Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210318:53210318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644C>G
AA Mutation	p.Ser215Cys(p.S215C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210675:53210675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001A>C
AA Mutation	p.Asp334Ala(p.D334A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53211005:53211005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331A>T
AA Mutation	p.Asp444Val(p.D444V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210714:53210714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040G>A
AA Mutation	p.Gly347Asp(p.G347D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210906:53210906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375957043
CDS Mutation	c.1232C>T
AA Mutation	p.Thr411Met(p.T411M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371486
Start	53210442:53210442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371486
Start	53210109:53210109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210842:53210842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168G>T
AA Mutation	p.Asp390Tyr(p.D390Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210422:53210422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748A>C
AA Mutation	p.Asn250His(p.N250H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371486
Start	53210714:53210714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040G>A
AA Mutation	p.Gly347Asp(p.G347D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript