Colon Cancer: Gene >> FOXC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320354
Start	86568654:86568654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1319T>G
AA Mutation	p.Phe440Cys(p.F440C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320354
Start	86567453:86567453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118G>A
AA Mutation	p.Val40Ile(p.V40I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320354
Start	86567739:86567739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320354
Start	86568787:86568787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320354
Start	86567711:86567711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376C>G
AA Mutation	p.Leu126Val(p.L126V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320354
Start	86568708:86568708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458Gln(p.R458Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript