Colon Cancer: Gene >> NOX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000388866
Start	69037141:69037141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302G>T
AA Mutation	p.Lys434Asn(p.K434N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000388866
Start	69055360:69055360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2026A>G
AA Mutation	p.Met676Val(p.M676V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000388866
Start	69028235:69028235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195C>A
AA Mutation	p.Phe65Leu(p.F65L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388866
Start	69031732:69031732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388866
Start	69056666:69056666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373378260
CDS Mutation	c.2268C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388866
Start	69056651:69056651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2253C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388866
Start	69035879:69035879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000388866
Start	69038886:69038886(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1407delT
AA Mutation	p.His470ThrfsTer10(p.H470Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NOX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000388866
Start	69031739:69031739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752341477
CDS Mutation	c.547G>C
AA Mutation	p.Gly183Arg(p.G183R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388866
Start	69049042:69049042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143553877
CDS Mutation	c.1983C>T
Mutation Classification	Silent
Feature Type	Transcript