Colon Cancer: Gene >> FBXW11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171900025:171900025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449T>C
AA Mutation	p.Val150Ala(p.V150A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171878063:171878063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856C>A
AA Mutation	p.Leu286Met(p.L286M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171899965:171899965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171910581:171910581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171878072:171878072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847G>A
AA Mutation	p.Val283Ile(p.V283I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171910652:171910652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778006732
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171868784:171868784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480C>T
AA Mutation	p.Arg494Cys(p.R494C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265094
Start	171900009:171900009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755955795
CDS Mutation	c.465G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265094
Start	171899002:171899002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265094
Start	171869809:171869809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FBXW11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265094
Start	171876402:171876402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041G>A
AA Mutation	p.Met347Ile(p.M347I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265094
Start	171878109:171878109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>C
Mutation Classification	Silent
Feature Type	Transcript