Mutation

Primary Site >> Stomach Cancer

Gene >> XPNPEP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371106
Start	129746649:129746649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780025939
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371106
Start	129744024:129744024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187A>G
AA Mutation	p.Thr63Ala(p.T63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371106
Start	129747630:129747630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>A
AA Mutation	p.Ala172Thr(p.A172T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371106
Start	129743980:129743980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143T>C
AA Mutation	p.Val48Ala(p.V48A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371106
Start	129745264:129745264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296C>T
AA Mutation	p.Ala99Val(p.A99V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371106
Start	129767687:129767687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762041216
CDS Mutation	c.1825G>A
AA Mutation	p.Glu609Lys(p.E609K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371106
Start	129745234:129745234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371093861
CDS Mutation	c.266G>A
AA Mutation	p.Arg89His(p.R89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371106
Start	129756541:129756542(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1359dupG
AA Mutation	p.Gln454AlafsTer35(p.Q454Afs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000371106
Start	129744073:129744073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript