Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TES

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116234603:116234603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199726977
CDS Mutation	c.97G>A
AA Mutation	p.Glu33Lys(p.E33K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116250486:116250486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>T
AA Mutation	p.Arg231Ile(p.R231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116234597:116234597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91G>A
AA Mutation	p.Gly31Arg(p.G31R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116251886:116251886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Asp277Asn(p.D277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116234598:116234598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92G>C
AA Mutation	p.Gly31Ala(p.G31A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116251920:116251920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863A>G
AA Mutation	p.Tyr288Cys(p.Y288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358204
Start	116252338:116252338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.939T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TES

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358204
Start	116234603:116234603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199726977
CDS Mutation	c.97G>A
AA Mutation	p.Glu33Lys(p.E33K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript