Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CCT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299300
Start	69597678:69597678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1143A>C
AA Mutation	p.Gln381His(p.Q381H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299300
Start	69589600:69589600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562C>T
AA Mutation	p.Leu188Phe(p.L188F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299300
Start	69597271:69597271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299300
Start	69588236:69588236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767503874
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299300
Start	69597979:69597979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1243A>C
AA Mutation	p.Met415Leu(p.M415L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299300
Start	69593519:69593519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888T>G
AA Mutation	p.Ile296Met(p.I296M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299300
Start	69597216:69597216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043T>G
AA Mutation	p.Leu348Arg(p.L348R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299300
Start	69588218:69588218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762745968
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript