Mutation

Primary Site >> Stomach Cancer

Gene >> SERPINE2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	224001747:224001747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154G>A
AA Mutation	p.Val52Met(p.V52M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	223977580:223977580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123A>G
AA Mutation	p.Arg375Gly(p.R375G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	224001725:224001725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769638840
CDS Mutation	c.176C>T
AA Mutation	p.Ala59Val(p.A59V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	223991815:223991815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766836069
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	223982739:223982739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927A>C
AA Mutation	p.Lys309Asn(p.K309N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	224001692:224001692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209A>G
AA Mutation	p.Asp70Gly(p.D70G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	224001860:224001860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373891026
CDS Mutation	c.41C>T
AA Mutation	p.Thr14Met(p.T14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258405
Start	223991890:223991890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>A
AA Mutation	p.Glu200Lys(p.E200K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000258405
Start	223998313:223998313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289A>T
AA Mutation	p.Lys97Ter(p.K97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript