Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OSGIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297438
Start	89924906:89924906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533674331
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Cys(p.R298C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297438
Start	89925102:89925102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1088A>G
AA Mutation	p.Gln363Arg(p.Q363R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297438
Start	89924754:89924754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740C>A
AA Mutation	p.Ser247Tyr(p.S247Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297438
Start	89924675:89924675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661A>C
AA Mutation	p.Lys221Gln(p.K221Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297438
Start	89914129:89914129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146570031
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OSGIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297438
Start	89924510:89924510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496A>G
AA Mutation	p.Lys166Glu(p.K166E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297438
Start	89924658:89924658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644A>G
AA Mutation	p.Asp215Gly(p.D215G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000297438
Start	89925380:89925380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366G>T
AA Mutation	p.Glu456Ter(p.E456*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000297438
Start	89921079:89921079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript