Colon Cancer: Gene >> CBX7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216133
Start	39138650:39138650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Trp(p.R78W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216133
Start	39134580:39134580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753630073
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216133
Start	39134491:39134491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567409810
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Trp(p.R170W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216133
Start	39134444:39134444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765884458
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216133
Start	39133984:39133984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CBX7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216133
Start	39134523:39134523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768808588
CDS Mutation	c.476G>A
AA Mutation	p.Arg159His(p.R159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216133
Start	39134571:39134571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Arg143Gln(p.R143Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript