Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CCR9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357632
Start	45901474:45901474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686T>C
AA Mutation	p.Val229Ala(p.V229A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357632
Start	45901685:45901685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357632
Start	45901856:45901856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201669237
CDS Mutation	c.1068G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357632
Start	45901400:45901400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771948402
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357632
Start	45901772:45901772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199687453
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000357632
Start	45900956:45900956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>A
AA Mutation	p.Trp56Ter(p.W56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCR9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357632
Start	45901629:45901629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199971970
CDS Mutation	c.841G>A
AA Mutation	p.Ala281Thr(p.A281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357632
Start	45901523:45901523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735G>T
AA Mutation	p.Lys245Asn(p.K245N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357632
Start	45901150:45901150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362T>G
AA Mutation	p.Val121Gly(p.V121G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript