Colon Cancer: Gene >> IFNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380232
Start	21077416:21077416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>A
AA Mutation	p.His152Asn(p.H152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380232
Start	21077395:21077395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475T>C
AA Mutation	p.Tyr159His(p.Y159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380232
Start	21077634:21077634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236C>T
AA Mutation	p.Thr79Ile(p.T79I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380232
Start	21077459:21077459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380232
Start	21077645:21077645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368199428
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IFNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380232
Start	21077636:21077636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234G>T
AA Mutation	p.Leu78Phe(p.L78F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript