Colon Cancer: Gene >> NOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372966
Start	100863540:100863540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197T>C
AA Mutation	p.Leu66Pro(p.L66P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372966
Start	100851261:100851261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772834730
CDS Mutation	c.869G>A
AA Mutation	p.Arg290His(p.R290H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372966
Start	100851255:100851255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875A>G
AA Mutation	p.Gln292Arg(p.Q292R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372966
Start	100849809:100849809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259A>G
AA Mutation	p.Lys420Arg(p.K420R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372966
Start	100844018:100844018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1629C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000372966
Start	100850218:100850218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369560908
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Ter(p.R356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372966
Start	100863529:100863529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208C>T
AA Mutation	p.Pro70Ser(p.P70S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000372966
Start	100843953:100843954(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1693dupT
AA Mutation	p.Ter565Leu(p.*565L)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript