Colon Cancer: Gene >> FBXL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355619
Start	77007683:77007683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749T>C
AA Mutation	p.Val250Ala(p.V250A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355619
Start	77021695:77021695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Trp(p.R56W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355619
Start	77007458:77007458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974G>A
AA Mutation	p.Gly325Asp(p.G325D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355619
Start	77007665:77007665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766494461
CDS Mutation	c.767G>A
AA Mutation	p.Arg256His(p.R256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355619
Start	77015455:77015455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355619
Start	77007373:77007373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355619
Start	77015566:77015576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.476_486delACTTTATCTCT
AA Mutation	p.His159ArgfsTer16(p.H159Rfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FBXL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355619
Start	77007552:77007552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.880T>G
AA Mutation	p.Phe294Val(p.F294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355619
Start	77015524:77015524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762454839
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript