Colon Cancer: Gene >> FBXO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354287
Start	11649819:11649819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577C>G
AA Mutation	p.Leu193Val(p.L193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354287
Start	11650538:11650538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319C>G
AA Mutation	p.Arg107Gly(p.R107G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354287
Start	11650049:11650049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354287
Start	11648766:11648766(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.819delG
AA Mutation	p.Gln274ArgfsTer14(p.Q274Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354287
Start	11649861:11649862(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.534dupA
AA Mutation	p.Ala179SerfsTer5(p.A179Sfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO2

No Mutation Annotation!