Colon Cancer: Gene >> NRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223190
Start	129657379:129657379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>A
AA Mutation	p.Glu10Lys(p.E10K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223190
Start	129711482:129711482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971C>T
AA Mutation	p.Thr324Met(p.T324M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000223190
Start	129727335:129727335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>T
AA Mutation	p.Gly440Ter(p.G440*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223190
Start	129710495:129710495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887G>T
AA Mutation	p.Ser296Ile(p.S296I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223190
Start	129717231:129717231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078T>C
AA Mutation	p.Trp360Arg(p.W360R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000223190
Start	129677639:129677639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Ter(p.R116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript