Colon Cancer: Gene >> FOXR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55624105:55624105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Pro132Ser(p.P132S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55624032:55624032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321T>G
AA Mutation	p.Ile107Met(p.I107M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55624174:55624174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463A>G
AA Mutation	p.Thr155Ala(p.T155A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55623740:55623740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29T>G
AA Mutation	p.Phe10Cys(p.F10C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55623788:55623788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77T>C
AA Mutation	p.Met26Thr(p.M26T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55624012:55624012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301A>G
AA Mutation	p.Lys101Glu(p.K101E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339140
Start	55623935:55623935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224A>T
AA Mutation	p.Glu75Val(p.E75V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript