Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOXF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259806
Start	1394768:1394768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244G>A
AA Mutation	p.Gly415Glu(p.G415E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259806
Start	1394746:1394746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222G>T
AA Mutation	p.Asp408Tyr(p.D408Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259806
Start	1394718:1394718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194T>A
AA Mutation	p.His398Gln(p.H398Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259806
Start	1390446:1390446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Trp(p.R167W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259806
Start	1394752:1394752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228G>A
AA Mutation	p.Val410Ile(p.V410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript