Colon Cancer: Gene >> TREX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334497
Start	153444965:153444965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781909660
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Cys(p.R199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334497
Start	153445177:153445177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782289254
CDS Mutation	c.383T>C
AA Mutation	p.Leu128Pro(p.L128P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334497
Start	153444976:153444976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>A
AA Mutation	p.Arg195Gln(p.R195Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334497
Start	153445146:153445146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377225993
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334497
Start	153445359:153445359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334497
Start	153447789:153447789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782750935
CDS Mutation	c.54T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334497
Start	153445173:153445173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370574683
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000334497
Start	153469262:153469262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.-1004-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TREX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334497
Start	153445321:153445321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782408064
CDS Mutation	c.239G>A
AA Mutation	p.Arg80His(p.R80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript