Colon Cancer: Gene >> FBXO6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376753
Start	11668746:11668746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746354058
CDS Mutation	c.88G>A
AA Mutation	p.Ala30Thr(p.A30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376753
Start	11673279:11673279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512T>C
AA Mutation	p.Phe171Ser(p.F171S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376753
Start	11671391:11671391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566510540
CDS Mutation	c.412G>A
AA Mutation	p.Glu138Lys(p.E138K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376753
Start	11668847:11668847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780663319
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376753
Start	11668934:11668934(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.276delG
AA Mutation	p.Cys93ValfsTer57(p.C93Vfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376753
Start	11668825:11668825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript