Colon Cancer: Gene >> FOS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303562
Start	75280883:75280883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746175046
CDS Mutation	c.602G>A
AA Mutation	p.Arg201Gln(p.R201Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303562
Start	75279896:75279896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303562
Start	75280581:75280581(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.418delA
AA Mutation	p.Arg140GlyfsTer22(p.R140Gfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303562
Start	75280600:75280600(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.436delA
AA Mutation	p.Arg146GlyfsTer16(p.R146Gfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303562
Start	75280825:75280825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Glu182Lys(p.E182K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript