Mutation

Primary Site >> Stomach Cancer

Gene >> OSBPL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62272161:62272161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295G>A
AA Mutation	p.Glu99Lys(p.E99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62279215:62279215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747912454
CDS Mutation	c.550G>A
AA Mutation	p.Ala184Thr(p.A184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62289306:62289306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773593916
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Cys(p.R409C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62289280:62289280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1199C>T
AA Mutation	p.Thr400Met(p.T400M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62284056:62284056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883C>T
AA Mutation	p.Leu295Phe(p.L295F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313733
Start	62263658:62263658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146206209
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313733
Start	62281097:62281097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748360123
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000313733
Start	62284045:62284045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000313733
Start	62289245:62289246(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1164_1165insGTGCTCTTCATT
AA Mutation	p.Glu388_Leu389insValLeuPheIle(p.E388_L389insVLFI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript