Mutation

Primary Site >> Stomach Cancer

Gene >> USP28

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113827285:113827285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1135C>G
AA Mutation	p.Pro379Ala(p.P379A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113840711:113840711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745453193
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Cys(p.R141C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113829258:113829258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>T
AA Mutation	p.Ala333Val(p.A333V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113808321:113808321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143699311
CDS Mutation	c.2281G>A
AA Mutation	p.Gly761Ser(p.G761S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113799316:113799316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3158C>A
AA Mutation	p.Ser1053Tyr(p.S1053Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113799325:113799325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3149G>A
AA Mutation	p.Arg1050Gln(p.R1050Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113840710:113840710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113808352:113808352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2250T>G
AA Mutation	p.Ile750Met(p.I750M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113833475:113833475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749927512
CDS Mutation	c.704C>T
AA Mutation	p.Pro235Leu(p.P235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113840725:113840725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554447859
CDS Mutation	c.407G>A
AA Mutation	p.Arg136His(p.R136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113815291:113815291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1555C>T
AA Mutation	p.Arg519Trp(p.R519W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113803849:113803849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770592432
CDS Mutation	c.2687G>A
AA Mutation	p.Arg896Gln(p.R896Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113801596:113801596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2945T>C
AA Mutation	p.Leu982Pro(p.L982P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000003302
Start	113823687:113823687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201A>T
AA Mutation	p.Ser401Cys(p.S401C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000003302
Start	113804700:113804700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2631A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000003302
Start	113803812:113803812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000003302
Start	113833474:113833474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528702166
CDS Mutation	c.705G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000003302
Start	113799399:113799399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3075C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000003302
Start	113813933:113813933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1695T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000003302
Start	113803202:113803202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2818delG
AA Mutation	p.Val940SerfsTer5(p.V940Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000003302
Start	113829263:113829263(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.993delA
AA Mutation	p.Ala333ProfsTer16(p.A333Pfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000003302
Start	113834269:113834269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>T
AA Mutation	p.Glu201Ter(p.E201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript