Mutation

Primary Site >> Stomach Cancer

Gene >> USP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63532653:63532653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98G>A
AA Mutation	p.Arg33Gln(p.R33Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63590795:63590795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532A>G
AA Mutation	p.His511Arg(p.H511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63570512:63570512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841A>T
AA Mutation	p.Asn281Tyr(p.N281Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63588768:63588768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201397735
CDS Mutation	c.1282G>A
AA Mutation	p.Val428Ile(p.V428I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380324
Start	63532654:63532654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380324
Start	63570514:63570514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380324
Start	63588788:63588788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768760655
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380324
Start	63590688:63590688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746051369
CDS Mutation	c.1425C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380324
Start	63537043:63537043(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.177delA
AA Mutation	p.Lys59AsnfsTer10(p.K59Nfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380324
Start	63553777:63553778(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.347_348delAA
AA Mutation	p.Glu116AlafsTer13(p.E116Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000380324
Start	63574045:63574045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript