Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CCR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32954072:32954072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650T>C
AA Mutation	p.Ile217Thr(p.I217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32954276:32954276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>A
AA Mutation	p.Ala285Asp(p.A285D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32954026:32954026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604A>G
AA Mutation	p.Ser202Gly(p.S202G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32953897:32953897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475T>A
AA Mutation	p.Leu159Met(p.L159M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330953
Start	32953773:32953773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330953
Start	32953434:32953434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32954141:32954141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200003145
CDS Mutation	c.719C>T
AA Mutation	p.Ala240Val(p.A240V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32954422:32954422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000C>A
AA Mutation	p.Leu334Ile(p.L334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330953
Start	32954393:32954393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971G>C
AA Mutation	p.Gly324Ala(p.G324A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript