Colon Cancer: Gene >> IRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245414
Start	132484422:132484422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793C>T
AA Mutation	p.Pro265Ser(p.P265S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245414
Start	132484458:132484458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>C
AA Mutation	p.Gly253Arg(p.G253R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245414
Start	132484450:132484450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.765delG
AA Mutation	p.Tyr256ThrfsTer34(p.Y256Tfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000245414
Start	132484499:132484499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000245414
Start	132484498:132484498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000245414
Start	132489484:132489484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-5-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000245414
Start	132486249:132486249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245414
Start	132487079:132487079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239A>G
AA Mutation	p.Asn80Ser(p.N80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245414
Start	132484020:132484020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript