Colon Cancer: Gene >> IRF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268638
Start	85918732:85918732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917G>A
AA Mutation	p.Cys306Tyr(p.C306Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268638
Start	85918596:85918596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Glu261Lys(p.E261K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268638
Start	85914488:85914488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140514602
CDS Mutation	c.569C>T
AA Mutation	p.Thr190Met(p.T190M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268638
Start	85918712:85918712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535845826
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268638
Start	85920162:85920162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268638
Start	85918673:85918673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201720336
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268638
Start	85909010:85909010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268638
Start	85920138:85920138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765523642
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Trp(p.R340W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript