Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50402300:50402300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897G>T
AA Mutation	p.Glu299Asp(p.E299D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50411225:50411225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355A>T
AA Mutation	p.Thr119Ser(p.T119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50403414:50403414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>T
AA Mutation	p.Gly214Val(p.G214V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50403447:50403447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769210568
CDS Mutation	c.608T>C
AA Mutation	p.Val203Ala(p.V203A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50405729:50405729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596T>C
AA Mutation	p.Val199Ala(p.V199A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303221
Start	50399871:50399871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50428173:50428173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167C>T
AA Mutation	p.Ser56Phe(p.S56F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303221
Start	50411227:50411227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749459608
CDS Mutation	c.353C>T
AA Mutation	p.Ala118Val(p.A118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000303221
Start	50411384:50411384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript