Mutation

Primary Site >> Stomach Cancer

Gene >> ZNF208

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973859:21973859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175C>A
AA Mutation	p.Thr392Asn(p.T392N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21987252:21987252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190A>C
AA Mutation	p.Asn64His(p.N64H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21971408:21971408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3626C>T
AA Mutation	p.Pro1209Leu(p.P1209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974694:21974694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340A>C
AA Mutation	p.Lys114Gln(p.K114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972938:21972938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2096G>A
AA Mutation	p.Gly699Asp(p.G699D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973642:21973642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392G>A
AA Mutation	p.Met464Ile(p.M464I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972644:21972644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2390G>T
AA Mutation	p.Arg797Ile(p.R797I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974031:21974031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>A
AA Mutation	p.His335Asn(p.H335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973319:21973319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715A>C
AA Mutation	p.Lys572Thr(p.K572T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973521:21973521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1513G>T
AA Mutation	p.Ala505Ser(p.A505S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973983:21973983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051A>G
AA Mutation	p.Ser351Gly(p.S351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974757:21974757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277G>A
AA Mutation	p.Asp93Asn(p.D93N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974456:21974456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578G>C
AA Mutation	p.Arg193Thr(p.R193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973557:21973557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477G>A
AA Mutation	p.Gly493Arg(p.G493R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974055:21974055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979A>G
AA Mutation	p.Thr327Ala(p.T327A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972526:21972526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2508A>C
AA Mutation	p.Lys836Asn(p.K836N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972227:21972227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2807A>T
AA Mutation	p.Lys936Met(p.K936M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972747:21972747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2287A>G
AA Mutation	p.Thr763Ala(p.T763A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973026:21973026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2008T>A
AA Mutation	p.Cys670Ser(p.C670S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973871:21973871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163A>G
AA Mutation	p.Lys388Arg(p.K388R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974086:21974086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948A>C
AA Mutation	p.Lys316Asn(p.K316N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974456:21974456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768540069
CDS Mutation	c.578G>T
AA Mutation	p.Arg193Ile(p.R193I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972452:21972452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2582A>G
AA Mutation	p.Tyr861Cys(p.Y861C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21971968:21971968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3066T>G
AA Mutation	p.Ile1022Met(p.I1022M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972599:21972599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435A>C
AA Mutation	p.Lys812Thr(p.K812T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972579:21972579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2455A>T
AA Mutation	p.Thr819Ser(p.T819S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21974375:21974375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372427595
CDS Mutation	c.659A>G
AA Mutation	p.Lys220Arg(p.K220R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21971604:21971604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3430G>C
AA Mutation	p.Glu1144Gln(p.E1144Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21973703:21973703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757778735
CDS Mutation	c.1331A>C
AA Mutation	p.Lys444Thr(p.K444T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000397126
Start	21972504:21972504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530A>G
AA Mutation	p.Lys844Glu(p.K844E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397126
Start	21973333:21973333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1701C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397126
Start	21973528:21973528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1506T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397126
Start	21971878:21971878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3156T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397126
Start	21972232:21972232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2802A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397126
Start	21974158:21974158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397126
Start	21974407:21974407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397126
Start	21974691:21974691(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.343delA
AA Mutation	p.Ile115LeufsTer23(p.I115Lfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000397126
Start	21971790:21971790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3244G>T
AA Mutation	p.Glu1082Ter(p.E1082*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000397126
Start	21974393:21974393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641C>A
AA Mutation	p.Ser214Ter(p.S214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000397126
Start	21974286:21974287(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.747_748insTCTTGCTTATGTAGTTTG
AA Mutation	p.Val249_Ile250insSerCysLeuCysSerLeu(p.V249_I250insSCLCSL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript