Mutation

Primary Site >> Stomach Cancer

Gene >> USP7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8915257:8915257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075A>T
AA Mutation	p.Asn359Tyr(p.N359Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8894095:8894095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3212C>T
AA Mutation	p.Ser1071Phe(p.S1071F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8915270:8915270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1062C>G
AA Mutation	p.Ile354Met(p.I354M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8923247:8923247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>A
AA Mutation	p.Phe117Leu(p.F117L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8894069:8894069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3238G>A
AA Mutation	p.Asp1080Asn(p.D1080N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8894588:8894588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3164A>C
AA Mutation	p.Glu1055Ala(p.E1055A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8902120:8902120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2009C>A
AA Mutation	p.Ala670Asp(p.A670D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8910780:8910780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126G>A
AA Mutation	p.Asp376Asn(p.D376N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8901172:8901172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2110C>T
AA Mutation	p.His704Tyr(p.H704Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8900994:8900994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2204A>G
AA Mutation	p.Tyr735Cys(p.Y735C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8904476:8904476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663C>T
AA Mutation	p.Arg555Trp(p.R555W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8902391:8902391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1931G>A
AA Mutation	p.Gly644Asp(p.G644D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8900588:8900588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2251G>A
AA Mutation	p.Val751Met(p.V751M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8902396:8902396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140316737
CDS Mutation	c.1926C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8923310:8923310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773674539
CDS Mutation	c.288A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8895112:8895112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2958T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8905251:8905251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776078669
CDS Mutation	c.1509C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8895091:8895091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757705172
CDS Mutation	c.2979G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8894004:8894004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3303T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8920409:8920409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344836
Start	8906535:8906535(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1319delC
AA Mutation	p.Thr440LysfsTer30(p.T440Kfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000344836
Start	8906551:8906551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303G>T
AA Mutation	p.Glu435Ter(p.E435*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344836
Start	8906535:8906536(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1318dupA
AA Mutation	p.Thr440AsnfsTer4(p.T440Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000344836
Start	8894783:8894783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3111+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	25
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000344836
Start	8899649:8899651(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2416_2418delGAT
AA Mutation	p.Asp806del(p.D806del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript