Colon Cancer: Gene >> NUDT14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392568
Start	105173197:105173197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201834263
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392568
Start	105173080:105173080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368844988
CDS Mutation	c.610G>A
AA Mutation	p.Val204Ile(p.V204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392568
Start	105173112:105173112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578C>T
AA Mutation	p.Ala193Val(p.A193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392568
Start	105176763:105176763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392568
Start	105173126:105173126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140616526
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392568
Start	105173039:105173039(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.651delC
AA Mutation	p.Asn218ThrfsTer11(p.N218Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NUDT14

No Mutation Annotation!