Colon Cancer: Gene >> CHORDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320585
Start	90202454:90202454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950T>C
AA Mutation	p.Leu317Pro(p.L317P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000320585
Start	90211230:90211230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>T
AA Mutation	p.Glu140Ter(p.E140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000320585
Start	90203364:90203365(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.732_733insCATAAAGAATGAT
AA Mutation	p.Val245HisfsTer4(p.V245Hfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000320585
Start	90210535:90210535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000320585
Start	90206274:90206274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000320585
Start	90215231:90215231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CHORDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320585
Start	90214082:90214082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265A>G
AA Mutation	p.Lys89Glu(p.K89E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320585
Start	90222922:90222922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320585
Start	90206216:90206216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549T>C
Mutation Classification	Silent
Feature Type	Transcript