Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FBXO8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393674
Start	174262962:174262962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760227265
CDS Mutation	c.131G>A
AA Mutation	p.Arg44His(p.R44H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393674
Start	174259780:174259780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393674
Start	174262907:174262907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772602892
CDS Mutation	c.186G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393674
Start	174262889:174262889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393674
Start	174241160:174241161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.514_515delAA
AA Mutation	p.Lys172ValfsTer18(p.K172Vfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393674
Start	174237516:174237516(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.856delA
AA Mutation	p.Arg286GlyfsTer19(p.R286Gfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393674
Start	174237478:174237479(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.893dupA
AA Mutation	p.Asn298LysfsTer3(p.N298Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393674
Start	174262911:174262911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182A>C
AA Mutation	p.Lys61Thr(p.K61T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393674
Start	174262787:174262787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763345340
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000393674
Start	174237504:174237504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Ter(p.R290*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript