Colon Cancer: Gene >> CNTF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361987
Start	58624456:58624456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537T>G
AA Mutation	p.Ile179Met(p.I179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361987
Start	58624226:58624226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>T
AA Mutation	p.Gly103Cys(p.G103C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361987
Start	58622842:58622842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361987
Start	58624321:58624321(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.406delC
AA Mutation	p.Arg136AlafsTer24(p.R136Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CNTF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361987
Start	58624320:58624320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401T>G
AA Mutation	p.Ile134Ser(p.I134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361987
Start	58624161:58624161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242G>A
AA Mutation	p.Arg81His(p.R81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript