Colon Cancer: Gene >> FOXO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71096775:71096775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247G>A
AA Mutation	p.Gly83Arg(p.G83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71101191:71101191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Trp(p.R321W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71096535:71096535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7C>G
AA Mutation	p.Pro3Ala(p.P3A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71100903:71100903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>A
AA Mutation	p.Gly225Ser(p.G225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71096833:71096833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Gly102Glu(p.G102E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71096820:71096820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Trp(p.R98W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71101573:71101573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343C>A
AA Mutation	p.Ala448Asp(p.A448D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71100836:71100836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>A
AA Mutation	p.Ser202Arg(p.S202R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71101236:71101236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Gly336Ser(p.G336S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374259
Start	71096788:71096788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260C>T
AA Mutation	p.Ala87Val(p.A87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374259
Start	71101076:71101076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript