Colon Cancer: Gene >> FOXO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40665651:40665651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Glu188Lys(p.E188K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40560655:40560655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377728010
CDS Mutation	c.836C>T
AA Mutation	p.Ser279Phe(p.S279F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40665622:40665622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>G
AA Mutation	p.Phe197Leu(p.F197L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40560850:40560850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>A
AA Mutation	p.Arg214His(p.R214H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40560551:40560551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940C>T
AA Mutation	p.Arg314Cys(p.R314C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40560386:40560386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>A
AA Mutation	p.Glu369Lys(p.E369K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379561
Start	40560753:40560753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374399783
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379561
Start	40560363:40560363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379561
Start	40559880:40559880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1611T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379561
Start	40665730:40665731(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.482dupG
AA Mutation	p.Asn162GlnfsTer39(p.N162Qfs*39)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FOXO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40560544:40560544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316Gln(p.R316Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379561
Start	40560550:40560550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760747458
CDS Mutation	c.941G>A
AA Mutation	p.Arg314His(p.R314H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript