mutation	p.Thr293Ile(p.T293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733211:130733211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Cys(p.R275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733375:130733375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659C>T
AA Mutation	p.Thr220Met(p.T220M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733432:130733432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602G>A
AA Mutation	p.Gly201Asp(p.G201D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733559:130733559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475G>A
AA Mutation	p.Ala159Thr(p.A159T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733087:130733087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782076927
CDS Mutation	c.947C>T
AA Mutation	p.Ala316Val(p.A316V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000583337
Start	130733086:130733086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000583337
Start	130733236:130733236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000583337
Start	130733404:130733404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782015781
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000583337
Start	130733159:130733159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875G>A
AA Mutation	p.Arg292Gln(p.R292Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript