Colon Cancer: Gene >> NCF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289473
Start	74777301:74777301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107C>T
AA Mutation	p.Ser36Leu(p.S36L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000289473
Start	74783060:74783060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573C>A
AA Mutation	p.Ser191Arg(p.S191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289473
Start	74783043:74783043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556G>A
AA Mutation	p.Val186Ile(p.V186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289473
Start	74782971:74782971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782730949
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289473
Start	74785228:74785228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NCF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289473
Start	74788662:74788662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Cys(p.R337C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289473
Start	74777339:74777339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>A
AA Mutation	p.Glu49Lys(p.E49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript