Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CD36

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309881
Start	80672032:80672032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1117A>G
AA Mutation	p.Ile373Val(p.I373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309881
Start	80661185:80661185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404T>C
AA Mutation	p.Phe135Ser(p.F135S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309881
Start	80671041:80671041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883C>A
AA Mutation	p.Leu295Ile(p.L295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309881
Start	80646816:80646816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309881
Start	80663094:80663094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309881
Start	80671109:80671109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309881
Start	80664477:80664477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371782363
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD36

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309881
Start	80672824:80672824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180A>G
AA Mutation	p.Lys394Glu(p.K394E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309881
Start	80671146:80671146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.988A>G
AA Mutation	p.Ile330Val(p.I330V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309881
Start	80656620:80656620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>A
Mutation Classification	Silent
Feature Type	Transcript