Colon Cancer: Gene >> FBXW4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331272
Start	101611361:101611361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148012023
CDS Mutation	c.1169G>A
AA Mutation	p.Arg390His(p.R390H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331272
Start	101611648:101611648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Cys(p.R367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331272
Start	101611393:101611393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556578828
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331272
Start	101611673:101611673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142927609
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331272
Start	101612342:101612342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574963392
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331272
Start	101672921:101672921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750444653
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331272
Start	101612444:101612444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.870delT
AA Mutation	p.Pro292GlnfsTer86(p.P292Qfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000331272
Start	101611626:101611626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FBXW4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331272
Start	101667898:101667898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>A
AA Mutation	p.Ser253Asn(p.S253N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331272
Start	101667897:101667897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript