Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CNOT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285896
Start	154871764:154871764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508A>G
AA Mutation	p.Thr170Ala(p.T170A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285896
Start	154870702:154870702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353A>T
AA Mutation	p.Asn118Ile(p.N118I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285896
Start	154865238:154865238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285896
Start	154872561:154872561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146858939
CDS Mutation	c.639T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000285896
Start	154870659:154870659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CNOT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285896
Start	154870689:154870689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>T
AA Mutation	p.Asp114Tyr(p.D114Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000285896
Start	154863363:154863363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>T
AA Mutation	p.Glu29Ter(p.E29*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000285896
Start	154865386:154865386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763685629
CDS Mutation	c.311+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript