Colon Cancer: Gene >> FOXE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375123
Start	97854344:97854344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430C>T
AA Mutation	p.Arg144Cys(p.R144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375123
Start	97854347:97854347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777292713
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Cys(p.R145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375123
Start	97854798:97854798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884C>T
AA Mutation	p.Ala295Val(p.A295V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375123
Start	97854351:97854351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375123
Start	97854146:97854146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>A
AA Mutation	p.Gly78Ser(p.G78S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375123
Start	97854260:97854260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Cys(p.R116C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375123
Start	97854268:97854268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXE1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375123
Start	97854112:97854112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript