Colon Cancer: Gene >> FOXO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663623:108663623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>A
AA Mutation	p.Arg264Ser(p.R264S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663840:108663840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007T>A
AA Mutation	p.Val336Asp(p.V336D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663747:108663747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914C>T
AA Mutation	p.Ala305Val(p.A305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108664587:108664587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1754A>C
AA Mutation	p.Asp585Ala(p.D585A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108664163:108664163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570814853
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108664444:108664444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108663781:108663781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108664459:108664459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747294855
CDS Mutation	c.1626C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108664474:108664474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343882
Start	108663858:108663859(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1030_1031delTC
AA Mutation	p.Ser344AlafsTer27(p.S344Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOXO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663855:108663855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022C>T
AA Mutation	p.Ala341Val(p.A341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108561821:108561821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>A
AA Mutation	p.Gly205Ser(p.G205S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108664475:108664475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642C>T
AA Mutation	p.Arg548Cys(p.R548C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript