Colon Cancer: Gene >> IFNA14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380222
Start	21239652:21239652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284A>G
AA Mutation	p.Asn95Ser(p.N95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380222
Start	21239878:21239878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58T>G
AA Mutation	p.Cys20Gly(p.C20G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380222
Start	21239654:21239654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>T
AA Mutation	p.Lys94Asn(p.K94N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000380222
Start	21239386:21239386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550A>T
AA Mutation	p.Arg184Ter(p.R184*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000380222
Start	21239498:21239498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>A
AA Mutation	p.Tyr146Ter(p.Y146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IFNA14

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380222
Start	21239630:21239630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript