Colon Cancer: Gene >> NCF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248899
Start	36864964:36864964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163A>G
AA Mutation	p.Ile55Val(p.I55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248899
Start	36867400:36867400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280T>G
AA Mutation	p.Tyr94Asp(p.Y94D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248899
Start	36876079:36876079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809T>C
AA Mutation	p.Leu270Pro(p.L270P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248899
Start	36877671:36877671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753588526
CDS Mutation	c.868G>A
AA Mutation	p.Ala290Thr(p.A290T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248899
Start	36877813:36877813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147550660
CDS Mutation	c.1010C>T
AA Mutation	p.Thr337Met(p.T337M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36864930:36864930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753635134
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36875727:36875727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745954906
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36864099:36864099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149998137
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36871673:36871673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000248899
Start	36877676:36877676(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.877delG
AA Mutation	p.Asp293IlefsTer11(p.D293Ifs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NCF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248899
Start	36877734:36877734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757937260
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36864924:36864924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369350039
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36864945:36864945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248899
Start	36877670:36877670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765893996
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript