Colon Cancer: Gene >> FBXO32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123531906:123531906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364G>A
AA Mutation	p.Val122Met(p.V122M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123513239:123513239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610C>A
AA Mutation	p.Leu204Ile(p.L204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123513254:123513254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Trp(p.R199W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123503417:123503417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370398489
CDS Mutation	c.1024G>A
AA Mutation	p.Val342Ile(p.V342I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123506519:123506519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707T>C
AA Mutation	p.Ile236Thr(p.I236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000517956
Start	123533223:123533224(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.246dupA
AA Mutation	p.Trp83MetfsTer10(p.W83Mfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123504729:123504729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853C>A
AA Mutation	p.Leu285Met(p.L285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517956
Start	123503380:123503380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061A>C
AA Mutation	p.Lys354Thr(p.K354T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript