Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OR6A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332601
Start	6794742:6794742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>T
AA Mutation	p.Ala323Ser(p.A323S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332601
Start	6794910:6794910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>T
AA Mutation	p.Pro267Ser(p.P267S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332601
Start	6795505:6795505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OR6A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332601
Start	6795075:6795075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634C>A
AA Mutation	p.Leu212Ile(p.L212I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332601
Start	6795543:6795543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
AA Mutation	p.Leu56Phe(p.L56F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332601
Start	6794821:6794821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript