Colon Cancer: Gene >> NQO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338130
Start	3010094:3010094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77C>G
AA Mutation	p.Ala26Gly(p.A26G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338130
Start	3015539:3015539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313T>C
AA Mutation	p.Tyr105His(p.Y105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338130
Start	3019592:3019592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338130
Start	3010093:3010094(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.76_77insT
AA Mutation	p.Ala26ValfsTer4(p.A26Vfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NQO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338130
Start	3012592:3012592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221A>G
AA Mutation	p.Glu74Gly(p.E74G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338130
Start	3010105:3010105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88C>T
Mutation Classification	Silent
Feature Type	Transcript