Colon Cancer: Gene >> EIF3F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309828
Start	7993000:7993000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371389618
CDS Mutation	c.629G>A
AA Mutation	p.Arg210His(p.R210H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309828
Start	7995069:7995069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309828
Start	7992997:7992997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.626G>A
AA Mutation	p.Gly209Asp(p.G209D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309828
Start	7991830:7991830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368962454
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309828
Start	7995010:7995010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309828
Start	7987588:7987588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236G>A
AA Mutation	p.Gly79Asp(p.G79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000309828
Start	7991818:7991818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402C>A
AA Mutation	p.Cys134Ter(p.C134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript