Colon Cancer: Gene >> NQO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320623
Start	69711170:69711170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114112422
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Cys(p.R211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320623
Start	69710981:69710981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820A>G
AA Mutation	p.Lys274Glu(p.K274E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320623
Start	69718494:69718494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376474672
CDS Mutation	c.48G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000320623
Start	69715067:69715068(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.311_313dupTGC
AA Mutation	p.Leu104dup(p.L104dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NQO1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320623
Start	69718249:69718249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177A>G
Mutation Classification	Silent
Feature Type	Transcript