Colon Cancer: Gene >> CBX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310942
Start	79784545:79784545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102G>A
AA Mutation	p.Val368Met(p.V368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310942
Start	79784829:79784829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1386G>T
AA Mutation	p.Glu462Asp(p.E462D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310942
Start	79781767:79781767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310942
Start	79784840:79784840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397G>A
AA Mutation	p.Ser466Asn(p.S466N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310942
Start	79783884:79783884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310942
Start	79784901:79784901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528502956
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CBX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310942
Start	79783852:79783852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Cys(p.R137C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000310942
Start	79783939:79783939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Ter(p.R166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript