Colon Cancer: Gene >> IDO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518237
Start	39925335:39925335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>A
AA Mutation	p.Asp274Asn(p.D274N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518237
Start	39922577:39922577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370075063
CDS Mutation	c.463C>T
AA Mutation	p.Arg155Cys(p.R155C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000518237
Start	39924756:39924756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774225205
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Cys(p.R231C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000518237
Start	39914009:39914009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87G>T
AA Mutation	p.Gln29His(p.Q29H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000518237
Start	39928080:39928080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107A>C
AA Mutation	p.Glu369Asp(p.E369D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000518237
Start	39927971:39927971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998A>G
AA Mutation	p.Asp333Gly(p.D333G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518237
Start	39913931:39913931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544291309
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518237
Start	39925344:39925344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518237
Start	39927966:39927966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000518237
Start	39925356:39925356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841C>T
AA Mutation	p.Gln281Ter(p.Q281*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IDO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518237
Start	39922577:39922577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370075063
CDS Mutation	c.463C>T
AA Mutation	p.Arg155Cys(p.R155C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518237
Start	39922621:39922621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript