Colon Cancer: Gene >> CBX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269397
Start	79837889:79837889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269397
Start	79835672:79835672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>T
AA Mutation	p.Pro74Ser(p.P74S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269397
Start	79834205:79834205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779400926
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269397
Start	79834742:79834742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758891335
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269397
Start	79834826:79834826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269397
Start	79834952:79834952(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.690delC
AA Mutation	p.Asn231ThrfsTer3(p.N231Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269397
Start	79834780:79834780(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.862delG
AA Mutation	p.Glu288ArgfsTer117(p.E288Rfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CBX4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269397
Start	79835087:79835087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269397
Start	79835117:79835117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript