Colon Cancer: Gene >> CBX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407418
Start	38867078:38867078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Cys(p.R124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407418
Start	38866829:38866829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Cys(p.R207C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000407418
Start	38871482:38871482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244A>G
AA Mutation	p.Lys82Glu(p.K82E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407418
Start	38867015:38867015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Gly145Arg(p.G145R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000407418
Start	38866963:38866963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485G>A
AA Mutation	p.Arg162His(p.R162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000407418
Start	38866964:38866964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407418
Start	38866275:38866275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407418
Start	38866827:38866827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407418
Start	38866254:38866254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407418
Start	38866724:38866724(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.724delC
AA Mutation	p.Leu242TrpfsTer2(p.L242Wfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407418
Start	38871730:38871740(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.131_141delCCGAGGAGAAC
AA Mutation	p.Pro44HisfsTer18(p.P44Hfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CBX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407418
Start	38871516:38871516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210G>T
AA Mutation	p.Lys70Asn(p.K70N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407418
Start	38866242:38866242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206T>G
Mutation Classification	Silent
Feature Type	Transcript