Colon Cancer: Gene >> NOXO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397280
Start	1980682:1980682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197C>T
AA Mutation	p.Ser66Phe(p.S66F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397280
Start	1979504:1979504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754C>A
AA Mutation	p.Arg252Ser(p.R252S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397280
Start	1980701:1980701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Ala60Thr(p.A60T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397280
Start	1980699:1980699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762383081
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NOXO1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397280
Start	1980007:1980007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761437131
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000397280
Start	1979887:1979902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.603_618delCTGGTGGCTGGTGGAG
AA Mutation	p.Trp202ThrfsTer29(p.W202Tfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript