Colon Cancer: Gene >> IDO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	39982667:39982667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331C>A
AA Mutation	p.Leu111Ile(p.L111I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	40015538:40015538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160T>G
AA Mutation	p.Val387Gly(p.V387G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	39987896:39987896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752076671
CDS Mutation	c.475C>T
AA Mutation	p.Pro159Ser(p.P159S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	40013695:40013695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765222349
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	40013689:40013689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844G>T
AA Mutation	p.Gly282Cys(p.G282C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	40013669:40013669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824A>G
AA Mutation	p.His275Arg(p.H275R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389060
Start	39989771:39989771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389060
Start	40013706:40013707(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.861_862insA
AA Mutation	p.Glu288ArgfsTer4(p.E288Rfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IDO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389060
Start	39949260:39949260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769653508
CDS Mutation	c.95C>T
AA Mutation	p.Ser32Phe(p.S32F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389060
Start	39979168:39979168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	start_lost
Transcription ID	ENST00000389060
Start	39949167:39949167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript