Mutation

Primary Site >> Stomach Cancer

Gene >> CUL7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052347:43052347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43037834:43037834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4951A>T
AA Mutation	p.Thr1651Ser(p.T1651S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43051337:43051337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>T
AA Mutation	p.Glu288Asp(p.E288D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052653:43052653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141692693
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Trp(p.R46W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43048368:43048368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199704962
CDS Mutation	c.2027C>T
AA Mutation	p.Pro676Leu(p.P676L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045607:43045607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749279996
CDS Mutation	c.2842C>T
AA Mutation	p.Arg948Cys(p.R948C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43038455:43038455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4585G>T
AA Mutation	p.Asp1529Tyr(p.D1529Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43051050:43051050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754112592
CDS Mutation	c.1151G>A
AA Mutation	p.Arg384Gln(p.R384Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052242:43052242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754739961
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Trp(p.R183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43042842:43042842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762601845
CDS Mutation	c.3605C>T
AA Mutation	p.Ala1202Val(p.A1202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045386:43045386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2879G>A
AA Mutation	p.Arg960His(p.R960H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045291:43045291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974C>T
AA Mutation	p.Arg992Trp(p.R992W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43050295:43050295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337A>T
AA Mutation	p.Tyr446Phe(p.Y446F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43043106:43043106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3430A>G
AA Mutation	p.Thr1144Ala(p.T1144A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052236:43052236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553A>C
AA Mutation	p.Ile185Leu(p.I185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43044757:43044757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3167C>T
AA Mutation	p.Ser1056Phe(p.S1056F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43040585:43040585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3968T>G
AA Mutation	p.Leu1323Arg(p.L1323R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43042957:43042957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201135654
CDS Mutation	c.3490C>T
AA Mutation	p.Arg1164Trp(p.R1164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052290:43052290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499A>G
AA Mutation	p.Met167Val(p.M167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43052741:43052741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774372821
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43046085:43046085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2667G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43050149:43050149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43051220:43051220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144880219
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43050071:43050071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754238136
CDS Mutation	c.1461A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43049630:43049630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778647248
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43052354:43052354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756779813
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43045605:43045605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2844C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43052522:43052522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201158458
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265348
Start	43050392:43050392(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1240delT
AA Mutation	p.Trp414GlyfsTer54(p.W414Gfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000265348
Start	43040580:43040580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3973C>T
AA Mutation	p.Gln1325Ter(p.Q1325*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265348
Start	43046602:43046602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript