Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IRF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309877
Start	49663382:49663382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.298C>A
AA Mutation	p.Pro100Thr(p.P100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309877
Start	49663250:49663250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>T
AA Mutation	p.Asp116Tyr(p.D116Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309877
Start	49662148:49662148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782T>C
AA Mutation	p.Val261Ala(p.V261A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309877
Start	49662318:49662318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309877
Start	49663362:49663362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309877
Start	49663404:49663404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309877
Start	49663438:49663438(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

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309877
Start	49663409:49663409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377410193
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309877
Start	49662318:49662318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309877
Start	49662201:49662201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript