Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CLEC4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7741521:7741521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135T>G
AA Mutation	p.Asn45Lys(p.N45K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7730881:7730881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413C>A
AA Mutation	p.Ser138Tyr(p.S138Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7729702:7729702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747788810
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7737461:7737461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Asp117Asn(p.D117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7746373:7746373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82T>C
AA Mutation	p.Ser28Pro(p.S28P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7730887:7730887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759515484
CDS Mutation	c.407G>T
AA Mutation	p.Arg136Ile(p.R136I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7741445:7741445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750777690
CDS Mutation	c.211G>A
AA Mutation	p.Val71Ile(p.V71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360345
Start	7730881:7730881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413C>A
AA Mutation	p.Ser138Tyr(p.S138Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360345
Start	7741446:7741446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360345
Start	7741500:7741500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>A
Mutation Classification	Silent
Feature Type	Transcript