Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FBXW8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	116964732:116964732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758915610
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	117010351:117010351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372814319
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423His(p.R423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	117028045:117028045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368052577
CDS Mutation	c.1670G>A
AA Mutation	p.Arg557His(p.R557H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	117024166:117024166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777410294
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	117024167:117024167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186364302
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463His(p.R463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309909
Start	116985396:116985396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183097307
CDS Mutation	c.1026G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FBXW8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	116928099:116928099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395A>G
AA Mutation	p.Asp132Gly(p.D132G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309909
Start	116928068:116928068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779200230
CDS Mutation	c.364G>A
AA Mutation	p.Glu122Lys(p.E122K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309909
Start	116945468:116945468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766290090
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript